Decline in CTL and antibody responses to HIV-1 p17 and p24 antigens in HIV-1-infected hemophiliacs irrespective of disease progression. A 5-year follow-up study

• Published in: AIDS research and human retroviruses Vol. 8; no. 8; p. 1361
• Main Authors: O'Toole, C M, Lowdell, M W, Chargelegue, D, Colvin, B T
• Format: Journal Article
• Language: English
• Published: United States 01-08-1992
• Subjects: Cell Line, Transformed; Epitopes - immunology; Follow-Up Studies; gag Gene Products, Human Immunodeficiency Virus; Gene Products, gag - immunology; Hemophilia A - complications; HIV Antibodies - biosynthesis; HIV Antibodies - blood; HIV Antigens - immunology; HIV Core Protein p24 - immunology; HIV Infections - complications; HIV Infections - immunology; HIV-1 - immunology; Humans; Peptide Fragments - immunology; T-Lymphocytes, Cytotoxic - immunology; Viral Proteins
• ISSN: 0889-2229
• DOI: 10.1089/aid.1992.8.1361

CTL and antibody responses to HIV-1 p17 and p24 antigens were monitored from 1986-1991, in 4 hemophiliacs. The patients had been infected with HIV-1 between 1980 and 1984. Two patients have remained asymptomatic while two progressed to AIDS in 1990. CTL were boosted by culturing with peptides from p17 aa 86-115, or p24 aa 265-279; and aa 270-373 or PHA. Lysis was measured on autologous or allogeneic targets pulsed with peptides or infected with recombinant vaccinia virus carrying HIV-1 gag or influenza A matrix genes. Antibodies to p17 and p24 were tested by ELISA using peptides and by Western blotting. High levels of CTL activity to p17 and p24 antigens could be generated only with lymphocytes from the two asymptomatic patients between 1986 and 1989, but these responses were absent in 1990 and 1991. Antibodies to p17 peptides disappeared in parallel with CTL activity. Antibodies to some p24 peptides also declined but most patients retained activity to others. In all patients a > or = 3-fold increase in CD8+ cell numbers occurred over time and accompanied the decline of CTL and antibody responses. The loss of CTL and p17 antibodies occurred irrespective of whether patients remained asymptomatic or progressed to AIDS in the intervening two years.