DISORDERS OF IMMUNITY III: IMMUNOLOGIC DEFICIENCY SYNDROMES R. HUGO MARTÍNEZ LOZANO, M.D. Aug-13-2009.
IMMUNOLOGIC DEFICIENCY SYNDROMES. I.- LEARNING OBJECTIVES: A.- IMMUNE RESPONSE AND INFECTIONS B.- IMMUNE DEFICIENCIES: TYPES: 1.- PRIMARY - ETIOLOGY - PATHOGENESIS - CHARACTERISTICS - RECOMMENDED STUDY - CLINICAL SIGNIFICANCE!!
IMMUNE DEFICIENCY SYNDROMES. I.- LEARNING OBJECTIVES: 2.- ACQUIRED: - CAUSES: -AGING -MEDICINE -CANCER -MALNUTRITION -AIDS -INFECTIONS -NEOPLASIA - MORPHOLOGY - CLINICAL SIGNIFICANCE!! REF: pp. 240-258
Adaptive immunity
Humoral (Abs.) -pyogenic bacteria. -some virus & protozoos (luminal) Cellular (cells & cytokines) -Many fungi -Many viruses -Other intracytoplasmic microbs
IMMUNE DEFICIENCY SYNDROMES. II.- PRIMARY: - CHARACTERISTICS - COMMON INHERITANCE - SPECIFIC VS NONSPECIFIC - TYPES OF INFECTION
PATHOGENESIS OF PRIMARY IMMUNEDEF.
IMMUNE DEFICIENCY SYNDROMES. II.- PRIMARY: RECOMMENDED STUDY: - X-LINKED AGAMMAGLOBULINEMIA - COMMON VARIABLE IMMUNODEF. - ISOLATED IgA DEF. - DiGEORGE SYNDROME - SEVERE COMBINED IMMUNODEF.
BRUTON’S AGAMMAGLOBULINEMIA
GIARDIA LAMBLIA
Mycoplasma & Arthritis
COMMON VARIABLE IMMUNODEFICIENCY DIFFERENCES (W/BRUTON’S): - GENDER - Ig LEVELS - PERIPHERAL B CELLS - CLINICAL – HERPES INF. - AUTOIMMUNE DIS. - MALIGNANCIES
ISOLATED IgA DEFICIENCY DIFFERENCES (W/BRUTON’S): - EPIDEMIOLOGY - Ig TYPES - FAMILIAL OR ACQUIRED - Ab VS IgA - GENDER, PERIPHERAL B CELLS, AUTOIMMUNE DIS.
SCID SPECTRUM OF DIFFERENT DISEASES - X-LINKED –R FOR IL - AR –ADA DEF. - OTHER. PROFOUND DEFECTS – HUMORAL - CELLULAR
CCR-5: M-TROPISM (vgr. APC) CXCR4: T-TROPISM
“ASPERGILLOMA”
PNEUMOCYSTOSIS
HISTOPLASMOSIS (LIVER)
IDEM: (KENYOUN STAIN)
Markers?. Genetics: t(8;14) or (2;8)