Important note: Information in this article was accurate in 1988. The state of the art may have changed since the publication date.
IMMUNOPHARMACOLOGY STUDIES RELATED TO IN VITRO INFECTION WITH HTLV-I
Dev Oncol; 44:309-19 1987. Unique Identifier : AIDSLINE ICDB/88639589 Grandori C; Graziani G; Perno CF; D'Onofrio C; Bonmassar E; Dept. of Experimental Medicine and Biochemical Science, Second; Univ. of Rome, Via Orazio Raimondo, I-00173 Rome, Italy
Abstract:
Ficoll-separated mononuclear cells from human umbilical cord blood (cord blood lymphocytes, CBL) or adult peripheral blood were treated with human beta interferon (IFN: 1,000 U/ml) or PCF-39 (N-9 arginil hypoxanthine derivative, 1 or 100 ug/ml) for 16 hr at 37 C. Cells were then tested for cell mediated-natural cytotoxicity against natural killer-susceptible K562 targets or a variety of human T-cell leukemia/lymphoma virus type I (HTLV-I)-positive lymphoblasts using a 4-hr 52Cr-release assay. Some pretreated lymphocytes also were cocultivated with irradiated virus-donor MT-2 cells (CBL cell line infected in vitro with HTLV-I), and later tested for nonspecific or MT-2-specific cytotoxicity and for virus infections monitored by cellular expression of HTLV-I P19 protein. The agents increased immune functions in selected experimental conditions and reduced virus infection by increasing target cell resistance and by decreasing MT-2 infectivity. Limited or no influence of the agents on virus transmission was found when target leukemic rather than immunocompetent cells were used in the donor-recipient cocultures. These preliminary results suggest a possible role of immunologic functions and immunomodulating agents on in vitro HTLV-I infection. (21 Refs)
Keywords: Adjuvants, Immunologic/*PHARMACOLOGY Cell Line Cytotoxicity, Immunologic/*DRUG EFFECTS Human Hypoxanthines/*PHARMACOLOGY HTLV-BLV Infections/*IMMUNOLOGY Interferon Type I/*PHARMACOLOGY T-Lymphocytes/DRUG EFFECTS JOURNAL ARTICLE
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