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 Bacteria  Fungi  Viruses  Parasites  Protozoa  Auto-immunity ?  Malignancy ?

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Presentation on theme: " Bacteria  Fungi  Viruses  Parasites  Protozoa  Auto-immunity ?  Malignancy ?"— Presentation transcript:

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3  Bacteria  Fungi  Viruses  Parasites  Protozoa  Auto-immunity ?  Malignancy ?

4  Innate system ( “old school”Castle with infantry defending )  - Castle : skin and mucous membrane  -infantry ( phagocytes )  Adaptive system (“modern “ intelligence gathering, IT and guided missiles and smart bombs)

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6 External epithelia: External surface Wounds & abrasions Insect bites Mucosal surfaces: Airway Gastrointestinal tract Reproductive tract (Fig. 2.2)

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10  Mucosa associated lymphoid tissue  80% of all immune cells  3 functions :  Protect mucous membranes  Prevent uptake of foreign antigens from food  Prevent pathological responses if foreign antigens cross the mucous membrane

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13  then the innate immune response begins.  The cells of the immune system determine “self” from “non- self” by recognizing molecules on the microbe surface.  Macrophages and dendritic cells are immune cells (phagocytes) that reside within the tissue. Neutrophils are phagocytes that reside in the blood but can extravagate into tissue during inflammation.  There are circulating proteins, called complement, that either kill microbes or mark them for effective phagocytization.

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15 Complement is a system of plasma proteins that interacts with pathogens to mark them for destruction. 1. Alternative pathway : pathogen surfaces 2. Mannan binding-lectin pathway : lectin binding to pathogen surfaces 3. Classical pathway : Ag:Ab complexes Functions: phagocytosis inflammation lysis

16  Through pattern recognition ( genetically programmed )  PAMPS  Toll like receptors

17    Activates vascular endothelium  Activates lymphocytes  Local tissue destruction  Increases access of effector cells    Fever,  production of IL-6

18    Activates vascular endothelium  Increases vascular permeability    Increased entry of IgG, complement, and cells to tissues  Increased fluid drainage to lymph nodes    Fever  Mobilization of metabolites  Shock

19    Lymphocyte activation  Increased antibody production    Fever  Induces acute-phase protein production

20    Activates NK cells  Induces the differentiation of CD4 T cells into T H 1 cells

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24  Hypothalamus  increased body temperature  Fat, muscle  protein & energy mobilization to allow increased body temperature   decreased viral & bacterial replication &  increased antigen processing & specific immune response

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28 Antigen specific response to antigen / pathogen Key feature if this system is that subsequent exposure to the initial antigen leads to more rapid and vigorous response ( Immunological memory) T and B lymphocytes drive this response from common stem cell

29  T-cell : cellular immunity through differentiation in TH-1 ( cellular )and TH-2 pathways ( humoral)  B-cell clonal response initially producing IgM and then IgG to infections : Memory cells produced that react much faster to future threats from the same pathogen.

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33  Positive and negative selection of t-cells  CD-4, CD-8 and T-killer cells emerge  Thymus continues to work in adult life especially when t-cell pool is damages as in AIDS and cancer chemotherapy

34  4 Major components :  Humoral immunity  Cell mediated immunity : lymphocytes  Phagocyts and polymorphnuclear cells  Complement

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