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Logo of nihpaAbout Author manuscriptsSubmit a manuscriptNIH Public Access; Author Manuscript; Accepted for publication in peer reviewed journal;
AIDS. Author manuscript; available in PMC Oct 18, 2009.
Published in final edited form as:
PMCID: PMC2635911
NIHMSID: NIHMS89950

A Call for Randomized Controlled Trials of Antiretroviral Therapy for HIV-2 Infection in West Africa

HIV-2 is endemic in West Africa, but unlike HIV-1 has had limited spread to other locales [1]. HIV-1 has emerged in West Africa more recently and because HIV-1 and HIV-2 co-circulate in this region, some individuals become dually infected with both viruses [2, 3]. Compared to HIV-1 infection, HIV-2 is characterized by a much longer asymptomatic stage, lower plasma viral loads, slower decline in CD4 count, decreased mortality rate due to AIDS, lower rates of mother to child transmission, genital tract shedding, and sexual transmission [1, 412]. Nonetheless, a significant proportion of HIV-2 infected individuals eventually progress to AIDS [6, 1315]. The clinical consequences of dual infection with both HIV-1 and HIV-2 need to be more fully understood, but current data suggest the majority of such patients also eventually progress to AIDS [2, 1620].

Antiretroviral therapy (ART) is becoming increasingly available in West Africa where HIV-2 infects up to 1–2 million people [21]. As ART “scale-up” programs proliferate in West Africa, significant numbers of HIV-2 and dually infected individuals will have access to and will be treated with antiretrovirals (ARV) developed against HIV-1 [2225]. However, HIV-2 is intrinsically resistant to the non-nucleoside reverse transcriptase inhibitors (NNRTI) and T-20 (enfurvirtide) and reports suggest that HIV-2 may be partially resistant to some protease inhibitors (PI) (e.g. Amprenavir, atazanavir and nelfinavir) and have a low genetic barrier to nucleoside reverse transcriptase inhibitors (NRTI) resistance [2639]. In addition, at least one recent report from Burkina Faso suggested the NRTI mutations M184V and Q151M may rarely be found in ARV-naïve individuals [40]. The presence of HIV-2 in dually infected patients complicates treatment, requiring drugs that are active against both HIV-1 and HIV-2.

Several observational cohort studies in developed countries have shown variable but generally poor outcomes of ART for HIV-2 infection [15, 4149] with similar results reported from the few small cohort studies from resource limited settings in Senegal, The Gambia and Cote d'Ivoire, West Africa [24, 25, 50].

Recently, there has been an effort in Europe to develop an international consortium (ACHIeV2E (A Collaboration on HIV-2 Infection)) of HIV-2 cohorts, to better study HIV-2 infection and standardize its management, including HIV-2 viral load testing, and treatment [51]. These efforts should ultimately lead to better care of HIV-2 infected individuals in the developed world and West Africa.

To date there has not been a single randomized clinical trial of ART for HIV-2 infection. This is despite greater than 20 years since the discovery of HIV-2 [52] and advent of AZT, greater than 10 years since the landmark studies showed the benefit of HAART for HIV-1 [5355], and currently 6 different classes of ARV available for HIV-1 (NRTI, NNRTI, PI, Fusion Inhibitors, CCR5-coreceptor blockers, and integrase inhibitors) of which 4 show in vitro and/or in vivo activity against HIV-2 [37, 38, 56-58]. The WHO currently recommends for first line therapy of HIV-2 infected patients, 2 NRTI and a protease inhibitor boosted by ritonavir [59]; they make no explicit recommendations for dually infected patients or for second line HIV-2 (or dual) infection regimens and little such data are available. In resource limited West Africa biological monitoring (CD4 counts) is limited and HIV-2 viral load and genotypic or phenotypic resistance testing are not commercially available, standardized nor routinely obtainable; thus assessing regimen failure is often made on clinical criteria and data suggest that CD4 count recovery with ART in HIV-2 infection is often poor [48, 49]. Consequently, an assessment of the relative efficacy of potential first line and salvage regimens including the newer generation of protease inhibitors, integrase inhibitors and CCR5 co-receptor blockers among HIV-2 (and dually) infected patients is needed. A key issue in West Africa where HIV and TB are common is to find the ART regimens for HIV-2 that can be given with concurrent treatment for TB, given interactions between protease inhibitors and rifampicin [59]. Finally, albeit rare, proven regimens to prevent mother to child transmission of HIV-2 (or dual infection) are needed [60].

We believe the 1–2 million HIV-2 infected people and communities in West Africa most affected by HIV-2 (and dual infection) deserve the same evidence-based medicine and efforts that those with HIV-1 have justly demanded [61]. Rigorous, well designed randomized controlled trials, that demonstrate which ARV regimens are effective in treating HIV-2 infected people, are urgently needed to guide patients and the clinicians who care for them. The outcome of such trials will also be beneficial in treating patients dually infected with HIV-1 and HIV-2, although ultimately trials of ART in dually patients are also needed. However, the apparent decline of HIV-2 in some West African locales [3, 61, 62] highlights the importance of involving multiple West African countries to establish large multi-center collaborative studies and trials. We believe the best place to carry out such trials is in West Africa, the locale where HIV-2 is endemic and effective treatment is most likely to serve the local population. We, therefore call on the wider AIDS community to support efforts for evidenced based treatment of HIV-2 infection.

Acknowledgments

We thank the editors and anonymous reviewers for their helpful comments.

Footnotes

Author Contributions: Geoffrey S. Gottlieb and Papa Salif Sow conceived of the opinion piece. All authors contributed to writing the paper.

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