Παρασκευή 28 Δεκεμβρίου 2012

Does ART Prevent HIV Transmission Among MSM? H XOΡΗΓΗΣΗ ΑΝΤΙΡΕΤΡΟΪΚΗΣ ΘΕΡΑΠΕΙΑΣ ΠΡΟΛΑΜΒΑΝΕΙ ΤΗ ΜΕΤΑΔΟΣΗ ΤΗΣ HIV ΛΟΙΜΩΞΗΣ ΜΕΤΑΞΥ ΤΩΝ ΟΜΟ/ΑΜΦΙΦΥΛΟΦΙΛΩΝ ΑΝΔΡΩΝ;

Kathryn E. Muessig, M. Kumi Smith, Kimberly A. Powers, Ying-Ru Lo, David N. Burns, Andrew E. Grulich, Andrew N. Phillips, Myron S. Cohen AIDS. 2012;26(18):2267-2273.

(Υπάρχει ερωτηματικό;
Εδώ κοντέψαμε να πάρουμε όλοι και όλες 
χάπια γνωστής Φαρμακευτικής Εταιρείας, για πρόληψη, 
πριν βγούμε βόλτα μήπως και κάνουμε σεξ, 
μήπως ο/η σύντροφος τύχει νάναι οροθετικός/ή.
Αντί της πρόληψης μας πρότειναν προληπτική φαρμακευτική αγωγή... 
Πολλά τα λεφτα...)



Σ.Σ.: Τα πλάγια γράμματα είναι δικά μας σχόλια..

 ...---...---...---...---...---...


Abstract and Introduction

Abstract

Objective: To review the evidence for antiretroviral 'treatment as prevention' for HIV transmission among MSM.

ΣΤΟΧΟΣ: η μελέτη στόχευσε στο να επανεξετάσει τις ενδείξεις για τη χορήγηση της αντιρετροϊκής θεραπείας ως τρόπου πρόληψης της μετάδοσης της HIV μεταξύ των ομο/αμφιφυλόφιλων ανδρών.

Methods: We reviewed studies that assess the biological plausibility that virally suppressive antiretroviral therapy (ART) reduces HIV infectiousness via anal intercourse and the epidemiologic evidence of whether ART has played a role in attenuating HIV incidence among MSM.

Results: Although ART treatment among MSM is likely to provide some preventive benefit, it is unknown whether it will reduce HIV infectiousness via anal intercourse to the same extent as via penile–vaginal intercourse. Additional research is needed on the pharmacokinetic properties of specific antiretroviral agents in the gastrointestinal tract. Estimates of risk behaviors and the incidence of HIV among MSM before and after the introduction and expansion of ART suggest that the population-level protective benefits of ART may be attenuated by a number of factors, most notably, continuing or increasing frequency of condomless anal intercourse and incidence of other sexually transmitted infections (STIs). Additional studies are needed on the impact of ART on HIV sexual risk behaviors and transmission among MSM outside of developed countries in North America, western Europe, and Australia.

ΑΠΟΤΕΛΕΣΜΑΤΑ:  
παρόλο που η χορήγηση αντιρετροϊκής θεραπείας  στους ομο/αμφιφυλόφιλους άνδρες φαίνεται να προσφέρει κάποιο πλεονέκτημα στην πρόληψη της μετάδοσης, είναι άγνωστο εαν μειώνει τη μολυσματικότητα του HIV κατά την πρωκτική επαφή τόσο όσο κατά την κολπική επαφή. ΑΠΑΙΤΟΥΝΤΑΙ ΠΕΡΑΙΤΕΡΩ ΜΕΛΕΤΕΣ ΓΙΑ ΤΙΣ ΦΑΡΜΑΚΟΚΙΝΗΤΙΚΕΣ ΙΔΙΟΤΗΤΕΣ ΕΙΔΙΚΩΝ ΑΝΤΙΡΕΤΡΟΪΚΩΝ ΣΤΟ ΓΑΣΤΡΕΝΤΕΡΙΚΟ ΣΩΛΗΝΑ
Εκτιμήσεις των επικινδυνων συμπεριφορών και της επίπτωσης του HIV μεταξύ των  ομο/αμφιφυλόφιλων ανδρών, πριν και μετά την χρήση και επέκτασή της χρήσης της αντιρετροϊκής θεραπείας υποδεικνύει οτι το προστατευτικό αποτέλεσμα της αντιρετροϊκής θεραπείας μπορεί να αλλοιωθεί από σειρά παραγόντων, κυρίως από τη συνεχιζόμενη και κλιμακούμενη απροφύλακτη πρωκτική επαφή αλλά και την επίπτωση άλλων ΣΜΝ.
ΧΡΕΙΑΖΟΝΤΑΙ ΚΑΙ ΑΛΛΕΣ ΜΕΛΕΤΕΣ για τη σημασία της αντιρετροϊκής θεραπείας στις επικίνδυνες σεξουαλικές συμπεριφορές και τη μετάδοαη του ΗΙV μεταξύ των ομο/αμφιφυλόφιλων ανδρών πλην των αναπτυγμένων χωρών της Β. Αμερικής, Δ. Ευρώπης και Αυστραλίας..

Τι φοβερό! 
Είναι άλλο το γαστρεντερικό σύστημα κι άλλο το γεννητικό! 
Οτι δουλεύει στο ένα δεν είναι υποχρεωτικό να δουλεύει με τον ίδιο τρόπο και στο άλλο! Κοινώς:  
άλλο το πέος...άλλο ο πρωκτός...!

Conclusion: The benefits of treatment as prevention for MSM are highly plausible, but not certain. In the face of these unknowns, treatment guidelines for earlier ART initiation should be considered within a combination prevention strategy that includes earlier diagnosis, expanded STI treatment, and structural and behavioral interventions.

ΣΥΜΠΕΡΑΣΜΑΤΑ
τα οφέλη της χορήγησης της θεραπείας ως πρόληψης της μετάδοσης στους ομο/αμφιφυλόφιλους άνδρες είναι σημαντικά ΑΛΛΑ ΔΕΝ ΕΛΙΝΑΙ ΒΕΒΑΙΑ. 
Μπροστά στα άγνωστα αυτά σημεία, οι κατευθυντήριες οδηγίες για την πρώϊμη έναρξη αντιρετροϊκής θεραπείας θα έπρεπε να συνδυαστούν με μια στρατηγική πρόληψης που περιλαμβάνει πρώϊμη διάγνωση, θεραπεία των ΣΜΝ και συμπεριφορικές παρεμβάσεις..

Κατάντησε πληκτικό! 
Πρόληψη, είναι η προσπάθεια αλλαγής συμπεριφορών..
Δεν μπόρεσε να τα καταργήσει το χάπι. 
Είναι κι αυτοί οι περίεργοι επιστήμονες που κάνουν ανασκοπήσεις στις δημοσιεύσεις..
Ξεφεύγει και κανένας..

Introduction

One randomized controlled trial [1] and numerous observational studies [2–6] 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), in which case 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 re-evaluating 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 study, we synthesize evidence from studies of MSM of the biological plausibility that virally suppressive ART reduces HIV infectiousness via anal intercourse and epidemiologic evidence of whether ART has played a role in attenuating HIV incidence.

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 20–300 acts of condomless anal intercourse, as compared to one in 200 to one in 2000 for penile–vaginal exposure. [8–13] Additionally, a higher median number of HIV variants are transmitted in MSM couples as compared to heterosexual couples, [14,15] potentially posing greater challenges for drug resistance. [16]

The pharmacology of antiretroviral agents also differs between the urogenital tract (vaginal intercourse) and the gastrointestinal tract (anal intercourse). Antiretroviral drugs can reduce – but not eliminate – the amount of HIV recovered from the genital tract [17–19] and gastrointestinal tract. [20–22] Higher levels of HIV DNA and RNA have been found in the gastrointestinal tract (duodenum, ileum, ascending colon, and rectum) as compared to the blood [23,24] and semen, [22] irrespective of ART use, although these levels may be positively correlated. [20,25,26] Some antiretrovirals such as tenofovir, tenofovir diphosphate, and maraviroc have been shown to penetrate rectal tissue with greater efficiency than blood or seminal plasma, [27,28] 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 antiretrovirals have shown different mutation profiles in the virus recovered from each site. [29] This would suggest that replication can persist in the rectum even if a patient appears otherwise virally suppressed. Although the results of the HIV Prevention Trials Network 052 randomized trial among serodiscordant couples (HPTN 052) demonstrated the capacity of antiretroviral drugs to markedly reduce the risk of penile–vaginal transmission [1] 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, [30–34] and these co-infections amplify HIV transmission. [35–40] Globally, there is evidence of increases in STIs among MSM including rectal gonorrhea, [30,32,33,41] urethral gonorrhea, [42] and syphilis. [32,33,43–45] Other behaviors such as serosorting (limiting sexual partners to those thought to be of the same HIV serostatus) [46] and rectal douching [47] 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) [48–51] and being on ART itself, [50,52,53] 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 nonsignificant association between taking ART and increased condomless anal intercourse among MSM [odds ratio (OR) 1.38, 95% confidence interval (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). [54] 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-naive, HIV-positive persons recruited from over 200 sites worldwide comparing initiation of ART at CD4 cell count greater than 500 cells/μl to initiation at less than 350 cells/μl. [55]

Observational studies of whether ART reduces HIV transmission among MSM produce mixed findings. Surveillance data and longitudinal cohort studies suggest that HIV incidence among MSM has fluctuated, in some cases increasing, in spite of widespread ART availability. [41–43,56–62] 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 highly active antiretroviral therapy (HAART). [13,63] 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 (). [42,56,64–66] 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. [56] 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 capture enzyme immunoassay was not statistically significant. [64] 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. [66] 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. [66] A study conducted in Vancouver reported similar associations between decreases in CVL and new HIV diagnoses [42] however, the role of injection drug use in driving these trends is unclear, [67,68] and government surveillance reports show fluctuations in new HIV diagnoses among MSM in British Columbia with no overall change compared to 2003. [62] Among Vancouver MSM specifically, HIV prevalence is steady and slightly rising, likely reflecting increases in survival as well as new diagnoses. [69] In contrast, a study 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. [65]
Table 1.  Ecological studies of antiretroviral therapy 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 [66]
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 et al. (2010); San Francisco, USA [64]
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 et al. (2002); San Francisco, USA [56]
City health department AIDS registry, stored samples from VCT and STI 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 et al. (2010); British Columbia, Canada [42]
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 et al. (2010); Denmark (national) [65]
National HIV surveillance data and behavioral studies of MSM
Estimated prevalence of HIVpositive 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
ART, antiretroviral therapy; CVL, community viral load; STARHS, serologic testing algorithm for recent HIV seroconversion; STI, sexually transmitted infection; UAI, unprotected (condomless) anal intercourse.

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 study utilizing phylogenetic methods among MSM in the UK identified the following characteristics as likely to contribute disproportionately to onward HIV transmission: recent infection, not receiving ART, and concomitant STI. [70] Whereas an individual-level randomized clinical trial to directly evaluate the efficacy of ART for prevention in MSM may not be feasible or ethical, [71] well designed observational studies of seroconcordant and discordant couples – as reported with heterosexual individuals [3,4] – allow researchers to measure the risk of acquiring and transmitting HIV. Two such studies involving MSM couples in Europe and Australia are currently enrolling or planned. [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. However, the impact of ART on HIV transmission via anal intercourse requires further evaluation due to 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, it will be critical to earlier treatment in combination with HIV diagnosis, continued structural and behavioral interventions, and expanded STI treatment and prevention.
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.

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.

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.

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.

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.

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.

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. 2012. http://www.who.int/hiv/pub/guidelines/9789241501972/en/index.html [Accessed 24 April 2012].

8.     Royce RA, Sena A, Cates W Jr, Cohen MS. Sexual transmission of HIV. N Engl J Med 1997; 336:1072–1078.

9.     Hladik F, McElrath MJ. Setting the stage: host invasion by HIV. Nat Rev Immunol 2008; 8:447–457.

10.  Baggaley RF, White RG, Boily MC. Systematic review of orogenital HIV-1 transmission probabilities. Int J Epidemiol 2008; 37:1255–1265.

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.

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.

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.

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.

15.  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.

16.  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.

17.  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.

18.  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.

19.  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.

20.  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.

21.  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.

22.  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.

23.  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.

24.  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.

25.  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 nonprogressors. AIDS 2008;22:1880–1882.

26.  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.

27.  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 HIVnegative men. J Infect Dis 2011; 203:1484–1490.

28.  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; 3:112re4.

29.  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.

30.  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.

31.  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.

32.  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.

33.  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.

34.  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.

35.  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.

36.  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.

37.  Cohen MS. Sexually transmitted diseases enhance HIV transmission: no longer a hypothesis. Lancet 1998; 351 (Suppl 3): 5–7.

38.  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.

39.  Cohen MS. HIV and sexually transmitted diseases: lethal synergy. Top HIV Med 2004; 12:104–107.

40.  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.

41.  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.

42.  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.

43.  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.

44.  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.

45.  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.

46.  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.

47.  Carballo-Dieguez A, Bauermeister JA, Ventuneac A, Dolezal C, Balan I, Remien RH. The use of rectal douches among HIVuninfected and infected men who have unprotected receptive anal intercourse: implications for rectal microbicides. AIDS Behav 2008; 12:860–866.

48.  Schwarcz S, Scheer S, McFarland W, Katz M, Valleroy L, Chen S, et al. Prevalence of HIV infection and predictors of hightransmission sexual risk behaviors among men who have sex with men. Am J Public Health 2007; 97:1067–1075.

49.  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 HIVinfected and uninfected homosexual men. AIDS 2002; 16:775–780.

50.  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.

51.  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.

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.

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.

54.  Crepaz N, Hart TA, Marks G. Highly active antiretroviral therapy and sexual risk behavior: a meta-analytic review. JAMA 2004; 292:224–236.

55.  U.S. National Institutes of Health and the University of Minnesota Clinical and Translational Science Institute. The START study (Strategic Timing of Antiretroviral Treatment). 2012. http://clinicaltrials.gov/ct2/show/study/NCT00867048#locn [Accessed 24 April 2012]

56.  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.

57.  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.

58.  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.

59.  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.

60.  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.

61.  San Francisco Department of Public Health. San Francisco Department of Public Health HIV/AIDS Epidemiology Annual Report HIV Epidemiology Section. 2010 http://sfhiv.org/documents/AnnualReport2010GreenSurveillance.pdf [Accessed 24 April 2012]

62.  BC Center for Disease Control. HIV and Sexually Transmitted Infections 2010 Annual Surveillance Report. 2010. http://www.bccdc.ca/util/about/annreport/default.htm#heading1 [Accessed 2 Feb 2012]

63.  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.

64.  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.

65.  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.

66.  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.

67.  Grebely J, Tyndall MW. Management of HCV and HIV infections among people who inject drugs. Curr Opin HIV AIDS 2011; 6:501–507.

68.  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.

69.  Tyndall M. Personal communication, December 4, 2011.

70.  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.

71.  Cohen MS, McCauley M, Sugarman J. Establishing HIV treatment as prevention in the HIV Prevention Trials Network 052 randomized trial: an ethical odyssey. Clin Trials 2012; 9:340–347.

72.  Rodger A, Bruun T, Vernazza P,Collins S, Estrada V, van Lunzen J, et al.Understandingwhy serodifferent couples do not always use condoms when the HIV Rpartner is on ART. 19th Conference on Retroviruses and Opportunistic Infections Seattle, USA; 2012.

73.  World Health Organization. WHO and U.S. NIH Working Group Meeting on Treatment for HIV Prevention among MSM: what additional evidence is required? Geneva, Switzerland; 2011 Oct. 26–27. http://www.who.int/hiv/pub/msm_meeting_report.pdf. [Accessed 24 April 2012]

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