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Published in final edited form as: AIDS. 2012 Nov 28;26(18):2267–2273. doi: 10.1097/QAD.0b013e328355713d

Does ART prevent HIV transmission among MSM?

Kathryn E Muessig a, M Kumi Smith b, Kimberly A Powers a,b, Ying-Ru Lo c, David N Burns d, Andrew E Grulich e, Andrew N Phillips f, Myron S Cohen a,b,g
PMCID: PMC3499670  NIHMSID: NIHMS408381  PMID: 22569019

One randomized controlled trial [1] and numerous observational studies [26] provide strong evidence that antiretroviral therapy (ART) can reduce or prevent the sexual transmission of HIV-1 within serodiscordant heterosexual couples. A key question remains: does ART reduce HIV transmission among men who have sex with men (MSM), where the primary mode of transmission is via condomless anal intercourse? New WHO guidelines for earlier initiation of ART among serodiscordant couples were released in April 2012 [7] and some countries, such as China, have already embraced treatment as prevention (TasP) for heterosexual couples. In the process of reevaluating current ART guidelines, we anticipate that for some countries, the issue of whether to recommend TasP for MSM will be under debate. The evidence supporting TasP for MSM is promising, but major gaps in our knowledge remain. To identify priority areas for research, in this paper we synthesize evidence of (a) the biological plausibility that virally suppressive ART reduces HIV infectiousness via anal intercourse and (b) epidemiologic evidence of whether ART has played a role in attenuating HIV incidence among MSM.

Some biological and epidemiological evidence suggests that ART for preventing transmission via anal intercourse may have more limited efficacy than via vaginal intercourse. Without ART, the probability of HIV transmission is estimated as 1 infection for every 20 to 300 acts of condomless anal intercourse, as compared to 1 in 200 to 1 in 2,000 for penile-vaginal exposure [813]. Additionally, a higher median number of HIV variants are transmitted in MSM couples as compared to heterosexual couples [1416] potentially posing greater challenges for drug resistance [17].

The pharmacology of antiretroviral (ARV) agents also differs between the urogenital tract (vaginal intercourse) and the gastrointestinal (GI) tract (anal intercourse). ARVs can reduce–—but not eliminate–—the amount of HIV recovered from the genital tract [1820] and GI tract [2123]. Higher levels of HIV DNA and RNA have been found in the GI tract (duodenum, ileum, ascending colon, and rectum) as compared to the blood [24,25] and semen [23] irrespective of ART use, although these levels may be positively correlated [21,26,27]. Some ARVs such as tenofovir, tenofovir diphosphate, and maraviroc have been shown to penetrate rectal tissue with greater efficiency than blood or seminal plasma [28,29] but the durability of this penetration and required levels for prevention are not yet established. Furthermore, paired blood and rectal biopsy samples tested for resistance to ARVs have shown different mutation profiles in the virus recovered from each site [30]. This would suggest that replication can persist in the rectum even if a patient appears otherwise virally suppressed. While the results of HPTN 052 demonstrated the capacity of ARVs to markedly reduce the risk of penile-vaginal transmission despite similar biological and pharmacokinetic uncertainties, we cannot be certain that this will be the case for anal intercourse given the much higher transmission probability in the absence of ART.

In addition, we do not know the extent to which sexual risk behaviors might offset the potential prevention benefits of ART. Increases in bacterial sexually transmitted infections (STIs) are compelling evidence of ongoing high-risk behaviors among MSM [3135] and these co-infections amplify HIV transmission [3641]. Globally, there is evidence of increases in STIs among MSM including rectal gonorrhea [31,33,34,42], urethral gonorrhea [43], and syphilis [33,34,4446]. Other behaviors such as serosorting (limiting sexual partners to those thought to be the same HIV serostatus) [47] and rectal douching [48] also alter the risk of HIV transmission among MSM.

We do not know the extent to which sexual risk behaviors among MSM are changing due to the increasing availability of ART. Positive beliefs about the protective ability of ART (treatment optimism) [4951] and being on ART itself [5154], irrespective of actual viral suppression, have been associated with increased condomless anal intercourse. A meta-analytic review of studies published between 1996 and 2003 found a non-significant association between taking ART and increased condomless anal intercourse among MSM (OR 1.38, 95% CI, 0.62–3.07); however, the belief that being on ART protects against transmission was associated with an almost two-fold increase in condomless anal intercourse (OR 1.84, 95% CI, 1.53–2.20) [55]. The number of studies on these impacts of ART on behavior has more than doubled since this review and an updated meta-analysis has been commissioned by the WHO with results anticipated in 2012. Changes in transmission risk behaviors are also being assessed as a secondary outcome in the randomized controlled START trial (Strategic Timing of Antiretroviral Treatment), a study among treatment naïve HIV-positive persons recruited from over 200 sites worldwide comparing initiation of ARTat CD4 >500 cells/mm3 to initiation at <350 cells/mm3 [56].

Observational evidence to support the idea that ART reduces HIV transmission among MSM is mixed. Surveillance data and longitudinal cohort studies suggest that HIV incidence among MSM has fluctuated, in some cases increasing, in spite of widespread availability of ART [4244,5763]. To estimate how ART has affected HIV transmission among MSM, some studies have calculated a per-partner or per-act transmission risk and compared these rates pre and post-HAART [13,64]. For example, the Health in Men Australian cohort (2001–2007) used behavioral risk data and annual HIV incident infections to estimate per-contact HIV transmission risk. In Sydney–—with overall stable incidence of HIV and increasing uptake of ART–—the authors conclude that the overall per-contact risk of transmission has not changed in spite of increased ART coverage and more effective regimens [13].

Other studies have combined HIV surveillance and/or cohort data from communities with high ART coverage to compare trends in ART use and transmission (Table 1) [43,57,6567]. For instance, one older study in San Francisco (1995–1999) using community surveillance and clinic data concluded that any decrease in HIV infectivity gained by widespread use of ART may have been offset by increases in condomless anal intercourse and/or STIs [57]. A more recent San Francisco study using HIV surveillance data (2004–2008) described a significant correlation between decreased annual mean community viral load (CVL, an aggregate measure of the total known viral load among a particular population) and decreases in newly diagnosed cases of HIV; however the association with HIV incidence measured with the BED assay was not statistically significant [65]. A similar study using surveillance data (2004–2008) from Washington DC found a decrease in mean CVL and an increase in the proportion of known HIV-positive persons virally suppressed, but a statistically significant increase in newly diagnosed cases of HIV [67]. In these data, MSM had the highest proportion of individuals with undetectable viral load compared with other risk groups; however, black MSM were less likely to have undetectable viral load compared to white MSM [67]. A study conducted in Vancouver reported similar associations between decreases in CVL and new HIV diagnoses [43]; however, the role of injection drug use in driving these trends is unclear [68,69] and government surveillance reports show fluctuations in new HIV diagnoses among MSM in British Columbia with no overall change compared to 2003 [63]. Among Vancouver MSM specifically, HIV prevalence is steady and slightly rising, likely reflecting increases in survival as well as new diagnoses [70]. In contrast, a report from Denmark using national HIV surveillance and clinic data showed that rising proportions of HIV-infected MSM on suppressive treatment were correlated with stable rates of new HIV diagnoses in spite of increasing proportions of MSM reporting condomless anal intercourse [66].

Table 1.

Ecological studies of ART and new diagnoses of HIV.

Citation Location Data Source Estimation of Suppressive ART Estimation of HIV Incidence Interpretation of Results
Castel et al. (2012); Washington DC; USA [67] District health department HIV/AIDS case surveillance system Annual mean and total of most recent viral load test, proportion of virally suppressed Number of new HIV diagnoses as reported through the District HIV/AIDS surveillance system No association was found between trends in the mean CVL and newly diagnosed HIV/AIDS cases. MSM had a higher proportion of virally suppressed cases
Das M et al. (2010); San Francisco, USA [65] City health department HIV/AIDS case surveillance system Annual measures of mean and total CVL Newly reported HIV diagnoses and HIV incidence estimated using the STARHS method Reductions in CVL were significantly associated with fewer annual HIV diagnoses, though not with estimated HIV incidence using the STARHS method
Katz M et al. (2002); San Francisco, USA [57] City health department AIDS registry, stored samples from VCT and STD clinics, and behavioral surveys of MSM Numbers of HIV infected individuals receiving HAART, reported sexual risk behaviors Trends in HIV incidence as determined by STARHS method Any decrease in per contact risk of HIV transmission due to HAART use appears to have been countered or overwhelmed by increases UAI
Montaner JSG et al. (2010); British Columbia, Canada [43] Provincial disease surveillance database; provincial treatment center database Numbers of HIV infected individuals receiving HAART New HIV positive tests per 100 population. Rising numbers of individuals receiving HAART and rising proportions of treated individuals with VL < 500 copies/mL were strongly associated with decreased number of HIV diagnoses per year
Cowan S et al. (2010); Denmark (national) [66] National HIV surveillance data and behavioral studies of MSM Estimated prevalence of HIV-positive MSM receiving HAART, sexual risk behaviors Annual numbers of MSM notified as HIV infected via serologic testing, used as proxy for incidence Increasing numbers of treated MSM coincides with stable numbers of newly notified HIV positive MSM and increasing STI diagnoses, suggesting reduced infectiousness among HIV infected MSM

Due to their reliance on aggregate data and on new diagnosis reports rather than on new incident infections, these ecological studies are unable to draw causal inferences about the individual-level processes driving transmission. Their mixed results suggest that characteristics of specific geographic epidemics as well as behavioral patterns likely contribute to the population-level impact of ART on HIV transmission among MSM.

The majority of data available for the impact of ART among MSM are from developed countries in North America, Western Europe and Australia. As a result, what we know about ART’s effect on HIV transmission comes from a small subset of MSM, limiting the generalizability of these results within other social, cultural and epidemic settings. While recognizing the barriers of stigma, discrimination and legal repercussions, it is clear that more research is needed in this regard among MSM populations in South America, Africa, Central Europe and Asia. In order to inform optimal ART recommendations, we also need to better understand the social and cultural environments in which new sexual behavioral trends are evolving.

Going forward, there are great opportunities to further our understanding of the individual- and population-level transmission dynamics of HIV and ART among MSM. For example, applying the tools of phylogenetic analysis, researchers may be able to identify the most likely source of an individual’s HIV infection, describe the size and distribution of clusters of new cases in the population, and assess the relative contributions to new transmissions by persons at various stages of infection. For example, a phylogenetic transmission cluster analysis with matched epidemiological and clinical data among MSM in the UK found that those who are recently infected, are untreated, and have a concomitant STI may be contributing disproportionately to secondary transmission [71]. While an individual-level randomized clinical trial to directly evaluate the efficacy of ART for prevention in MSM may not be feasible or ethical (Cohen et al., in press CLIN Trials), well-designed observational studies of seroconcordant and discordant couples–—as reported with heterosexual subjects [3,4]–—allow researchers to measure both the risk of acquiring as well as transmitting HIV. Two such studies involving MSM couples are currently enrolling or planned in Europe and Australia [72,73].

The benefits of TasP for MSM are highly plausible, but not certain. The results of HPTN 052 have generated great urgency for maximizing the prevention benefit of ART. The impact of ART on HIV transmission via anal intercourse requires further evaluation, however, given the inconclusive observational data currently available for MSM and the challenging biological and behavioral risk factors that may be present. If TasP becomes part of prevention policy for MSM, implementation of early treatment in combination with other prevention methods including promotion of condom use to prevent other STIs, expanded STI treatment, structural and behavioral interventions, and earlier diagnosis will be critical.

Acknowledgements

Source of Funding: Kathryn E. Muessig and M. Kumi Smith are supported by an NIH institutional training grant (5T32AI007001-35). Kimberly A. Powers is supported by the NIH (R01 AI083059, R01 DA025885). Myron S. Cohen is supported by the Center for AIDS Research (CFAR) and the NIH HIV Prevention Trials Network (HPTN-052). The views expressed herein do not reflect the official stance of any funding agencies.

Footnotes

AUTHOR CONTRIBUTIONS: Myron S. Cohen, Ying-Ru Lo and David Burns conceived of the primary idea for this article. Kathryn E. Muessig and M. Kumi Smith completed the literature review, data analysis, and crafted the first draft. All authors identified additional relevant literature and studies and contributed substantively throughout the subsequent development of the manuscript.

Conflicts of Interest: We have no conflicts of interests to declare.

REFERENCES

  • 1.Cohen MS, Chen YQ, McCauley M, Gamble T, Hosseinipour MC, Kumarasamy N, et al. Prevention of HIV-1 infection with early antiretroviral therapy. N Engl J Med. 2011;365:493–505. doi: 10.1056/NEJMoa1105243. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Bunnell R, Ekwaru JP, Solberg P, Wamai N, Bikaako-Kajura W, Were W, et al. Changes in sexual behavior and risk of HIV transmission after antiretroviral therapy and prevention interventions in rural Uganda. AIDS. 2006;20:85–92. doi: 10.1097/01.aids.0000196566.40702.28. [DOI] [PubMed] [Google Scholar]
  • 3.Donnell D, Baeten JM, Kiarie J, Thomas KK, Stevens W, Cohen CR, et al. Heterosexual HIV-1 transmission after initiation of antiretroviral therapy: A prospective cohort analysis. Lancet. 2010;375:2092–2098. doi: 10.1016/S0140-6736(10)60705-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Del Romero J, Castilla J, Hernando V, Rodriguez C, Garcia S. Combined antiretroviral treatment and heterosexual transmission of HIV-1: cross sectional and prospective cohort study. BMJ. 2010;340:c2205. doi: 10.1136/bmj.c2205. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Musicco M, Lazzarin A, Nicolosi A, Gasparini M, Costigliola P, Arici C, et al. Antiretroviral treatment of men infected with human immunodeficiency virus type 1 reduces the incidence of heterosexual transmission. Italian Study Group on HIV Heterosexual Transmission. Arch Intern Med. 1994;154:1971–1976. [PubMed] [Google Scholar]
  • 6.Castilla J, Del Romero J, Hernando V, Marincovich B, Garcia S, Rodriguez C. Effectiveness of highly active antiretroviral therapy in reducing heterosexual transmission of HIV. J Acquir Immune Defic Syndr. 2005;40:96–101. doi: 10.1097/01.qai.0000157389.78374.45. [DOI] [PubMed] [Google Scholar]
  • 7.World Health Organization. Guidance on couples HIV testing and counselling, including antiretroviral therapy for treatment and prevention in serodiscordant couples: Recommendations for a public health approach. [Accessed 24 April 2012];2012 http://www.who.int/hiv/pub/guidelines/9789241501972/en/index.html. [PubMed]
  • 8.Royce RA, Sena A, Cates W, Jr, Cohen MS. Sexual transmission of HIV. N Engl J Med. 1997;336:1072–1078. doi: 10.1056/NEJM199704103361507. [DOI] [PubMed] [Google Scholar]
  • 9.Hladik F, McElrath MJ. Setting the stage: host invasion by HIV. Nat Rev Immunol. 2008;8:447–457. doi: 10.1038/nri2302. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Baggaley RF, White RG, Boily MC. Systematic review of orogenital HIV-1 transmission probabilities. Int J Epidemiol. 2008;37:1255–1265. doi: 10.1093/ije/dyn151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Boily MC, Baggaley RF, Wang L, Masse B, White RG, Hayes RJ, et al. Heterosexual risk of HIV-1 infection per sexual act: systematic review and meta-analysis of observational studies. Lancet Infect Dis. 2009;9:118–129. doi: 10.1016/S1473-3099(09)70021-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Powers KA, Poole C, Pettifor AE, Cohen MS. Rethinking the heterosexual infectivity of HIV-1: a systematic review and meta-analysis. Lancet Infect Dis. 2008;8:553–563. doi: 10.1016/S1473-3099(08)70156-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Jin F, Jansson J, Law M, Prestage GP, Zablotska I, Imrie JC, et al. Per-contact probability of HIV transmission in homosexual men in Sydney in the era of HAART. AIDS. 2010;24:907–913. doi: 10.1097/QAD.0b013e3283372d90. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Keele BF, Giorgi EE, Salazar-Gonzalez JF, Decker JM, Pham KT, Salazar MG, et al. Identification and characterization of transmitted and early founder virus envelopes in primary HIV-1 infection. Proc Natl Acad Sci U S A. 2008;105:7552–7557. doi: 10.1073/pnas.0802203105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Saathoff E, Pritsch M, Geldmacher C, Hoffmann O, Koehler RN, Maboko L, et al. Viral and host factors associated with the HIV-1 viral load setpoint in adults from mbeya region, Tanzania. J Acquir Immune Defic Syndr. 2010;54:324–331. doi: 10.1097/qai.0b013e3181cf30ba. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Bar KJ, Li H, Chamberland A, Tremblay C, Routy JP, Grayson T, et al. Wide variation in the multiplicity of HIV-1 infection among injection drug users. J Virol. 2010;84:6241–6247. doi: 10.1128/JVI.00077-10. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Truong HH, Kellogg TA, McFarland W, Louie B, Klausner JD, Philip SS, et al. Sentinel Surveillance of HIV-1 Transmitted Drug Resistance, Acute Infection and Recent Infection. PLoS One. 2011;6:e25281. doi: 10.1371/journal.pone.0025281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Graham SM, Holte SE, Peshu NM, Richardson BA, Panteleeff DD, Jaoko WG, et al. Initiation of antiretroviral therapy leads to a rapid decline in cervical and vaginal HIV-1 shedding. AIDS. 2007;21:501–507. doi: 10.1097/QAD.0b013e32801424bd. [DOI] [PubMed] [Google Scholar]
  • 19.Leruez-Ville M, Dulioust E, Costabliola D, Salmon D, Tachet A, Finkielsztejn L, et al. Decrease in HIV-1 seminal shedding in men receiving highly active antiretroviral therapy: an 18 month longitudinal study (ANRS EP012) AIDS. 2002;16:486–488. doi: 10.1097/00002030-200202150-00023. [DOI] [PubMed] [Google Scholar]
  • 20.Eron JJ, Jr, Smeaton LM, Fiscus SA, Gulick RM, Currier JS, Lennox JL, et al. The effects of protease inhibitor therapy on human immunodeficiency virus type 1 levels in semen (AIDS clinical trials group protocol 850) J Infect Dis. 2000;181:1622–1628. doi: 10.1086/315447. [DOI] [PubMed] [Google Scholar]
  • 21.Kelley CF, Haaland RE, Patel P, Evans-Strickfaden T, Farshy C, Hanson D, et al. HIV-1 RNA rectal shedding is reduced in men with low plasma HIV-1 RNA viral loads and is not enhanced by sexually transmitted bacterial infections of the rectum. J Infect Dis. 2011;204:761–767. doi: 10.1093/infdis/jir400. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Lampinen TM, Critchlow CW, Kuypers JM, Hurt CS, Nelson PJ, Hawes SE, et al. Association of antiretroviral therapy with detection of HIV-1 RNA and DNA in the anorectal mucosa of homosexual men. AIDS. 2000;14:F69–F75. doi: 10.1097/00002030-200003310-00001. [DOI] [PubMed] [Google Scholar]
  • 23.Zuckerman RA, Whittington WL, Celum CL, Collis TK, Lucchetti AJ, Sanchez JL, et al. Higher concentration of HIV RNA in rectal mucosa secretions than in blood and seminal plasma, among men who have sex with men, independent of antiretroviral therapy. J Infect Dis. 2004;190:156–161. doi: 10.1086/421246. [DOI] [PubMed] [Google Scholar]
  • 24.Yukl SA, Gianella S, Sinclair E, Epling L, Li Q, Duan L, et al. Differences in HIV burden and immune activation within the gut of HIV-positive patients receiving suppressive antiretroviral therapy. J Infect Dis. 2010;202:1553–1561. doi: 10.1086/656722. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Di Stefano M, Favia A, Monno L, Lopalco P, Caputi O, Scardigno AC, et al. Intracellular and cell-free (infectious) HIV-1 in rectal mucosa. J Med Virol. 2001;65:637–643. doi: 10.1002/jmv.2084. [DOI] [PubMed] [Google Scholar]
  • 26.Avettand-Fenoel V, Prazuck T, Hocqueloux L, Melard A, Michau C, Kerdraon R, et al. HIV-DNA in rectal cells is well correlated with HIV-DNA in blood in different groups of patients, including long-term non-progressors. AIDS. 2008;22:1880–1882. doi: 10.1097/QAD.0b013e32830fbdbc. [DOI] [PubMed] [Google Scholar]
  • 27.Anton PA, Mitsuyasu RT, Deeks SG, Scadden DT, Wagner B, Huang C, et al. Multiple measures of HIV burden in blood and tissue are correlated with each other but not with clinical parameters in aviremic subjects. AIDS. 2003;17:53–63. doi: 10.1097/00002030-200301030-00008. [DOI] [PubMed] [Google Scholar]
  • 28.Brown KC, Patterson KB, Malone SA, Shaheen NJ, Prince HM, Dumond JB, et al. Single and multiple dose pharmacokinetics of maraviroc in saliva, semen, and rectal tissue of healthy HIV-negative men. J Infect Dis. 2011;203:1484–1490. doi: 10.1093/infdis/jir059. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Patterson KB, Prince HA, Kraft E, Jenkins AJ, Shaheen NJ, Rooney JF, et al. Penetration of Tenofovir and Emtricitabine in Mucosal Tissues: Implications for Prevention of HIV-1 Transmission. Sci Transl Med. 2011;3:112re114. doi: 10.1126/scitranslmed.3003174. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Monno L, Punzi G, Scarabaggio T, Saracino A, Brindicci G, Fiore JR, et al. Mutational patterns of paired blood and rectal biopsies in HIV-infected patients on HAART. J Med Virol. 2003;70:1–9. doi: 10.1002/jmv.10354. [DOI] [PubMed] [Google Scholar]
  • 31.Hogg RS, Weber AE, Chan K, Martindale S, Cook D, Miller ML, et al. Increasing incidence of HIV infections among young gay and bisexual men in Vancouver. AIDS. 2001;15:1321–1322. doi: 10.1097/00002030-200107060-00020. [DOI] [PubMed] [Google Scholar]
  • 32.van der Bij AK, Stolte IG, Coutinho RA, Dukers NH. Increase of sexually transmitted infections, but not HIV, among young homosexual men in Amsterdam: are STIs still reliable markers for HIV transmission? Sex Transm Infect. 2005;81:34–37. doi: 10.1136/sti.2003.007997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Truong HM, Kellogg T, Klausner JD, Katz MH, Dilley J, Knapper K, et al. Increases in sexually transmitted infections and sexual risk behaviour without a concurrent increase in HIV incidence among men who have sex with men in San Francisco: a suggestion of HIV serosorting? Sex Transm Infect. 2006;82:461–466. doi: 10.1136/sti.2006.019950. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Stolte IG, Dukers NH, de Wit JB, Fennema JS, Coutinho RA. Increase in sexually transmitted infections among homosexual men in Amsterdam in relation to HAART. Sex Transm Infect. 2001;77:184–186. doi: 10.1136/sti.77.3.184. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Zablotska IB, Kippax S, Grulich A, Holt M, Prestage G. Behavioural surveillance among gay men in Australia: methods, findings and policy implications for the prevention of HIV and other sexually transmissible infections. Sex Health. 2011;8:272–279. doi: 10.1071/SH10125. [DOI] [PubMed] [Google Scholar]
  • 36.Fleming DT, Wasserheit JN. From epidemiological synergy to public health policy and practice: the contribution of other sexually transmitted diseases to sexual transmission of HIV infection. Sex Transm Infect. 1999;75:3–17. doi: 10.1136/sti.75.1.3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Cohen MS, Hoffman IF, Royce RA, Kazembe P, Dyer JR, Daly CC, et al. Reduction of concentration of HIV-1 in semen after treatment of urethritis: implications for prevention of sexual transmission of HIV-1. AIDSCAP Malawi Research Group. Lancet. 1997;349:1868–1873. doi: 10.1016/s0140-6736(97)02190-9. [DOI] [PubMed] [Google Scholar]
  • 38.Cohen MS. Sexually transmitted diseases enhance HIV transmission: no longer a hypothesis. Lancet. 1998;351(Suppl 3):5–7. doi: 10.1016/s0140-6736(98)90002-2. [DOI] [PubMed] [Google Scholar]
  • 39.Chen L, Jha P, Stirling B, Sgaier SK, Daid T, Kaul R, et al. Sexual risk factors for HIV infection in early and advanced HIV epidemics in sub-Saharan Africa: systematic overview of 68 epidemiological studies. PLoS One. 2007;2:e1001. doi: 10.1371/journal.pone.0001001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Cohen MS. HIV and sexually transmitted diseases: lethal synergy. Top HIV Med. 2004;12:104–107. [PubMed] [Google Scholar]
  • 41.Jin F, Prestage GP, Imrie J, Kippax SC, Donovan B, Templeton DJ, et al. Anal sexually transmitted infections and risk of HIV infection in homosexual men. J Acquir Immune Defic Syndr. 2010;53:144–149. doi: 10.1097/QAI.0b013e3181b48f33. [DOI] [PubMed] [Google Scholar]
  • 42.Dukers NH, Spaargaren J, Geskus RB, Beijnen J, Coutinho RA, Fennema HS. HIV incidence on the increase among homosexual men attending an Amsterdam sexually transmitted disease clinic: using a novel approach for detecting recent infections. AIDS. 2002;16:F19–F24. doi: 10.1097/00002030-200207050-00001. [DOI] [PubMed] [Google Scholar]
  • 43.Montaner JS, Lima VD, Barrios R, Yip B, Wood E, Kerr T, et al. Association of highly active antiretroviral therapy coverage, population viral load, and yearly new HIV diagnoses in British Columbia, Canada: a population-based study. Lancet. 2010;376:532–539. doi: 10.1016/S0140-6736(10)60936-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Sullivan PS, Hamouda O, Delpech V, Geduld JE, Prejean J, Semaille C, et al. Reemergence of the HIV epidemic among men who have sex with men in North America, Western Europe, and Australia, 1996–2005. Ann Epidemiol. 2009;19:423–431. doi: 10.1016/j.annepidem.2009.03.004. [DOI] [PubMed] [Google Scholar]
  • 45.Cicconi P, Cozzi-lepri A, Orlando G, Matteelli A, Girardi E, Degli Esposti A, et al. Recent acquired STD and the use of HAART in the Italian Cohort of Naive for Antiretrovirals (I.Co.N. A): analysis of the incidence of newly acquired hepatitis B infection and syphilis. Infection. 2008;36:46–53. doi: 10.1007/s15010-007-6300-z. [DOI] [PubMed] [Google Scholar]
  • 46.Jin F, Prestage GP, Kippax SC, Pell CM, Donovan BJ, Kaldor JM, et al. Epidemic syphilis among homosexually active men in Sydney. Med J Aust. 2005;183:179–183. doi: 10.5694/j.1326-5377.2005.tb06989.x. [DOI] [PubMed] [Google Scholar]
  • 47.Golden MR, Stekler J, Hughes JP, Wood RW. HIV serosorting in men who have sex with men: is it safe? J Acquir Immune Defic Syndr. 2008;49:212–218. doi: 10.1097/QAI.0b013e31818455e8. [DOI] [PubMed] [Google Scholar]
  • 48.Carballo-Dieguez A, Bauermeister JA, Ventuneac A, Dolezal C, Balan I, Remien RH. The use of rectal douches among HIV-uninfected and infected men who have unprotected receptive anal intercourse: implications for rectal microbicides. AIDS Behav. 2008;12:860–866. doi: 10.1007/s10461-007-9301-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Schwarcz S, Scheer S, McFarland W, Katz M, Valleroy L, Chen S, et al. Prevalence of HIV infection and predictors of high-transmission sexual risk behaviors among men who have sex with men. Am J Public Health. 2007;97:1067–1075. doi: 10.2105/AJPH.2005.072249. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Ostrow DE, Fox KJ, Chmiel JS, Silvestre A, Visscher BR, Vanable PA, et al. Attitudes towards highly active antiretroviral therapy are associated with sexual risk taking among HIV-infected and uninfected homosexual men. AIDS. 2002;16:775–780. doi: 10.1097/00002030-200203290-00013. [DOI] [PubMed] [Google Scholar]
  • 51.Rawstorne P, Fogarty A, Crawford J, Prestage G, Grierson J, Grulich A, et al. Differences between HIV-positive gay men who ’frequently’, ’sometimes’ or ’never’ engage in unprotected anal intercourse with serononconcordant casual partners: positive Health cohort, Australia. AIDS Care. 2007;19:514–522. doi: 10.1080/09540120701214961. [DOI] [PubMed] [Google Scholar]
  • 52.Dukers NH, Goudsmit J, de Wit JB, Prins M, Weverling GJ, Coutinho RA. Sexual risk behaviour relates to the virological and immunological improvements during highly active antiretroviral therapy in HIV-1 infection. AIDS. 2001;15:369–378. doi: 10.1097/00002030-200102160-00010. [DOI] [PubMed] [Google Scholar]
  • 53.Hasse B, Ledergerber B, Hirschel B, Vernazza P, Glass TR, Jeannin A, et al. Frequency and determinants of unprotected sex among HIV-infected persons: the Swiss HIV cohort study. Clin Infect Dis. 2010;51:1314–1322. doi: 10.1086/656809. [DOI] [PubMed] [Google Scholar]
  • 54.Ostrow DG, Silverberg MJ, Cook RL, Chmiel JS, Johnson L, Li X, et al. Prospective study of attitudinal and relationship predictors of sexual risk in the multicenter AIDS cohort study. AIDS Behav. 2008;12:127–138. doi: 10.1007/s10461-007-9223-x. [DOI] [PubMed] [Google Scholar]
  • 55.Crepaz N, Hart TA, Marks G. Highly active antiretroviral therapy and sexual risk behavior: a meta-analytic review. JAMA. 2004;292:224–236. doi: 10.1001/jama.292.2.224. [DOI] [PubMed] [Google Scholar]
  • 56.U.S. National Institutes of Health and the University of Minnesota Clinical and Translational Science Institute. The START study (Strategic Timing of Antiretroviral Treatment) [Accessed 24 April 2012];2012 http://clinicaltrials.gov/ct2/show/study/NCT00867048#locn.
  • 57.Katz MH, Schwarcz SK, Kellogg TA, Klausner JD, Dilley JW, Gibson S, et al. Impact of highly active antiretroviral treatment on HIV seroincidence among men who have sex with men: San Francisco. Am J Public Health. 2002;92:388–394. doi: 10.2105/ajph.92.3.388. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Jansen IA, Geskus RB, Davidovich U, Jurriaans S, Coutinho RA, Prins M, et al. Ongoing HIV-1 transmission among men who have sex with men in Amsterdam: a 25-year prospective cohort study. AIDS. 2011;25:493–501. doi: 10.1097/QAD.0b013e328342fbe9. [DOI] [PubMed] [Google Scholar]
  • 59.Prejean J, Song R, Hernandez A, Ziebell R, Green T, Walker F, et al. Estimated HIV incidence in the United States, 2006–2009. PLoS One. 2011;6:e17502. doi: 10.1371/journal.pone.0017502. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.He Q, Xia Y, Raymond HF, Peng R, Yang F, Ling L. HIV trends and related risk factors among men having sex with men in mainland China: findings from a systematic literature review. Southeast Asian J Trop Med Public Health. 2011;42:616–633. [PubMed] [Google Scholar]
  • 61.Finlayson TJ, Le B, Smith A, Bowles K, Cribbin M, Miles I, et al. HIV risk, prevention, and testing behaviors among men who have sex with men–National HIV Behavioral Surveillance System, 21 U.S. cities, United States, 2008. MMWR Surveill Summ. 2011;60:1–34. [PubMed] [Google Scholar]
  • 62.San Francisco Department of Public Health. San Francisco Department of Public Health HIV/AIDS Epidemiology Annual Report HIV Epidemiology Section. [Accessed 24 April 2012];2010 http://sfhiv.org/documents/AnnualReport2010GreenSurveillance.pdf.
  • 63.BC Center for Disease Control. HIV and Sexually Transmitted Infections 2010 Annual Surveillance Report. [Accessed 2 Feb 2012];2010 http://www.bccdc.ca/util/about/annreport/default.htm#heading1.
  • 64.Porco TC, Martin JN, Page-Shafer KA, Cheng A, Charlebois E, Grant RM, et al. Decline in HIV infectivity following the introduction of highly active antiretroviral therapy. AIDS. 2004;18:81–88. doi: 10.1097/01.aids.0000096872.36052.24. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Das M, Chu PL, Santos GM, Scheer S, Vittinghoff E, McFarland W, et al. Decreases in community viral load are accompanied by reductions in new HIV infections in San Francisco. PLoS One. 2010;5:e11068. doi: 10.1371/journal.pone.0011068. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Cowan S, Christiansen A, Haff J. New Paradigm for Positive Prevention: “Test and Treat”: Testing for and Treating HIV has Lowered Transmission Rate in Denmark in Spite of Increased Unsafe Sex Among MSM. 18th International AIDS Conference; Vienna, Austria. 2010. [Google Scholar]
  • 67.Castel AD, Befus M, Willis S, Griffin A, West T, Hader S, et al. Use of the community viral load as a population-based biomarker of HIV burden. AIDS. 2012;26:345–353. doi: 10.1097/QAD.0b013e32834de5fe. [DOI] [PubMed] [Google Scholar]
  • 68.Grebely J, Tyndall MW. Management of HCV and HIV infections among people who inject drugs. Curr Opin HIV AIDS. 2011;6:501–507. doi: 10.1097/COH.0b013e32834bcb36. [DOI] [PubMed] [Google Scholar]
  • 69.Wood E, Montaner J, Yip B, Tyndall M, Schechter M, O’Shaughnessy Mea. Adherence and plasma HIV RNA responses to highly active antiretroviral therapy among HIV-1 Infected injection drug users. CMAJ. 2003;169:656–661. [PMC free article] [PubMed] [Google Scholar]
  • 70.Tyndall M. 2011:Personal communication, December 4, 2011 [Google Scholar]
  • 71.Fisher M, Pao D, Brown AE, Sudarshi D, Gill ON, Cane P, et al. Determinants of HIV-1 transmission in men who have sex with men: a combined clinical, epidemiological and phylogenetic approach. AIDS. 2010;24:1739–1747. doi: 10.1097/QAD.0b013e32833ac9e6. [DOI] [PubMed] [Google Scholar]
  • 72.Rodger A, Bruun T, Vernazza P, Collins S, Estrada V, van Lunzen J, et al. Understanding Why Serodifferent Couples Do Not Always Use Condoms When the HIV+ Partner Is on ART. 19th Conference on Retroviruses and Opportunistic Infections; Seattle, USA. 2012. [Google Scholar]
  • 73.World Health Organization. Geneva, Switzerland: 2011. Oct. [Accessed 24 April 2012]. WHO and U.S. NIH Working Group Meeting on Treatment for HIV Prevention among MSM: What Additional Evidence is Required? http://www.who.int/hiv/pub/msm_meeting_report.pdf. [Google Scholar]

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