Immunodeficiency K.J. Goodrum 2006. Origins of Immunodeficiency Primary or Congenital –Inherited genetic defects in immune cell development or function,

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Presentation transcript:

Immunodeficiency K.J. Goodrum 2006

Origins of Immunodeficiency Primary or Congenital –Inherited genetic defects in immune cell development or function, or inherited deficiency in a particular immune molecule Secondary or acquired –A loss of previously functional immunity due to infection, toxicity, radiation, splenectomy, aging, malnutrition, etc.

Infectious Consequences of Immunodeficiency Antibody deficiency, Phagocyte deficiencies, or Complement protein deficiencies are associated with recurrent infections with extracellular pyogenic bacteria (pneumonia, otitis media, skin infections) Deficiency in Cell-mediated immunity is associated with recurrent or chronic viral, fungal, or protozoal diseases.

Immunodeficiency Syndromes

B cell Deficiencies Congenital hypogammaglobulinemia –Symptoms at 9 mo. to 2 yr of age –Treat with intravenous immunoglobulin (IVIG) Hyper IgM: defective CD-40L expression Selective IgA deficiency –Occurs in 1:600-1:800 people –Possible connection with increased sinopulmonary infections and allergies

Immunoglobulin Levels vs. Age

T Cell Deficiencies Congenital Thymic aplasia Chronic Mucocutaneous Candidiasis

Severe Combined Immunodeficiency X-linked SCID: –Defect in IL-2 receptor Swiss-Type SCID –Adenosine deaminase deficiency Bare Lymphocyte syndrome –Absence of MHC Class II gene products

Phagocyte Deficiencies Chronic Granulomatous Disease –NADPH oxidase defect Chediak -Higashi Syndrome –Abnormal lysosome formation Leukocyte Adhesion Deficiency –Absence of leukocyte adhesion molecules

Complement Deficiencies Single component deficiencies –Example: C3 deficiency Hereditary Angioedema –C1 Inhibitor deficiency C5,C6,C7,C8, or C9 deficiency –Recurrent bacterial meningitis due defective membrane attack complex

Causes of Acquired Immunodeficiency Cancer (immunoproliferative diseases) Cytotoxic drugs or radiation Malnutrition Splenectomy Immunosuppressive therapies Stress/emotions Aging (thymic atrophy) Infection

Immunopathogenesis of HIV- Infection HIV infects and ultimately destroys CD4+, CCR5+ or CXCR4+ T cells, monocytes, & dendritic cells. Primary HIV Infection : A vigorous immune response to HIV controls the primary infection. ( clonal Cytotoxic T cells, suppressive chemokines, poorly neutralizing antibody)

Immunopathogenesis of HIV- Infection. (continued) Chronic Asymptomatic Phase: Viral trapping & replication in lymphoid tissues, high rate turnover of virus and CD4 T cells, loss of CD4 functional help to CTL and antibody responses, destruction of lymph tissue,, viral mutation and escape from recognition, exhaustion or viral inhibition of CD4 T cell renewal.

Immunopathogenesis of HIV- Infection. (continued) Overt AIDS: CD4 count declines, viral load increases, opportunistic infections.

Dendritic Cells transport HIV from Mucosal to Lymphoid Tissues

HIV binds CD4 and co-receptor (chemokine receptor) to enter host cells

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CD4 T cell depletion over the course of HIV infection

Mechanisms of CD4+ T cell depletion- Dysfunction Accumulation of unintegrated viral DNA Loss of plasma membrane integrity due to viral budding Elimination of infected cells by HIV- specific immune effectors Syncytium formation Autoimmunity

Mechanisms of CD4+ T cell depletion- Dysfunction(continued) Superantigenic stimulation Apoptosis Infection of stem cells and interference with lymphopoiesis

Opportunistic Infections in AIDS Patients