( Major histocompatibility complex.)
The immune system is regulated by
molecules coded by some genes.These are genes of the histocompatibility system which code For Human leukocyte antigens (HLA).
Impact of MHC class I diversity on immune control of Immuno-deficiency virus ...Ramesh Pothuraju
This document summarizes a presentation on the impact of MHC class I diversity on immune control of HIV replication. It discusses how MHC class I molecules present antigens to T cells, and their role in distinguishing self from non-self. It then focuses on the central role of MHC class I molecules, particularly HLA-B alleles, in controlling HIV viral loads through CD8+ T cell responses targeting conserved HIV proteins like Gag. Polyfunctional and HLA-B restricted CD8+ T cell responses targeting Gag seem to be most effective at control of HIV replication.
The major histocompatibility complex (MHC) is a collection of genes located on chromosome 6 in humans that encode MHC molecules. MHC molecules present peptide fragments on the cell surface to help the immune system identify infected or damaged cells. There are two main classes of MHC molecules: class I molecules present peptides from intracellular proteins on most nucleated cells to cytotoxic T cells, while class II molecules present peptides from extracellular proteins on antigen-presenting cells to helper T cells. MHC molecules play a key role in immune system functions like regulating T cell development and activating immune responses against pathogens.
Some potential causes of the immune system attacking the self in autoimmune diseases include:
- Genetic predisposition - Genes coding for the variety of MHC molecules can influence susceptibility. A T cell's ability to respond is determined by MHC genotype. Differences in MHC alleles' ability to present autoantigens can play a role.
- Environmental triggers - Factors like infections, drugs, trauma, etc. may trigger autoimmunity in genetically susceptible individuals by molecular mimicry or other mechanisms.
- Loss of tolerance - Failure to eliminate self-reactive lymphocytes during development or maintain peripheral tolerance can allow self-reactivity.
- Hormonal factors - Many autoimmune diseases are more common in women and fluctuate with horm
The MHC complex is a cluster of genes present in all mammals that plays an important role in self/non-self discrimination. MHC genes code for cell surface antigens that present antigens to T cells and are highly polymorphic between individuals. There are four classes of MHC molecules: Class I presents endogenous antigens to CD8+ T cells on all nucleated cells; Class II presents exogenous antigens to CD4+ T cells on antigen presenting cells; Class III proteins have immune functions; Class IV is no longer used. The MHC complex is crucial for immune recognition and response.
Major Histo compatibility Complex of Genes /certified fixed orthodontic cours...Indian dental academy
The document provides information about the major histocompatibility complex (MHC), a set of genes that encodes antigen-presenting molecules that play a key role in the immune system's response to foreign substances. It discusses how MHC genes were discovered through studies of transplant rejection between inbred mouse strains, and how MHC molecules present peptide antigens to T cells, triggering an immune response. The document also summarizes the structure and function of MHC class I and class II molecules, how they bind peptides, and their extensive polymorphism in human populations, which helps protect against rapidly mutating pathogens.
The major histocompatibility complex (MHC) plays a key role in the immune system by presenting antigens and distinguishing self from non-self. It is located on chromosome 6 in humans and contains genes like HLA that determine disease susceptibility. MHC molecules come in two classes: class I present intracellular peptides and class II present extracellular peptides. Variants in MHC genes can increase risk for certain diseases, like a variant in HLA-DQ increasing susceptibility to type 1 diabetes. Loss of MHC diversity in some populations like cheetahs can also lead to increased disease emergence due to a less broad range of antigens recognized.
Impact of MHC class I diversity on immune control of Immuno-deficiency virus ...Ramesh Pothuraju
This document summarizes a presentation on the impact of MHC class I diversity on immune control of HIV replication. It discusses how MHC class I molecules present antigens to T cells, and their role in distinguishing self from non-self. It then focuses on the central role of MHC class I molecules, particularly HLA-B alleles, in controlling HIV viral loads through CD8+ T cell responses targeting conserved HIV proteins like Gag. Polyfunctional and HLA-B restricted CD8+ T cell responses targeting Gag seem to be most effective at control of HIV replication.
The major histocompatibility complex (MHC) is a collection of genes located on chromosome 6 in humans that encode MHC molecules. MHC molecules present peptide fragments on the cell surface to help the immune system identify infected or damaged cells. There are two main classes of MHC molecules: class I molecules present peptides from intracellular proteins on most nucleated cells to cytotoxic T cells, while class II molecules present peptides from extracellular proteins on antigen-presenting cells to helper T cells. MHC molecules play a key role in immune system functions like regulating T cell development and activating immune responses against pathogens.
Some potential causes of the immune system attacking the self in autoimmune diseases include:
- Genetic predisposition - Genes coding for the variety of MHC molecules can influence susceptibility. A T cell's ability to respond is determined by MHC genotype. Differences in MHC alleles' ability to present autoantigens can play a role.
- Environmental triggers - Factors like infections, drugs, trauma, etc. may trigger autoimmunity in genetically susceptible individuals by molecular mimicry or other mechanisms.
- Loss of tolerance - Failure to eliminate self-reactive lymphocytes during development or maintain peripheral tolerance can allow self-reactivity.
- Hormonal factors - Many autoimmune diseases are more common in women and fluctuate with horm
The MHC complex is a cluster of genes present in all mammals that plays an important role in self/non-self discrimination. MHC genes code for cell surface antigens that present antigens to T cells and are highly polymorphic between individuals. There are four classes of MHC molecules: Class I presents endogenous antigens to CD8+ T cells on all nucleated cells; Class II presents exogenous antigens to CD4+ T cells on antigen presenting cells; Class III proteins have immune functions; Class IV is no longer used. The MHC complex is crucial for immune recognition and response.
Major Histo compatibility Complex of Genes /certified fixed orthodontic cours...Indian dental academy
The document provides information about the major histocompatibility complex (MHC), a set of genes that encodes antigen-presenting molecules that play a key role in the immune system's response to foreign substances. It discusses how MHC genes were discovered through studies of transplant rejection between inbred mouse strains, and how MHC molecules present peptide antigens to T cells, triggering an immune response. The document also summarizes the structure and function of MHC class I and class II molecules, how they bind peptides, and their extensive polymorphism in human populations, which helps protect against rapidly mutating pathogens.
The major histocompatibility complex (MHC) plays a key role in the immune system by presenting antigens and distinguishing self from non-self. It is located on chromosome 6 in humans and contains genes like HLA that determine disease susceptibility. MHC molecules come in two classes: class I present intracellular peptides and class II present extracellular peptides. Variants in MHC genes can increase risk for certain diseases, like a variant in HLA-DQ increasing susceptibility to type 1 diabetes. Loss of MHC diversity in some populations like cheetahs can also lead to increased disease emergence due to a less broad range of antigens recognized.
The document discusses the major histocompatibility complex (MHC), which plays a key role in immune response and organ transplantation. It describes the structure of MHC class I and II molecules, which present peptide fragments to T cells. MHC molecules are highly polymorphic and this variability allows recognition of diverse pathogens. The T cell receptor engages peptide-MHC complexes and accessory molecules provide costimulatory signals for T cell activation. Certain MHC alleles are associated with increased risk of various autoimmune diseases.
The document provides an overview of major histocompatibility complex (MHC) and human leukocyte antigen (HLA) typing. It discusses that MHC molecules present antigen fragments to T cells and are classified into classes I, II, and III. MHC proteins in humans are called HLA genes and are located on chromosome 6. The document describes HLA classification, functions in infectious disease, graft rejection, and autoimmunity, as well as genetics and methods of HLA typing including serotyping, phenotyping, and allele names.
This document provides information on MHC class I and class II molecules, including their structure, function, and role in antigen presentation. It discusses that MHC class I molecules are expressed on all nucleated cells and present intracellular antigens to CD8+ T cells. MHC class II molecules are expressed primarily on antigen presenting cells and present extracellular antigens to CD4+ T cells. The peptide binding grooves of MHC class I and II molecules differ in their structure and the size of peptides they can bind.
The document discusses the major histocompatibility complex (MHC) and its role in immune recognition. It notes that Gorer and Snell in the 1930s discovered that mouse skin grafts were rejected between mice of different blood groups, showing tissue recognition is based on genetics. They coined the term MHC to describe the genes controlling this tissue recognition. MHC molecules present peptides and are highly polymorphic within and between species, allowing an organism to distinguish self from non-self. The MHC in humans is called the HLA complex.
The document summarizes the HLA system and major histocompatibility complex. It discusses that MHC antigens are located on chromosome 6 and have 4 loci (A, B, C, D). MHC antigens are divided into 3 classes - Class I antigens regulate cytotoxic T cells, Class II antigens regulate helper T cells, and Class III antigens are components of the complement system but not associated with HLA expression. The HLA complex plays important roles in organ transplantation by matching donors and recipients, regulating the immune system through Class I and II antigens, and being associated with certain diseases.
The document summarizes key aspects of the major histocompatibility complex (MHC):
1) The MHC was discovered through studies of transplant rejection in inbred mouse strains, which showed that rejection depended on the genetics of the donor and recipient strains.
2) MHC molecules present peptide antigens to T cells and play a crucial role in immune responses, including transplant rejection.
3) MHC molecules are highly polymorphic and polygenic, with multiple variants of each type, which allows populations to recognize a wide variety of pathogens.
The Major Histocompatibility Complex (MHC):
- Is located on chromosome 6 and contains genes such as HLA that play a role in distinguishing self from non-self.
- Genes are organized into three classes: class I present antigens to T cells, class II present antigens to T helper cells, and class III genes produce immune system proteins.
- MHC molecules are highly polymorphic and inherited as sets (haplotypes) from each parent, allowing presentation of a wide variety of antigens.
The MHC encodes antigen presenting molecules that display peptide fragments to T cells to initiate immune responses. It contains three regions - Class I MHC presents intracellular peptides to CD8+ T cells, Class II MHC presents extracellular peptides to CD4+ T cells, and Class III MHC encodes complement proteins. MHC molecules are highly polymorphic and individuals inherit multiple alleles from each parent. This polymorphism allows presentation of a wide range of peptides and enhances immune responses against pathogens. MHC matching is important for transplantation, as mismatch can lead to graft rejection through T cell recognition of foreign MHC.
The Major Histocompatibility Complex (MHC) is a cluster of genes found in all mammals that plays a key role in the immune system by helping distinguish self from non-self. MHC genes are organized into three classes: Class I presents antigens to cytotoxic T cells, Class II presents antigens to helper T cells, and Class III encodes proteins involved in immune functions. MHC molecules are highly polymorphic and vary considerably between individuals, helping the immune system recognize a wide variety of pathogens.
This document discusses the major histocompatibility complex (MHC) and its class I and class II molecules. It describes the structure and components of MHC class I and II molecules, including their peptide binding grooves. MHC class I molecules are expressed on nearly all nucleated cells and present peptides from intracellular pathogens to cytotoxic T cells. MHC class II molecules are only expressed on antigen-presenting cells and present peptides from extracellular pathogens to helper T cells. The MHC genes are highly polymorphic in human populations, contributing to diversity in antigen presentation.
The document discusses the major histocompatibility complex (MHC), which consists of glycoproteins found on cell surfaces that present antigens to T cells. MHC molecules are divided into class I and class II. Class I molecules are found on all nucleated cells and present antigens to CD8+ T cells, while class II molecules are found on antigen-presenting cells and present antigens to CD4+ T cells. The MHC was first identified as important for tissue graft compatibility.
The document summarizes key concepts about the major histocompatibility complex (MHC):
1) The MHC was discovered through studies of transplant rejection in mice, which showed that rejection was dependent on the genetics of the donor and recipient strains.
2) MHC molecules present peptide antigens to T cells and play a key role in immune responses, including transplant rejection.
3) MHC molecules are highly polymorphic, with many variants within populations, in order to allow populations to recognize a wide variety of pathogens.
MAJOR HISTOCOMPATIBILITY COMPLEX AND HEAT SHOCK PROTEINSiva Ramakrishnan
The document discusses major histocompatibility complex (MHC) and heat shock proteins (HSP) in chickens. MHC genes encode proteins that present antigens and are involved in immune response and recognition. HSPs help proteins fold correctly and prevent aggregation. Both MHC and HSP play important roles in immune function, disease resistance, and stress response in chickens. Manipulation of these genes may help improve production traits and resistance to disease.
MHC genes evolve through duplication, followed by diversification, co‐evolution, and sequence exchange. The focus, for HLA in transplantation, has been the specific classical class I and class II human leukocyte antigen (HLA) molecules and alleles. Importantly, anti‐HLA antibodies developed after the organ transplants play a role in acute and chronic allograft rejection, highlighting the need to detect these antibodies in a clinically relevant manner. Although the immune response to HLA antigens plays a pivotal role in allograft rejection, evidence shows that non‐HLA antigens also contribute to the pathogenesis of acute and chronic rejection, which limits long‐term graft survival of the solid organ transplants.
The document discusses the major histocompatibility complex (MHC) in mammals. It notes that MHC acts as antigen presenting receptors and are involved in cell-cell interaction, antigen presentation, and recognition of self and non-self molecules. MHC is found on chromosome 6 in humans and is referred to as the HLA complex. MHC molecules are divided into three main classes - Class I MHC present antigens to cytotoxic T cells, Class II MHC present antigens to helper T cells, and Class III MHC genes encode complement components and cytokines. The structures and functions of Class I and Class II MHC molecules are described in detail.
The document summarizes the major histocompatibility complex (MHC). It discusses how the MHC was discovered through studies of tissue transplantation in mice. The MHC locus contains genes that encode MHC class I and class II molecules that present antigens to T cells and play a key role in immune responses. MHC molecules are expressed on nearly all nucleated cells for class I and specifically on antigen presenting cells for class II. The genomic organization and structures of MHC class I and II molecules allow them to present peptides to CD8+ or CD4+ T cells, respectively.
The seminar presented discussed the major histocompatibility complex (MHC). MHC molecules are surface proteins located on nucleated cells that play an important role in identifying antigens and presenting them to T cells to trigger an immune response. The seminar covered the definition of MHC, its history of discovery, the different classes of MHC molecules including their structure and function, examples in humans (HLA) and mice (H-2 complex), and concluded with a summary of how MHC molecules recognize both endogenous and exogenous antigens to initiate an immune response. The seminar was presented by Miss. Sandhya Sahu and guided by her professor Mr. Shishir Vind Sharma at Rungta College of Science & Technology,
The major histocompatibility complex (MHC) is a set of genes found in all mammals that encodes cell surface proteins essential for the immune system to distinguish self from non-self. The MHC is involved in antigen presentation, immune cell interactions, and determining compatibility for transplantation. In humans, MHC genes are located on chromosome 6 and are divided into three main classes: Class I presents antigens to cytotoxic T cells, Class II presents antigens to helper T cells, and Class III encodes proteins involved in inflammation. Differences in MHC proteins determine an individual's ability to mount immune responses to pathogens.
The document discusses the major histocompatibility complex (MHC), which controls a major part of the immune system. It defines MHC as a set of cell surface proteins expressed on all nucleated cells and encoded by a large gene family. MHC molecules play a role in antigen presentation, autoimmune diseases, and transplantation. MHC genes in humans are found on chromosome 6 and are divided into three classes - class I expressed on all tissues, class II expressed mainly by antigen presenting cells, and class III encoding complement and TNF proteins. MHC molecules participate in discriminating self from non-self and in both humoral and cell-mediated immunity by presenting antigens.
Major Histocompatibility complex & Antigen Presentation and ProcessingSreeraj Thamban
The document discusses the major histocompatibility complex (MHC) and antigen processing and presentation. It describes MHC molecules as polymorphic glycoproteins that play a role in discriminating self from non-self and participate in both humoral and cell-mediated immunity. MHC class I molecules present endogenous antigens on most nucleated cells and interact with CD8+ T cells. MHC class II molecules present exogenous antigens on antigen-presenting cells and interact with CD4+ T cells. Antigens are processed into peptides of appropriate size and bound motifs to be presented in the binding groove of MHC molecules.
The document outlines an orthopedics marketing campaign for Ascension across three regions from June to September 2016. The campaign's goal is to grow the orthopedics program through increased new patient volume. It will use the theme "Be Active for Life" and incorporate Olympic messaging to promote the system's expert orthopedic care. Tactics include websites, online/social media ads, radio, TV, billboards, and print ads directing patients to landing pages. The campaign will be measured by engagement metrics and increases in calls, appointments, and patient volume.
This document discusses fever of unknown origin (FUO) and adult onset Still's disease (AOSD). FUO is defined as a fever over 38.3°C on multiple occasions for more than 3 weeks without an initial obvious cause. Common causes of FUO include infections like tuberculosis, cancers like lymphoma, and collagen vascular diseases like SLE. AOSD is a rare condition characterized by daily high spiking fevers, arthritis, and an evanescent rash. Diagnosis is based on characteristic features and exclusion of other conditions. Treatment involves NSAIDs, steroids, methotrexate, and TNF blocking agents. Prognosis varies from self-limited to intermittent to chronic arthritis.
The document discusses the major histocompatibility complex (MHC), which plays a key role in immune response and organ transplantation. It describes the structure of MHC class I and II molecules, which present peptide fragments to T cells. MHC molecules are highly polymorphic and this variability allows recognition of diverse pathogens. The T cell receptor engages peptide-MHC complexes and accessory molecules provide costimulatory signals for T cell activation. Certain MHC alleles are associated with increased risk of various autoimmune diseases.
The document provides an overview of major histocompatibility complex (MHC) and human leukocyte antigen (HLA) typing. It discusses that MHC molecules present antigen fragments to T cells and are classified into classes I, II, and III. MHC proteins in humans are called HLA genes and are located on chromosome 6. The document describes HLA classification, functions in infectious disease, graft rejection, and autoimmunity, as well as genetics and methods of HLA typing including serotyping, phenotyping, and allele names.
This document provides information on MHC class I and class II molecules, including their structure, function, and role in antigen presentation. It discusses that MHC class I molecules are expressed on all nucleated cells and present intracellular antigens to CD8+ T cells. MHC class II molecules are expressed primarily on antigen presenting cells and present extracellular antigens to CD4+ T cells. The peptide binding grooves of MHC class I and II molecules differ in their structure and the size of peptides they can bind.
The document discusses the major histocompatibility complex (MHC) and its role in immune recognition. It notes that Gorer and Snell in the 1930s discovered that mouse skin grafts were rejected between mice of different blood groups, showing tissue recognition is based on genetics. They coined the term MHC to describe the genes controlling this tissue recognition. MHC molecules present peptides and are highly polymorphic within and between species, allowing an organism to distinguish self from non-self. The MHC in humans is called the HLA complex.
The document summarizes the HLA system and major histocompatibility complex. It discusses that MHC antigens are located on chromosome 6 and have 4 loci (A, B, C, D). MHC antigens are divided into 3 classes - Class I antigens regulate cytotoxic T cells, Class II antigens regulate helper T cells, and Class III antigens are components of the complement system but not associated with HLA expression. The HLA complex plays important roles in organ transplantation by matching donors and recipients, regulating the immune system through Class I and II antigens, and being associated with certain diseases.
The document summarizes key aspects of the major histocompatibility complex (MHC):
1) The MHC was discovered through studies of transplant rejection in inbred mouse strains, which showed that rejection depended on the genetics of the donor and recipient strains.
2) MHC molecules present peptide antigens to T cells and play a crucial role in immune responses, including transplant rejection.
3) MHC molecules are highly polymorphic and polygenic, with multiple variants of each type, which allows populations to recognize a wide variety of pathogens.
The Major Histocompatibility Complex (MHC):
- Is located on chromosome 6 and contains genes such as HLA that play a role in distinguishing self from non-self.
- Genes are organized into three classes: class I present antigens to T cells, class II present antigens to T helper cells, and class III genes produce immune system proteins.
- MHC molecules are highly polymorphic and inherited as sets (haplotypes) from each parent, allowing presentation of a wide variety of antigens.
The MHC encodes antigen presenting molecules that display peptide fragments to T cells to initiate immune responses. It contains three regions - Class I MHC presents intracellular peptides to CD8+ T cells, Class II MHC presents extracellular peptides to CD4+ T cells, and Class III MHC encodes complement proteins. MHC molecules are highly polymorphic and individuals inherit multiple alleles from each parent. This polymorphism allows presentation of a wide range of peptides and enhances immune responses against pathogens. MHC matching is important for transplantation, as mismatch can lead to graft rejection through T cell recognition of foreign MHC.
The Major Histocompatibility Complex (MHC) is a cluster of genes found in all mammals that plays a key role in the immune system by helping distinguish self from non-self. MHC genes are organized into three classes: Class I presents antigens to cytotoxic T cells, Class II presents antigens to helper T cells, and Class III encodes proteins involved in immune functions. MHC molecules are highly polymorphic and vary considerably between individuals, helping the immune system recognize a wide variety of pathogens.
This document discusses the major histocompatibility complex (MHC) and its class I and class II molecules. It describes the structure and components of MHC class I and II molecules, including their peptide binding grooves. MHC class I molecules are expressed on nearly all nucleated cells and present peptides from intracellular pathogens to cytotoxic T cells. MHC class II molecules are only expressed on antigen-presenting cells and present peptides from extracellular pathogens to helper T cells. The MHC genes are highly polymorphic in human populations, contributing to diversity in antigen presentation.
The document discusses the major histocompatibility complex (MHC), which consists of glycoproteins found on cell surfaces that present antigens to T cells. MHC molecules are divided into class I and class II. Class I molecules are found on all nucleated cells and present antigens to CD8+ T cells, while class II molecules are found on antigen-presenting cells and present antigens to CD4+ T cells. The MHC was first identified as important for tissue graft compatibility.
The document summarizes key concepts about the major histocompatibility complex (MHC):
1) The MHC was discovered through studies of transplant rejection in mice, which showed that rejection was dependent on the genetics of the donor and recipient strains.
2) MHC molecules present peptide antigens to T cells and play a key role in immune responses, including transplant rejection.
3) MHC molecules are highly polymorphic, with many variants within populations, in order to allow populations to recognize a wide variety of pathogens.
MAJOR HISTOCOMPATIBILITY COMPLEX AND HEAT SHOCK PROTEINSiva Ramakrishnan
The document discusses major histocompatibility complex (MHC) and heat shock proteins (HSP) in chickens. MHC genes encode proteins that present antigens and are involved in immune response and recognition. HSPs help proteins fold correctly and prevent aggregation. Both MHC and HSP play important roles in immune function, disease resistance, and stress response in chickens. Manipulation of these genes may help improve production traits and resistance to disease.
MHC genes evolve through duplication, followed by diversification, co‐evolution, and sequence exchange. The focus, for HLA in transplantation, has been the specific classical class I and class II human leukocyte antigen (HLA) molecules and alleles. Importantly, anti‐HLA antibodies developed after the organ transplants play a role in acute and chronic allograft rejection, highlighting the need to detect these antibodies in a clinically relevant manner. Although the immune response to HLA antigens plays a pivotal role in allograft rejection, evidence shows that non‐HLA antigens also contribute to the pathogenesis of acute and chronic rejection, which limits long‐term graft survival of the solid organ transplants.
The document discusses the major histocompatibility complex (MHC) in mammals. It notes that MHC acts as antigen presenting receptors and are involved in cell-cell interaction, antigen presentation, and recognition of self and non-self molecules. MHC is found on chromosome 6 in humans and is referred to as the HLA complex. MHC molecules are divided into three main classes - Class I MHC present antigens to cytotoxic T cells, Class II MHC present antigens to helper T cells, and Class III MHC genes encode complement components and cytokines. The structures and functions of Class I and Class II MHC molecules are described in detail.
The document summarizes the major histocompatibility complex (MHC). It discusses how the MHC was discovered through studies of tissue transplantation in mice. The MHC locus contains genes that encode MHC class I and class II molecules that present antigens to T cells and play a key role in immune responses. MHC molecules are expressed on nearly all nucleated cells for class I and specifically on antigen presenting cells for class II. The genomic organization and structures of MHC class I and II molecules allow them to present peptides to CD8+ or CD4+ T cells, respectively.
The seminar presented discussed the major histocompatibility complex (MHC). MHC molecules are surface proteins located on nucleated cells that play an important role in identifying antigens and presenting them to T cells to trigger an immune response. The seminar covered the definition of MHC, its history of discovery, the different classes of MHC molecules including their structure and function, examples in humans (HLA) and mice (H-2 complex), and concluded with a summary of how MHC molecules recognize both endogenous and exogenous antigens to initiate an immune response. The seminar was presented by Miss. Sandhya Sahu and guided by her professor Mr. Shishir Vind Sharma at Rungta College of Science & Technology,
The major histocompatibility complex (MHC) is a set of genes found in all mammals that encodes cell surface proteins essential for the immune system to distinguish self from non-self. The MHC is involved in antigen presentation, immune cell interactions, and determining compatibility for transplantation. In humans, MHC genes are located on chromosome 6 and are divided into three main classes: Class I presents antigens to cytotoxic T cells, Class II presents antigens to helper T cells, and Class III encodes proteins involved in inflammation. Differences in MHC proteins determine an individual's ability to mount immune responses to pathogens.
The document discusses the major histocompatibility complex (MHC), which controls a major part of the immune system. It defines MHC as a set of cell surface proteins expressed on all nucleated cells and encoded by a large gene family. MHC molecules play a role in antigen presentation, autoimmune diseases, and transplantation. MHC genes in humans are found on chromosome 6 and are divided into three classes - class I expressed on all tissues, class II expressed mainly by antigen presenting cells, and class III encoding complement and TNF proteins. MHC molecules participate in discriminating self from non-self and in both humoral and cell-mediated immunity by presenting antigens.
Major Histocompatibility complex & Antigen Presentation and ProcessingSreeraj Thamban
The document discusses the major histocompatibility complex (MHC) and antigen processing and presentation. It describes MHC molecules as polymorphic glycoproteins that play a role in discriminating self from non-self and participate in both humoral and cell-mediated immunity. MHC class I molecules present endogenous antigens on most nucleated cells and interact with CD8+ T cells. MHC class II molecules present exogenous antigens on antigen-presenting cells and interact with CD4+ T cells. Antigens are processed into peptides of appropriate size and bound motifs to be presented in the binding groove of MHC molecules.
The document outlines an orthopedics marketing campaign for Ascension across three regions from June to September 2016. The campaign's goal is to grow the orthopedics program through increased new patient volume. It will use the theme "Be Active for Life" and incorporate Olympic messaging to promote the system's expert orthopedic care. Tactics include websites, online/social media ads, radio, TV, billboards, and print ads directing patients to landing pages. The campaign will be measured by engagement metrics and increases in calls, appointments, and patient volume.
This document discusses fever of unknown origin (FUO) and adult onset Still's disease (AOSD). FUO is defined as a fever over 38.3°C on multiple occasions for more than 3 weeks without an initial obvious cause. Common causes of FUO include infections like tuberculosis, cancers like lymphoma, and collagen vascular diseases like SLE. AOSD is a rare condition characterized by daily high spiking fevers, arthritis, and an evanescent rash. Diagnosis is based on characteristic features and exclusion of other conditions. Treatment involves NSAIDs, steroids, methotrexate, and TNF blocking agents. Prognosis varies from self-limited to intermittent to chronic arthritis.
This document discusses pyrexia of unknown origin (PUO), also known as fever of unknown origin (FUO). It provides definitions of PUO, outlines the normal human body temperature, and categorizes different types of PUO including classical, nosocomial, neutropenic, HIV-associated, and transplant-associated PUO. It also discusses common causes of PUO including infections, malignancies, and collagen vascular diseases. The document emphasizes the importance of a thorough history and physical examination to identify potential etiologies and key physical signs.
Sjögren's syndrome is an autoimmune disease that causes inflammation of the exocrine glands, most commonly the salivary and lacrimal glands, leading to dry eyes and dry mouth. It exists as either a primary form that occurs alone or a secondary form associated with other connective tissue diseases like rheumatoid arthritis. Diagnosis involves evaluating symptoms of dry eyes and dry mouth along with tests like salivary gland biopsy, salivary flow tests, and lab tests for autoantibodies. Treatment focuses on managing symptoms while complications can involve other organ systems.
Adult-onset Still's disease is a form of rheumatoid arthritis that was characterized by Bywaters in 1971. Its main feature is a combination of symptoms such as high fever, cutaneous rash during fever peaks, joint and muscle pain, lymph node enlargement, increased white cell count especially polymorphonuclear neutrophils and abnormalities of liver metabolism. None of these symptoms is sufficient to establish the diagnosis and infact may be present in several other diseases such as neoplastic and infectious diseases. Thus AOSD is a “diagnosis of exclusion”.
Polymyalgia rheumatica and giant cell arteiritisdattasrisaila
Polymyalgia rheumatica (PMR) and giant cell arteritis (GCA) are two closely related inflammatory conditions that often occur in the same patient population. GCA causes inflammation of medium and large arteries and can lead to vision loss, strokes, and other ischemic symptoms. It predominantly affects women over 50 and is diagnosed based on clinical features, elevated inflammatory markers like ESR, and positive temporal artery biopsy. Imaging plays an important role in diagnosis and monitoring disease involving large arteries like the aorta. High-dose corticosteroids are the primary treatment.
A 71-year-old woman presented with aching pain and stiffness in her arms, hands, knees and feet for several months. She responded well initially to steroid treatment but had difficulty tapering off the dose. Examination found symmetrical joint swelling. Tests showed elevated inflammatory markers. She was diagnosed with possible polymyalgia rheumatica or late-onset rheumatoid arthritis. Treatment with methotrexate and gradual steroid tapering was recommended.
Brad Cohen is a motivational speaker who has Tourette syndrome. He wrote a book about growing up with the condition that was named Education Book of the Year and adapted into a Hallmark Hall of Fame movie. Cohen has been featured in major media sharing his experiences overcoming challenges through his work as a teacher determined to provide the support for students he never received.
El documento repite la frase "MATEMÁTICAS NIVEL INTRODUCTORIO - UIS SEDE BARRANCABERMEJA" doce veces, indicando que se refiere a un curso de matemáticas de nivel introductorio que se imparte en la sede de Barrancabermeja de la Universidad Industrial de Santander.
The document discusses the benefits of meditation for reducing stress and anxiety. Regular meditation practice can help calm the mind and body by lowering heart rate and blood pressure. Making meditation a part of a daily routine, even if just 10-15 minutes per day, can have mental and physical health benefits over time by helping people feel more relaxed and focused.
major histocompatibility cells and its role in immunity. one of the main mechanisms of innate and acquired immunity in human body defense mechanism. it includes both the major and minor forms and different types of cells that are involved in. difference between innate and acquired immunity and its role in autoimmune disorders. the concept of advanced immunology. modern concepts in immunology.
minor histocompatibility molecules. definition and functions of major histocompatibilty molecules. role in autoimmune disorders. immunology and micro-invironment. role of genetics in immunity. minor cells are lymphocytes and plasma cells. acute cells are neutrophils or PMNLS. ROLE OF INFLAMMATIO IN IMMUNITY. role of cell membrane receptors in immunity and immune-mediated diseases.
This document discusses MHC haplotypes, immune responsiveness, and disease susceptibility. It begins by outlining topics including inheritance of MHC haplotypes in mice (H-2) and humans (HLA), the relationship between MHC and immune responsiveness, and the association between MHC and disease susceptibility. It then provides details on MHC polymorphism and haplotype inheritance, the role of MHC in determining immune responses, and examples of diseases linked to specific MHC alleles.
This document discusses HLA typing and its role in tissue transplantation. It begins by introducing the major histocompatibility complex (MHC) and its role in transplant rejection. It then describes MHC polymorphism, HLA nomenclature, and various methods for HLA typing including serology and molecular techniques. The document concludes by discussing the applications of HLA typing in organ transplantation, including the mechanisms of allograft recognition and rejection.
Major histocompatibility complex and antigen presentation & processingAISHUJ3
The major histocompatibility complex (MHC) was discovered through studies of transplant rejection in inbred mouse strains. The MHC encodes three classes of molecules - class I molecules present peptides to CD8+ T cells, class II molecules present peptides to CD4+ T cells, and class III molecules play roles in immune responses. MHC molecules have a peptide-binding cleft that binds peptides derived from antigens. The polymorphisms in MHC genes allow presentation of a wide variety of peptides and help populations respond to diverse pathogens.
The document discusses HLA typing and its implications. It begins with a brief history of the discovery of the major histocompatibility complex (MHC) in mice and humans. It then describes the structure and functions of the MHC, including the class I, class II, and class III regions. The document discusses methods of HLA typing, including serological testing using microcytotoxicity and molecular methods. It notes some implications of HLA typing, such as its role in organ transplant matching and susceptibility to autoimmune disease.
Transplantation : Introduction to immunology part of Major Histocompatability complex(MHC) that facilitates you to understand the basic principles or issues of graft rejection and How it occurs.
The document discusses the major histocompatibility complex (MHC), which are surface proteins that play an important role in identifying antigens and presenting them to T cells. It covers the different classes of MHC molecules, their structures, functions in immunity, and examples in humans (HLA) and mice (H-2 complex). MHC molecules present peptide fragments on their surface and interact specifically with T cells through anchor residues on the peptides. They are essential for self/non-self discrimination, defense against infection, and transplantation compatibility.
Human Leukocyte Antigen (HLA) typing involves determining the presence of HLA antigens on white blood cells. HLA antigens are encoded by genes in the major histocompatibility complex located on chromosome 6. HLA typing was originally done using serology to detect antibodies binding to HLA antigens, but now molecular techniques are more commonly used. HLA antigens are highly polymorphic and inherited as haplotypes from each parent, contributing to diversity in transplantation compatibility.
IT CONTAINS THE LATEST INFORMATION ABOUT MHC MOLECULE WHICH WILL BE HELPFUL FOR B.SC /M.SC/CSIR-NET/DBT-JRF/GATE STUDENTS. THIS IS IN VERY SIMPLE AND LUCID MANNER TO UNDERSTAND AND ONE CAN EASILY OPT FOR THIS TO PREPARE NOTES.
1. The document discusses the major histocompatibility complex (MHC), a gene complex encoding cell surface molecules that present antigens and are responsible for graft rejection.
2. MHC molecules exist in two main classes, MHC class I and II. Class I presents antigens to CD8+ T cells and is found on all nucleated cells. Class II presents antigens to CD4+ T cells and is found on antigen presenting cells.
3. MHC molecules are highly polymorphic, with many alleles present within populations, ensuring a diverse ability to present a wide range of antigens and defend against pathogens.
The document discusses hypersensitivity reactions and the mechanisms of immunologically mediated diseases. It describes the four main types of hypersensitivity reactions: Type I (immediate) involves IgE antibodies and mediators like histamine; Type II (antibody-mediated) involves IgG and IgM antibodies binding to cells and tissues; Type III (immune complex-mediated) involves deposition of antigen-antibody complexes activating complement; Type IV (delayed) is mediated by T cells and involves reactions that develop over 24-48 hours. The document also provides examples of prototype disorders for each type and their characteristic immune mechanisms and pathologic lesions.
General principles of immunology and MHC - converted.pdfsubhankar9366
1. The document discusses principles of immunology including recognition, effector response, memory response, antigens, immunogens, epitopes, and types of immunity.
2. It describes the major classes of antigens that can induce an immune response and examples of cross-reactivity between antigens.
3. The roles and expression of MHC class I and II molecules are summarized, including their involvement in antigen processing and presentation to T cells.
The major histocompatibility complex (MHC) is a set of surface proteins that present antigens to T cells. MHC molecules are classified into two groups: Class I MHC molecules are expressed on all nucleated cells and present intracellular antigens to CD8+ T cells. Class II MHC molecules are mainly expressed on antigen-presenting cells and present extracellular antigens to CD4+ T cells. MHC molecules play an important role in organ transplantation by determining tissue compatibility and in the immune response by ensuring the correct response is mounted against different pathogens.
1) Antigen processing and presentation involves extracellular and intracellular proteins being degraded into peptides and bound to MHC class I or II molecules. These peptide-MHC complexes are expressed on antigen presenting cells and recognized by T cells to initiate an immune response.
2) T cells are activated through recognition of peptide-MHC complexes by their T cell receptors along with co-stimulatory signals. Activated T cells proliferate and differentiate into effector and memory T cells.
3) Effector T cells stimulate immune responses like activating macrophages to kill intracellular pathogens, leading to delayed type hypersensitivity reactions which can cause tissue damage if infection is not resolved.
The major histocompatibility complex (MHC) genes code for cell surface proteins that present antigens to T cells. In humans, MHC genes are located on chromosome 6 and are highly polymorphic. There are three main MHC classes - class I presents intracellular antigens to CD8+ T cells, class II presents extracellular antigens to CD4+ T cells, and class III encodes complement and cytokine proteins. MHC matching is important for transplant acceptance, as mismatches can lead to graft rejection through cellular and antibody-mediated immune responses.
Major Histocompatibility Complex (MHC) molecules display antigen peptides on the surface of cells to be recognized by T cells. There are two main types of MHC molecules: class I molecules present intracellular peptides to CD8+ T cells on most nucleated cells, while class II molecules present extracellular peptides to CD4+ T cells on antigen-presenting cells like dendritic cells and macrophages. MHC molecules bind peptides promiscuously but polymorphisms among individuals influence peptide binding. Dendritic cells are especially effective at antigen capture and presentation to initiate primary T cell responses.
This document provides an overview of immunogenetics. It begins with an agenda that defines immunogenetics and discusses immune responses, diversity mechanisms, and immunodeficiency diseases. The document then defines immunogenetics as the study of genetic control of immune cells and molecules. It focuses on structure and organization of immune response genes, HLA antigens and disease association, generation of antibody and T cell diversity. Mechanisms creating diversity for B cell receptors, T cell receptors and HLA are described. Finally, immunodeficiency diseases associated with impaired immune function are briefly discussed.
Describing and Interpreting an Immersive Learning Case with the Immersion Cub...Leonel Morgado
Current descriptions of immersive learning cases are often difficult or impossible to compare. This is due to a myriad of different options on what details to include, which aspects are relevant, and on the descriptive approaches employed. Also, these aspects often combine very specific details with more general guidelines or indicate intents and rationales without clarifying their implementation. In this paper we provide a method to describe immersive learning cases that is structured to enable comparisons, yet flexible enough to allow researchers and practitioners to decide which aspects to include. This method leverages a taxonomy that classifies educational aspects at three levels (uses, practices, and strategies) and then utilizes two frameworks, the Immersive Learning Brain and the Immersion Cube, to enable a structured description and interpretation of immersive learning cases. The method is then demonstrated on a published immersive learning case on training for wind turbine maintenance using virtual reality. Applying the method results in a structured artifact, the Immersive Learning Case Sheet, that tags the case with its proximal uses, practices, and strategies, and refines the free text case description to ensure that matching details are included. This contribution is thus a case description method in support of future comparative research of immersive learning cases. We then discuss how the resulting description and interpretation can be leveraged to change immersion learning cases, by enriching them (considering low-effort changes or additions) or innovating (exploring more challenging avenues of transformation). The method holds significant promise to support better-grounded research in immersive learning.
PPT on Direct Seeded Rice presented at the three-day 'Training and Validation Workshop on Modules of Climate Smart Agriculture (CSA) Technologies in South Asia' workshop on April 22, 2024.
ESA/ACT Science Coffee: Diego Blas - Gravitational wave detection with orbita...Advanced-Concepts-Team
Presentation in the Science Coffee of the Advanced Concepts Team of the European Space Agency on the 07.06.2024.
Speaker: Diego Blas (IFAE/ICREA)
Title: Gravitational wave detection with orbital motion of Moon and artificial
Abstract:
In this talk I will describe some recent ideas to find gravitational waves from supermassive black holes or of primordial origin by studying their secular effect on the orbital motion of the Moon or satellites that are laser ranged.
Authoring a personal GPT for your research and practice: How we created the Q...Leonel Morgado
Thematic analysis in qualitative research is a time-consuming and systematic task, typically done using teams. Team members must ground their activities on common understandings of the major concepts underlying the thematic analysis, and define criteria for its development. However, conceptual misunderstandings, equivocations, and lack of adherence to criteria are challenges to the quality and speed of this process. Given the distributed and uncertain nature of this process, we wondered if the tasks in thematic analysis could be supported by readily available artificial intelligence chatbots. Our early efforts point to potential benefits: not just saving time in the coding process but better adherence to criteria and grounding, by increasing triangulation between humans and artificial intelligence. This tutorial will provide a description and demonstration of the process we followed, as two academic researchers, to develop a custom ChatGPT to assist with qualitative coding in the thematic data analysis process of immersive learning accounts in a survey of the academic literature: QUAL-E Immersive Learning Thematic Analysis Helper. In the hands-on time, participants will try out QUAL-E and develop their ideas for their own qualitative coding ChatGPT. Participants that have the paid ChatGPT Plus subscription can create a draft of their assistants. The organizers will provide course materials and slide deck that participants will be able to utilize to continue development of their custom GPT. The paid subscription to ChatGPT Plus is not required to participate in this workshop, just for trying out personal GPTs during it.
(June 12, 2024) Webinar: Development of PET theranostics targeting the molecu...Scintica Instrumentation
Targeting Hsp90 and its pathogen Orthologs with Tethered Inhibitors as a Diagnostic and Therapeutic Strategy for cancer and infectious diseases with Dr. Timothy Haystead.
When I was asked to give a companion lecture in support of ‘The Philosophy of Science’ (https://shorturl.at/4pUXz) I decided not to walk through the detail of the many methodologies in order of use. Instead, I chose to employ a long standing, and ongoing, scientific development as an exemplar. And so, I chose the ever evolving story of Thermodynamics as a scientific investigation at its best.
Conducted over a period of >200 years, Thermodynamics R&D, and application, benefitted from the highest levels of professionalism, collaboration, and technical thoroughness. New layers of application, methodology, and practice were made possible by the progressive advance of technology. In turn, this has seen measurement and modelling accuracy continually improved at a micro and macro level.
Perhaps most importantly, Thermodynamics rapidly became a primary tool in the advance of applied science/engineering/technology, spanning micro-tech, to aerospace and cosmology. I can think of no better a story to illustrate the breadth of scientific methodologies and applications at their best.
Immersive Learning That Works: Research Grounding and Paths ForwardLeonel Morgado
We will metaverse into the essence of immersive learning, into its three dimensions and conceptual models. This approach encompasses elements from teaching methodologies to social involvement, through organizational concerns and technologies. Challenging the perception of learning as knowledge transfer, we introduce a 'Uses, Practices & Strategies' model operationalized by the 'Immersive Learning Brain' and ‘Immersion Cube’ frameworks. This approach offers a comprehensive guide through the intricacies of immersive educational experiences and spotlighting research frontiers, along the immersion dimensions of system, narrative, and agency. Our discourse extends to stakeholders beyond the academic sphere, addressing the interests of technologists, instructional designers, and policymakers. We span various contexts, from formal education to organizational transformation to the new horizon of an AI-pervasive society. This keynote aims to unite the iLRN community in a collaborative journey towards a future where immersive learning research and practice coalesce, paving the way for innovative educational research and practice landscapes.
The debris of the ‘last major merger’ is dynamically youngSérgio Sacani
The Milky Way’s (MW) inner stellar halo contains an [Fe/H]-rich component with highly eccentric orbits, often referred to as the
‘last major merger.’ Hypotheses for the origin of this component include Gaia-Sausage/Enceladus (GSE), where the progenitor
collided with the MW proto-disc 8–11 Gyr ago, and the Virgo Radial Merger (VRM), where the progenitor collided with the
MW disc within the last 3 Gyr. These two scenarios make different predictions about observable structure in local phase space,
because the morphology of debris depends on how long it has had to phase mix. The recently identified phase-space folds in Gaia
DR3 have positive caustic velocities, making them fundamentally different than the phase-mixed chevrons found in simulations
at late times. Roughly 20 per cent of the stars in the prograde local stellar halo are associated with the observed caustics. Based
on a simple phase-mixing model, the observed number of caustics are consistent with a merger that occurred 1–2 Gyr ago.
We also compare the observed phase-space distribution to FIRE-2 Latte simulations of GSE-like mergers, using a quantitative
measurement of phase mixing (2D causticality). The observed local phase-space distribution best matches the simulated data
1–2 Gyr after collision, and certainly not later than 3 Gyr. This is further evidence that the progenitor of the ‘last major merger’
did not collide with the MW proto-disc at early times, as is thought for the GSE, but instead collided with the MW disc within
the last few Gyr, consistent with the body of work surrounding the VRM.
Mending Clothing to Support Sustainable Fashion_CIMaR 2024.pdfSelcen Ozturkcan
Ozturkcan, S., Berndt, A., & Angelakis, A. (2024). Mending clothing to support sustainable fashion. Presented at the 31st Annual Conference by the Consortium for International Marketing Research (CIMaR), 10-13 Jun 2024, University of Gävle, Sweden.
The technology uses reclaimed CO₂ as the dyeing medium in a closed loop process. When pressurized, CO₂ becomes supercritical (SC-CO₂). In this state CO₂ has a very high solvent power, allowing the dye to dissolve easily.
Travis Hills of MN is Making Clean Water Accessible to All Through High Flux ...Travis Hills MN
By harnessing the power of High Flux Vacuum Membrane Distillation, Travis Hills from MN envisions a future where clean and safe drinking water is accessible to all, regardless of geographical location or economic status.
4. .MHC
( Major histocompatibility complex.)
The immune system is regulated by
molecules coded by some genes.
These are genes of the
histocompatibility system
which code
For Human leukocyte antigens.
(HLA).
5. HLA : located in the short arm
of chromosome 6.( part of MHC.)
MHC: divided into 3 classes.
MHC class 1 : code the molecules
HLA-A, HLA-B, HLA-C.
(present in almost all somatic cells)
MHC class11 : code the molecules
HLA-DR, HLA-DQ, HLA-DP.
(expressed in APC , B- cells, activated
T-cells, macrophages, dendritic cells,
Thymic epith.cells.)
6.
7.
8.
9. Each individual have:
* 2 antigens in each locus.
* one half inherited from each parent.
Expression of MHC alleles is
Codominant.
each ( one haplotype inherited from
parent .)
10. HLA: the most polymorphic
genetic system in man.
* numerous alleles.
* various possible combinations.
* Polymorphism contribute to :
- the genetic diversity of the species.
- differences in susceptibility to diseases.
(among genetically distinct groups.)
* this make it difficult for large-scale
epidemics to occur.
11. MHC polymorphism &polygeny.
Polymorphism of MHC loci ensure the
diversity in MHC gene expression
in the population as a whole.
Polygeny (the presence of several different
related genes with similar functions) , ensures
that each individual produces a number
of different MHC molecules .
12.
13. The antigenic universe.
Scientists estimate that the antigenic universe
contain between 106- 107
epitopes.(antigens.)
This mean that there are at least
106- 107 epitope –specific T-cell
and B-cell.
(specific mean that there is a cell, T or
B for each of the 106- 107 epitopes.)
14.
15.
16. T-cells only recognize microbial
peptides in association with
MHC.(restricted)
* MHC control :
-resistance to infections.
-susceptibility to infections.
Stimulation require 2 signals.
*Antigen peptide.
* Co-stimulatory signal.
(2 key system .)
17.
18.
19.
20.
21.
22.
23.
24.
25.
26.
27.
28. *HLA-DRB1*7 and HLA-DQA1*0101:
are associated with greater susceptibility
to develop pulmonary T.B.
*HLA-DQA1*0301 &HLA-DQA1*0501:
are associated with protection against T.B
.
29.
30. Conclusion
* HLA may act alone (or with other genes )
in conferring susceptibility to , or protection
against , infectious diseases.
* Knowledge about genetic mechanisms
contribute to our understanding of the
pathogenesis of infectious diseases.
* The mechanism of immune responses to
infections that are influenced by HLA
may be the key to future vaccines.
31. * Future vaccines aim to use peptides
of the organisms that mimic the HLA
antigens