Clastogenic factors in plasma of HIV-1 infected patients activate HIV-1 replication in vitro: Inhibition by superoxide dismutase

被引:33
作者
Edeas, MA
Emerit, I
Khalfoun, Y
Lazizi, Y
Cernjavski, L
Levy, A
Lindenbaum, A
机构
[1] SCH PHARM, DEPT CLIN PHARM, CHATENAY MALABRY, FRANCE
[2] UNIV PARIS 06, INST BIOMED CORDELIERS,FREE RAD RES GRP,CNRS, DEPT CLIN PHARM, PARIS, FRANCE
[3] HOP ANTOINE BECLERE, DEPT IMMUNOVIROL, CLAMART, FRANCE
关键词
AIDS; chromosome damaging materials; superoxide dismutase; oxidative stress; neoplastic disorders;
D O I
10.1016/S0891-5849(97)00002-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The frequent neoplastic disorders present in HIV-infected patients and the implication of oxidative stress in AIDS-Kaposi's sarcoma pathogenesis prompted us to study whether the mechanisms implicated in genotoxic effects of clastogenic factors (CFs) (i.e., chromosome damaging materials released by cells under conditions of oxidant stress) can play a role in HIV-1 expression and whether exogenous superoxide dismutase can inhibit the clastogenic and HIV-inducing effects of CFs. CFs were found in the plasma of all HIV-1 infected patients (n = 21) of this study group, in asymptomatic (CDC II) as well as in symptomatic patients (CDC II). In addition to their chromosome damaging effect, CFs are able to upregulate HIV-1 expression in U1 cells and in PBMCs activated with PHA and IL2 at all time points (p <.05). Their formation, therefore, is an early event in the disease. It occured despite antiviral medication in these patients. Superoxide dismutase inhibited the clastogenic and the viral inducing effects (p <.05). On the basis of our findings, association of SOD mimetics or superoxide scavengers with antiviral drugs may be a new therapeutic approach. This polytherapy, if started early enough after infection, may prolong the latency period and limit the emergence of drug-resistant viral strains. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:571 / 578
页数:8
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