How Freund's Incomplete Adjuvant Stimulates Immune Cells and Pathways. Delve into the intricate process of how Freund's Incomplete Adjuvant triggers activation in immune cells and pathways.
Freund's Complete Adjuvant in Research and its Path to Clinical Applications.pdfChangyu Bio
https://www.changyubio.com/freunds-complete-adjuvant/ | In the intricate realm of immunology, Freund's Complete Adjuvant (FCA) stands as an indispensable tool, a catalyst that sparks robust immune responses and propels vaccine development forward. This essay embarks on a comprehensive exploration of FCA, navigating through its composition, mechanism of action, applications in research, and the intricate regulatory landscape that shapes its journey toward clinical applications.
The document summarizes a seminar presentation on vaccines. It begins with an introduction to vaccines and defines them as biological preparations that provide active acquired immunity against diseases. It then discusses different types of vaccines such as live attenuated, killed, subunit, and DNA vaccines. The mechanisms of how vaccines work and provide immunization are also summarized. Common immunization programs for diseases like BCG, polio, hepatitis B, measles are outlined. The presentation concludes with emphasizing the importance of vaccines in providing protection from pathogens and immunity.
This document discusses vaccine drug delivery systems. It provides an introduction to vaccines and their history. It describes the types of vaccines and how they work, as well as ideal vaccine properties. It discusses uptake of antigens and different delivery methods for vaccines, including single shot vaccines, mucosal delivery, and transdermal delivery. It also lists previous exam questions related to these vaccine delivery topics.
Vaccines work by exposing the immune system to weakened or killed forms of pathogens to stimulate antibody production against them. There are several types of vaccines including live attenuated vaccines using weakened live pathogens, inactivated vaccines using killed pathogens, subunit vaccines using pathogen proteins, DNA vaccines using genetic material, synthetic peptide vaccines, and toxoid vaccines using inactivated bacterial toxins. Vaccines provide active immunity and are the most effective method of preventing infectious diseases.
The document discusses vaccines and immunization. It provides details on what vaccines are, how they work, different types of vaccines, vaccine production methods, and the risks and benefits of vaccines. It also discusses immunization programs like EPI Pakistan, which aims to vaccinate children against 8 diseases through routine vaccination schedules. The overall goal of vaccines and immunization programs is to safely establish immunity in populations against harmful pathogens.
This document discusses immunization and different types of vaccines. It defines immunization as the process by which the immune system becomes fortified against an agent. Vaccinology is the science of vaccine development, and an ideal vaccine provides long-lasting immunity, induces both antibody and cellular immune responses, is safe, inexpensive to produce and store, and easy to administer. The document outlines different types of vaccines including killed, attenuated, toxoid, subunit, recombinant protein, conjugate, DNA, and recombinant vector vaccines. It also discusses the use of synthetic peptides as immunogens and recombinant protein production using specialized vectors.
1) Vaccine delivery systems aim to improve the immune response to vaccines. Virosomes are a type of delivery system that are biodegradable, biocompatible, and non-toxic. They enable drug delivery into target cells and protect drugs from degradation. However, virosomes have short shelf lives and scaling up poses challenges.
2) Vaccines work by exposing the immune system to antigens from pathogens in a way that stimulates antibody production without causing illness. Antibodies bind to antigens and help the immune system recognize and destroy pathogens. Vaccines contain antigens along with other ingredients like adjuvants to enhance the immune response.
3) There are various types of traditional and innovative vaccines that target different
Freund's Complete Adjuvant in Research and its Path to Clinical Applications.pdfChangyu Bio
https://www.changyubio.com/freunds-complete-adjuvant/ | In the intricate realm of immunology, Freund's Complete Adjuvant (FCA) stands as an indispensable tool, a catalyst that sparks robust immune responses and propels vaccine development forward. This essay embarks on a comprehensive exploration of FCA, navigating through its composition, mechanism of action, applications in research, and the intricate regulatory landscape that shapes its journey toward clinical applications.
The document summarizes a seminar presentation on vaccines. It begins with an introduction to vaccines and defines them as biological preparations that provide active acquired immunity against diseases. It then discusses different types of vaccines such as live attenuated, killed, subunit, and DNA vaccines. The mechanisms of how vaccines work and provide immunization are also summarized. Common immunization programs for diseases like BCG, polio, hepatitis B, measles are outlined. The presentation concludes with emphasizing the importance of vaccines in providing protection from pathogens and immunity.
This document discusses vaccine drug delivery systems. It provides an introduction to vaccines and their history. It describes the types of vaccines and how they work, as well as ideal vaccine properties. It discusses uptake of antigens and different delivery methods for vaccines, including single shot vaccines, mucosal delivery, and transdermal delivery. It also lists previous exam questions related to these vaccine delivery topics.
Vaccines work by exposing the immune system to weakened or killed forms of pathogens to stimulate antibody production against them. There are several types of vaccines including live attenuated vaccines using weakened live pathogens, inactivated vaccines using killed pathogens, subunit vaccines using pathogen proteins, DNA vaccines using genetic material, synthetic peptide vaccines, and toxoid vaccines using inactivated bacterial toxins. Vaccines provide active immunity and are the most effective method of preventing infectious diseases.
The document discusses vaccines and immunization. It provides details on what vaccines are, how they work, different types of vaccines, vaccine production methods, and the risks and benefits of vaccines. It also discusses immunization programs like EPI Pakistan, which aims to vaccinate children against 8 diseases through routine vaccination schedules. The overall goal of vaccines and immunization programs is to safely establish immunity in populations against harmful pathogens.
This document discusses immunization and different types of vaccines. It defines immunization as the process by which the immune system becomes fortified against an agent. Vaccinology is the science of vaccine development, and an ideal vaccine provides long-lasting immunity, induces both antibody and cellular immune responses, is safe, inexpensive to produce and store, and easy to administer. The document outlines different types of vaccines including killed, attenuated, toxoid, subunit, recombinant protein, conjugate, DNA, and recombinant vector vaccines. It also discusses the use of synthetic peptides as immunogens and recombinant protein production using specialized vectors.
1) Vaccine delivery systems aim to improve the immune response to vaccines. Virosomes are a type of delivery system that are biodegradable, biocompatible, and non-toxic. They enable drug delivery into target cells and protect drugs from degradation. However, virosomes have short shelf lives and scaling up poses challenges.
2) Vaccines work by exposing the immune system to antigens from pathogens in a way that stimulates antibody production without causing illness. Antibodies bind to antigens and help the immune system recognize and destroy pathogens. Vaccines contain antigens along with other ingredients like adjuvants to enhance the immune response.
3) There are various types of traditional and innovative vaccines that target different
1. Biotechnology applications can help in the discovery of new vaccines through recombinant DNA technology. This allows for the production of recombinant protein vaccines and DNA vaccines.
2. Recombinant protein vaccines involve isolating the gene for an immunogenic protein, expressing it in a host organism to produce the protein, which is then purified and used in a vaccine. DNA vaccines use the isolated gene itself as the vaccine.
3. While biotechnology offers advantages like safety and immune response, developing new vaccines faces challenges like high costs, storage requirements, and producing vaccines for diseases with many variable strains. Extensive research and testing is still required.
This document summarizes key aspects of vaccine development and production. It discusses the types of vaccines including live-attenuated, inactivated, subunit, recombinant peptide, DNA, and viral vector vaccines. Production involves growing microorganisms or cells, purification, formulation with adjuvants or stabilizers, characterization, storage, and licensing. New technologies aim to develop vaccines for diseases lacking vaccines, and improve safety, efficacy, and heat stability of existing vaccines.
There are several types of vaccines: polysaccharide vaccines stimulate B cells without T cells but are not effective for children. Conjugate vaccines link polysaccharides to proteins, inducing T cell responses and memory. Recombinant subunit vaccines produce antigens through genetic engineering, allowing mass production without live organisms. Acellular vaccines use purified bacterial antigens to induce immunity with fewer side effects than whole cell vaccines, which use live attenuated pathogens and pose risks of reversion or contamination. DNA vaccines deliver DNA encoding antigens to generate immune responses without replication.
SYNTHETIC PEPTIDE VACCINES AND RECOMBINANT ANTIGEN VACCINED.R. Chandravanshi
This document discusses synthetic peptide vaccines and recombinant antigen vaccines. It begins with definitions of vaccines and how they work to induce an immune response. It then describes two types of modern vaccines: synthetic peptide vaccines and recombinant antigen vaccines. Synthetic peptide vaccines use short fragments of viral or bacterial proteins that contain epitopes to induce an immune response, while recombinant antigen vaccines produce antigens through DNA technology by inserting viral or bacterial DNA into cells that then express the antigen protein. Both types of modern vaccines offer advantages over traditional vaccines like easier production and stability without refrigeration.
Vaccines work by enhancing the body's immune response to disease-causing microorganisms. They contain weakened or killed forms of viruses or bacteria, or purified components, which trigger an immune response and develop antibodies without causing illness. Vaccines are formulated with antigens, fluids, preservatives and adjuvants to ensure potency over the shelf life. They are prepared from isolated microbial strains grown in culture and tested in clinical trials before use in vaccine production. The immune response triggered by vaccination mimics natural infection and prepares the body to fight the disease if exposed in the future.
This document provides an overview of vaccine drug delivery systems. It discusses various types of vaccines including traditional vaccines like killed, live attenuated, toxoid, and subunit vaccines as well as innovative conjugate, recombinant vector, and T-cell receptor peptide vaccines. It also describes single shot vaccines, transdermal vaccine delivery using microneedles and jet injectors, as well as mucosal vaccine delivery through intranasal, oral, oral cavity, and intrapulmonary routes. Design strategies for mucosal delivery including emulsion, liposome, polymeric nanoparticles, and virosome-based systems are also summarized.
Most developments in biotechnology originated for their potential applications in health care.
Contributions of biotechnology are more frequent, more notable and more rewarding in health sector.
Recombinant vaccines are more effective than conventional vaccines. They have several advantages: they are reliable and safer since only a single protein is used rather than the whole organism; this also reduces the risk of illness. Recombinant technology allows scientists to control the type of vector used and choose specific antigens. While only one recombinant vaccine has been approved by the FDA so far, the technology produces a strong protective immune response similar to a natural infection and may be less expensive to produce in the future. However, developing recombinant vaccines is currently very expensive and some ethical concerns remain regarding the use of human subjects in testing.
Vaccines work by inducing active immunity through antibody and cell-mediated immune responses. Antibodies are produced by B cells to help eliminate antigens, while T cells have cytotoxic and helper functions. There are two main types of vaccines - live attenuated vaccines, which activate all phases of the immune system but carry a risk of mutation; and inactivated vaccines, which are safer but require boosters. An ideal vaccine would provide lifelong protection against all variants of a pathogen by preventing disease transmission through rapid, effective, and safe induction of immunity in all individuals.
This document discusses vaccines and the potential for using plants as bioreactors to produce vaccines. It notes that vaccines provide active immunity against diseases and typically contain weakened or killed forms of pathogens. Vaccination is an effective public health measure. Recently, genetically engineering plants to express antigen proteins from pathogens has emerged as a way to develop subunit vaccines more economically than traditional methods. The document outlines opportunities like safety, immune response, stability, low cost, and challenges like regulatory concerns for plant-based vaccines. It provides examples of plant-made influenza vaccines in development that could allow rapid production in response to pandemics.
The document discusses various COVID-19 vaccine candidates and types. It describes four main types - whole virus vaccines, protein subunit vaccines, nucleic acid vaccines, and viral vector vaccines. For each type it explains how they work, potential advantages and disadvantages, and examples of vaccines that use each approach. It provides details on some of the leading COVID-19 vaccine candidates in clinical trials, including Pfizer/BioNTech, Moderna, Oxford/AstraZeneca, and discusses the clinical trial process, recommendations for distribution, and efforts to scale up production and distribution of approved vaccines.
vaccine train user immune system to create antibodies, just as it when it is exposed to a disease. However, because vaccine contain only killed or weakened forms of germs like viruses or bacteria, they do not cause the disease or put you at the risk of complications.
vaccine is a biological preparation that improve immunity to a particular disease.
A vaccine typically contain an agent that resembles a disease causing microorganisms and is often made from weakened or killed forms of the microbes.
This document discusses new generation vaccines and the role of bioinformatics in their development. It defines vaccines and describes problems with conventional vaccines. New generation vaccines include recombinant, DNA, and peptide-based vaccines. Recombinant vaccines use proteins from pathogens produced using genetic engineering. DNA vaccines use only pathogen DNA. Peptide vaccines are built from defined peptide antigens. Bioinformatics plays a key role through genomic analysis, epitope prediction, reverse vaccinology, vaccine design, immunoinformatics, adjuvant prediction, and vaccine surveillance. It integrates various omics data to gain insights into host-pathogen interactions and immune responses to aid vaccine development.
1) The document discusses new generation vaccines, including DNA vaccines, recombinant vaccines, and peptide-based vaccines.
2) It explains how bioinformatics plays a key role in various aspects of developing these new generation vaccines, such as genomic data analysis, epitope prediction, reverse vaccinology, vaccine antigen design, and immunoinformatics.
3) New generation vaccines aim to address limitations of conventional vaccines and leverage cutting-edge technologies enabled by bioinformatics.
The word “Immuis” means free from burden and “immunitas” means exemption from government taxes and this provided the English terminology Immunity.
Immunity is a broad definition: This is a protective or defense mechanism of our body, which leads us to a healthy life.
Inborn or Innate immunity: It is present at birth; This is our First Line Of Defense.
Acquired or Specific: It is not present at birth but becomes part of our immune system as the lymphoid system develops.
1970: WHO defined immunity as immune response to antigen ( Foreign body) in form of:-
Humoral (activation of B-lymhocytes).
Cellular (by activation of T-lymphocytes).
This document discusses different types of vaccines that can be developed for aquaculture, including live attenuated, inactivated, subunit, DNA, and RNA vaccines. It notes the advantages and disadvantages of each type. First generation vaccines include live attenuated and inactivated whole pathogens, while second generation are subunit vaccines containing purified proteins. DNA and RNA vaccines are third generation vaccines that induce immune responses by encoding pathogen antigens intracellularly. The document also discusses novel vaccine types such as biofilm and egg yolk vaccines produced from chickens.
A vaccine is a biological preparation that provides active acquired immunity to a particular infectious disease.Vaccine contains certain agents that not only resembles a disease-causing microorganism but it also stimulates body’s immune system recognize the foreign agents.Vaccines can be prophylactic or therapeutic.
The administration of vaccines is called vaccination.
British physician Edward Jenner, who in 1796 used the cowpox virus (Latin variola vaccinia) to confer protection against smallpox. In 1885 the French microbiologist Louis Pasteur and Emile Roux developed the first vaccine against rabies.
There are several types of vaccines like Whole-Organism vaccine, recombinant vaccine,dna vaccine, multivalent subunit vaccines etc.
The document discusses different types of vaccines, including live attenuated vaccines, inactivated vaccines, subunit vaccines, recombinant vaccines, DNA vaccines, and conjugate vaccines. Live attenuated vaccines use weakened live pathogens to induce immunity, while inactivated vaccines use killed pathogens. Subunit vaccines contain purified antigens from pathogens. Recombinant vaccines produce antigens using genetic engineering, while DNA vaccines use DNA encoding antigens. Conjugate vaccines chemically link bacterial coat proteins to carrier proteins to generate stronger immune responses.
Lecture 4 : Animal Diseases for Veterinary Scienceal.pptxWiseAcademy
This document provides an overview of veterinary immunization principles and methods against specific diseases. It discusses various types of vaccines including live attenuated, inactivated/killed, toxoid, bacterins, subunit/conjugate, peptide, recombinant DNA, DIVA/marker vaccines. Key points covered include active vs passive immunity, advantages and disadvantages of different vaccine types, and immunization schedules for poultry birds. Mucosal immunity and its role in disease protection is also summarized. The document concludes with addressing causes of vaccination failure and strategies to avoid it.
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
1. Biotechnology applications can help in the discovery of new vaccines through recombinant DNA technology. This allows for the production of recombinant protein vaccines and DNA vaccines.
2. Recombinant protein vaccines involve isolating the gene for an immunogenic protein, expressing it in a host organism to produce the protein, which is then purified and used in a vaccine. DNA vaccines use the isolated gene itself as the vaccine.
3. While biotechnology offers advantages like safety and immune response, developing new vaccines faces challenges like high costs, storage requirements, and producing vaccines for diseases with many variable strains. Extensive research and testing is still required.
This document summarizes key aspects of vaccine development and production. It discusses the types of vaccines including live-attenuated, inactivated, subunit, recombinant peptide, DNA, and viral vector vaccines. Production involves growing microorganisms or cells, purification, formulation with adjuvants or stabilizers, characterization, storage, and licensing. New technologies aim to develop vaccines for diseases lacking vaccines, and improve safety, efficacy, and heat stability of existing vaccines.
There are several types of vaccines: polysaccharide vaccines stimulate B cells without T cells but are not effective for children. Conjugate vaccines link polysaccharides to proteins, inducing T cell responses and memory. Recombinant subunit vaccines produce antigens through genetic engineering, allowing mass production without live organisms. Acellular vaccines use purified bacterial antigens to induce immunity with fewer side effects than whole cell vaccines, which use live attenuated pathogens and pose risks of reversion or contamination. DNA vaccines deliver DNA encoding antigens to generate immune responses without replication.
SYNTHETIC PEPTIDE VACCINES AND RECOMBINANT ANTIGEN VACCINED.R. Chandravanshi
This document discusses synthetic peptide vaccines and recombinant antigen vaccines. It begins with definitions of vaccines and how they work to induce an immune response. It then describes two types of modern vaccines: synthetic peptide vaccines and recombinant antigen vaccines. Synthetic peptide vaccines use short fragments of viral or bacterial proteins that contain epitopes to induce an immune response, while recombinant antigen vaccines produce antigens through DNA technology by inserting viral or bacterial DNA into cells that then express the antigen protein. Both types of modern vaccines offer advantages over traditional vaccines like easier production and stability without refrigeration.
Vaccines work by enhancing the body's immune response to disease-causing microorganisms. They contain weakened or killed forms of viruses or bacteria, or purified components, which trigger an immune response and develop antibodies without causing illness. Vaccines are formulated with antigens, fluids, preservatives and adjuvants to ensure potency over the shelf life. They are prepared from isolated microbial strains grown in culture and tested in clinical trials before use in vaccine production. The immune response triggered by vaccination mimics natural infection and prepares the body to fight the disease if exposed in the future.
This document provides an overview of vaccine drug delivery systems. It discusses various types of vaccines including traditional vaccines like killed, live attenuated, toxoid, and subunit vaccines as well as innovative conjugate, recombinant vector, and T-cell receptor peptide vaccines. It also describes single shot vaccines, transdermal vaccine delivery using microneedles and jet injectors, as well as mucosal vaccine delivery through intranasal, oral, oral cavity, and intrapulmonary routes. Design strategies for mucosal delivery including emulsion, liposome, polymeric nanoparticles, and virosome-based systems are also summarized.
Most developments in biotechnology originated for their potential applications in health care.
Contributions of biotechnology are more frequent, more notable and more rewarding in health sector.
Recombinant vaccines are more effective than conventional vaccines. They have several advantages: they are reliable and safer since only a single protein is used rather than the whole organism; this also reduces the risk of illness. Recombinant technology allows scientists to control the type of vector used and choose specific antigens. While only one recombinant vaccine has been approved by the FDA so far, the technology produces a strong protective immune response similar to a natural infection and may be less expensive to produce in the future. However, developing recombinant vaccines is currently very expensive and some ethical concerns remain regarding the use of human subjects in testing.
Vaccines work by inducing active immunity through antibody and cell-mediated immune responses. Antibodies are produced by B cells to help eliminate antigens, while T cells have cytotoxic and helper functions. There are two main types of vaccines - live attenuated vaccines, which activate all phases of the immune system but carry a risk of mutation; and inactivated vaccines, which are safer but require boosters. An ideal vaccine would provide lifelong protection against all variants of a pathogen by preventing disease transmission through rapid, effective, and safe induction of immunity in all individuals.
This document discusses vaccines and the potential for using plants as bioreactors to produce vaccines. It notes that vaccines provide active immunity against diseases and typically contain weakened or killed forms of pathogens. Vaccination is an effective public health measure. Recently, genetically engineering plants to express antigen proteins from pathogens has emerged as a way to develop subunit vaccines more economically than traditional methods. The document outlines opportunities like safety, immune response, stability, low cost, and challenges like regulatory concerns for plant-based vaccines. It provides examples of plant-made influenza vaccines in development that could allow rapid production in response to pandemics.
The document discusses various COVID-19 vaccine candidates and types. It describes four main types - whole virus vaccines, protein subunit vaccines, nucleic acid vaccines, and viral vector vaccines. For each type it explains how they work, potential advantages and disadvantages, and examples of vaccines that use each approach. It provides details on some of the leading COVID-19 vaccine candidates in clinical trials, including Pfizer/BioNTech, Moderna, Oxford/AstraZeneca, and discusses the clinical trial process, recommendations for distribution, and efforts to scale up production and distribution of approved vaccines.
vaccine train user immune system to create antibodies, just as it when it is exposed to a disease. However, because vaccine contain only killed or weakened forms of germs like viruses or bacteria, they do not cause the disease or put you at the risk of complications.
vaccine is a biological preparation that improve immunity to a particular disease.
A vaccine typically contain an agent that resembles a disease causing microorganisms and is often made from weakened or killed forms of the microbes.
This document discusses new generation vaccines and the role of bioinformatics in their development. It defines vaccines and describes problems with conventional vaccines. New generation vaccines include recombinant, DNA, and peptide-based vaccines. Recombinant vaccines use proteins from pathogens produced using genetic engineering. DNA vaccines use only pathogen DNA. Peptide vaccines are built from defined peptide antigens. Bioinformatics plays a key role through genomic analysis, epitope prediction, reverse vaccinology, vaccine design, immunoinformatics, adjuvant prediction, and vaccine surveillance. It integrates various omics data to gain insights into host-pathogen interactions and immune responses to aid vaccine development.
1) The document discusses new generation vaccines, including DNA vaccines, recombinant vaccines, and peptide-based vaccines.
2) It explains how bioinformatics plays a key role in various aspects of developing these new generation vaccines, such as genomic data analysis, epitope prediction, reverse vaccinology, vaccine antigen design, and immunoinformatics.
3) New generation vaccines aim to address limitations of conventional vaccines and leverage cutting-edge technologies enabled by bioinformatics.
The word “Immuis” means free from burden and “immunitas” means exemption from government taxes and this provided the English terminology Immunity.
Immunity is a broad definition: This is a protective or defense mechanism of our body, which leads us to a healthy life.
Inborn or Innate immunity: It is present at birth; This is our First Line Of Defense.
Acquired or Specific: It is not present at birth but becomes part of our immune system as the lymphoid system develops.
1970: WHO defined immunity as immune response to antigen ( Foreign body) in form of:-
Humoral (activation of B-lymhocytes).
Cellular (by activation of T-lymphocytes).
This document discusses different types of vaccines that can be developed for aquaculture, including live attenuated, inactivated, subunit, DNA, and RNA vaccines. It notes the advantages and disadvantages of each type. First generation vaccines include live attenuated and inactivated whole pathogens, while second generation are subunit vaccines containing purified proteins. DNA and RNA vaccines are third generation vaccines that induce immune responses by encoding pathogen antigens intracellularly. The document also discusses novel vaccine types such as biofilm and egg yolk vaccines produced from chickens.
A vaccine is a biological preparation that provides active acquired immunity to a particular infectious disease.Vaccine contains certain agents that not only resembles a disease-causing microorganism but it also stimulates body’s immune system recognize the foreign agents.Vaccines can be prophylactic or therapeutic.
The administration of vaccines is called vaccination.
British physician Edward Jenner, who in 1796 used the cowpox virus (Latin variola vaccinia) to confer protection against smallpox. In 1885 the French microbiologist Louis Pasteur and Emile Roux developed the first vaccine against rabies.
There are several types of vaccines like Whole-Organism vaccine, recombinant vaccine,dna vaccine, multivalent subunit vaccines etc.
The document discusses different types of vaccines, including live attenuated vaccines, inactivated vaccines, subunit vaccines, recombinant vaccines, DNA vaccines, and conjugate vaccines. Live attenuated vaccines use weakened live pathogens to induce immunity, while inactivated vaccines use killed pathogens. Subunit vaccines contain purified antigens from pathogens. Recombinant vaccines produce antigens using genetic engineering, while DNA vaccines use DNA encoding antigens. Conjugate vaccines chemically link bacterial coat proteins to carrier proteins to generate stronger immune responses.
Lecture 4 : Animal Diseases for Veterinary Scienceal.pptxWiseAcademy
This document provides an overview of veterinary immunization principles and methods against specific diseases. It discusses various types of vaccines including live attenuated, inactivated/killed, toxoid, bacterins, subunit/conjugate, peptide, recombinant DNA, DIVA/marker vaccines. Key points covered include active vs passive immunity, advantages and disadvantages of different vaccine types, and immunization schedules for poultry birds. Mucosal immunity and its role in disease protection is also summarized. The document concludes with addressing causes of vaccination failure and strategies to avoid it.
Similar to Deciphering How Freund's Incomplete Adjuvant Activates Immune Cells.pdf (20)
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
TEST BANK For Community Health Nursing A Canadian Perspective, 5th Edition by...Donc Test
TEST BANK For Community Health Nursing A Canadian Perspective, 5th Edition by Stamler, Verified Chapters 1 - 33, Complete Newest Version Community Health Nursing A Canadian Perspective, 5th Edition by Stamler, Verified Chapters 1 - 33, Complete Newest Version Community Health Nursing A Canadian Perspective, 5th Edition by Stamler Community Health Nursing A Canadian Perspective, 5th Edition TEST BANK by Stamler Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Pdf Chapters Download Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Pdf Download Stuvia Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Study Guide Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Ebook Download Stuvia Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Questions and Answers Quizlet Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Studocu Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Quizlet Test Bank For Community Health Nursing A Canadian Perspective, 5th Edition Stuvia Community Health Nursing A Canadian Perspective, 5th Edition Pdf Chapters Download Community Health Nursing A Canadian Perspective, 5th Edition Pdf Download Course Hero Community Health Nursing A Canadian Perspective, 5th Edition Answers Quizlet Community Health Nursing A Canadian Perspective, 5th Edition Ebook Download Course hero Community Health Nursing A Canadian Perspective, 5th Edition Questions and Answers Community Health Nursing A Canadian Perspective, 5th Edition Studocu Community Health Nursing A Canadian Perspective, 5th Edition Quizlet Community Health Nursing A Canadian Perspective, 5th Edition Stuvia Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Pdf Chapters Download Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Pdf Download Stuvia Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Study Guide Questions and Answers Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Ebook Download Stuvia Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Questions Quizlet Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Studocu Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Quizlet Community Health Nursing A Canadian Perspective, 5th Edition Test Bank Stuvia
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
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Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
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Does Over-Masturbation Contribute to Chronic Prostatitis.pptxwalterHu5
In some case, your chronic prostatitis may be related to over-masturbation. Generally, natural medicine Diuretic and Anti-inflammatory Pill can help mee get a cure.
Cell Therapy Expansion and Challenges in Autoimmune DiseaseHealth Advances
There is increasing confidence that cell therapies will soon play a role in the treatment of autoimmune disorders, but the extent of this impact remains to be seen. Early readouts on autologous CAR-Ts in lupus are encouraging, but manufacturing and cost limitations are likely to restrict access to highly refractory patients. Allogeneic CAR-Ts have the potential to broaden access to earlier lines of treatment due to their inherent cost benefits, however they will need to demonstrate comparable or improved efficacy to established modalities.
In addition to infrastructure and capacity constraints, CAR-Ts face a very different risk-benefit dynamic in autoimmune compared to oncology, highlighting the need for tolerable therapies with low adverse event risk. CAR-NK and Treg-based therapies are also being developed in certain autoimmune disorders and may demonstrate favorable safety profiles. Several novel non-cell therapies such as bispecific antibodies, nanobodies, and RNAi drugs, may also offer future alternative competitive solutions with variable value propositions.
Widespread adoption of cell therapies will not only require strong efficacy and safety data, but also adapted pricing and access strategies. At oncology-based price points, CAR-Ts are unlikely to achieve broad market access in autoimmune disorders, with eligible patient populations that are potentially orders of magnitude greater than the number of currently addressable cancer patients. Developers have made strides towards reducing cell therapy COGS while improving manufacturing efficiency, but payors will inevitably restrict access until more sustainable pricing is achieved.
Despite these headwinds, industry leaders and investors remain confident that cell therapies are poised to address significant unmet need in patients suffering from autoimmune disorders. However, the extent of this impact on the treatment landscape remains to be seen, as the industry rapidly approaches an inflection point.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Top 10 Best Ayurvedic Kidney Stone Syrups in India
Deciphering How Freund's Incomplete Adjuvant Activates Immune Cells.pdf
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Deciphering How Freund's Incomplete
Adjuvant Activates Immune Cells and
Pathways
Freund's incomplete adjuvant, a well-known immunological tool, plays a crucial role in
enhancing the immune response to antigens, thereby amplifying the effectiveness of
vaccines and immunotherapies. Understanding how Freund's incomplete adjuvant
activates immune cells and pathways provides insights into its mechanism of action and
its potential applications in various research and medical fields. In this article, we delve
into the intricate processes through which Freund's incomplete adjuvant stimulates
immune cells and orchestrates immune pathways for optimal immunogenicity.
Priming the Immune System
Freund's incomplete adjuvant, composed of mineral oil and emulsifying agents, serves
as a potent immune activator. When introduced alongside antigens, it triggers a
cascade of immune responses that collectively enhance the body's ability to recognize
and combat potential threats.
Activation of Antigen-Presenting Cells
One of the key roles of Freund's incomplete adjuvant is to activate antigen-presenting
cells (APCs) such as dendritic cells and macrophages. These cells recognize antigens,
internalize them, and present them to immune cells, initiating a coordinated immune
response.
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Enhancing T Cell Responses
Freund's incomplete adjuvant promotes the activation of T cells, a critical component of
adaptive immunity. Activated T cells initiate various immune responses, including
cytotoxic T cell responses that target infected or abnormal cells.
Induction of Humoral Immunity
The adjuvant's unique formulation stimulates B cells, leading to the production of
antibodies. This humoral immune response is crucial for neutralizing pathogens and
preventing infections.
Shift towards Cell-Mediated Immunity
Freund's incomplete adjuvant is known to skew the immune response towards cell-
mediated immunity. This type of immunity involves the activation of cytotoxic T cells,
which play a crucial role in combating intracellular infections and abnormal cells.
Inflammatory Response Activation
The adjuvant's introduction triggers a controlled inflammatory response at the injection
site. This inflammation attracts immune cells to the site, facilitating antigen uptake and
immune cell activation.
Cytokine Signaling
Freund's incomplete adjuvant promotes the release of cytokines, signaling molecules
that coordinate immune responses. These cytokines enhance immune cell
communication, recruitment, and activation.
Long-Term Immunological Memory
By activating immune pathways and cells, Freund's incomplete adjuvant contributes to
the establishment of immunological memory. This memory ensures that the immune
system can recognize and respond rapidly to the same antigen in the future.
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Applications in Research and Medicine
Understanding how Freund's incomplete adjuvant activates immune cells and pathways
has implications across various fields. It has been used in vaccine development,
immunotherapy research, and the study of immune responses in experimental models.
Freund's incomplete adjuvant serves as a potent activator of immune cells and
pathways, fostering a heightened immune response to antigens. By orchestrating a
cascade of immune events, it primes the body for robust protection against infections
and diseases. As researchers continue to unravel the complexities of immune activation
by this adjuvant, its potential applications in vaccines, therapies, and immune system
studies remain promising avenues for advancing both basic science and clinical
practice.
Exploring Different Versions of Freund's
Incomplete Adjuvant and Their Diverse Effects
Freund's incomplete adjuvant (FIA) has been a cornerstone in immunology research
and vaccine development for decades. This adjuvant, known for its ability to enhance
immune responses, comes in different versions, each tailored to produce specific
effects on the immune system. In this article, we delve into the various versions of
Freund's incomplete adjuvant and explore their distinct impacts on immune activation,
antibody production, and cellular responses.
Freund's Incomplete Adjuvant: A Brief Overview
Before delving into the different versions, let's recap the basics of Freund's incomplete
adjuvant. It's an oil-in-water emulsion composed of mineral oil and surfactants. It's a
well-established tool for enhancing the immunogenicity of antigens, making them more
effective in triggering immune responses.
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FIA Version 1- Immune Boosting and Antibody Production
FIA Version 1, also known as Complete Freund's Adjuvant (CFA), contains killed
Mycobacterium tuberculosis. It is a powerful immune stimulant that induces a robust
and persistent immune response. When used with antigens, it leads to strong antibody
production, especially of the IgG class. However, due to its potency, CFA is primarily
used in research settings and not in human vaccines due to potential adverse effects.
FIA Version 2 - Enhancing Cellular Immunity
FIA Version 2, or Incomplete Freund's Adjuvant (IFA), is devoid of Mycobacterium
tuberculosis. It focuses on enhancing cellular immunity, including the activation of T
cells. IFA is less potent than CFA, making it safer for use in experimental models and, in
some cases, veterinary vaccines. It stimulates milder inflammation while still boosting
immune responses.
Tailoring Immune Responses
The effects of different versions of Freund's incomplete adjuvant can be tailored based
on the specific goals of research or vaccine development. CFA's robust antibody
response is ideal for certain infectious diseases, while IFA's focus on cellular immunity
is more suitable for conditions where T cell responses are critical.
Use in Immunotherapy and Allergy Research
Both versions of Freund's incomplete adjuvant have found applications beyond
vaccines. They are used in immunotherapy research, including cancer immunotherapy,
where boosting immune responses against tumor antigens is crucial. They are also
employed in allergy research to study immune mechanisms and develop potential
treatments.
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Considerations and Caution
While Freund's incomplete adjuvant can greatly enhance immune responses, it's
important to note that its use requires careful consideration. The strong inflammation it
induces can lead to adverse effects in some cases, and its application should adhere to
ethical and safety guidelines.
Freund's incomplete adjuvant exists in multiple versions, each with distinct effects on
immune responses. From inducing robust antibody production to enhancing cellular
immunity, these versions play a pivotal role in research, vaccine development, and
immunotherapy. As we continue to explore the immunological landscape, the diverse
impacts of these adjuvants remain invaluable tools for understanding and manipulating
the immune system for beneficial outcomes.
Deciphering How Freund's Incomplete Adjuvant
Modulates Immunity
Freund's incomplete adjuvant (FIA) has long been recognized as a pivotal tool in
immunology research and vaccine development. Its ability to enhance immune
responses and amplify the effectiveness of antigens has made it a cornerstone in
understanding and modulating the immune system. In this article, we delve into the
intricate mechanisms through which Freund's incomplete adjuvant modulates immunity,
shedding light on its role in shaping immune responses for optimal protection against
diseases.
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Priming the Immune System
At the core of Freund's incomplete adjuvant modulation of immunity is its capacity to
prime the immune system. When introduced alongside antigens, it creates a localized
environment that stimulates a heightened immune response, allowing the body to
recognize and respond more effectively to potential threats.
Activation of Antigen-Presenting Cells
One of the key steps in modulating immunity is the activation of antigen-presenting cells
(APCs). Freund's incomplete adjuvant activates dendritic cells and macrophages,
prompting them to capture and process antigens. These activated APCs then present
antigens to other immune cells, initiating a coordinated immune response.
Inflammatory Microenvironment
The introduction of Freund's incomplete adjuvant triggers controlled inflammation at the
injection site. This inflammatory microenvironment recruits immune cells, enhances
antigen uptake, and fosters immune cell activation, thereby amplifying the overall
immune response.
Cytokine Signaling
Cytokines, signaling molecules that facilitate immune cell communication, play a crucial
role in modulating immunity. Freund's incomplete adjuvant stimulates the release of
various cytokines, which coordinate immune responses, attract immune cells to the site
of injection, and influence the nature of the immune reaction.
T Cell Activation
The modulation of immunity by Freund's incomplete adjuvant involves the activation of T
cells, a central component of adaptive immunity. Activated T cells play a pivotal role in
orchestrating immune responses, including the production of cytokines, the destruction
of infected cells, and the regulation of other immune cells.
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Enhanced Antibody Production
Another facet of immunity modulation involves Freund's incomplete adjuvant influence
on antibody production. The adjuvant stimulates B cells, leading to increased production
of antibodies. These antibodies recognize and neutralize pathogens, bolstering the
body's defense mechanisms.
Long-Term Immune Memory
A critical outcome of Freund's incomplete adjuvant's modulation of immunity is the
establishment of immunological memory. Immune cells exposed to the adjuvant develop
memory responses, ensuring a swift and effective reaction upon subsequent encounters
with the same antigen.
Tailoring Immune Responses:
Freund's incomplete adjuvant's ability to modulate immunity enables researchers and
vaccine developers to tailor immune responses. Depending on the type of immune
reaction desired—such as antibody production or cellular immunity—the adjuvant can
be strategically employed to achieve specific outcomes.
Freund's incomplete adjuvant's modulation of immunity offers a deeper understanding
of how the immune system can be harnessed for disease prevention and treatment. By
influencing immune cells, signaling molecules, and immune pathways, this adjuvant
contributes to a heightened and targeted immune response. As we continue to unveil
the intricacies of immune modulation, the potential applications of Freund's incomplete
adjuvant in vaccines, immunotherapies, and immunological research remain promising
avenues for advancing both scientific understanding and clinical practice.
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Exploring the Evolution and Initial Applications
of Freund's Incomplete Adjuvant
Freund's incomplete adjuvant (FIA) stands as a pioneering innovation in the field of
immunology, revolutionizing our approach to vaccine development and immune system
modulation. The journey of its development and early uses sheds light on the dynamic
interplay between scientific exploration and medical advancement. In this article, we
delve into the origins of Freund's incomplete adjuvant, its evolution, and its initial
applications that paved the way for modern immunological breakthroughs.
Genesis of Freund's Incomplete Adjuvant
The story of Freund's incomplete adjuvant begins in the early 20th century, when Dr.
Jules Freund and his colleagues at the College of Physicians and Surgeons of
Columbia University embarked on a quest to enhance the potency of vaccines. The goal
was to find a way to amplify immune responses to antigens, ultimately leading to more
effective disease prevention strategies.
Early Formulation and Discoveries
In their pursuit, Dr. Freund and his team formulated an emulsion containing mineral oil
and killed Mycobacterium tuberculosis, which was to become known as Complete
Freund's Adjuvant (CFA). The researchers observed that this formulation induced a
powerful immune response and heightened antibody production, making it a valuable
tool for immunology research.
Innovative Evolution
However, due to safety concerns associated with CFA, Freund's incomplete adjuvant
(IFA) was developed. IFA omitted the use of the bacterium and focused on emulsifying
agents and mineral oil. This new formulation still exhibited immune-stimulating
properties, albeit with a milder inflammatory response.
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Early Applications
Freund's incomplete adjuvant quickly found applications in various fields. Researchers
explored its potential in vaccine development, immunotherapy, and the study of immune
responses in experimental models. It enabled scientists to unlock new insights into
immune cell activation, antigen processing, and immune memory formation.
Foundation for Modern Immunology
The development and early uses of Freund's incomplete adjuvant laid the groundwork
for modern immunology research and vaccine development. These advancements
paved the way for our current understanding of immune responses, adjuvant
mechanisms, and the optimization of vaccine formulations.
Ethical Considerations
While Freund's incomplete adjuvant contributed significantly to scientific progress, its
early versions, particularly CFA, raised ethical concerns due to potential side effects. As
a result, its use in human vaccines and clinical settings was limited.
Continued Impact
The legacy of Freund's incomplete adjuvant lives on in the numerous discoveries and
breakthroughs it facilitated. It remains a vital tool in laboratories, enabling researchers to
unravel the complexities of immune activation and optimize vaccine formulations for
maximum efficacy.
Freund's incomplete adjuvant journey from its inception to early applications illustrates
the dynamic interplay between scientific ingenuity, medical innovation, and ethical
considerations. While the early versions posed challenges, they spurred the
development of safer and more effective adjuvants that continue to shape modern
immunology and contribute to our collective ability to combat diseases. The legacy of
Freund's incomplete adjuvant reminds us of the profound impact that dedicated
research and pioneering discoveries can have on advancing medical knowledge and
improving global health.