Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
innate immunity- first line of defence
physical barriers, cellular components, inflamation, anatomical barriers, skin, mucuos, mucous membranes.
for more refer to www.faunafondness.com
innate immunity- first line of defence
physical barriers, cellular components, inflamation, anatomical barriers, skin, mucuos, mucous membranes.
for more refer to www.faunafondness.com
Mechanisms of innate immunity in invertebrates (hemocytes)Abhijeet2509
Provides an overview of the mechanism of innate immunity in invertebrates, particularly insects. Types of hemocytes present in insects and their roles in innate immunity.
This slide covers briefly how intracellular and extracellular bacteria elicits an immune response, how bacteria evade from the immune system, what complement system is, opsonization, neutralisation, septic shock, sepsis, superantigens, phagocytosis, interleukins, Toll-like receptors, a list of diseases caused by bacterias and their names etc.
Mechanisms of innate immunity in invertebrates (hemocytes)Abhijeet2509
Provides an overview of the mechanism of innate immunity in invertebrates, particularly insects. Types of hemocytes present in insects and their roles in innate immunity.
This slide covers briefly how intracellular and extracellular bacteria elicits an immune response, how bacteria evade from the immune system, what complement system is, opsonization, neutralisation, septic shock, sepsis, superantigens, phagocytosis, interleukins, Toll-like receptors, a list of diseases caused by bacterias and their names etc.
As a periodontist, I have included the basics of immunity from the periodontist point of view that will help in understanding the immunological basis of periodontal disease...
Toll-like receptors (TLRs) are a class of proteins that play a key role in the innate immune system. They are single-spanning receptors usually expressed on sentinel cells such as macrophages and that recognize structurally conserved molecules derived from microbes. TLRs are pattern recognition receptors (PRRs) that recognize pathogen-associated molecular patterns (PAMPs) and damage-associated molecular patterns (DAMPs). PAMPs are molecular structures associated with pathogens, such as bacteria, viruses, and fungi, that are recognized by the innate immune system. DAMPs are molecules that are released into the extracellular space when cells are injured or damaged. TLRs play a crucial role in the recognition of PAMPs and DAMPs and the initiation of immune responses, such as the production of pro-inflammatory cytokines, type I interferons, and other molecules that enhance the immune response. TLRs are a bridge between the innate and adaptive immune systems by regulating the activation of antigen-presenting cells and key cytokines. Upon recognition of their specific ligands, TLRs initiate downstream signaling cascades, leading to the production of pro-inflammatory and antiviral factors and the upregulation of co-stimulatory molecules, promoting the maturation of antigen-presenting cells and linking innate immunity to adaptive immunity. TLRs are widely distributed in both immune and other body cells and are a critical target for the development of immunotherapies and vaccines. Further research is needed to fully understand the .mechanisms underlying TLR signaling and its potential applications in the field of immunology.Toll-like receptors (TLRs) are a bridge between the innate and adaptive immune systems. TLRs are expressed on all innate immune cells and a large majority of non-hematopoietic cells, such as macrophages, neutrophils, dendritic cells, natural killer cells, mast cells, basophils, eosinophils, and epithelial cells. Importantly, TLRs can also be detected on adaptive immune cells, including T and B cells. Adaptive immunity consists of humoral immunity and cell-mediated immunity, which are mainly mediated by B lymphocytes and T lymphocytes, respectively. TLRs critically link innate immunity to adaptive immunity by regulating the activation of antigen-presenting cells and key cytokines. Upon recognition of pathogen-associated molecular patterns (PAMPs) or damage-associated molecular patterns (DAMPs) by TLRs, downstream signaling cascades are initiated, leading to the production of pro-inflammatory cytokines, such as IL-6 and INF-α, and the upregulation of co-stimulatory molecules, promoting the maturation of antigen-presenting cells and linking innate immunity to adaptive immunity. TLR signaling is also being studied for its direct regulatory roles in effector T cells and regulatory T cells, as well as its involvement in various diseases, including infectious diseases, autoimmune conditions, and cancer.
This presentation answers the following questions!!
How Immune Cells communicate with each other?
Receptors of Immune System?
Receptors of Innate Immune System?
What are PRRS?
What are PAMPS?
What are DAMPS?
What is the structure of PRRS?
What is the mechanism of PRRS?
What are the types of PRRS?
What is the role of PRRS in Immunology?
Immunity is the ability of the body to defend itself against disease-causing organisms.
The immune system refers to a collection of cells, chemicals and processes that function to protect the body from foreign antigens, such as microbes (organisms, such as bacteria, fungi, and parasites), viruses, cancer cells, and toxins.
The structural and chemical barriers which protect us from infection, the immune system can be classified into two “lines of defense”: innate immunity and adaptive immunity
Book Chapter published at may 2021
From the Edited Volume "Innate Immunity in Health and Disease" by Prof. Shailendra K. Saxena
Via IntechOpen
DOI: http://dx.doi.org/10.5772/intechopen.97502
A brief covering basics of immunity understanding and also allowing students to understand with ease the concepts of innate immunity, adaptive immunity, Tcell, Bcell, MHC molecular genetics, and also cytokines and also its role in various disease.
Similar to Evaluation and importance of innate & adaptive immunity Dr. ihsan edan abdulkareem alsaimary (20)
2021 laboratory diagnosis of infectious diseases dr.ihsan alsaimarydr.Ihsan alsaimary
2021 laboratory diagnosis of infectious diseases
dr. ihsan alsaimary
university of basrah - college of medicine- DEPARTMENT OF MICROBIOLOGY
POBOX 696 ASHAR
BASRAH 42001
IRAQ
Src jbbr-21-125 Dr. ihsan edan abdulkareem alsaimary PROFESSOR IN MEDICAL M...dr.Ihsan alsaimary
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Src jbbr-20-120 Dr. ihsan edan abdulkareem alsaimary PROFESSOR IN MEDICAL M...dr.Ihsan alsaimary
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Doi10.18535ijmsciv7i11.06 Dr. ihsan edan abdulkareem alsaimary PROFESSOR I...dr.Ihsan alsaimary
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Assessment of immunomolecular_expression_and_prognostic_role_of_tlr7_among_pa...dr.Ihsan alsaimary
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Estimation of Dr. ihsan edan abdulkareem alsaimary PROFESSOR IN MEDICAL MICR...dr.Ihsan alsaimary
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Tolerance & autoimmunity and organ specific autoimmune diseasesdr.Ihsan alsaimary
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Pathogenesis of microbial infections dr. ihsan alsaimarydr.Ihsan alsaimary
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Dr. ihsan edan abdulkareem alsaimary
PROFESSOR IN MEDICAL MICROBIOLOGY AND MOLECULAR IMMUNOLOGY
ihsanalsaimary@gmail.com
mobile : 009647801410838
university of basrah - college of medicine - basrah -IRAQ
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
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The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
These lecture slides, by Dr Sidra Arshad, offer a quick overview of 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 leads (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
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. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
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Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
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New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
2.
Protection from foreign macromolecules or invading
organisms (viruses, bacteria, protozoa or even larger
parasites).
Tumor immunity
Against our own aberrant cells.
Autoimmunity
immune responses against our own proteins.
The Immune System
5.
INNATE IMMUNITY:
Defense mechanisms used by the host immediately after
encountering a foreign ligand
Composed of hereditary components that provide an
immediate "first-line" of defense to continuously protect
against pathogens.
ADAPTIVE (ACQUIRED) IMMUNITY:
The body can develop a specific immunity Humoral or
cell-mediated to target particular pathogens.
This response takes days to develop, and so is not
effective at preventing an initial invasion, but it will
normally prevent any subsequent infection, and also
aids in clearing up longer-lasting infections.
Immune system
6. INNATE: Two Intrinsic
Defense
Systems
Non specific and consists of:
A. EXTERNAL (SURFACE) DEFENSES -FIRST LINE OF
DEFENSE:
prevent entry of microorganisms
(1) Skin
(2) Mucosa
And their secretions
B. INTERNAL DEFENSES -SECOND LINE OF DEFENSE:
(1) Biochemical factors e.g. C, cytokines
(2) Cells, phagocytes, and other cells
Inhibit spread of invaders throughout the body
Inflammation is its hallmark and most important mechanism
8.
Activated by three pathways:
1) Classical pathway: stimulated by antigen antibody
complex.
2) Alternative pathway: stimulated by polysaccharides
of microbial cell walls.
3) Lectin pathway: by the binding of the microbial
carbohydrates with mannose binding lectin (MBL).
1. The Complement system
10.
On the organism:
Pathogen associated molecular patterns (PAMPS),
On the effector cells:
Pattern recognition receptors
(PRR).
Identification Of The Invader
2. Toll-like receptors (TLR)
11.
Toll-like receptors (TLRs) are transmembrane
proteins that serve as a key part of the innate
immune system considered pattern recognition
receptors (PRRs), binding to pathogen-associated
molecular patterns (PAMPs). Their function is the
recognition of pathogens and the activation of
immune responses directed against those pathogens.
2. Toll-like receptors (TLR)
12. PAMPS recognized by the innate immune system:
Cell wall constituents or microbial nucleic acids
1. Lipopolysaccharide (LPS) from the gram -ve cell wall.
2. Peptidoglycan found abundantly in the gram-positive cell wall and to a
lesser degree in the gram-negative cell wall .
3. Lipoteichoic acids in the gram +ve bacterial cell walls
4. Lipoarabinomannum (LAM) in mycobacterial wall
5. Mannose-rich glycans (common in microbial glycoproteins and
glycolipids but rare in those of humans).
6. Flagellin found in bacterial flagella.
7. Pilin from bacterial pili.
8. Bacterial and viral nucleic acid. Bacterial and viral genomes contain a
high frequency of unmethylated cytosine-guanine dinucleotide
sequences (a cytosine lacking a methyl or CH3 group and located
adjacent to a guanine). Mammalian DNA has a low frequency of
cytosine-guanine dinucleotides and most are methylated.
9. Double-stranded RNA unique to most viruses.
10. Lipoteichoic acids, glycolipids, and zymosan from yeast cell walls.
PAMPS
13.
To recognize microbial molecules,
various body defense cells have on
their surface a variety of receptors
called
Pattern-recognition Receptors
capable of binding specifically to
PAMPS
Pattern-recognition Receptors (PRR)
15.
Found on the surface of phagocytes and
promote the attachment of microorganisms
to phagocytes and their subsequent
engulfment and destruction.
ENDOCYTIC PRR
16.
Binding of microbial molecules to the
receptor promotes the synthesis and
secretion of intracellular regulatory
molecules such as cytokines that is crucial
to initiating innate immunity and adaptive
immunity.
1. Toll-like receptors
2. CD14.
3. NOD (nucleotide-binding oligomerization
domain proteins)
Signaling PRR
17.
Secreted pattern-recognition receptors. These
bind to microbial cell walls and enable them to
be recognized by the complement pathways
and phagocytes.
E.g. mannose-binding lectin is synthesized by
the liver and released into the bloodstream. MBL
recognizes carbohydrate patterns, found on the
surface of a large number of pathogenic micro-
organisms, including bacteria, viruses, protozoa
and fungi.
Secreted PRR
18. Classes of PRRs
four different classes of PRR
families have been identified :
Toll-like receptors(TLRs)
C-type lectin receptors (CLRs)
RIG-I-like receptors (RLRs)
NOD-like receptors (NLRs).
19.
TLRs belong to the IL-1 receptor family.
Linked to a signaling pathway that involves the
IL-1 receptor-associated kinase-4 (IRAK-4)
transcription NF-κB .
Upon binding of the extracellular ligand
recognition domain to PAMPs, changes in the
intracellular domain result in initiation of
signaling events leading to
Inflammatory responses and/or
Release of antimicrobial agents.
2. Toll like receptors (TLR(
20.
TLRs are found both on the surface and within the
phagolysosomes of phagocytes.
21. ROLE IN INNATE IMMUNITY
1.The binding of a microbial molecule to its TLR
transmits a signal to the cell's nucleus inducing the
expression of genes coding for the synthesis of
cytokines. Many of the TLRs, especially those that bind
to BACTERIAL AND FUNGAL cell wall components
stimulate IL -1, TNF-alpha, and IL-8. triggering innate
immune defenses such as inflammation, fever, and
phagocytosis in order to provide an immediate
response against the invading microorganism.
2.Most of the TLRs that bind to VIRAL components
trigger the synthesis of interferons via activation of
interferon regulatory factor 3 (IRF-3) that block viral
replication within infected host cells..
2. Toll like receptors (TLR(
22.
TLR Responding to Lipopolysaccharide (LPS)
from the Gram-Negative Cell Wall
23. TLRstrigger various secondary signals needed for
- Humoral immunity (the production of antibodies).
- Cell-mediated immunity (the production of cytotoxic T-
lymphocytes and additional cytokines).
Dendritic cells express several types of TLRs. Upon activation
of these receptors by microbial components, the dendritic cells
mature and migrate to the lymph nodes, where they present
pathogen-derived antigens to
naive T cells differentiate into TH-1, TH-2 or T-reg
TLRs thereby bridge the gap between the innate and adaptive
immune systems
Without innate immune responses there could be no adaptive
immunity.
2. Toll like receptors (TLR(
ROLE IN ADAPTIVE IMMUNITY
24.
1. Human β-defensin hBD 1-4 attract immature dendritic
cells and memory T cells via the chemokine receptor
(CCR)-6
2. Antileukoproteases (ALP)
3. Dramcidin (DCD)-1 (SWEAT GLANDS)
4. Lysosyme
5. Psoriasin (SEBOCYTES) prevents E. coli infection
6. RNase7 (ribonucleotidase)
7. LL-37 A.K.A Cathelicidin antimicrobial peptide
(CAMP)/hCAP18 (UROGENITAL TRACT) mediates
dendritic cell activation in psoriasis
3. Antimicrobial peptides (AMPs)
26. FAMILIES OF CYTOKINES:
1.Interleukins (ILs): (interaction bet. leukocytes), Cytokines produced by
leukocytes and exert effects preferentially on other WBCs.
2.Interferons )IFNs): interfere with viral replication.
3.Tumor necrosis factor (TNF(
4.CSFs (Colony stimulating factors) induce differentiation and
proliferation of hematopoietic progenitor cells.
5.Chemokines: Cytokines that have chemoattractant activity, and
they play a crucial role in leukocyte migration.
6.Inflammatory chemokines: Chemokines that recruit leukocytes.
7.Lymphoid chemokines: Chemokines that regulate trafficking within
lymphoid tissues.
4. Cytokines
28. CYTOKINES OF THE INNATE IMMUNE SYSTEM
Mainly cytokines with
1.Inflammatory capacity (e.g. IL-1, IL-6, IL-18, tumor necrosis factor-α
[TNF-α], inflammatory chemokines)
2.Antiviral capacity (e.g. IFN-α, IFN-β(.
CYTOKINES OF THE ADAPTIVE IMMUNITY:
Dependent on cytokineswith
Immunomodulatory capacities (e.g. IL-2, IL-4, IL-12, IL-13, IL-17, IL-
22, IL-23, IFN-γ(.
However, since most of these mediators exhibit multiple and
sometimes overlapping activities, a strict separation into
inflammatory and immunomodulatory cytokines is not possible.
4. Cytokines
29.
Phagocytic cells derived from blood-borne monocytes.
Expresses PRR to identify organisms.
Receptors for antibodies and complement that enhances
phagocytosis.
Destroy the organisms by toxic intracellular molecules as:
superoxide anions, hydroxyl radicals, nitrous oxide,
lysozyme.
Antigen presenting capacity present processed antigens to
T and B cells. (much less than Langerhans cells)
Releases G-CSF, & GM-CSF that stimulate the division
and release of neutrophils from the bone marrow.
5. Macrophages
30.
They enter the blood stream to enter the site of infection
through the complex effect of proinflammatory mediators, G-
CSF, GM-CSF, adhesion molecules chemoattractants and
chemokines
Phagocytosis is enhanced by coating the organism by
antibodies and complement that bind to their receptors on the
neutrophils
kills the organisms within phagolysosomes by:
a) Oxygen dependent mechanisms (e.g. H2O2 and hydroxyl
radicals)
b) Oxygen independent mechanisms (e.g. lysozyme).
6. Neutrophils
31.
Major function protective against parasites.
Weak phagocytic activity.
Important in allergic reactions.
IgE antibodies coat the parasite eosinophils bind to IgE
antibodies and become activated Release toxic substances
to the parasite as:
Major basic protein
Eosinophilic cationic protein,
Eosinophil peroxidase
Eosinophil-derived neurotoxin,
which can kill parasites, together with prostaglandins,
leukotrienes and various cytokines
7. Eosinophils
32.
Basophil in the blood and mast cell in the tissues have
similar functional and morphologic characteristics.
Both express high-affinity receptors for IgE (FcεRI)
Two populations of mast cells
1. Mucosal mast cells: contain only trypsin,
2. Connective tissue mast: cells contain both trypsin an
chymotrypsin
Mast cells are involved in TLR-mediated responses against
Gram-negative bacteria.
8. Basophils & mast cells
33.
When a specific antigen binds to mast cell-bound IgE, the
FcεRI becomes activated, which leads to degranulation and
release of preformed mediators, including:
1. Histamine
2. Serotonin.
3. Prostaglandins
4. Leukotrienes (B4, C4, D4 and E4),
5. Platelet activating factor
They enhance
i. vascular permeability
ii. bronchoconstriction
iii. induction of an inflammatory response
Thus both play an important role in immediate allergic
reaction, urticaria and angioedema.
Only cutaneous mast cells express receptors for the
anaphylatoxin C5 a so when activated by binding antigen
specific antibodies only a local reaction occur in the skin, but
8. Basophils & mast cells
34.
• It’s major task to identify and eliminate virally
infected or malignant cells.
• Pattern recognition receptors (TLR 3,9)
• NK cells can recognize their targets in two
ways:
1. Adhere and kill target cells coated with IgG as they carry
receptors for it (antibody dependent cellular cytotoxicity
ADCC).
2. Activation of killer activating receptors that recognize
the abnormal cells and kills them by secreting perforin
and injecting granzyme that kills the cells by inducing
apoptosis.
9. Natural killer cells
35.
10. Inflammation
The inflammatory response is triggered whenever
body tissues are injured, infected or irritated.
physical barrier against the spread of infection
Prevents the spread of damaging agents to nearby
tissues
Disposes of cell debris and pathogens
Sets the stage for repair processes promote healing of
any damaged tissue following the clearance of
pathogens
The 5 cardinal signs of acute inflammation are
redness, heat, swelling, tenderness and pain
37. 3
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Chapter 21, Immune
System
The adaptive immune system is antigen-specific,
systemic, and has memory
It has two separate but overlapping arms
Humoral, or antibody-mediated (B Cell) immunity
Cellular, or cell-mediated (T Cell) immunity
Adaptive Immune Defenses
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System
Important functional properties:
Immunogenicity – the ability to stimulate
proliferation of specific lymphocytes and antibody
production
Reactivity – the ability to react with the products of
the activated lymphocytes and the antibodies
released in response to them
Complete antigens include foreign protein, nucleic
acid, some lipids, and large polysaccharides
Complete Antigens
39. 3
9
Chapter 21, Immune
System
Small molecules, such as peptides, nucleotides, and
many hormones,
not immunogenic (does not stimulate a response)
reactive when attached to protein carriers
If they link up with the body’s proteins, the adaptive
immune system may recognize them as foreign and
mount a harmful attack (allergy)
Haptens are found in poison ivy, dander, some
detergents, and cosmetics
Haptens (Incomplete Antigens)
40. have little or no immunogenicity 38
Chapter 21, Immune
System
Only certain parts of an entire antigen are
immunogenic
Antibodies and activated lymphocytes bind to these
antigenic determinants
Most naturally occurring antigens have numerous
antigenic determinants that:
Mobilize several different lymphocyte populations
Form different kinds of antibodies against it
Large, chemically simple molecules (e.g., plastics)
Antigenic Determinants
41. 4
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Chapter 21, Immune
System
Our cells are dotted with protein molecules (self-
antigens) that are not antigenic to us but are strongly
antigenic to others (reason for transplant rejection)
One type of these, MHC proteins, mark a cell as self
The two classes of MHC proteins are:
Class I MHC proteins – found on virtually all body
cells
Class II MHC proteins – found on certain cells in
the immune response
Self-Antigens: MHC Proteins
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Chapter 21, Immune
System
Two types of lymphocytes
B lymphocytes – oversee humoral immunity
T lymphocytes – non-antibody-producing cells that
constitute the cell-mediated arm of immunity
Antigen-presenting cells (APCs):
Do not respond to specific antigens
Play essential auxiliary roles in immunity
Cells of the Adaptive Immune System
43. 4
3
Chapter 21, Immune
System
T cells mature in the thymus under negative and
positive selection pressures
Negative selection – eliminates T cells that are
strongly anti-self
Positive selection – selects T cells with a weak
response to self-antigens, which thus become both
immunocompetent and self-tolerant
T Cells
44. 4
4
Chapter 21, Immune
System
B cells become immunocompetent and self-tolerant
in bone marrow
Some self-reactive B cells are inactivated (anergy)
while others are killed
Other B cells undergo receptor editing in which
there is a rearrangement of their receptors
B Cells
45. 4
5
Chapter 21, Immune
System
Major roles in immunity are:
To engulf foreign particles
To present fragments of antigens on their own
surfaces, to be recognized by T cells
Major APCs are dendritic cells (DCs), macrophages,
and activated B cells
The major initiators of adaptive immunity are DCs,
which actively migrate to the lymph nodes and
secondary lymphoid organs and present antigens to
T and B cells
Antigen-Presenting Cells (APCs)
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Chapter 21, Immune
System
Secrete soluble proteins that activate T cells
Activated T cells in turn release chemicals that:
Rev up the maturation and mobilization of DCs
Prod macrophages to become activated
macrophages, which are insatiable phagocytes that
secrete bactericidal chemicals
Macrophages and Dendritic Cells
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Chapter 21, Immune
System
Antigen challenge – first encounter between an
antigen and a naive immunocompetent cell
Takes place in the spleen or other lymphoid organ
If the lymphocyte is a B cell:
The challenging antigen provokes a humoral
immune response
Antibodies are produced against the challenger
Humoral Immunity Response
49. 4
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Chapter 21, Immune
System
Primary immune response – cellular differentiation
and proliferation, which occurs on the first exposure
to a specific antigen
Lag period: 3 to 6 days after antigen challenge
Peak levels of plasma antibody are achieved in 10
days
Antibody levels then decline
Immunological Memory
50. 5
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Chapter 21, Immune
System
Secondary immune response – re-exposure to the
same antigen
Sensitized memory cells respond within hours
Antibody levels peak in 2 to 3 days at much higher
levels than in the primary response
Antibodies bind with greater affinity, and their
levels in the blood can remain high for weeks to
months
Immunological Memory
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Chapter 21, Immune
System
Differs from active immunity in the antibody source
and the degree of protection
B cells are not challenged by antigens
Immunological memory does not occur
Protection ends when antigens naturally degrade in
the body
Naturally acquired – from the mother to her fetus via
the placenta
Artificially acquired – from the injection of serum,
such as gamma globulin
Passive Humoral Immunity
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Chapter 21, Immune
System
Commercially prepared antibodies are used:
To provide passive immunity
In research, clinical testing, and treatment of certain
cancers
Monoclonal antibodies are pure antibody
preparations
Specific for a single antigenic determinant
Produced from descendents of a single cell
Monoclonal Antibodies
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Chapter 21, Immune
System
Hybridomas – cell hybrids made from a fusion of a
tumor cell and a B cell
Have desirable properties of both parent cells –
indefinite proliferation as well as the ability to
produce a single type of antibody
Monoclonal Antibodies
55. 5
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Chapter 21, Immune
System
Since antibodies are useless against intracellular antigens,
cell-mediated immunity is needed
Two major populations of T cells mediate cellular immunity
CD4 cells (T4 cells) are primarily helper T cells (TH)
CD8 cells (T8 cells) are cytotoxic T cells (TC) that destroy
cells harboring foreign antigens
Other types of T cells are:
Suppressor T cells (TS)
Memory T cells
Cell-Mediated Immune Response
57. 5
7
Chapter 21, Immune
System
Soluble antibodies
The simplest ammunition of the immune response
Interact in extracellular environments such as body
secretions, tissue fluid, blood, and lymph
Importance of Humoral Response
58. 5
8
Chapter 21, Immune
System
T cells recognize and respond only to processed
fragments of antigen displayed on the surface of
body cells
T cells are best suited for cell-to-cell interactions,
and target:
Cells infected with viruses, bacteria, or intracellular
parasites
Abnormal or cancerous cells
Cells of infused or transplanted foreign tissue
Importance of Cellular Response
59. 5
9
Chapter 21, Immune
System
Immunocompetent T cells are activated when the V
regions of their surface receptors bind to a
recognized antigen
T cells must simultaneously recognize:
Nonself (the antigen)
Self (a MHC protein of a body cell)
Antigen Recognition and MHC
Restriction
60. 6
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Chapter 21, Immune
System
Endogenous antigens are:
Degraded by proteases and enter the endoplasmic
reticulum
Transported via TAP (transporter associated with
antigen processing)
Loaded onto class I MHC molecules
Displayed on the cell surface in association with a
class I MHC molecule
Class I MHC Proteins
62. 6
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Chapter 21, Immune
System
Class II MHC proteins are found only on mature B
cells, some T cells, and antigen-presenting cells
A phagosome containing pathogens (with exogenous
antigens) merges with a lysosome
Invariant protein prevents class II MHC proteins
from binding to peptides in the endoplasmic
reticulum
Class II MHC Proteins
63. Class II MHC Proteins
Figu8re621.15b
Chapter 21, Immune System
64. Regulatory cells that play a central role in the
adaptive immune response
Once primed by APC presentation of antigen, they:
Chemically or directly stimulate proliferation of
other T cells
Stimulate B cells that have already become bound
to antigen
Without TH,there is no immuneresponse
64
Chapter 21, Immune
System
Helper T Cells (TH
66. TCcells, or killer T cells, are the only T cells that can directly
attack and kill other cells
They circulate throughout the body in search of body cells
that display the antigen to which they have been sensitized
Their targets include:
Virus-infected cells
Cells with intracellular bacteria or parasites
Cancer cells
Foreign cells from blood transfusions or transplants
66
Chapter 21, Immune
System
Cytotoxic T Cell (Tc
67. In some cases, TCcells:
Bind to the target cell and release perforin into its
membrane
In the presence of Ca2+perforin causes cell lysis
by creating transmembrane pores
Other TC cells induce cell death by:
Secreting lymphotoxin, which fragments the target
cell’s DNA
Secreting gamma interferon, which stimulates
phagocytosis by macrophages
67
Chapter 21, Immune
System
Mechanisms of Tc Action
68. Mechanisms of Tc Action
107
Chapter 21, Immune System
Figure 21.18a, b
69. Summary of the Primary Immune Response
Fig10u9re21.19
Chapter 21, Immune System
70. • Molecular markers of innate immunity and
inflammation in therapeutic intervention
71. TLRs in cancer and anti-cancer
immunotherapy
The TLR3 has been shown to be receptor for
viral dsRNA, and also seems to be potentially
promising in anti-cancer therapy. Reports have
shown that cancer cells themselves express
TLR3 in vivo
and agonist ploy (I:C) is activating the signalling
pathway leading to the anticancer effects (O'Neill
et al., 2011)
72. NF-κB and cancer therapy
NF-kB regulates the expression of genes involved
in many processes that play a key role in the
development and progression of cancer such as
proliferation, migration and apoptosis.
constitutive NF-kB activation has been
detected in many human malignancies.
some anti-inflammatory drugs may inhibit NF-kB
by interfering with IKK activity.
73. Tumor necrosis factor(TNF) as
therapeutic target
In patients with meningococcal meningitis serum levels
of TNF-α have been shown to correlate with
mortality(Arditi,1990) , but other authors have failed to
show significant increases in TNF-α in septic
patients(Casey,1993).
In a rodent model, mortality after an injection of
endotoxin was signifantly decreased by pre-treatment
with TNF-a antibodies.(Beutler,1987)
the antibody approach has produced little
evidence of benefit in man although
improvements in the haemodynamics of patients
have been observed.(Exley,1990)