MicroBIO-Immunology – Flashcards
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Organs of the immune system -Bone Marrow -Thymus |
Residence |
Organs of the immune system -Lymph Nodes -Peyer's Patches -Spleen ; |
Circulation |
Organs of the immune system -Lymphatic Vessels -Blood Vessels |
Self-Renewal |
Abilitly of a stem cell to go through numerous cell divisions while maintaing the undifferentiated state |
Potency (specializing) |
capacity of the stem cell to differentiate into specialized cell types |
Totipotent |
embryonic stem cells are produced from the fusion of an egg and sperm cell and can produce a complete organism |
Pluripotent |
Both embryonic and adult stem cells are the descendants of totipotents cells and can differentiate into cells of any tissue |
Mulitpotent |
Adult stem cells can produce only cells of a closely related family of cells (lineage-restricted) |
A Skin B Neurons C Blood D Liver |
Pluripotent depends on signal, growth under diff. conditions: A. B. C. D. |
Multipotent HSC |
____---->differentiate----> Only specialized types of blood cells; -red blood cells -white blood cells -platelets |
Hematopoisesis |
Mechanism that ensures that continous and regulated replacement of blood cells
-generated in bone marrow |
Primitive Hematopoiesis |
-transient program -begins in early embryogenesis (first 8 weeks) |
Definitive Hematopoiesis |
-what we see in adults -begins during fetal life (placenta) -expands in the fetal liver and spleen -establishes in the bone marrow in the late fetus and remains at this site for life |
HSC |
____are multipotent stem cells that give rise to all cells of the immune system
-found in the bone marrow of adults (femurs, hips, ribs, sternum) |
- Self Renewal - Potency - Exist in small numbers - Relies on cell surface markers for identification |
What are some properties of HSC? |
Common Lymphoid and Common Myeloid Progenitors (CLP and CMP) |
Same as stem cells because have capacity to differentiate into a specific type of cell
Different then stem cells because pushed to differentiate into their "target" cell and are in the "center" between stem cells and fully differentiated cell |
T Cells B Cells NK Cells |
The 3 types of lymphocytes that are dervied from CLP? (part of lymphopoiesis) |
-Dendritic Cells -Monocytes/Macrophages -Granulocytes (neutrophils, eosinophils, and basophils) -Mast Cells |
CMP during myelopoiesis give rise to what? |
T Cell B Cell |
What are the 2 adaptive cells? |
NK Cell Immature Dendritic Cell Macrophage Granulocytes (neutrophils, basophils, eosinophil, mast cell, monocytes) |
What are the innate cells? |
The Immune System |
- Distinguishes between self and non-self and protects us from our hostile environment
-Detects and eliminates w/ great selectivity a large variety of immune challenges
-Memorizes previous challenges and increases defense to pathogens- function (goal of vaccine)
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phylogenetically |
origin of innate immunity |
Innate Immunity |
-non-specific -occurs w/in hours -recognition of motif patterns -limited # of specialties |
Adaptive Immunity |
-Specific -Develops after days -Recognition of structural details -Large # of specificities |
What is innate Immunity? |
-Referes to the basic resistance to infection that an individual possesses by virtue of his/her birth
(potential pathogens are encountered routinely, but rarely cause disease. the vast majority of microorganisms are destroyed within minutes or hours by innate defenses) |
Eyes |
a barrier of innnate immunity-tearss wash out pathogens and also contain an enzyme that can kill bacteria |
Skin |
barrier of innate immunity- the outer layer of skin is dead and difficult for pathogens to grow on or penetrate. Cuts allow pathogens to gain entry to body |
Stomach |
Barrier of innate immunity- Acid helps to sterilize food |
Large Intestine |
Barrier of innate immunity- Friendly bacteria help to stop the growth of harmful pathogens. Feces contail over 30% live bacteria |
Reproductive System |
Barrier of innate immunity- slightly acidic conditions in the vagina and urethra help to stop the growth of pathogens |
Lungs |
Barrier of innate immunity- Mucus in the lungs trap bacteria and fungal spores. Tiny hairs, called cilia, move the mucus to the back of the throat where it is swallowed |
Mouth |
Barrier of innate immunity- Friendly bacteria help to prevent the growth of harmful pathogens. Saliva cleans and removes bacteria |
Nose |
Barrier of innate immunity- Mucus traps pathogens, which are then swallowed or blown out in coughs and sneezes |
Anatomic Barriers |
Skin (largest organ protecting oneself) and Mucus (cilia, tears, saliva, sneezing) |
Physiological Barriers |
1. Temp- normal body temp. inhibits the growht of some pathogens
2. Fever- inhibits growth of pathogens by elevating body's temp
3. pH- Acidity of stomach content kills most ingested microorganisms (gastric juice) |
Chemical Barriers |
-both skin and mucous membranes are protected by variety of antimibrobial substances including:
1. Lysozyme- degrade peptidoglycans of bacterial cell wall -tears mucous secretions
2. Lactoferm- sequesters iron from microorganisms -saliva, phagoctyes, blood and tissue fluids
3. Defensins- damage cell membrane of microbes -mucous membranes (skin, small intestines, and respiratory tract) |
Microflora Barrier |
-Populationof microorganisms found on the body surface of healthy indivduals is called microbiota- healthy bacteria
-Friendly microorganisms protect through Competivite Exclusion (space and nutrients) |
Inflammatory Barrier |
Attracts Phagocytes -Tissue damage, caused by a wound or by an invading pathogen microorganism, induces a complex sequence of events, known as inflammatory response 3 major events of inflammatory response are: 1. Vasodilation- (red) due to chemical release 2. Increase in capillary permeability 3. Influx of phagocytes from the blood into the tissues
(redness comes due to eradication-as a defense) |
Which cells are components of innate immune defense? |
•Innate immune system includes A. NK cells B. Dendritic cells C. Macrophages D. Granulocytes •Generated in the bone marrow •Found in the blood, spleen and lymph nodes, liver, lung, intestine |
How soon after infection is the innate immune response triggered? |
9-96 hours |
Natural Killer Cells (NK) |
-attack unhealthy cells (infected) -Large granular lymphocytes -specialized in killing -develop in the bone marrow - dervie from CLP and HSC -major surface markers are NK1.1 and NKp46 -found in spleen, blood, liver, lymph nodes -exist in small numbers in lymphoid organs |
Killing tumor and infected cells |
What is the major function of NK cells? |
1. Recognition of infected cells 2. Release of perforins and granzymes 3. Induction of cell death "apoptosis" |
What do NK cells do? (3 steps) |
Dendritic Cells (DC) |
-cells with several denrites - specialized in ANTIGEN PRESENTATION -develop in the bone marrow - derive from CMP and HSC -major surface markers are CD11c & MHC class II -exist in small numbers in lymphoid organs |
sampling and presenting antigens to T-Lymphocytes |
What is the major function of Dendritic cells? |
it involves degrading pathogens into small pieces than presentation of antigens by MHC molecules |
What is the mechanism involved in Dendritic Cells? |
TRUE |
TRUE or FALSE: Dendritic cell is the most potent of all the antigen-presenting cells |
Macrophages |
-Big Eaters -special in Phagocytosis -develop in the bone marrow -dervie from HSC-CMP-GMP-monocytes -major surface markers are CD11b & MHC Class II -exist in small number in lymphoid organs -can present Antigen presentation -mainly in lymph nodes |
1. in the liver 2. in the lungs 3. in connective tissues 4. in the bones 5. in the kidney 6. in the brain |
mononuclear cells: macrophages are dispersed throughout the body and are named according to their tissue location: 1. Kupffer cells-? 2. Alveolar Macrophages- ? 3. Histiocytes- ? 4. Osteoclasts- ? 5. Messanglal cells- ? 6. Macroglial cells- ? |
Major function: to engulf and digest cellular debris and pathogens= phagocytosis
-processing and presentation of antigens to T-Lymphoctyes |
What are the functions of Macrophages? |
Granulocytes |
-characterized by presence of granules in cytoplasm -called Polymorphonuclear Leukocytes (PMN or PML)= nuclear lobed into three segments 3. derived from HSC-CMP-GMP 4. 3 types: Neutrophils, Eosinophils, Basophils |
Neutrophils: -Predominant in acute inflammation - 50-70% of circulating whitle blood cells
Eosinophils: -Associated with allergic inflammation and parasitic infection - found predominantly in tissues rather than bloodstream
Basophils: -Associated with anaphylactic allergy -found in blood or in tissues (as Mast Cells) |
What are Neutrophils?
What are Eosinophils?
What are Basophils? |
- it is the release of anti-mibrobial molecules from secretory vesicules "granules" |
Macrophages=Granulation
What is Granulation? |
through Cytokines (which are messengers=secreted proteins) |
How do cells communicate? |
1. Bind to a specific cell-surface receptor & then signaling takes place, which alters cell functions: -increasing the # of surface receptors for other molecules - suppressing their own effect by feedback inhibition - results in production of other cytokines
2. cytokines can share similar functions: Redundant
3. Are pleiotopic- diff. cell types to secrete the same cytokine or for single cytokine to act on several diff. cell types
4. act synergistically (two or more cytokines acting together) or anagonistically (causing opposing activities) |
What are the functions of cytokines? |
Autocrine- if the cytokine acts on the cell that secretes it
Paracrine- if the cytokine acts on closed neighbor cell
Endocrine- if the cytokine diffuses to distant regions of the body (carried by blood) |
Cytokine Action
What is Autocrine?
What is Paracrine?
What is Endocrine?
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Pathogen Associated Molecular Pattern
Pattern Recognition Receptor |
Ligand is on the pathogen and contians a PAMP. What is PAMP?
Receptor is on the innate cells and contains a PRR. What is PRR? |
human cells |
PAMP are signature molecules expressed only in microbes not in ____? |
Bacteria, Virus, Parasite, Fungi |
name some types of pathogens? |
Flagellin |
a structure by itself, on a bacteria. part of PAMP that helps recognize patterns. |
Zymosan |
Yeast is a PAMP. and is recognized by ? |
True |
True or False: Innate cells can also sense intracellular virus- the double stranded RNA |
Pattern Recognition Receptors |
What is PAR? |
PAR- Pattern Recognition Receptors |
- Represent the sensor system for pathogens -Are receptors for PAMPS -Are mainly expressed in innate cells -Can be found at the surface or inside the innate cells |
B1. Toll-like Receptor (TLR) B2. Nod Like-Receptor (NLR) B3. Macrohpage-Mannose Recepor (MMR) |
What are the types of PAR? |
-Membrane Associated receptor -Expressed on surface -Expressed inside cell/vacoules |
What are a Toll-Like Receptors (TLR)? |
-cyosolic receptors -Not expressed on the surface -Expressed inside cell/free in the cytoplasm |
What are Nod-Like Receptors (NLR)? |
-Mannose-rich glycans are short carbohydrate chains with the sugar mannose or fructose as the terminal sugar -They are commonly found in microbial glycoproteins and glycolipids but are rare in those humans |
What are Macrophage-Mannose Receptor (MMR)? |
Phagocytosis |
1: Bacteria binding to MMR 2: Microbe is ingested by phagocytosis 3: Phagosome is formed 4: Phagolysosome is formed by fusion between phagosome and lysosome 5: Enzymes digest the microbe 6: Residual body is formed 7: Discharge of waste material |
After phagocytosis, macrophages and dendritic cells can participate in antigen presentation, in which the phagocyte moves parts of the ingested material back to its surface |
What happens after phagocytosis? |
which recruit other phagocytes to the site of infections or stimulate “dormant” lymphocytes (naïve T cells) |
Phagocytes can communicate with other cells by producing cytokines, which do what? |
1. Destroy invading pathogens and any toxic molecules they produce 2. Highly specific to the particular pathogen that induced them 3. The innate responses call the adaptive immunce responses into play,and they both work together to eliminate the pathogens 4. Provide long-lasting protection. A person who recovers from measles, for ex. is protected for life against measles by the adaptive immune system 5. The ability to distinguish forgeign from self is afundamental feature of the adaptive immune system |
Functions of Adaptive Immunity? |
Neutrophils |
Which type of granulocytes is most abundant in the blood? |
Senses pathogens by recognition of PAMPs |
What is the function of Toll-like receptors in the immune response? |
Dendritic cells, Macrophages |
Which cells of the immune system are phagocytes? |
Cytotoxicity- Kills infected cells
Phagocytosis- Kills pathogens directly |
What are the differences between killing by phagocytosis and killing by cytotoxicity? |
1. T-cells develop in the bone marrow and migrate to thymus 2. Positive selection- T cells that can interact with MHC 3. Negative Selection- T cells that can interact with MHC with only low avidity(entusiasm) 4. Maturation and seeding in the lymphoid system 5. Binding of pathogenic peptides to MHC leads to high-avidity interactions with the TCR and results in T-cell activiation
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What is negative and positive selection of T cells? |
1. Exogenous Antigens Foreign antigens that enter the body from the outside by injection, ingestion, or inhalation MHC II 2. Endogenous Antigens Foreign antigens that are generated within the cell because of viral or intracellular bacterial infection MHC I |
What are MHC I and MHC II? |
-All cells express MHC I because if virus infects cell can alert CD8 T cells to kill infected cell
-MHC II only expressed by innate cells that are able to phagocytose pathogen and present it on MHC II which binds to TCR on CD4 T cells= Helper T cells |
What are the differences between MHC I and MHC II? |
Macrophages, B cells, and Dendritic cells |
What are antigen-presenting cells? |
ü Small round cells
ü Derive from HSC - CLP - T cell progenitor
ü Develop in the thymus ü Express a special receptor called T cell receptor (TCR)
ü Major surface markers are TCR, CD4, and CD8
ü Found in spleen, lymph nodes, blood
ü Represent 60% of lymph Nodes |
What are T-Lymphocytes? |
- The V region of the TCR a(alpha) and b(beta) regions - highly variable from one t-cell clone to the next -reflecting their role in antigen presentation -recognize peptide fragments presented with MHC I and MHC II molecules found on APCs or target cells |
What are the functions of TCR (T cell receptors)? |
with CD3 to form TCR complex |
TCR is associated with what? |
Co-receptor CD4 and CD8 allows prolonged engagement between the antigen presenting cell and the T cell |
what does the receptors CD4 and CD8 do in the T Lymphoctye? |
Th- which expresses CD4 glycoproteins on their surfaces
Tc- which expresses CD8 glycoproteins on their surfaces
(therefore, acquired immunity is composed of activated CD4(Th) and CD8(Tc) cellular responses)
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what are the T cell subsets on T Lymphocytes? |
Naive Cells- are cells that have matured, in the central lymphoid organ, have entered the lymphatic system, but that have yet to encounter their cognate antigen
Effector Cells- are cells that have been activated by their cognate antigen, and are actively involved in eliminating a pathogen Memory Cells- are long-lived survivors of past infections |
In state of Activation for T Lymphocytes, what are Naive Cells, Effector Cells, and Memory cells? |
1. progenitor T Cells leave the bone marrow and enter the thymus 2. After arriving at the thymus, these cells enter the outer cortex and begin to proliferate slowly 3. During 3wks of development in the thymus, the differentiating T-Cells progress through a series of stages marked by the changes in their cell surface phenotype |
How are T cells developed? |
-T cell progenitors (pre-T cells) derive from CLP and HSC -Pre-T cells leave bone marrow and populate thymus -Pre-T cells develop into CD4+CD8+ thymocytes and express TCR and CD3 -CD4+CD8+ thymocyteslose CD4 or CD8 and mature into CD4+ and CD8+ T cells -Mature CD4+ and CD8+ T cells leave thymus to peripheral lymphoid organs |
How do T Cells achieve maturation? |
üTCR is formed during T cell development in the thymus ü Without TCR a T cell cannot develop
ü TCR undergo sequence of gene recombination
ü Gene recombination produces limitless assortment of TCR responsible for T cell diversity ONE T cell = SEVERAL copies of same TCR ONE clone of T cells = ONE specificity for TCR ONE thymus = LIMITLESS clones of T cells ONE thymus = LIMITLESS specificity of TCR |
How is the T Cell diverse from other cells? |
ANTIGEN = IMMUNOGEN Large foreign molecules that can elicit an immune response -Proteins and polysaccharides are more immunogenic than lipids and nucleic acids -Antigens from individuals of same species are less immunogenic than those from distant species |
What is an antigen? |
Immunologically active portion of the antigen |
What is an epitope? |
Immunogenicity-The ability of an antigen to induce an Immune Response Antigenicity-The ability of an antigen to bind specifically to an Antibody |
Name some properties of an Antigen? |
Exogenous Antigens |
a foreign antigen that enters the body from the outside by injection, ingestion, or inhalation? |
Endogenous Antigens |
a foregin antigen that are generated within the bell because of ciral or intracellular bacterial infection? |
Auto-Antigens |
self antigens that are recognized by the immune system? |
Antigens must be degraded into small peptides and bound to protein called MHC proteins |
What is antigen processing? |
They are specialized for the presentation of intracelluar antigens to the TCR of CD8+ T-Cells
(Endogenous Peptides) |
What is MHC class I? |
They are specialized for the presentation of extracellular antigens to the TCR of CD4+ T-Cells
(Exogenous Peptides) |
What is MHC class II? |
Specialized cells = Antigen Presenting Cells (APC) FDendritic cells FMacrophages FB cells |
All cells express MHC-I but only specialized cells express MHC-II, What are those cells? |
1. Present endogenously derived peptides
2. Peptide (antigen) can be either self-derived or derived from viruses
3. Because MHC class I is present on all cells, any cell can interact with T-Cells if infected by a virus |
What are the properties of MHC Class I? |
1. Present exogenous antigens
2. Antigen has been phagocytosed and processed, ex. bacteria
3. This is performed by professional antigen-presenting cells. ex. macrophages |
What are the properties of MHC class II? |
The sequence of events involved in the formation of peptide. MHC complexes would require degradation of antigen into peptides |
What is the definition of antigen presentation? |
Humoral Immune Response |
-Aspect of immunity that is mediated by secreted antibidoes, produced in the cells of the B lymphocyte lineage (B Cell) -Involves substances found in the humors or body fluids -Secreted antibodies bind to antigens on the surfaces of invading microbes (such as viruses or bacteria), which flags them for destruction |
Immunoglobulins (Ig) |
Antibodies are known as what? |
Variable Region |
Which region of the Ig accounts for antigen-binding specificty? |
IgG IgA IgM IgD IgE |
What are the 5 classes of Ig? |
Soluble Form |
-a form of antibody where the antibodies are: -called free antibodies -secreted into the blood and other fluids |
Surface Bound Form |
a form of antibody where antibodies are: -attached to the surface of a B Cell -called surface immunoglobulin (sIg) or membrane immunoglobuling (mIg) -sIg is part of the B Cell receptor (BCR) composed of surface-bound IgD or IgM and associated Ig-ab hetero dimers |
It is determined by the amino acids sequence in the variable regions of the heavy and light chains. |
How is an Immunoglobulin (Ig) specificity determined? |
Paratopes
Epitopes |
Antigen Binding Site?
Antigenic Determinants on an antigen? |
Antigenic Determinants are in variable regions, and they both have millions of different specificities
|
What are the similarities between Ig and TCR? |
Ig- Form is free or surface bound -No antigen presentation by MHC -Free Antigens -No Antigen Processing
TCR- Form is ONLY surface bound -Antigen presentation by MHC -Antigen processing required |
What are the differences of Ig and TCR? |
IgG |
an Ig that: -makes up 75% of total serum antibodies -only antibody that crosses placenta -responsible for protection of newborns -provides defense against bacterial toxins |
IgA |
an Ig that: -is found in mucosa (GI, respiratory, urogenital tracts) and secretions (saliva, tears, nasal fluids, breast milk) -contribute to protection of newborns -defends external surface body against attachment of microorganisms -FOUND IN THE GUT |
IgM |
an Ig that: -is expressed on the surface of B Cells (BCR) and in secreted form -first antibody to appear in the serum after exposure to antigen (acute infection) -mainly found in bloodstream -presence in the cord blood indicates acute fetal infection (does not cross placenta in a healthy situation) |
IgD |
an Ig that: -is mostly present on B Cell Surface (BCR) -present in serum (soluble form) in trace amounts -needed for B Cell maturation |
IgE |
an Ig that: -is present in low concentration in serum -found in respiratory and gastro-intestinal tracks -involved in parasitic infections, allergic and hypersensitive reactions |
Opsonization |
Step in antibodies mediated host defense for IgG: 1. Antibodies bind epitopes on the surface of bacteria= COATING bacteria 2. Antibody-coated antigen attach to macrophages= Fc-Rc receptor binding 3. Engulfment of bacteria by phagocytosis |
Immobilization & Prevention of Adherence (won't let bacteria Adhere) |
Step in Antibodies Mediated Host Defense for IgA: 1. Bind on cover surface structure (important in adherence) 2. Bind structure in the flagella to block motility
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Toxin Neutralization
(the toxin will damage the cell so IgG will neutralize it) |
Step in Antibodies Mediated Host Defense for IgG: 1. Antibodies bind soluble bacterial toxins and block interactions of toxins with target cell
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1. Agglutination
2. Precipitation |
Step in Antibodies Mediated Host Defense for IgM:
1. antibodies bind surface of microorganisms and form clumps of particles of large size which will be removed by phagocytosis- (functions towards bacteria)
2. antibodies bind soluble toxin and from aggregates of neutralized toxin which will be removed by phagocytosis- (functions toward soluble molecules)1. |
B Lymphoctyes |
üSmall round cells ü Derive from HSC – CLP ü Develop in the bone marrow ü“B’ comes from Boursa of Fabricus(organ of B cell maturation in birds) üMake antibodies against soluble antigens ü Major surface markers are Immunoglobulins and MHC class II ü Found in spleen, lymph nodes, blood ü Represent 30% of lymph Nodes |
- immunoglobulin selection of B Cell |
-Immunoglobulin recognizes the cell and the B- Cell will go through an “exam” |
Diversity Diversity of antibodies (and TCR in T cells) |
-from the bone marrow you will have migration of different clones -the immunoglobulin will recognize only one structure. 1. Random rearrangement of segment genes VDJ 2. Random mutation at joining segment genes VDJ
|
Transition from membrane-bound Ig to secreted Ig is Called “Class Switching |
üPlasma B cell produce antibody in a secreted form rather than a membrane-bound form ü Class Switching allows Plasma B cells to switch from membrane-bound antibody to production of other classes (IgE, IgA, IgG)
üEx: circulating B cells switch to IgG production while B cells in mucosal tissues switch to IgA to provide mucosal ****The plasma B cells will change the class from IgE and IgG to IgA in the gut
In the respiratory tract you will want to switch to an IgE |
Activation of B Cell |
- doe NOT require presentation of antigen by MHC but requires a “help / confirmation” from a T helper cell |
B Lymphocytes Development: Self/Non-Self Seletion -Ig Diversity -No MHC restriction Activation: Recognition of free antigens Proliferation: Differentiation: Plasma B Cells -Class Switching Memory
T Lymphocytes Development: Self/Non-Self Seletion -TCR Diversity -MHC restriction Activation: Recognition of MHC-Peptides Proliferation: Differentiation: Th & Tc Cells -No Class Switching Memory
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B VS. T Lymphocytes Development Activation Proliferation Differentiation Memory |
Specificity of Innate and Adaptive Immune Response |
Specific structural components of pathogens are recognized. F Innate immune receptors (TLR and NLR) recognize general molecular patterns. Adaptive immune receptors (BCR and TCR) recognize specific structural components of pathogens |
Diversity of Innate and Adaptive Immune Response |
The total number of foreign molecules recognizable by T and B cells is very large ~ 109 distinct molecular determinants. F VDJ recombination of BCR and TCR is responsible for immunological diversity |
Discrimination of self from non-self of Innate and Adaptive Immune Response |
The immune system of normal individuals is able to recognize foreign agents while not reacting to components of “self” F During their development, B and T cells go through selection processes that eliminate cells with receptors that recognize self |
Memory of Innate and Adaptive Immune Response |
Ability to respond more vigorously and rapidly to repeated exposures of the same microbe. F The formation of memory B and T cells accounts for immunological memory and the success of vaccination |
: Disorder in which cells of the immune system are missing (B and T Cell)
Increased susceptibility to INFECTIONs |
What is Immunodeficiency? |
Full Blood Count
Antibodies against surface markers of immune cells (T cells = CD4, CD8, CD3, TCR B cells = BCR (IgM, IgD), MHC class II)
|
How is Immunodeficiency is diagnosed? |
Genetic Factor= Primary Immunodeficiency Lymphocyte Deficiencies Antibody Deficiencies Phagocyte Disorders Innate Immunity Deficiencies SCID = Severe Combined ImmunoDeficiency MHC class II deficiency CD3γ deficiency CD8 deficiency External Factor= Acquired Immunodeficiency Chemotherapy Drug treatment Other diseases
AIDS = Acquired ImmunoDeficiency Syndrome |
What causes Immunodeficiency? |
SCID (Severe Combined ImmunoDeficiency) |
üis a severe form of primary immunodeficiency in which both T and B cells are absent due to a genetic defect
ü Enfant born with this condition, if untreated, usually die within one year due to severe recurrent infections |
SCID is due to mutations in γc gene leading to lack of T and B cells |
What is the cause of SCID? |
Bone marrow transplant |
What is a treatment for SCID? |
Acquired Immunodeficiency Syndrome (AIDS) |
ü AIDS is caused by the Human Immunodeficiency Virus (HIV) which is responsible for damping numbers of CD4 T cells
ü HIV is transmitted through direct contact of blood, semen, vaginal fluid, and breast milk |
HIV infects and destroy CD4+ T cells and as result of killing so many CD4+ T cells Immunity is lost CD4+T cells are very important in cellular immunity CD4+ T cells provide HELP to B cells and cytotoxic T cells |
What is the cause of AIDS? |
The failure of an organism to recognize its own constituent parts as SELF which results in an immune response against its own cells and tissues*** Do REACT to SELF*** |
What is Autoimmunity? |
Systemic Autoimmunity(effects the nervous system)- Immune system attacks different organs of the body -Systemic Lupus Erythematosis -Rheumatoid Arthritis - Systemic Sclerosis Dermatomyositis Autoantibodies directed against contents of the cell nucleus Organ-specific Autoimmunity-Immune system affects only one organ or tissue type -Diabetes mellitus type 1 (Pancreas) -Hashimoto's thyroiditis (Thyroid gland) -Multiple sclerosis (Brain) -Myasthenia gravis (Muscles) Autoreactive T cells with a TCR specific to myelin components
|
What causes Autoimmunity? |
Type 1 diabetes |
- is an autoimmune disease that results in destruction of insulin-producing beta cells of the pancreas |
In Autoreactivity- CD8 recognizes cells represented by B Cells -need a MHC-I (class I)
In Cytotoxicity- B-cell is dead |
Cause of Diabetes Mellitus Type 1? |