The anti-HIV-1 activity of chloroquine

被引:85
作者
Savarino, A
Gennero, L
Sperber, K
Boelaert, JR
机构
[1] Algemeen Ziekenhuis St Jan, Unit Renal & Infect Dis, B-8000 Brugge, Belgium
[2] Mt Sinai Sch Med, Dept Clin Immunol, New York, NY USA
[3] Univ Turin, Dept Med & Surg Sci, Turin, Italy
关键词
chloroquine; HIV; developing world; antiretroviral treatment;
D O I
10.1016/S1386-6532(00)00139-6
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: there is a dramatic need for drugs with anti-HIV-1 activity that are affordable for resource-poor countries. Chloroquine (CQ) is one such drug. Objectives: to review the data indicating that CQ has anti-HIV-1 activity. Results: chloroquine (CQ) and its derivative hydroxychloroquine (HCQ) are endowed with a broad anti-HIV-1 activity inhibiting X4, R5, and X4/R5 stains in lymphocytic and monocytic cells. Interestingly, CQ is capable of inhibiting HIV-1 replication at concentrations within the range reported in plasma of individuals chronically treated with doses of the drug which have well-known and limited toxicity. These effects have been confirmed in vivo in two clinical trials. The principal mechanism of HIV-1 inhibition by CQ seems to be an effect on gp120 on a post-transcriptional level. Because CQ and HCQ appear to have a novel site of action (i.e. post-transcriptional inhibition of gp120), these drugs may be particularly useful in combination with other anti-retroviral agents (e.g. ZDV, ddI and HU). Conclusion: combining these drugs with other anti-HIV-1 agents, especially HU and ddI, may be an interesting option for the treatment for HIV-1 infected individuals in the developing world. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:131 / 135
页数:5
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