CD8(-LYMPHOCYTES IN THE LUNG OF ACQUIRED-IMMUNODEFICIENCY-SYNDROME PATIENTS HARBOR HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1() T)

Citation
G. Semensato et al., CD8(-LYMPHOCYTES IN THE LUNG OF ACQUIRED-IMMUNODEFICIENCY-SYNDROME PATIENTS HARBOR HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1() T), Blood, 85(9), 1995, pp. 2308-2314
Citations number
39
Categorie Soggetti
Hematology
Journal title
BloodACNP
ISSN journal
00064971
Volume
85
Issue
9
Year of publication
1995
Pages
2308 - 2314
Database
ISI
SICI code
0006-4971(1995)85:9<2308:CITLOA>2.0.ZU;2-Q
Abstract
Human immunodeficiency virus-1 (HIV-1) infection of CD8(+) lymphocytes has been described in several in vitro culture systems, but whether C D8(+) cells are a target and also serve as a reservoir for infection i n vivo as yet is unknown. We addressed this issue in patients with acq uired immunodeficiency syndrome (AIDS)-related lower respiratory tract chronic inflammation, which is characterized by a massive influx of C D8(+) HIV-1-specific cytotoxic T lymphocytes (CTL). Proviral load in l ung T lymphocytes and their subpopulations was evaluated by using the DNA-polymerase chain reaction (PCR) technique on cells retrieved by br onchoalveolar lavage. To avoid the possibility that the presence of HI V-1 DNA could be caused by contaminating CD4(+) cells, serial dilution s of highly purified CD8(+) cells were also analyzed by PCR. Our findi ngs showed that lung CD8(+) cells harbor and express HIV-1. To explore the possible mechanisms leading to pulmonary CD8(+) lymphocyte infect ion, we evaluated CD4 gene expression on highly purified CD8(+) cells by means of reverse transcriptase PCR, Despite the lack of membrane CD 4 reactivity, we could show that CD8(+) cells may express CD4 RNA, Coi nfection of lung CD8(+) cells harboring proviral HIV-1 sequences by vi ral agents capable of inducing CD4 expression (ie, HHV-6) was not dete cted. Our data indicate that not only CD4(+) T lymphocytes and macroph ages, but also CD8(+) cells, may represent a target and/or a reservoir for HIV-1 in vivo, and suggest that lung CD8(+) lymphocytes could der ive from precursors equipped with enough CD4 molecules to become HIV-1 permissive, Aside from the cell-to-cell contact between activated HIV -1 specific CTL and relevant targets, the infection of precursors coul d represent an additional mechanism accounting for the infection of pu lmonary CD8(+) cells and their functional impairment. (C) 1995 by The American Society of Hematology.