Effect of presumptive co-trimoxazole prophylaxis on pneumococcal colonization rates, seroepidemiology and antibiotic resistance in Zambian infants: a longitudinal cohort study
CJ Gill a, V Mwanakasale b, MP Fox a, R Chilengi c, M Tembo b, M Nsofwa b, V Chalwe b, L Mwananyanda d, D Mukwamataba b, B Malilwe b, D Champo b, WB Macleod a, DM Thea a & DH Hamer a
a. Department of International Health, Boston University School of Public Health, 710 Albany Street, Boston, MA, United States of America.
b. Tropical Diseases Research Centre (TDRC), Ndola, Zambia.
c. Africa Malaria Network Trust (AMANET), Dar es Salaam, United Republic of Tanzania.
d. Zambia-Emory HIV Research Project, Ndola, Zambia.
Correspondence to Christopher J Gill (e-mail: firstname.lastname@example.org).
(Submitted: 16 November 2007 – Revised version received: 18 March 2008 – Accepted: 10 April 2008 – Published online: 05 August 2008.)
Bulletin of the World Health Organization 2008;86:929-938. doi: 10.2471/BLT.07.049668
In 2000, the WHO and Joint United Nations Programme on HIV/AIDS (UNAIDS) secretariats recommended that infants in resource-poor settings with perinatal HIV exposure from an infected mother should receive co-trimoxazole (trimethoprim-sulfamethoxazole) prophylaxis presumptively.1,2 Co-trimoxazole prophylaxis would continue until two conditions are satisfied: (i) the child has been fully weaned and is no longer being exposed to maternal HIV; and (ii) the child can be proven uninfected with HIV. In resource-poor settings, presumptive prophylaxis would be necessary for at least a year in most cases. While WHO’s policy is intended to protect the subset of HIV-exposed infants who are (or become) HIV-infected in their first year, the majority of infants so targeted will escape HIV infection.3
In an earlier commentary on this policy,4 we drew attention to multiple potential adverse consequences of presumptive co-trimoxazole prophylaxis, with a particular focus on antimicrobial resistance. To better understand how co-trimoxazole prophylaxis affects microbial colonization and resistance rates, we implemented the co-Trimoxazole in Zambian Infants (TZI) project, a longitudinal cohort study designed to measure selected microbiological consequences of WHO’s policy. We selected Streptococcus pneumoniae as our sentinel pathogen for several reasons. First, the pneumococcus is a leading cause of morbidity/mortality among infants worldwide. Second, drug-resistant pneumococci are increasingly common and of particular public health concern. Third, multiple aspects of pneumococcal epidemiology can be assessed conveniently via nasopharyngeal colonization surveys. Lastly, the effectiveness of antibiotics and vaccines, our two main tools for combating pneumococcal disease, could both be degraded by widespread presumptive co-trimoxazole prophylaxis. Exposure to sulfonamides is presumably the dominant force behind the emergence of co-trimoxazole-resistant pneumococci and might induce cross-resistance to other antibiotics.5–8 Moreover, because antibiotic resistance is often linked with specific serotypes,9–12 exposure to co-trimoxazole might shift the prevailing pneumococcal serotypes away from those represented by the 7-valent conjugate pneumococcal vaccine.
Hence, this analysis addressed the following questions:
The TZI project was a two-arm longitudinal cohort study whose principal objective was to measure the microbiological consequences of implementing WHO guidelines2 for presumptive co-trimoxazole prophylaxis on pneumococcal colonization, drug resistance and seroepidemiology. The project was conducted at three antenatal clinics in Ndola, Zambia. Ndola is Zambia’s third-largest city, with most of its inhabitants living below the poverty level in periurban compounds. All mother/infant pairs were enrolled at the study clinics. Eligibility criteria were: (i) residence within the catchment zone of our study clinics; (ii) signed maternal informed consent; and (iii) maternal willingness to undergo HIV testing. “Case” infants were those born to HIV-positive women and thus requiring prophylaxis per WHO guidelines. “Comparison” infants were infants born to HIV-negative women, unexposed to HIV and hence not requiring prophylaxis per WHO guidelines. Comparison infants were recruited contemporaneously 1:1 with case infants, and were age- and clinic-matched. Our sample size of 260 mother/infant pairs was powered to detect a 30% reduction in colonization and a twofold increase in co-trimoxazole resistance as a function of co-trimoxazole exposure, while accommodating up to 30% attrition.
As per WHO guidelines, case infants received daily prophylactic oral co-trimoxazole from 6 weeks until ≥ 12 months of age, dosed at 10 mg/kg daily for trimethoprim and 50 mg/kg daily for sulfamethoxazole. Case infants still on study at 12 months were tested for HIV infection. If positive at 12 months and again at 15 months, they were considered true positives and offered co-trimoxazole prophylaxis indefinitely. Case infants who tested negative at 12 or 15 months and had fully weaned were considered HIV-negative and co-trimoxazole was stopped.
All infants were enrolled at 6 weeks of age and followed according to a seven-visit, well-child care schedule at prespecified intervals (Fig. 1). At visit 1, no infants had started co-trimoxazole prophylaxis. From visits 2 to 5, all case infants received co-trimoxazole. After visit 5, most case infants tested negative for HIV and stopped co-trimoxazole. This schedule creates three distinct periods for comparison (Fig. 1): pre-co-trimoxazole (period 1), on co-trimoxazole (period 2), and post-co-trimoxazole (period 3).
Fig. 1. Design of longitudinal cohort study of co-trimoxazole prophylaxis among Zambian infants
The TZI project was jointly approved by the ethical review boards at Boston University and the Tropical Diseases Research Centre (TDRC) in Ndola. All mothers provided written informed consent.
Mothers attending antenatal clinics underwent HIV voluntary counselling and testing according to local standards. HIV screening used the Determine® 1 + 2 test (Abbott Laboratories, Abbott Park, IL, United States of America) and confirmed using the Capillus® test (Cambridge Biotech Ltd, Galway, Ireland),13 with the Bioline® test (Bionor AS, Skien, Norway) to resolve indeterminate/discrepant results. The sensitivity/specificity of this protocol exceeds 99%. This same protocol was used for case infants at 12 and 15 months.14 HIV-positive mothers and their infants received peripartum nevirapine prophylaxis according to the HIVNET 012 protocol.3 Antiretroviral drugs were virtually unavailable in Ndola during TZI.
At every visit, we screened for S. pneumoniae colonization using posterior nasopharyngeal samples obtained with sterile calcium-alginate-tipped aluminium swabs advanced into both nostrils until meeting resistance and then rotated 180°.15 To maximize yields, swabs were plated immediately on to room temperature soy-trypticase agar plates with 5% sheep’s blood/5% gentamicin (gent/BAP) and streaked later for optimal colony separation at the TDRC microbiology laboratory.15–17 Gentamicin increases the yield for S. pneumoniae by approximately 40%.16,17 Screening plates were incubated at 37 °C under 5% CO2 atmosphere for 48 hours. Colonies were presumptively identified as S. pneumoniae by colony morphology (small grey “draftsman” mucoid α-haemolytic colonies), and typical diplococcoid morphology on Gram stain.18 For confirmation, colonies from the screening gent/BAP plates were subcultured onto gentamicin-free BAP, and defined as S. pneumoniae on the basis of ≥ 14 mm optochin (ethylhydrocupreine, Difco, Detroit,. MI, USA) inhibition zones, or bile-solubility for isolates with < 14 mm optochin inhibition.19
Drug resistance was determined using the elipsometer method (Etest®, AB Biodisk, Solna, Sweden).20,21 We measured the minimum inhibitory concentration (MIC) for each isolate against co-trimoxazole, penicillin, tetracycline, erythromycin, chloramphenicol and clindamycin. Subcultures of pure pneumococcal isolates were used to create a bacterial lawn on 150 mm Mueller–Hinton broth agar plates, each plate accommodating all Etests® simultaneously. Diameters of inhibition were measured at 24 hours of incubation. The point on the Etest® strip where inhibition was first noted indicated the MIC for that isolate and was read directly off the calibration guide printed on each strip. Classification of inhibition zones for isolates into sensitive, intermediately and highly resistant pneumococci was per the National Committee for Clinical Laboratory Standards guidelines.18
Subcultured isolates were characterized to the serogroup and serotype level using the Statens Serum Institute (Copenhagen, Denmark) latex slide agglutination system, with subsequent factor typing of the dominant serotypes.
Data were dual entered at TDRC and cleaned/reconciled at Boston University. We conducted univariate estimates of risk ratios (RRs) with 95% confidence intervals (CI), t-tests, and/or tests of proportions (χ2 or Fisher’s exact). Because MICs for antibiotic resistance operate on a logarithmic scale, we log transformed MICs before conducting t-tests on the means and back-transformed the result using the exponent of the difference in the log means. Note that this procedure yields the ratio of the two medians of the back-transformed MICs, not their means [exp(Ln mean1 - Ln mean2) = median1/median2].22
In univariate analyses, we assumed that case infants received co-trimoxazole during period 2 but not in periods 1 or 3 (adjusting for the handful who tested positive for HIV and remained on co-trimoxazole), and no comparison infants received co-trimoxazole. However, we also tested the effect on colonization and drug resistance of intercurrent short-term sulfonamide treatment among the comparisons, such as brief courses of co-trimoxazole for acute infections or malaria treatment with sulfadoxine-pyrimethamine, a pharmacologically similar drug to co-trimoxazole that has been linked to increased colonization with co-trimoxazole-resistant pneumococci.23 Lacking a priori knowledge about what exposure level would be sufficient to induce resistance, we categorized any level of sulfonamide exposure during the preceding interval as ‘exposed to co-trimoxazole’ under this expanded definition. Conversely, only those infants with no reported exposure to sulfonamides were categorized as unexposed to co-trimoxazole. Owing to the longitudinal structure of the data set with multiple observations on individuals, we recalculated the RRs using a log-linear model with robust standard errors to adjust for the clustering effect of repeated measures to see if our results changed significantly.22 Our sample size was based on a projected 30% reduction in colonization between the two arms from a typical baseline of 60% colonized, while adjusting for predicted rates of attrition of up to 50% by study end.
Between December 2003 and September 2004, we enrolled 132 HIV-exposed (case) and 128 HIV-unexposed (comparison) infants (260 total). We followed the mother/infant pairs for a total of 3096 person-months with the last patient visit in November 2005. Baseline characteristics were similar between the two groups (Table 1); 25 case versus 44 comparison infants were lost to follow-up (P < 0.01); 1 case versus 6 comparison infants withdrew (P = 0.05); 10 case versus 0 comparison infants died by study end (P = 0.001). Of these 10 case infants, only 2 had reached the 12-month visit and had undergone HIV testing; neither was HIV-positive. Fifteen of 105 HIV-exposed infants still on study by 12 months were HIV seropositive (14.3%, standard error: 3.0%). One tested positive at 12 months but negative at 15 months, presumably a false positive due to residual maternal antibody. Although 48 versus 42 unscheduled clinical illness visits occurred in the case and comparison arms respectively, the rates did not differ statistically after adjusting for person-time at risk. Intercurrent sulfonamide use occurred frequently among the comparison infants. By study end, 56.6% of the comparison infants had been treated at least once with a sulfonamide, occurring at 137 of 648 visits (21.1%).
Table 1. Baseline demographic and clinical characteristics of infants and mothers in longitudinal cohort study of the effect of co-trimoxazole prophylaxis on pneumococcal colonization rates, seroepidemiology and antibiotic resistance in Zambian infants
From 1394 nasopharyngeal swabs, 360 tested positive for S. pneumoniae (25.8%). Of the 360 isolates, 45 (12.5%) were from period 1; 231 (64.2%) from period 2; and 84 (23.3%) from period 3. The sample positivity rate did not vary by the time of year of sampling (data not shown). By contrast, nasopharyngeal colonization was strongly associated with the infants’ age (P < 0.001), peaking in both groups at 12 months (Fig. 2).
Fig. 2. Nasopharyngeal pneumococcal colonization among Zambian infants given co-trimoxazole prophylaxis and comparison group in longitudinal cohort study, by age
Co-trimoxazole exposure modestly suppressed colonization among case infants. Colonization rates were 6.8% higher for cases than comparisons during period 1 (20.9% versus 14.1%, RR: 1.5; 95% CI: 0.9–2.6) and 7.1% higher in period 3 (28.7% versus 21.6%, RR: 1.3; 95% CI: 0.9–1.9). After combining the non-exposure periods (periods 1 and 3), case infants were significantly more likely to be colonized than comparisons (25.3% versus 18.1%, RR: 1.4; 95% CI: 1.0–1.9, P = 0.04). Adjusting for intercurrent sulfonamide treatments among the controls did not change this risk substantially (RR: 1.5; 95% CI: 1.2–1.9). By contrast, during co-trimoxazole exposure (period 2), colonization rates were similar between the two groups (29.8% case versus 27.2% comparison infants, RR: 1.1; 95% CI: 0.9–1.4, P = 0.41; Fig. 2).
The onset of co-trimoxazole prophylaxis led to a rapid increase in co-trimoxazole-resistant pneumococci from the case infants. During period 1, the mean Ln MICs for co-trimoxazole were comparable between the two groups (difference in means: –0.11; 95% CI: –1.2 to 1.0, P = 0.12). In period 2, the mean Ln MICs for co-trimoxazole increased in the case arm but stayed constant in the comparison arm (difference: +0.35; 95% CI: –0.03 to 0.73, P = 0.07). During period 3, the difference in the mean Ln MICs for co-trimoxazole declined among case infants, though it remained elevated relative to the comparison infants (difference: +0.26; 95% CI: –0.54 to 1.05, P = 0.52). During period 2, the median co-trimoxazole MICs were 1.4 times higher for case than comparison infants (P = 0.08) but were similar during periods 1 or 3. The median MICs did not differ significantly for any of the other antibiotics tested during the three periods (Table 2).
Table 2. Case:comparison ratios of median antibiotic MICs in pneumococci isolated from nasopharyngeal cultures taken from Zambian infants in longitudinal cohort study of co-trimoxazole prophylaxis, by study perioda
When categorizing the MICs as sensitive (S), intermediately resistant (I) or resistant (R), the distributions were similar between cases and comparisons during period 1 but diverged during period 2 (Table 3). This was largely explained by rapid increases in co-trimoxazole resistance between visits 1 and 2 (P = 0.04). At baseline (visit 1), the distribution was virtually identical between the two arms (14.8% S, 25.9% I, 59.3% R in cases, versus 16.7% S, 22.2% I, 61.1% R in comparisons; P = 0.96). By visit 2, 6 weeks later, all isolates from case infants were intermediately or highly resistant to co-trimoxazole (case versus comparison infants, RR: 2.2; 95% CI: 1.6–2.9), whereas the comparisons showed only a modest shift towards more highly resistant pneumococci (0.0% S, 7.4% I, 93.6% R in cases, versus 25.0% S, 16.7% I, 76.5% R in comparisons; P < 0.01). Thereafter, resistance rates increased in both groups so that after visit 3, intermediately or highly resistant isolates occurred in similar proportions between the two groups (Fig. 3).
Table 3. Degree of sensitivity to co-trimoxazole among pneumococci isolated from nasopharyngeal cultures taken from Zambian infants (n = 359)a given co-trimoxazole prophylaxis and comparison group, by study periodb
Fig. 3. Proportion of nasopharyngeal pneumococcal isolates classified as sensitive, intermediately resistant or resistant to co-trimoxazole, over time, in longitudinal cohort study of co-trimoxazole prophylaxis among Zambian infants
When combining both I and R categories together as non-susceptible, the relationship between co-trimoxazole prophylaxis and colonization with co-trimoxazole-resistant pneumococci became even stronger (RR: 3.2; 95% CI: 1.3–7.8, P = 0.01). Overall, approximately 10% of all co-trimoxazole non-susceptibility in this population was accounted for by co-trimoxazole prophylaxis (attributable risk: 12%; 95% CI: 6– 18). When also considering intercurrent non-prophylaxis exposure to sulfonamides among the controls, the risk of colonization with a co-trimoxazole non-susceptible pneumococcus increased further (RR: 4.4; 95% CI: 1.9–10.4).
Repeating these analyses for the other antibiotics, co-trimoxazole prophylaxis led to a small but statistically significant increase of colonization with clindamycin non-susceptible pneumococci (RR: 1.6; 95% CI: 1.0–2.6, P = 0.04). Co-trimoxazole use did not increase the risk of non-susceptibility to penicillin (RR: 1.1; 95% CI: 0.7–1.7), erythromycin (RR: 1.0; 95% CI: 0.6–1.7), tetracycline (RR: 0.9; 95% CI: 0.6–1.5) or chloramphenicol (RR: 0.8; 95% CI: 0.3–2.3).
In each of these analyses, the adjusted values after controlling for repeated measures and for baseline demographic variables were virtually identical to the results presented above (data not shown).
We had serotype data for 354/360 samples (98%), of which 44% were covered by the 7-valent conjugate vaccine. The probability that a given isolate would be a 7-valent vaccine strain was not altered by whether the infant was exposed or not to co-trimoxazole (RR: 1.0; 95% CI: 0.7–1.6). However, 7-valent vaccine strain isolates were more likely to be non-susceptible to co-trimoxazole than non-vaccine isolates (RR: 2.2; 95% CI: 1.0–4.8). The distribution of serotypes between the two groups across the three exposure periods is summarized in Fig. 4, Fig. 5 and Fig. 6. The five most common serotypes were: 19f (16.0%), 6b (9.9%), 23f (7.5%), 15 (7.0%) and 14 (6.4%), with 5.9% untypable. The most striking differences were a predominance of serotype 6 among the case infants (6b = 5, 6a = 3, 6 unfactorable = 3) during period 1 (Fig. 4), and an apparent loss of serotype diversity over time (Fig. 6): serotypes 2, 3, 5, 8, 12, 17, 18 and 33 were all found in period 1 and/or period 2, but were absent from both groups in period 3.
Fig. 4. Frequency of nasopharyngeal pneumococcal serotypes in period 1 (pre-cotrimoxazole) of longitudinal cohort study of co-trimoxazole prophylaxis among Zambian infants (n = 45)
Fig. 5. Frequency of nasopharyngeal pneumococcal serotypes in period 2 (on co-trimoxazole) of longitudinal cohort study of co-trimoxazole prophylaxis among Zambian infants (n = 228)
Fig. 6. Frequency of nasopharyngeal pneumococcal serotypes in period 3 (post-cotrimoxazole) of longitudinal cohort study of co-trimoxazole prophylaxis among Zambian infants (n = 84)
In this cohort of mostly HIV-negative Zambian infants followed from age 6 weeks through 18 months, pneumococcal colonization was common, peaked in incidence during the first year of life, and was dominated by serotypes represented by the conjugate 7-valent pneumococcal vaccine. These findings are all consistent with what is generally understood to be typical for colonization patterns of pneumococci in young infants24 and thus increase our level of confidence in interpreting our subsequent findings.
Co-trimoxazole prophylaxis had the following effects on pneumococcal colonization dynamics. First, co-trimoxazole exposure significantly reduced colonization rates, though not below the rate in the comparison infants. While the magnitude of this effect was modest (~ 7% on an absolute scale), it may still be relevant at a population level, insofar as nasopharyngeal colonization is considered a precondition to invasive pneumococcal disease.25,26
Second, co-trimoxazole prophylaxis induced a rapid rise in intermediate and particularly high-level co-trimoxazole resistance. This was our most striking finding. On the one hand, co-trimoxazole-resistant pneumococci were exceedingly common in this population, cases and comparisons alike. While co-trimoxazole resistance in the colonizing pneumococci occurred rapidly with the onset of prophylaxis, resistance to co-trimoxazole increased over time in the comparison infants also, albeit somewhat later. Thus, in a setting of widespread sulfonamide exposure, one could argue that co-trimoxazole prophylaxis merely accelerated a process that was already under way. On the other hand, the induction of co-trimoxazole resistance clearly validates concerns about rising drug resistance from presumptive co-trimoxazole prophylaxis. Moreover, co-trimoxazole prophylaxis accounted for slightly over 10% of the total increase in co-trimoxazole resistance in this study, a surprisingly large fraction given the already high background prevalence of resistance and frequency of sulfonamide exposure. This necessarily prompts the question of whether co-trimoxazole prophylaxis might have a more profound effect in settings where co-trimoxazole resistance is uncommon and/or where other sulfonamide use is less widespread.
Third, co-trimoxazole exposure marginally increased the odds of non-susceptibility to clindamycin but did not appear to induce cross-resistance to other classes of antibiotics. Given that co-trimoxazole and clindamycin come from unrelated drug classes, this is unlikely to be explained by pharmacological cross-tolerance. An alternative explanation is co-selection of linked antibiotic-resistance genes. Supporting this hypothesis is the fact that multiple antibiotic-resistance genes among pneumococci have been demonstrated in clusters grouped together on transposons and that such transposons are linked with specific strains or clones of S. pneumoniae.27–29 Our results contrast with those obtained by Abdel-Haq et al., who noted that co-trimoxazole prophylaxis selected for colonization with multidrug resistant pneumococci.30 However, such selection presumably depends on whether such strains are already circulating in a given community, so we do not feel that our results necessarily conflict with their findings. For the same reason, we would be cautious in inferring whether the pattern of cross-induction of clindamycin resistance observed in the context of this study and population should be extrapolated externally. In our view, a more generalizable interpretation is that our data provide additional evidence that co-trimoxazole exposure has consequences that may extend beyond induction of co-trimoxazole resistance alone but may include unrelated drug classes in patterns that are difficult to predict a priori.
Fourth, co-trimoxazole exposure was not associated with any notable shifts in the distribution of pneumococcal serotypes. Thus, our data provide no support for concerns that co-trimoxazole prophylaxis might reduce the future effectiveness of pneumococcal vaccines by shifting the distribution of prevailing serotypes away from vaccine strains.
The loss of serotype diversity that occurred in both study arms during period 3 was curious. This is unlikely to be explained by sample size, since there was a far greater diversity of serotypes during period 1, despite there being roughly half as many isolates as in period 3. More plausibly, this narrowed spectrum reflects the maturation of the infants’ mucosal immunity, with infants becoming refractory to colonization by certain serotypes over time. In partial support of this theory, Simell et al. noted that nasopharyngeal pneumococcal colonization in infants was inversely correlated with development of strain-specific immunoglobulin A.31
Of concern, co-trimoxazole resistance was extremely common even at baseline, indicating a high community background prevalence of co-trimoxazole-resistant pneumococci – perhaps unsurprising given how frequent sulfonamide exposure was in this population. Though most of our infants were HIV negative, colonization rates were significantly higher among case infants even at baseline. Because this occurred so early in life and because so few of the infants proved to be infected with HIV, HIV-induced immunodeficiency is unlikely to be the explanation. More plausibly, it might reflect other aspects of these infants’ home/environments that increase their pneumococcal exposure risk or susceptibility to colonization, or qualitative/quantitative differences in passive immunity from residual maternal antibody.
The TZI study was conducted to generate empirical population-level evidence about the possible microbiological effects of presumptive co-trimoxazole prophylaxis among HIV-exposed infants, but was not intended to study the efficacy of co-trimoxazole for reducing clinical disease. Clearly, we could have selected any number of pathogens to study, but we felt that the pneumococcus was a logical choice. Studying colonization dynamics in a relatively small cohort closely over an extended period of time reduced the risk that secular events (time of year, intercurrent outbreaks of pneumococcal disease in the community) would confound our results, and allowed us to evaluate the effect of starting and stopping co-trimoxazole prophylaxis, further strengthening inferences regarding cause and effect. However, an obvious limitation is that studying colonization dynamics is not equivalent to studying invasive pneumococcal disease. Another limitation is that the higher rates of study attrition in the comparison-arm infants could have introduced some degree of bias into our measurements. That said, given that pneumococcal colonization is generally asymptomatic, it seems unlikely that colonization and attrition would be confounded.
Co-trimoxazole prophylaxis modestly suppresses nasopharyngeal colonization with S. pneumoniae. Unfortunately, this comes at the price of accelerated acquisition of high-level resistance to co-trimoxazole and potentially other antibiotic classes as well (i.e. clindamycin). The clinical significance of the co-trimoxazole resistance is uncertain, particularly in settings where co-trimoxazole-resistant pneumococci are highly prevalent and sulfonamide exposure extremely common, as in this African community. The lack of effect of co-trimoxazole exposure on the distribution of pneumococcal serotypes is reassuring from the perspective of the future effectiveness of conjugate pneumococcal vaccines. Taken in the context of recent reports of co-trimoxazole’s ancillary benefits in African populations,32,33 on balance, our findings support WHO’s current policy on presumptive co-trimoxazole prophylaxis. That said, our data reinforce the pressing need for a refined strategy for early diagnosis of infant HIV infection, both to minimize unnecessary drug exposure and to optimize the use of precious resources. ■
We thank Ms Anne Bolmström, president of AB-Biodisk for donating a portion of the Etests® used in this study; Mr Theo Leuenberger of Roche Pharmaceuticals for donating co-trimoxazole; also Dr Anne von Gottberg; Ms Christine Ayash, Ms Anna Knapp; Ms Sushma Hyoju and Dr Stephen Pelton. We also thank the study nurses Victoria Luo, Joyce M Mulenga, Joyce W Mulenga, Rosaline Kapupa, Edna Mungwa and Sister Kasongo. The nevirapine and Determine® tests were donated by Boehringer Ingelheim and Abbott Laboratories through the Axios Corporation. Some of these data were presented in abstract form at the 2004 American Society of Tropical Medicine and Hygiene conference in Miami, FL, USA.
Funding: TZI was supported by NIH/NIAID K23 AI 62208 and a cooperative agreement between Boston University and the Office of Health and Nutrition of the United States Agency for International Development: GHS-A-00-03-00020-00. The funders and commercial donors listed above played no role in the design, implementation, analysis/interpretation of the data, or writing of the manuscript.
Competing interests: None declared.
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