Sexually transmitted infections (STIs) including Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), Treponema pallidum (TP), and cytomegalovirus (CMV) may lead to adverse pregnancy and infant outcomes. The role of combined maternal STIs in HIV mother-to-child transmission (MTCT) was evaluated in mother-infant pairs from NICHD HPTN 040.
Urine samples from HIV-infected pregnant women during labor were tested by polymerase chain reaction (PCR) for CT, NG, and CMV. Infant HIV infection was determined by serial HIV DNA PCR testing. Maternal syphilis was tested by VDRL and confirmatory treponemal antibodies.
A total of 899 mother-infant pairs were evaluated. Over 30% had at least one of the following infections (TP, CT, NG, and/or CMV) detected at the time of delivery. High rates of TP (8.7%), CT (17.8%), NG (4%), and CMV (6.3%) were observed. HIV MTCT was 9.1% (n = 82 infants). HIV MTCT was 12.5%, 10.3%, 11.1%, and 26.3% among infants born to women with CT, TP, NG or CMV respectively. Forty-two percent of HIV-infected infants were born to women with at least one of these 4 infections. Women with these infections were nearly twice as likely to have an HIV-infected infant (aOR 1.9, 95% CI 1.1–3.0), particularly those with 2 STIs (aOR 3.4, 95% CI 1.5–7.7). Individually, maternal CMV (aOR 4.4 1.5–13.0) and infant congenital CMV (OR 4.1, 95% CI 2.2–7.8) but not other STIs (TP, CT, or NG) were associated with an increased risk of HIV MTCT.
HIV-infected pregnant women identified during labor are at high risk for STIs. Co-infection with STIs including CMV nearly doubles HIV MTCT risk. CMV infection appears to confer the largest risk of HIV MTCT.
Citation: Adachi K, Xu J, Yeganeh N, Camarca M, Morgado MG, Watts DH, et al. (2018) Combined evaluation of sexually transmitted infections in HIV-infected pregnant women and infant HIV transmission. PLoS ONE 13(1): e0189851. https://doi.org/10.1371/journal.pone.0189851
Editor: Jacobus P. van Wouwe, TNO, NETHERLANDS
Received: July 25, 2017; Accepted: November 30, 2017; Published: January 5, 2018
This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: The NICHD HPTN 040 study was supported by NICHD Contract #HHSN267200800001C (NICHD Control # N01-HD-8-0001) and U01 AI047986 (Brazilian AIDS Prevention Trials International Network), NIAID/ NIH. Overall support for the International Maternal Pediatric Adolescent AIDS Clinical Trials Group (IMPAACT) was provided by the National Institute of Allergy and Infectious Diseases (NIAID) U01 AI068632, UM1AI068632 (IMPAACT LOC), UM1AI068616 (IMPAACT SDMC) and UM1AI106716 (IMPAACT LC), with co-funding from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) and the National Institute of Mental Health (NIMH) AI068632. The original parent study was supported in part by Boehringer Ingelheim Pharmaceuticals Inc. (BIPI), and GlaxoSmithKline, on behalf of ViiV Healthcare and support was also received from Cepheid for the testing of CT and NG in a prior HPTN 040 sub-study. Support was also provided by the UCLA Children’s Discovery and Innovation Institute (CDI) through the Harry Winston Fellowship Award, the UCLA AIDS Institute, the UCLA Center for AIDS Research (CFAR) NIH/ NIAID AI02869 and AI28697, the UCLA Pediatric AIDS Coalition, and Westat contract with NIH/NICHD HHSN275201300003C. The content, conclusions and opinions expressed in this article are those of the authors and do not necessarily represent those of the National Institutes of Health, the U.S. Department of Health and Human Services, or the U.S. Department of State, affiliated universities, programs or companies. Co-authors Margaret Camarca and Jiahong Xu were employed by Westat. Westat provided support in the form of salary for the co-authors MC and JX but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors, themselves, did play a role in the study design, data collection, analysis, preparation of the manuscript. The specific roles of these authors to the study are articulated in the ‘author contributions’ section.
Competing interests: We have the following interests: Co-author Margaret Camarca is employed by Westat, and co-author Jiahong Xu is a former employee of Westat. Funding was received from commercial sources for the parent study HPTN 040 clinical trial from Boehringer Ingelheim Pharmaceuticals Inc. (BIPI), and GlaxoSmithKline, on behalf of ViiV Healthcare, all of which donated antiretrovirals for the conduct of the primary parent study evaluating neonatal prophylaxis. Support was also received from Cepheid for the testing of CT and NG during the implementation of another previous HPTN 040 sub-study. There are no patents, products in development or marketed products to declare. This does not alter our adherence to all the PLOS ONE policies on sharing data and materials.
Abbreviations: HIV, human immunodeficiency virus; NICHD, National Institute of Child Health and Human Development; HPTN, HIV Prevention Trials Network; STI, sexually transmitted infection; CT, Chlamydia trachomatis (chlamydia); NG, Neisseria gonorrhoeae (gonorrhea); TP, Treponema pallidum (syphilis); CMV, cytomegalovirus; MTCT, mother-to-child transmission
Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), and Treponema pallidum (TP) contribute to formidable global burden of treatable bacterial sexually transmitted infections (STIs) with nearly a quarter of a billion of new cases reported annually. These treatable STIs disproportionately impact the health of pregnant women, particularly adolescents and young women in low and middle-income countries.[1–3] Untreated CT, NG, and TP are associated with adverse pregnancy outcomes including spontaneous abortion, stillbirth, preterm labor and delivery. Maternal infection with these conditions has also been associated with neonatal infections such as conjunctivitis (CT, NG), pneumonia (CT), and disseminated infection (TP, NG); TP may be particularly devastating given its associations with multi-organ involvement, failure to thrive, and neonatal death.[4–11] Apart from these bacterial STIs, other sexually transmitted infections including viruses such as cytomegalovirus (CMV)[12, 13] are often overlooked but can also have profound infant sequelae including neurodevelopmental anomalies and sensorineural hearing loss when acquired in-utero.[14, 15] CMV, which can be transmitted by close or sexual contact, is the major infectious etiology of sensorineural hearing loss and developmental delay, and congenital infection globally may be as high as 1–5%.[16–18] Routine antenatal screening for these conditions is not routine practice in many regions of the world, particularly in low and middle-income countries. These practices may have particular importance for high-risk groups such as HIV-infected pregnant women and their infants.
Given earlier findings of our HPTN 040 sub-studies evaluating the individual effects of STIs on HIV MTCT (CT and NG and HIV MTCT; TP and HIV MTCT; and CMV and HIV MTCT),[19–22] the following analysis provides a more comprehensive evaluation of the risk factors associated with these STIs (CT, NG, TP, and CMV) and the impact of these combined untreated infections on HIV MTCT in a high-risk cohort of late-presenting HIV-infected pregnant women who did not receive antiretroviral drugs (ARV) during pregnancy.
This study was a retrospective, cross-sectional clinical trial sub-study of the National Institute of Child Health and Human Development (NICHD) HIV Prevention Trials Network (HPTN) 040 trial, which is also known as the International Maternal Pediatric Adolescent AIDS Clinical Trials Network (IMPAACT) P1043. Clinical data and specimens were collected from NICHD/HPTN 040 (P1043), a phase 3, triple-arm, randomized, open-label, multi-center study aimed at the prevention of intrapartum HIV transmission to infants born to HIV-infected pregnant women, who had not received antiretroviral drugs until labor and delivery due to late diagnosis of infection. Enrollment in the HPTN 040 parent study occurred from April 2004 through July 2010 with the last patients followed until 2011, which included 1684 HIV-infected pregnant women, including the majority who were diagnosed as HIV-infected at the time of labor and delivery. All mothers provided written informed consent. Enrollment occurred at multiple sites in Brazil, South Africa, Argentina, and the United States. Infants <32 weeks of age were excluded from the study. All HIV-exposed infants enrolled in the study were formula-fed. Infants were randomized at birth to one of three neonatal prophylactic ARV regimens. The primary endpoint was HIV infection status at 3 months of age.
Women were enrolled during labor and delivery with information obtained on maternal sociodemographics, obstetric history including prior prenatal care, prior stillbirths, and risk behaviors during pregnancy. Maternal plasma HIV RNA levels and T lymphocyte subsets were collected. Syphilis testing was performed using Venereal Disease Research Laboratory (VDRL) titers with confirmatory treponemal syphilis antibody tests performed, as per standard of care. Infants were followed until 6 months of age for safety and toxicity monitoring in the parent study with serious adverse events (SAEs) recorded as previously described.
HIV testing of infants occurred within 48 hours of birth, 14 days, 4–6 weeks, 3, and 6 months of age. Confirmatory HIV DNA testing was done for positive results. Testing procedures have been previously described.
Chlamydia, gonorrhea, and CMV testing.
Stored maternal urine samples collected at the time of labor and delivery or within 48 hours of giving birth were frozen and stored at study sites. Aliquots (7 mL each) of stored frozen urine were shipped for testing at Cepheid, Sunnyvale, CA. Urines were tested for the presence of CT and NG using the Xpert® CT/NG assay. Results were reported as positive, negative or indeterminate. Indeterminate test results were repeated up to two times, and those that remained indeterminate were excluded from data analysis. Remaining 1mL aliquots of maternal and infant urines (also collected within 48 hours of delivery) were tested by qualitative Real-time PCR for CMV DNA (FOCUS Diagnostics CMV Analyte Specific Reagent), and those with positive results were tested by quantitative CMV PCR. In this study, given the limited number of maternal urines available for CMV PCR testing, primarily infant CMV urine results were used in the analysis, (although analysis was also done with maternal urine CMV PCR results when available as indicated in our Tables). The STIs were not treated in pregnancy because the women had not presented for care, and STI testing was done retrospectively on stored specimens.
All computations were done using SAS software v9.3 (Cary, NC, USA). Two-sample t-test or Kruskal-Wallis test was used to compare mean or median differences for continuous variables as appropriate. Chi-squared or Fisher’s exact test was used to compare differences of proportions for categorical variables. Univariate and multivariate logistic regression modeling was used to examine the relationship of HIV MTCT and maternal STI infection (CT, NG, TP, CMV) with potential risk factors respectively. The risk factors include maternal demographic, alcohol, tobacco, illegal substance use, pregnancy and delivery characteristics, and HIV-related clinical characteristics. Covariates with a p-value of 0.15 or less from univariate models were selected for the initial multivariable model. Covariates with an overall p-value <0.05 were retained in the final model.
The study was approved by the institutional review boards and national ethics committees at each of the participating study sites. The study was approved by the OHRP, the HPTN ethics board and the NICHD. It was also approved by the IRBs of the following institutions locally: Fiocruz, Rio de Janeiro, Hospital dos Servidores do Estado, Rio de Janeiro, Hospital Geral de Nova Iguacu, Rio de Janeiro, Grupo Hospitalar Conceicao in Porto Alegre (Hospital Conceicao and Hospital Femina), Santa Casa da Misericordia, Porto Alegre, Universidade Federal de Minas Gerais, Belo Horizonte, Universidade Federal de Sao Paulo, Sao Paulo and Ribeirao Preto, all in Brazil; Foundation for Maternal and Infant Health, Buenos Aires, Argentina, SAMRC and Perinatal HIV Research Unit, Soweto, South Africa, Tygerberg Hospital, Cape Town, South Africa, Boston University School of Medicine, MA, USA. UCLA IRB #02-04-86-12 approved the NICHD HPTN 040 study and was the lead IRB for the overall study. This particular study was a secondary endpoint analysis of the parent study and evaluated previously collected data and specimens from NICHD HPTN 040. As such, it received the UCLA IRB approval exemption number 14–001348.
Baseline characteristics of mother-infant pairs
Among 1684 mother-infant pairs enrolled in the parent study, 899 pairs (53.4%) had specimens available for maternal CT, NG, TP, and infant CMV testing. Specimen availability for testing of all four potential co-infections determined inclusion in the present analysis. As such, 785 mother-infant pairs (approximately 47% of the original HPTN 040 cohort) were excluded. We evaluated potential differences in both populations and determined that both groups were very similar in most parameters (S1 Table). Most women in this analysis (86.2%) were from the Americas (Brazil, Argentina, and the U.S.) compared to South Africa (13.8%). (Table 1) The mean maternal age was 26.5 (SD 6.3) years, and the majority received some prenatal care during pregnancy (69.4%). High rates of alcohol (36.5%), tobacco (37%), and illegal substance (9.8%) usage were noted during pregnancy. There were also high rates of prior poor pregnancy outcomes reported such as stillbirth (4.8%). Median log10 HIV plasma viral load at the time of delivery was 4.2 (interquartile range = IQR 1.7–6.5) copies/mL, with 58% having HIV viral load >10,000 copies/mL; the median CD4 count was 465 (IQR 12–2160) cells/mm3. Preterm delivery (<37 weeks) occurred in 9.2% of infants, and 15.8% were of low birth weight (<2500 grams). Approximately 38.9% of infants experienced a serious adverse event (SAE) during the study period.
Rates of co-infections were high in this sub-cohort; over 30% of women had at least one of the infections of interest (TP, CT, NG, and/or CMV). High rates of TP (8.7%), CT (17.8%), and NG (4%) were found. Based on a positive infant urine CMV PCR at birth, which revealed the presence of congenital CMV (cCMV) infection and was used as a surrogate for active maternal CMV infection, 6.3% of women had CMV infection during pregnancy. (Table 1)
Characteristics of STI positive and STI negative HIV-infected pregnant women
Characteristics of mother-infant pairs were compared for women with and without STIs (TP, CT, NG, and/or CMV). (Table 2) Most women with STIs were under 30 years of age (77.3%). Rates of STIs (35.6%) were highest among young women (13–24 years). The results from the adjusted multivariable model indicated that younger women were 1.6 to nearly two times more likely to have an STI (aOR 1.9, 95% CI 1.3–2.8 for those 13–24 years of age and aOR 1.6, 95% CI 1.1–2.5 for those 25–29 years of age) when compared with older women ages 30 years and above. Infants with any SAEs were 2.4-times more likely to born to mothers with STIs (aOR 2.4, 95% CI: 1.8–3.2). Cesearean delivery prior to rupture of membranes was less frequent in women with maternal STIs (aOR 0.55, 95% CI 0.37–0.83). (Table 2) In addition, frequent alcohol use (≥ 1/week) (OR 1.7, 95% CI 1.2–2.5), frequent tobacco use (>10/day) (OR 1.5, 95% CI 1.0–2.3), and illegal substance use (OR 1.7, 95% CI 1.1–2.6) as well as low birth weight infants (OR 1.5, 95% CI 1.0–2.2) were also associated with maternal STI-infection. However, these risk factors were not significant in the adjusted multivariate models.
Syphilis, chlamydia, gonorrhea, CMV and HIV mother-to-child transmission (MTCT)
82 infants of 899 (9.1%) HIV-infected mothers acquired HIV (in utero or intrapartum). Fifty (61%) infants were HIV-infected in utero, while 32 (39%) were infected intrapartum. Thirty-five (42.7%) HIV-infected infants were born to women with at least one of the STIs of interest (TP, CT, NG and/or CMV), whereas maternal STI rates among HIV-uninfected infants were 29.1%. (Table 3) Of the 35 HIV-infected infants born to women with STIs, 11 (31.4%) were born to women with multiple STIs, among whom in utero infection was the more common means of infant HIV acquisition (73%). (S2 Table includes additional details of HIV in utero, intrapartum transmission and specific maternal STIs). While HIV MTCT rates were higher among women with individual TP, CT, and NG infections compared to women without these STIs at delivery, this was not statistically significant: TP (10.3% vs 9%, p = 0.7), CT (12.5% vs 8.4%, p = 0.1), NG (11.1% vs 9%, p = 0.7). In contrast, HIV MTCT rates were significantly different in the presence of infant cCMV infection (i.e. congenital CMV infection), (26.3% vs 8%, p<0.0001)] and maternal CMV infection [(i.e. maternal CMV viruria), (30.4% vs 8.3%, p = 0.01)] compared to those without CMV. (Table 3) Infants born to women with one of these STIs (CT, NG, TP, and/or CMV) were nearly twice as likely to be HIV-infected (OR 1.8, 95% CI 1.1–2.9) compared to those born to women without these infections; these findings (aOR 1.9, 95% CI 1.1–3.0) persisted after adjusting for risk factors including maternal HIV viral load, maternal HIV log10 viral load, maternal CD4 count, prolonged rupture of membranes (either 12–24 hours or >24 hours), illegal substance use during pregnancy, and infant death.
Detectable CMV from the urine of women and infants were important risk factors for infant HIV acquisition. Women with CMV detected at the time of labor and delivery were over four times more likely to have an HIV-infected infant than those without CMV viruria in adjusted analyses (aOR 4.4, 95% CI 1.5–13.0). Similarly, women whose infants had CMV detected in urine after birth (i.e. congenital CMV; cCMV) were more likely to also have infants with HIV-infected than those without CMV viruria (i.e. without congenital CMV) in the unadjusted analysis (OR 4.1, 95% CI 2.2–7.8), but this did not remain statistically significant in adjusted analysis. (Table 3) Other factors associated with infant HIV acquisition included log10 HIV maternal viral load (aOR 1.9, 95% CI 1.4–2.5), illegal substance use during pregnancy (aOR 2.3, 95% CI 1.2–4.6), and subsequent infant death (aOR 7.1, 95% CI 2.7–18.8), whereas higher maternal CD4 count was protective (OR 0.90, 95% CI 0.82–0.98) in the unadjusted analysis. (Table 3)
Further evaluation was done to compare the proportion of maternal STI infections (0 vs 1 vs 2 vs 3 STIs) between HIV-infected and HIV-uninfected infants. (Table 4) Of the 35 HIV-infected infants born to women with STIs (CT, NG, TP, and/or CMV), the majority were those born to women with one STI (n = 24, 68.6%) as opposed to two (n = 10, 28.6%) or three STIs (n = 1, 2.9%). However, significant differences were noted in the proportion of maternal STI infections (0 vs 1, 2 or 3 STIs) and infant HIV-infection, which ranged from 7.5% (47/626) for 0 STIs to 23.8% (10/42) for 2 STIs. Additional regression analyses were done to elucidate these relationships between the number of STIs and HIV MTCT. Women with two STIs were 3.4 times more likely to transmit HIV to their infants than those without STIs (aOR 3.4, 95% CI 1.5–7.7). (Table 3)
The results of this study were notable for the high prevalence of overall STIs (TP, CT, NG, and CMV) in this sub-cohort of HIV-infected pregnant women. The presence of at least one of these STIs represented an increased risk for HIV MTCT, particularly two STIs, with CMV being the most important co-infection contributing to HIV perinatal transmission.
In general, limited published studies have focused on evaluating the impact of untreated maternal STIs such as CT, NG, TP, and active CMV infection in pregnancy on HIV mother-to-child transmission (MTCT), nor have they comparatively evaluated the potential contribution of individual co-infections within the same cohort on perinatal HIV transmission. The biological plausibility for STIs increasing HIV MTCT risk was suggested in studies of non-pregnant women which demonstrated increased HIV genital shedding in the presence of STIs.[24, 25] Chorioamnionitis has also been demonstrated to increase the risk of HIV MTCT.[26–33] Selected studies have demonstrated a link between specific STIs with HIV MTCT, including results from our prior individual HPTN 040 analyses.[19–22, 34–37]
Over 30% of HIV-infected pregnant women in the present analysis had at least one STI (TP, CT, NG, and/or CMV). Our findings re-emphasize that women in our study were at high-risk for multiple STIs apart from HIV, particularly younger women. Predictors of STIs such as younger maternal age has been previously well-documented.[38–43] Women enrolled in the parent study were a high-risk group by definition; they were late to present for HIV diagnosis and not on antiretrovirals (ARVs) during pregnancy because they were only diagnosed with HIV at the time of labor and delivery. Nearly 30% did not receive antenatal care and more than a third of women engaged in tobacco, alcohol, and/or illegal substance use during pregnancy.
Collectively, results of this analysis provide additional support that STIs (TP, CT, NG, and/or CMV) increase the risk of HIV MTCT by nearly two-fold and for those with two STIs, possibly more than three-fold. Forty-three percent of infants with HIV were born to women with at least one of these STIs, while rates of HIV MTCT were most pronounced in women with CMV (>26% but possibly as high as >30% for those with CMV viruria) and CT (12.5%) infection.
Our previous studies of individual STIs also demonstrated that these conditions were associated with an increased risk of HIV MTCT. In our earlier individual analyses, 10% of the original NICHD HPTN 040 maternal cohort had positive syphilis results and were twice as likely to transmit HIV to their infants (adjusted OR 2.1, 95% CI 1.3–1.4). Among 1373 HIV-infected pregnant women with high rates of CT (18.1%) and NG (4.6%), CT appeared to pose a possible 1.5-fold increased risk of HIV MTCT (OR 1.5, 95% CI 0.94–2.3). We believe that the present study did not highlight this MTCT risk as clearly due to the reduction in sample size required to perform a combined analysis, which included testing of subjects for all four co-infections. Apart from our own published results from HPTN 040, literature focusing on the impact of STIs (TP, CT, and NG) and the risk of HIV MTCT has also demonstrated mixed results, particularly for CT and NG.[33, 34, 36, 40]
In the present study, maternal CMV (especially CMV viruria) was significantly associated with an increased risk of HIV MTCT (more than four-fold). A prior analysis of the same cohort demonstrated high rates of CMV viruria (9.2%) among HIV-infected pregnant women at the time of delivery, with maternal CMV viruria being associated with a similar but higher risk of HIV MTCT (aOR 5.6, 95% CI 1.9–16.8). The clinical significance of detectable CMV viruria at the time of labor and delivery in HIV-infected pregnant women not on ARVs, however, is not well-understood. Considering that it is very likely that most of the studied women were already CMV seropositive before pregnancy due to the frequent exposure to CMV in these populations, CMV viruria might result from CMV reactivation in the genitourinary tract or reinfection with a new virus strain.
The relationship between HIV and CMV perinatal infections is complex, since infection with one may be a risk factor for infection with the other pathogen. Yet, while several studies have shown that HIV-exposure in pregnancy is a risk factor for congenital CMV, fewer have demonstrated that congenital CMV acquisition is also a risk factor for HIV perinatal transmission.[31, 37, 45, 46] To our knowledge, the only other primary study to address this aspect of the relationship was a retrospective case-control study of 293 HIV-infected and HIV-exposed, uninfected infants from Thailand.[37, 47] They found that congenital CMV was a risk factor for HIV MTCT, particularly for in utero HIV (OR 8.1, 95% CI 1.5–63.7).
In summary, maternal co-infections such as TP, CT, NG, and CMV facilitate HIV perinatal transmission by a variety of means. Genital tract infections from these organisms may lead to cervicitis, which may trigger increased cervico-vaginal HIV viral shedding [24, 25, 48–52] or may cause acute or chronic placental inflammation. [26, 30–34] This inflammation at the maternal-fetal interface may induce immune activation and alter cytokine production, increasing viral load, and upregulating the expression of CCR5 T-cell receptors as well as CCR5 HIV co-receptors on Hofbauer cells (macrophages) in the placenta, which contribute towards increased HIV tropism and infectivity.[46, 53] It has been suggested that many of these factors are especially important in understanding the role CMV infection plays as a risk factor for HIV MTCT, particularly at the placental interface. These pathogens appear to effectively overcome inherent placental antiviral mechanisms that safeguard against fetal infection.[46, 53]
As discussed previously in our results section, specimen availability for testing for potential co-infections determined inclusion in the present analysis. While study inclusion and exclusion populations were similar, some differences were noted in maternal age, mode of delivery, prenatal care, alcohol use, tobacco use, and maternal HIV viral load. In addition, in the parent study, 28% of subjects came from South Africa and 72% from the Americas. This proportion was not maintained in the sub-analysis as specimen availability was limited for South African subjects. Therefore, 13.8% of subjects were from South Africa and the remainder from the Americas in the present analysis, p < 0.0001. This implies that our results might not be as generalizable to the South African site. Additional limitations include inability to test for other STIs and genital tract infections such as bacterial vaginosis, Trichomonas vaginalis, and Herpes simplex virus.
We conducted this analysis to explore the potential synergy between several co-infections and increased risk for HIV MTCT in a large cohort of HIV-infected mothers and HIV-exposed infants. HIV-infected pregnant women in this cohort were at very high risk for STIs (TP, CT, NG, and/or CMV). The presence of one or more infections nearly doubled the odds of HIV MTCT, and the presence of two co-infections tripled the odds. In particular, CMV in HIV-infected pregnant women, especially the presence of maternal CMV viruria at delivery, appeared to confer the largest risk of perinatal HIV transmission. Our study’s results emphasize the importance that undiagnosed STIs may play in pregnancy as risk factors for HIV MTCT. Our data underscores the need to augment current existing antenatal care programs to include STI screening, particularly for high-risk women such as young, HIV-infected pregnant women as well as ensuring that HIV-infected women have consistent access to antiretroviral treatment and monitoring, particularly during pregnancy.
S1 Table. Comparison of included vs. excluded HPTN 040 study mother-infant pairs.
In addition to the authors, members of the NICHD/HPTN 040/PACTG 1043 protocol team include the following: Argentina, Buenos Aires- Foundation for Maternal and Infant Health (FUNDASAMIN): Edgardo Szyld, Silvia Marzo. Brazil, Belo Horizonte- Federal University of Minas Gerais: Flavia Faleiro Ferreira, Fabiana Kakehasi. Porto Alegre-Hospital Nossa Senhora da Conceicao: Rita Lira. Porto Alegre-Hospital Femina: Carla Franceschini de Fraga, Rita Lira. Porto Alegre-Irmandade da Santa Casa de Misericordia de Porto Alegre: Debora Fernandes Coelho, Alberto Sanseverino, Luis Carlos Ribeiro. Rio de Janeiro-Hospital dos Servidores do Estado: M. Leticia Santos Cruz, Ezequias Martins, Jacqueline Anita de Menezes, Luisa Andrea Torres Salgado. Rio de Janeiro- Hospital Geral de Nova Iguaçu: Ana Valeria Cordovil, Andréa Gouveia, Priscila Mazzucanti, Jorge Eurico Ribeiro. Ribeirao Preto -Universidade de São Paulo: Geraldo Duarte, Adriana Aparecida Tiraboschi Barbaro, Carolina Sales Vieira. São Paulo-Universidade Federal de São Paulo: Regina Succi. South Africa, Capetown-Stellenbosch University and Tygerberg Hospital: Mark Cotton, Jeanne Louw, Elke Maritz. Johannesburg-Perinatal HIV Research Unit, University of Witwatersrand and Chris Hani Baragwanath Hospital: Sarita Lalsab, Shini Legoete, James Alasdair McIntyre, Mandisa Nyati. United States, Baltimore-Johns Hopkins University: Allison Agwu, Jean Anderson, Joan Bess, Jonathan Ellen, Todd Noletto, Nancy Hutton. Gainesville-Shands Hospital: Carol Delany, Robert M. Lawrence. Jacksonville-University of Florida: Chas Griggs, Mobeen Rathore, Kathleen Thoma, Michelle Tucker. Long Beach- Miller Childrens Hospital: Audra Deveikis, Susan Marks. Newark-University Medical and Dental School of NJ: Linda Bettica, James M. Oleske. San Juan City-San Juan City Hospital: Midnela Acevedo Flores, Elvia Pérez. Oswaldo Cruz Foundation, Rio de Janeiro (FIOCRUZ): Ronaldo I. Moreira, Marilia Santini de Oliveira, Monica Derrico, Valéria Ribeiro, Thiago Torres e FIOTEC (Fundação para o Desenvolvimento Científico e Tecnológico). Westat, Inc.: James Bethel, Emmanuel Aluko, Yolanda Bertucci, Jennifer Bryant, Patty Chen, Barbara Driver, Ruby Duston, Adriana Ferreira, Priya Guyadeen, Sarah Howell, Marsha Johnson, Linda Kaufman, Naomi Leshabane, Lilya Meyerson, Rita Patel, Lubima Petrova, Georgine Price, Susan Raitt, Scott Watson, Yiling Xu, Eunice Yu. Other protocol team members included Jennifer Read from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), Elizabeth Smith and Sheryl Zwerski from the National Institute of Allergy and Infectious Diseases (NIAID). Please note that Karin Nielsen-Saines is the NICHD HPTN 040 Study Group Protocol Chair (email@example.com).
The authors thank the patients and their families who enrolled in this trial. We would like to acknowledge laboratory personnel who conducted all of the urine specimen preparation and shipment (for chlamydia, gonorrhea, and CMV sub-studies), Bonnie Ank, Mary Ann Hausner, and Jessica Liu. We also thank Marita McDonough and Lauren Petrella from Boehringer Ingelheim Pharmaceuticals and Helen Watson from GlaxoSmithKline (on behalf of ViiV Healthcare) for assistance with the donation of study drugs from their respective companies for the conduct of the parent study.
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