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Clinical and Diagnostic Laboratory Immunology, Sep 1994, 538-544, Vol 1, No. 5
BG Brenner, M Gornitsky and MA Wainberg
The functions of natural killer (NK) cells and their interleukin-2-
deducible counterparts, lymphokine-activated killer (LAK) cells, are often
impaired in human immunodeficiency virus (HIV)-infected individuals. A
statistical approach was used to establish if changes in LAK activity were
associated with antiviral drug therapy, HIV-1 burden, or lymphocyte subset
alterations. Our study group included 61 HIV- positive subjects without any
opportunistic infections (OI-), 16 of whom received zidovudine (AZT), and
97 HIV-positive individuals with AIDS-related infection (OI+), 50 of whom
received AZT. As expected, there was a stepwise decrease in total
lymphocyte numbers in OI+ groups as a result of the selective loss of CD4+
cells. The groups receiving AZT therapy had fewer CD4+ cells but lower
circulating p24 antigen levels than corresponding untreated groups did. No
significant changes in the relative proportions or absolute numbers of
CD56+ subsets in HIV- positive groups could be ascribed to OI status or AZT
intervention. LAK cell cytotoxic responses, measured as LU20 values (which
give a measure of 20% cytolysis of target cells), lysis per unit CD56+ NK
cell, or lysis per unit blood volume, declined in OI+ groups. No main or
interactive effects of AZT therapy on LAK activities were observed.
Multivariate general linear models were used to determine the interactive
effects of NK- and T-cell subsets on measured LAK cell numbers were added
negative and positive predictors of LAK activity, respectively. These
findings indicate that declines in NK-mediated LAK cell responses serve as
functional correlates of progression in HIV- infected individuals.
Copyright © 1994 by the American Society for Microbiology. All rights reserved.
Interleukin-2-inducible natural immune (lymphokine-activated killer cell) responses as a functional correlate of progression to AIDS
McGill AIDS Centre, Lady Davis Institute--Jewish General Hospital, Montreal, Quebec, Canada.
| Antimicrob. Agents Chemother. | Clin. Microbiol. Rev. | Infect. Immun. |
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