Article Text
Abstract
Objective: To understand the changing impact of herpes simplex 2 (HSV2) and other sexually transmitted infections (STIs) on HIV incidence over time in four subSaharan African cities, using simulation models.
Methods: An individualbased stochastic model was fitted to demographic, behavioural and epidemiological data from crosssectional populationbased surveys in four African cities (Kisumu, Kenya; Ndola, Zambia; Yaoundé, Cameroon; and Cotonou, Benin) in 1997. To estimate the proportion of new HIV infections attributable to HSV2 and other STIs over time, HIV incidence in the fitted model was compared with that in model scenarios in which the cofactor effect of the STIs on HIV susceptibility and infectivity were removed 5, 10, 15, 20 and 25 years into the simulated HIV epidemics.
Results: The proportion of incident HIV attributable to HSV2 infection (the model estimated population attributable fraction (PAF_{M})) increased with maturity of the HIV epidemic. In the different cities, the PAF_{M} was 8–31% 5 years into the epidemic, but rose to 35–48% 15 years after the introduction of HIV. In contrast, the proportion of incident HIV attributable to chancroid decreased over time with strongest effects five years after HIV introduction, falling to no effect 15 years after. Sensitivity analyses showed that, in the model, recurrent HSV2 ulcers had more of an impact on HIV incidence than did primary HSV2 ulcers, and that the effect of HSV2 on HIV infectivity may be more important for HIV spread than the effect on HIV susceptibility, assuming that HSV2 has similar cofactor effects on HIV susceptibility and infectivity. The overall impact of other curable STIs on HIV spread (syphilis, gonorrhoea and chlamydia) remained relatively constant over time.
Conclusions: Although HSV2 appears to have a limited impact on HIV incidence in the early stages of subSaharan African HIV epidemics when the epidemic is concentrated in core groups, it has an increasingly large impact as the epidemic progresses. In generalised HIV epidemics where control programmes for curable STIs are already in place, interventions against HSV2 may have a key role in HIV prevention.
 HSV2, herpes simplex virus 2
 STD, sexually transmitted disease
 STI, sexually transmitted infection
 HIV
 Herpesvirus 2 (HSV2)
 subSaharan Africa
 STI
 STD
 epidemiology
 mathematical model
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Infection with herpes simplex virus type 2 (HSV2) is associated with a threefold increase in risk of HIV acquisition in both men and women in the general population.^{1} Given the high prevalence of HSV2 in subSaharan Africa,^{2} HSV2 may have an important role in the spread of HIV in these regions. Understanding the proportion of new HIV infections attributable to HSV2, and how and why this proportion may change over time, will provide insight into current epidemic dynamics, and will help in designing and evaluating future HSV2 interventions.
This paper uses model simulations of populations in four African cities as described by Orroth et al in this supplement.^{3} The individualbased stochastic model STDSIM was used to model the demography, sexual behaviour and STI/HIV epidemiology of four subSaharan Africa cities (Cotonou, Benin; Yaoundé, Cameroon; Ndola, Zambia; and Kisumu, Kenya), based on data from crosssectional surveys in 1997 and other sources.^{4,}^{5,}^{6,}^{7,}^{8,}^{9,}^{10,}^{11,}^{12,}^{13,}^{14,}^{15} Although many mathematical models have been used to simulate HIV, few models have been used to simultaneously simulate the transmission and interaction of HSV2 and HIV.^{16–}^{18}STDSIM allows for the simultaneous and interactive simulation of up to 16 different STIs.
In the present study, HIV, HSV2, chancroid, syphilis, gonorrhoea and chlamydia were simulated in each of the four populations. Using STDSIM, we compared the proportion of HIV incidence attributable to HSV2 over time with that due to chancroid and other curable STIs (syphilis, chlamydia and gonorrhoea) over the same time period in the four African cities. We also examined the sensitivity of model predictions to assumptions made regarding the association of HSV2 with HIV, including assumptions relating to HSV2 effects on HIV during periods of subclinical shedding of HSV2. Finally, we looked at the relative importance to HIV spread of primary versus recurrent HSV2 ulcers, and of HSV2 effects on HIV infectivity compared with susceptibility.
METHODS
The mathematical model STDSIM was fitted to data collected from four subSaharan African cities and other data sources, as explained in detail by Orroth et al in this supplement.^{3} The model was primarily fitted to data from the Four Cities Study^{4} for the year 1997 and to available data on trends over time.^{5,}^{6,}^{7,}^{8,}^{9,}^{10,}^{11,}^{12,}^{13,}^{14,}^{15} The population attributable fractions of incident HIV due to HSV2 and other STIs were then calculated for different time periods during the epidemic.
Quantification of model parameters: HSV2
The modelassumed parameter values for HSV2 are based on previous reviews and are shown in detail in the companion paper by Orroth et al in this supplement.^{3,}^{17,}^{18} Infection with HSV2 is followed by a primary ulcer lasting three weeks.^{17,}^{19,}^{20} All individuals are assumed to pass through this primary stage following infection with HSV2, although in empirical studies some individuals fail to report a primary ulcer, perhaps due to lack of recognition rather than true absence. In this paper, the term ulcer refers to clinically recognisable herpetic lesions, whether or not they are recognised by the infected individual.
After the “primary stage”, ulcers recur with decreasing frequency over time.^{20–}^{22} In the early latent stage, ulcers recur on average every 2.5 months for men and every three months for women, and in the latent stage, ulcers recur every six months for men and eight months for women. We assumed a sex difference in ulcer recurrence rates,^{21} although modelling this effect assumes the higher recurrence in men is not due to differences in symptom recognition. Ulcer recurrence rates were assumed to vary widely between individuals,^{23} so the duration of periods between ulcers and the duration of early latent and latent stages were sampled from an exponential distribution.^{17} Recurrent ulcers were assumed to last on average one week; a Weibull distribution (shape parameter = 2) was used to reflect the relative homogeneity of ulcer durations.^{17}
After “early latent” and “latent” stages with recurrent ulcers, individuals enter the “late latent” stage, in which they are still HSV2 positive but no longer experience recurrent ulcers.^{17} Stage duration is, on average, 3 weeks for primary, 2 years for early latent, 10 years for latent, with the rest of life in the late latent phase. Transmission probabilities for maletofemale transmission in all HSV2 phases were assumed to be twice those of femaletomale transmission, as for HIV.^{24,}^{25} There are limited data on per contact transmission probabilities of HSV2 due to the difficulties in measurement and problems of generalisability to the general population of results from wellcounselled but highrisk study populations. We assumed the primary HSV2 stage to have the highest level of HSV2 transmission (per contact maletofemale transmission probability 0.30), followed by periods of ulcer recurrence (maletofemale 0.20).^{19} In addition, there is evidence that subclinical shedding of HSV2 occurs during periods between ulcers.^{23,}^{26,}^{27} HSV2 transmission may occur during these periods of subclinical shedding^{24}; therefore, a low (conservative) level of HSV2 transmission was modelled continuously during the early latent (maletofemale 0.01) and latent (maletofemale 0.005) stages between ulcers to take this shedding effect into account.^{17,}^{18,}^{23,}^{27–}^{32} Any effect of HSV1 on HSV2 was ignored, because HSV1 infection is almost universal in subSaharan African populations.^{2}
Per contact cofactor effects of HSV2 on HIV susceptibility and infectivity were estimated using data from observational studies of Kenyan commercial sex workers and their clients.^{33,}^{34} From this work, primary herpetic ulcers were estimated to be associated with a 25fold increase in the per contact transmission probability of HIV (as were chancroid ulcers). Recurrent HSV2 ulcers were estimated to be associated with a 10fold increase in the transmission probability of HIV, to match the reduced severity of these ulcers in comparison with the primary ulcer.^{17} HIV transmission probabilities per act have been found to increase with the presence of recent genital ulceration in an HIVpositive source partner.^{35,}^{36} Cofactor effect values were chosen to be at the lower end of the range of estimates from the Kenyan study (3–300)^{34} to account for possible bias.
The magnitudes of the stagespecific cofactor effects were assumed to be constant across all sites, but varied by stage of HSV2 infection. For example, if a male was simultaneously in the primary stage of HSV2 infection and the primary stage of HIV infection, then the per contact HIV transmission probability from that male to an uninfected female would be the product of the maletofemale transmission probability during primary HIV (0.028) and the cofactor effect for primary HSV2 infection (25)—that is, 0.688. This overall per contact HIV transmission probability would quickly reduce either when the individual entered a HSV2 stage with a lower cofactor for HIV transmission, or when the individual entered an HIV stage associated with lower infectivity. Equal cofactor effects were assumed for HIV infectivity and HIV susceptibility, increasing the risk of HIV transmission to an HIVnegative partner either when the HIVpositive source partner was also infected with HSV2 (increased infectivity) or when the HIVnegative partner had an HSV2 ulcer (increased HIV susceptibility). As there was a lack of definitive evidence that HSV2 increases HIV infectivity more than HIV susceptibility, we were interested in comparing the populationlevel impacts of HSV2 cofactor effects on infectivity and susceptibility acting through population mixing and sexual behaviour.
Conservatively, no increase in the risk of HIV susceptibility or infectivity was initially assumed for the periods of subclinical shedding of HSV2 between ulcers. Coinfection with HIV in HSV2 positive individuals has been shown to increase both the HSV2 shedding rate and quantity (taken account of in the model, see below),^{35,}^{37–}^{39} with several studies finding a significant correlation between genital HIV RNA and HSV2 DNA in those HIV positive women who were shedding HSV2, without finding the same correlation between HIV RNA and HSV2 DNA in those dually infected overall.^{38,}^{40,}^{41} New evidence (currently in preparation) from Burkina Faso and Peru suggests that HSV2 therapy can reduce the frequency and quantity of HIV shedding as well as plasma HIV loads. We still await the definitive trial results on whether this decreased shedding is associated with reduced HIV transmission. The importance of this assumption of no increased risk of acquisition or transmission during subclinical shedding of HSV2, as well as the importance of the values assumed for cofactors during ulcerative periods, were examined in a sensitivity analysis (see below).
HIV infection was also assumed to alter the natural history of HSV2 infection. In line with evidence on increased HSV2 shedding in HIVpositive individuals ^{35,}^{37–}^{41} and increased HSV ulcer recurrence rates in HIVpositive individuals^{39,}^{42–}^{45} and with previous assumptions in STDSIM,^{17} we assumed a fourfold increase in HSV2 ulcer duration and recurrence rate with the onset of symptomatic HIV.
Quantification of model parameters: other STIs, demography and sexual behaviour
Other model parameter values, for the demography, sexual behaviour and natural history of the other STIs and their interaction with HIV were as reported in our companion paper in this supplement.^{3} Briefly, chancroid infection was assumed to be associated with a cofactor effect of 25 on HIV susceptibility and infectivity. Gonorrhoea and chlamydia infection were assumed to have a cofactor effect of 3 on HIV, and primary stage syphilis was assumed to have a cofactor effect of 7.5 on HIV.^{3} It is important to note that in a sexual encounter when there is more than one STI present (one individual with two different STIs or two individuals with different STIs), only the highest of the relevant cofactor effects is assumed to act on the probability of HIV transmission in that sexual act. Cofactor effects were not assumed to be additive or multiplicative.
Simulated population composition and growth rate are determined in STDSIM by inputs relating to fertility, mortality and migration (see companion paper). Inmigration is modelled by creating a simulated copy of an individual in the population in a specified age and relationship (risk) group. This simulated migration pattern allows us to adequately fit the population composition and observed patterns of behaviour.
Population attributable fraction calculation
The modelled population attributable fractions (PAF_{M}) of incident HIV attributable to HSV2, chancroid and other curable STIs (syphilis, chlamydia and gonorrhoea) were calculated from the STDSIM model simulations in the following manner. The cofactor effects on HIV for a given STI were removed from the model for a twoyear period—for example, during 1997 and 1998. HIV incidence in adults (15–49 years) over this twoyear period was then compared with the HIV incidence in the default scenario in which the default cofactor effects were assumed. By removing cofactor effects for susceptibility, the PAF_{M} can be calculated for effects of the STI on HIV acquisition. By simultaneously removing the cofactor effects for susceptibility and infectivity, overall PAF_{M} can be calculated for effects of the STI on HIV acquisition and transmission. The following equation was used for the simulated PAF_{M} calculations:
where IR_{nocofactor} is the incidence rate of HIV in model scenarios with the cofactor effect removed, and IR_{defaultcofactor} is the incidence rate in model scenarios with the default cofactor effects of HSV2 or other STIs on HIV.^{46}
The PAF_{M} for different time points in the epidemic was calculated by removing the STI cofactor effect on HIV over twoyear periods starting 5, 10, 15, 20 and 25 years after the introduction of HIV into each population (each in a separate set of simulations). Due to the earlier introduction of HIV assumed for Kisumu (1980) than the other cities (1984), the cofactors were removed during 1985/6, 1990/1, 1995/6, 2000/1 and 2005/6 in Kisumu and in 1989/90, 1994/5, 1999/2000, 2004/5 and 2009/10 in the other sites. The HIV incidence over the twoyear period during the removal of the STI cofactor effects was averaged and was compared with HIV incidence over the same period in the default scenario for each site. This process was undertaken for the effects on HIV due to HSV2, chancroid and other curable STIs combined (gonorrhoea, chlamydia and syphilis).
Sensitivity analysis
A sensitivity analysis was undertaken to assess the influence of the strength of the assumed HSV2 cofactor effect on the proportion of new HIV cases attributable to HSV2. Simulated PAF_{M} were calculated with the HSV2 cofactor effects on HIV during primary HSV2 and recurrent ulcerative periods at 50%, 150%, 200% and 300% of their default values by removing the cofactor effects starting in 1998, the last year of the Four Cities Study, and comparing HIV incidence in these simulations with incidence in simulations without these new cofactors removed.
The effects of HSV2 cofactors on HIV susceptibility and on HIV infectivity were compared to assess which had the greater impact on HIV spread. HIV incidence was calculated from simulations with the cofactors on susceptibility removed (with the cofactor effects on infectivity still in place), and then for simulations with cofactors on infectivity removed (with effects for susceptibility still in place). The PAF_{M} was calculated by comparing these incidence levels to default simulations with the effects for infectivity and susceptibility in place. The sensitivity analysis also investigated the relative contribution of cofactor effects during primary HSV2 with those assumed during ulcerative recurrent HSV2 on HIV incidence. The PAF_{M} was calculated for primary HSV2 only (by selectively removing the cofactor effects during that period and comparing the incidence rates as above) and was then calculated for recurrent ulcerative periods of HSV2 in a similar manner.
The effect of an additional inclusion of an HSV2 cofactor effect on HIV during periods of subclinical HSV2 shedding between ulcers was also explored. Various scenarios were explored including: cofactor effects between ulcers of 2 or 5; effects only during the early latent stage, or during both the early latent and latent stages and thus persisting many years into the course of HSV infection; and effects on susceptibility only, or on both susceptibility and infectivity.
RESULTS
The fit of the model simulations to data for demography, sexual behaviour and prevalence levels of STI is presented in our companion paper in this supplement.^{3} The fit of model simulated HSV2 prevalence to data from the four cities can be seen in figure 1. Prevalence of HSV2 in younger age groups was fitted preferentially, because younger individuals account for a higher proportion of new HIV and HSV2 infections. As a result, HSV2 prevalence in older adults was slightly overestimated in Yaoundé and Ndola, and underestimated in Cotonou. In all the sites, prevalence of HSV2 in younger males was allowed to be overestimated in favour of fitting the prevalence of HSV2 in younger females, because higherrisk males may not have been completely captured in the original surveys.^{47} The fit of HSV2 prevalence reflects the general age trends in HSV2 prevalence and the important differences between the four sites, such as the difference in HSV2 prevalence in females aged 15–19 years in Cotonou (9%) and Kisumu (39%).^{48} Due to the sensitivity of simulated HIV prevalence and shortduration STI prevalence to the alteration of sexual behaviour parameters, these parameters could not be further altered to improve the fit. Natural history parameters were held constant across all four sites.
Figure 2 shows the proportion of new HIV infections attributable to other STIs over time (PAF_{M}). The results were similar for males and females when examined separately by sex; the PAF_{M} shown are for males and females aged 15–49 years combined. Figure 2A shows the proportion of HIV incidence due to HSV2, which increased with the maturity of the epidemic in all four sites. The PAF_{M} across the four cities rose from 8.2–30.9% five years after the introduction of HIV to 35.4–48.2% 15 years after, as the HIV epidemic spread from core groups to the general population. The proportion of new HIV infections due to HSV2 was highest in Cotonou, especially earlier on in the epidemic. This effect is due to the relative lack of other (ulcerative) STIs in Cotonou (see fig 3), so that HSV2 accounted for proportionately more of the HIV transmission in that site. Although the PAF_{M} in Yaoundé increased dramatically between five years and 10 years after the introduction of HIV, it levelled off at around 37% after this 10year mark. This pattern matches the concurrent decrease observed in other STIs besides HSV2 in Yaoundé, which were highly prevalent five years after the introduction of HIV (corresponding to 1989 in fig 3) but had declined by 10 years after HIV introduction (1994). This was due simulated condom use and implementation of syndromic treatment in the early 1990s in the Yaoundé scenario. In all four sites, whereas the PAF_{M }of incident HIV due to HSV2 increased over time, the HSV2 prevalence remained constant.
The rapid increase in new HIV infections attributable to HSV2 over time contrasted markedly with the rapid decrease in HIV infections due to chancroid over time, as shown in figure 2B. Fifteen years after the introduction of HIV, all the chancroid PAF_{M} for HIV infection had fallen to zero due to the simulated decline in chancroid prevalence over time because of the simulated implementation of condom use and syndromic treatment^{3} starting in the early 1990s (fig 3). Overall, the drop in PAF_{M} of HIV due to chancroid and rise in PAF_{M} of HIV due to HSV2 occurred while the HIV incidence continued to rise (the effective reproduction number remaining >1). As can be expected from the explanations above, the PAF_{M} of HIV due to chancroid were the inverse of those for HSV2 in terms of sitespecific value, with the PAF_{M} in Cotonou for HIV due to chancroid much lower than in the other sites.
The PAF_{M} of HIV attributable to other curable STIs (syphilis, chlamydia and gonorrhoea) can be seen in figure 2C. In three sites, the proportion of HIV incidence due to these STIs remained relatively constant throughout the HIV epidemic. In Cotonou, in contrast, this proportion decreased rapidly from a little over 40% five years into the HIV epidemic to less than 5% 15 years into the epidemic.
The simulated prevalence of curable STIs over time is presented in figure 3. There are no consistent empirical timetrend data available from the four cities with which to compare these prevalence levels, but the figure is included to provide insight into the simulated PAF_{M} over time seen in figure 2. The irregularity in the prevalence levels of curable STIs is due to simulated improvements in syndromic management over time (introduced in the model in 1992 in Kisumu, Ndola and Yaoundé, and in 1995 in Cotonou) and the use of condoms (introduced at a low level in 1990, increased in 1993 and 1995 in commercial sex workers, and increased in 1995 for general population casual relationships). An initial dip can be seen in the curable STI prevalences in 1990, corresponding to the introduction of lowlevel condom use, followed by further decreases due to the introduction of improved syndromic management and higher condom use. By 1995, simulated chancroid had all but disappeared in the four sites.
Overall, the HSV2 PAF_{M} were relatively insensitive to changes in assumed cofactor strength. Figure 4 shows the PAF_{M} as a function of assumed cofactor strength in 1998. Reducing all of the HSV2 cofactor effects on HIV by half only decreased the proportion of new HIV infections from the default value of 36.1–47.9% to 21.3–30.5%, suggesting that HSV2 would still have a large role in HIV transmission even if our assumed default cofactor values were too large. As the magnitude of HSV2 cofactor effects on HIV was increased substantially, to 200% and 300% of default values, the PAF_{M} began to slowly level off, suggesting that, as could be expected, the proportion of new HIV infections attributable to HSV2 will reach its maximum well below 100%.
Further sensitivity analyses of the HSV2 PAF_{M} are presented by sex in table 1. The PAF_{M} was similar for males and females. An analysis of the contribution of primary HSV2 compared with recurrent HSV2 ulcers to new HIV infections can be seen in this table. The proportion of new HIV infections due to recurrent HSV2, ranging from 26.4% to 36.0%, was much higher than the proportion due to primary HSV2, ranging from 6.3% to 11.2%. This effect was observed because primary HSV2, while assumed to have a much higher cofactor on HIV susceptibility and transmission, is also much shorter in duration than the combined total of all recurrent ulcerative episodes.
The contribution to new HIV infections of the effect of HSV2 on HIV susceptibility as compared to HIV infectivity can also be seen in table 1. Assuming cofactor effects of equal strength, the cofactor effects on HIV transmissibility/infectivity contributed substantially more than those on susceptibility to the overall effect that HSV2 has on the spread of HIV. In Cotonou, for example, the overall PAF_{M} of incident HIV due to HSV2 was 47.9% in 1998, with a PAF_{M} of 9.7% due to the cofactors on HIV susceptibility and 31.8% due to the cofactors on HIV infectivity.
Finally, the sensitivity of the PAF_{M} to the introduction of an additional cofactor effect of HSV2 on HIV due to HSV subclinical shedding can also be seen in table 1. An assumed cofactor effect of 2 during subclinical shedding results in a negligible increase in the PAF_{M} when the cofactor is assumed only to act during early latency (not shown). A slightly stronger effect is seen if the cofactor is assumed for both early latency and latency. As expected, an even stronger assumed cofactor effect during periods of subclinical shedding increases the PAF_{M} of HIV due to HSV2, but a large increase is seen only if cofactor effects of 5 or greater are assumed for both HIV susceptibility and infectivity.
DISCUSSION
The present study showed HSV2 to have an increasingly important role in HIV spread in these four urban African populations. We estimate that more than a third of new HIV cases were attributable to HSV2 infection (PAF_{M} of >30%) at the time of the Four Cities Study. This was larger than the PAF_{M} for syphilis, gonorrhoea and chlamydia taken together, and also for chancroid. The PAF_{M} for HSV2 was low at the start of the HIV epidemic in all four cities but increased rapidly over time as the epidemic became more generalised and as the prevalence of other STIs with high cofactor effects on HIV acquisition and transmission decreased (with STI treatment and preventative measures in place). In Yaoundé, for example, the early decrease in prevalence of other ulcerative STIs in response to simulated interventions was matched by an early increase and then stabilisation in the PAF_{M} for HSV2. In contrast, the simulations showed that chancroid had an important role in establishing the HIV epidemics in three of the four cities, but its effect decreased rapidly over time with simulated implementation of condom use and syndromic treatment, the simulated PAF for HIV incidence falling to zero by 15 years into the HIV epidemic. Chancroid has a low basic reproduction number and tends to cluster in groups at high risk, explaining its strong effect on HIV transmission during the growth phase of an HIV epidemic. As HIV spreads beyond highrisk groups into the general population, chancroid plays a less important part in transmission. It is also highly symptomatic and therefore amenable to improvements in STI treatment services, disappearing rapidly once these services are in place.
The combined PAF_{M} for syphilis, chlamydia and gonorrhoea declined over time in Cotonou. In this site, high levels of STI treatment were introduced for commercial sex workers in model simulations in line with empirical data.^{3,}^{49,}^{50} As Cotonou is still a concentrated epidemic, STI treatment in this particular group had a large effect on prevalence levels of curable STIs. The PAF_{M} due to syphilis, chlamydia and gonorrhoea was relatively constant over time in the other sites, falling only slightly after the assumed introduction of more limited STI treatment services in these populations. At the current stage of the HIV epidemics, and given the current level of condom use and provision of STI treatment services, further strengthening of treatment services for curable STIs may be expected to produce little additional gain, except possibly in Yaoundé where the PAF_{M} approached 30%. However, withdrawing these services would most likely result in increased prevalence of curable STIs and increased HIV transmission.
Key messages

The impact of HSV2 and other STIs on the spread of the simulated HIV epidemic in four subSaharan African cities has changed over time.

The proportion of incident HIV attributable to HSV2 increased over time with the maturity of the epidemic, whereas the proportion of incident HIV attributable to chancroid and other curable STIs diminished over time.

In generalised HIV epidemics with control programmes for curable STIs already in place, interventions against HSV2 may have a key role in HIV prevention.
The modelsimulated PAF_{M} for HIV attributable to HSV2 were similar to those calculated from relative risks. A recent metaanalysis estimated that 38–60% of new HIV infections in subSaharan African women and 8–49% of new HIV infections in men could be due to HSV2,^{1} depending on HSV2 prevalence levels that ranged from 29% to 71% in women and 5% to 53% in men.^{2} However, these empirical estimates would not include those incident HIV infections due to increased transmissibility/infectivity of HIV, as the simulations do, because cohort studies measure incidence among HIVnegative individuals. Our major findings from the model were the robust assumptions about the strength of the interaction between HIV and HSV2. Although the absolute value of the PAF_{M} was somewhat sensitive to the cofactor values assumed, even reducing all cofactor values to half of their originally assumed value still resulted in a high proportion of new HIV cases due to HSV2 at the time of the Four Cities Study. Increasing HSV2 cofactor effects on HIV resulted in higher PAF_{M}, although the proportion of new HIV cases attributable to HSV2 became saturated at around 60%. Model simulations showed that recurrent HSV2 ulcers contributed more to HIV incidence than did primary HSV2 ulcers, probably because of the longer duration over which the recurrent ulcerative HSV2 cofactors acted on HIV, despite recurrent ulcers being less severe than primary ulcers.
HSV2 cofactor effects on HIV, assumed to be at the same per contact level for susceptibility and infectivity, appear to increase HIV incidence at the population level more through their effect on HIV infectivity than on their effect on HIV susceptibility. This effect may have been observed because increased susceptibility to HIV only increases that particular individual’s probability of contracting HIV (passing it on to another individual is another step), whereas increased infectivity of HIV in an individual could more immediately influence multiple transmissions if that individual had multiple partners. In addition, HIVinfected individuals are also more likely to be coinfected with HSV2 due to the strong association between HIV and HSV2^{1,}^{51}; therefore, in discordant partnerships, more of the HIVpositive partners will be HSV2 positive. This finding suggests that empirically calculated PAF, relying on relative risks of HIV acquisition only, may underestimate the effect of HSV2 on HIV incidence.^{46}
Introducing hypothetical, low level cofactor effects during subclinical shedding of HSV2 had little impact on HIV spread. A cofactor almost equivalent to that applied during recurrent ulcers would have to be assumed before making a large impact on HIV spread. This effect is understandable considering the nonadditive way in which the STDSIM model uses cofactors to increase HIV susceptibility and transmissibility, with the strongest cofactor in a given sexual encounter taken as the only cofactor. If only a low cofactor effect is assumed during subclinical shedding, only in partnerships with neither partner having additional active STIs would subclinical shedding of HSV2 begin to increase the likelihood for HIV transmission, although this may already be the case in more generalised epidemics. The current STDSIM model does not allow for more than one cofactor to have an effect during a given sexual encounter. Further work will be done on the implications of this assumption, and alternative methods of combination of cofactor effects need to be explored.
Another effect of note was the consistently high proportion of HIV cases due to HSV2 in Cotonou compared with the other sites. Cotonou had the lowest levels of other ulcerative STIs, even lower than in Yaoundé, due to STI treatment in commercial sex workers and to comparatively less risky sexual behaviour in the general population. In addition, examining the time trend of other STIs over time, the rise in the proportion of HIV due to HSV2 was concurrent with the decrease in other STIs in that site. In other sites, the cofactor effects of other STIs competed with those of HSV2, because the model only took into account the highest cofactor effect for a given sexual encounter. The simulated PAF_{M} should be interpreted with care, because it calculates the total effect of HSV2 on HIV acquisition and transmission. Although it is not directly comparable with PAF calculated from empirical relative risks of HIV acquisition, it may, however, give us a better idea of the “true” PAF of HIV incidence due to effects on both HIV susceptibility and transmissibility.^{46} The fit of the HIV epidemic and HSV2 epidemic was based on the best available data from the four cities, and, where unavailable, from outside sources. Further data on STI prevalence trends over time in the four cities would have been informative. Importantly, the prevalence of chancroid in the four cities was unknown historically and at the time of the Four Cities Study.
The model used in this study was primarily parameterised using crosssectional data, the limitations of which are well known. Crosssectional data provide little information on epidemiological or behavioural trends over time. Incorrect assumptions regarding the historic trends may alter our estimates of the proportion of new HIV cases due to STIs over time. However, the model did successfully replicate the observed time trends in HIV for the four cities.^{3}
The findings of this paper have potential implications for ongoing and future trials of HSV2 interventions. That the proportion of incident HIV due to HSV2 may change over time along with the changing prevalence of other STIs in the population suggests that the timing of an intervention in a population, and the prevalence of other cofactors for HIV transmission present in that population at that given timepoint, may be very important. Our simulations suggest that HSV2 is now responsible for a large proportion of new HIV infections in these African settings, highlighting the potential impact of herpes control for HIV prevention. Empirical trials of such interventions are now underway, and their results are eagerly awaited.
Acknowledgments
The authors would like to thank the Wellcome Trust (Grant 069509/Z/02/Z) and the Marshall Scholarship Commission for their financial support. We also extend our gratitude to the original participants of the Four Cities Study.
REFERENCES
This paper is freely available online under the BMJ Journals unlocked scheme, see http://sti.bmj.com/info/unlocked.dtl.
Footnotes

Published Online First 3 April 2007

Competing interests: None.

Edited by: Sevgi O Aral and James Blanchard
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