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7th International AIDS ConferenceFlorence, Italy — June 16-21, 1991 |
Int Conf AIDS 1991 Jun 16-21; 7:102 (abstract no. M.A.1040)
Dolei A, Serra C, Arca MV, Toniolo A; Institute of Microbiology and Virology, University of Sassari, Italy
OBJECTIVE: To correlate the permissiveness to HIV of adherent cells to the expression of surface molecules.
METHODS: HIV-1 (strain HTLV-IIIB) was given to human diploid lung embryo fibroblasts and to other adherent human cell lines, either untreated or pre-treated with recombinant interferon (IFN) gamma. Modulation of membrane molecules was evaluated by radiobinding to living cells of a panel of MAbs directed against membrane markers, or by immunofluorescence. HIV infection was monitored by syncytium assays, RT activity and p24 ELISA.
RESULTS: Pre-treatment of cells with IFNgamma increased the surface expression of Class I, beta2-microglobulin, and CD4 molecules, and induced de novo Class II DR and DP antigens; HIV adsorption was increased by a factor of 2-4. Virus yield was reduced only in those cells which completed virus cycle within 2-3 days. Infectivity of adsorbed particles lasted longer in IFN-treated cells, suggesting delayed uncoating. Newly formed p24 and infectious virus were detected 48-72 hrs p.i. in continuous cell lines. Diploid fibroblasts started to produce low levels of HIV only 20-30 days p.i., which were not influenced by pre-treatment with IFNgamma, whereas physiological doses of TNF enhanced p24 production. No matter of pre-exposure to IFN, persistent infection with HIV could be established in diploid fibroblasts, with chronic production of HIV antigens and low levels of infectivity.
Copyright © 1991 - International AIDS Society (IAS). Reproduction of this abstract (other than one copy for personal reference) must be cleared through the IAS.