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Principles of Immunology Immunodeficiency 4/20/06 ”Wise people talk because they have something to say; fools, because they have to say something” Plato
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Word/Terms List AIDS SCID Primary immunodeficiency Secondary immunodeficiency
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Immunodeficiency Primary-usually genetic, congenital Secondary-Acquired
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Mechanisms of Immunodeficiency Loss or reduction of: Cell type Cell numbers Cell function
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Loss of Cell Function Receptors Cell signaling Cytokine production Ig production Co stimulation impairment Intracellular killing Extravasation impairment
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Primary Immunodeficiency Myeloid lineage Congenital agranulocytosis Leukocyte-adhesion deficiency Lymphoid lineage Severe combined immunodeficiency (SCID) B cells Agammaglobulinemia Hypogammaglobulinemia Specific Ig Deficiencies T cells DiGeorge Syndrome Wiskott Aldrich Syndrome
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Secondary Immunodeficiency Drug related Disease related Cancer AIDS HIV T helper cell as target
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SCID Various genetic defects No TCR or defective TCR Defective cell signaling Defective IL 2 Recurrent infections Death at early age
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Wiskott Aldrich Syndrome X linked disorder Affects platelet numbers/function Affects T cell function Cytoskeleton of lymphocytes affected Lower amounts of IgM Increased susceptibility to certain bacterial infections
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Bruton’s Agammaglobulinemia Low levels of IgG B cell signal transduction affected Defective BCR Recurrent bacterial diseases starting at end of first year of life Short life span
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DiGeorge Syndrome Poorly developed or functioning thymus Associated with other developmental conditions Depression of T cell numbers Absence of T cell response Humoral response to T independent antigens only
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Secondary Immunodeficiency Drugs Irradiation Cancer AIDS
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AIDS HIV as agent T helper as target cell Attacked by own CD8 cells Susceptible to opportunistic infections Kaposi’s sarcoma CMV Candida Pneumocystis carinii
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