Document 0572 DOCN M9480572 TI Mycobacterium avium infection in HIV-1-infected subjects increases monokine secretion and is associated with enhanced viral load and diminished immune response to viral antigens. DT 9410 AU Denis M; Ghadirian E; Pulmonary Research Unit, Faculty of Medicine, University of; Sherbrooke, Canada. SO Clin Exp Immunol. 1994 Jul;97(1):76-82. Unique Identifier : AIDSLINE MED/94306756 AB The complex interaction between HIV-1 infection and Mycobacterium avium was studied. Viral burden was assessed, as well as immune response to HIV-1 in the context of Myco. avium infections. We also examined serum cytokine levels and cytokine release by blood mononuclear cells in HIV-1-infected subjects, infected or not with Myco. avium. Undetectable serum levels of IL-1, tumour necrosis factor-alpha (TNF-alpha) and IL-6 were found in normal controls and in groups I, II and III of HIV-1-infected subjects. Moderate levels of TNF-alpha, IL-1 and IL-6 were found in the sera of group IV patients. When group IV was subdivided into subjects with and without Myco. avium infections, subjects with Myco, avium infections were shown to have higher serum levels of TNF-alpha, IL-1 beta and IL-6 than those with other infections. Blood mononuclear cells from controls and HIV subjects were stimulated with bacterial lipopolysaccharide, and cytokine levels assessed. Cells from group II patients were shown to secrete normal levels of TNF-alpha and IL-6, and lower levels of IL-1 beta; group III subjects released higher levels of IL-6. Patients in group IV had blood cells that released elevated levels of IL-6 and TNF-alpha, and lower levels of IL-1 beta. Group IV subjects with Myco. avium infections had blood cells that released higher levels of TNF-alpha, IL-6 and IL-1 than group IV subjects with other infections. Assessment of viral burden in cells of HIV-1-infected subjects revealed that Myco. avium-infected subjects had a higher level of virus burden and a lower level of lymphoproliferative response to an inactivated gp120-depleted HIV-1 antigen than AIDS subjects with other infections. These data suggest that Myco. avium infections in HIV-1-infected subjects hasten the progression of viral disease, enhance cytokine release and contribute to the anergy to viral antigens. DE beta 2-Microglobulin/METABOLISM AIDS-Related Opportunistic Infections/*COMPLICATIONS/*IMMUNOLOGY/ MICROBIOLOGY Cytokines/BLOOD/SECRETION Human HIV Antigens/IMMUNOLOGY HIV Core Protein p24/BLOOD *HIV-1/IMMUNOLOGY/ISOLATION & PURIF Immunity, Cellular In Vitro Leukocytes, Mononuclear/IMMUNOLOGY Lymphocyte Transformation Monokines/*SECRETION Mycobacterium avium-intracellulare Infection/*COMPLICATIONS/ *IMMUNOLOGY/MICROBIOLOGY Support, Non-U.S. Gov't JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).