Department of Obstetrics & Gynecology, Christiana Care Health Services, 4755 Ogletown Stanton Road, Newark, DE, 19713, USA.
Center for Global Health, Department of Medicine and Obstetrics & Gynecology, Weill Cornell Medicine, 402 E 67th Street, 2nd floor, New York, NY, 10021, USA.
Curr HIV/AIDS Rep. 2022 Dec;19(6):455-470. doi: 10.1007/s11904-022-00641-x. Epub 2022 Oct 29.
Pregnant people living with HIV (PLWH) are at especially high risk for progression from latent tuberculosis infection (LTBI) to active tuberculosis (TB) disease. Among pregnant PLWH, concurrent TB increases the risk of complications such as preeclampsia, intrauterine fetal-growth restriction, low birth weight, preterm-delivery, perinatal transmission of HIV, and admission to the neonatal intensive care unit. The grave impact of superimposed TB disease on maternal morbidity and mortality among PLWH necessitates clear guidelines for concomitant therapy and an understanding of the pharmacokinetics (PK) and potential drug-drug interactions (DDIs) between antitubercular (anti-TB) agents and antiretroviral therapy (ART) in pregnancy.
This review discusses the currently available evidence on the use of anti-TB agents in pregnant PLWH on ART. Pharmacokinetic and safety studies of anti-TB agents during pregnancy and postpartum are limited, and available data on second-line and newer anti-TB agents used in pregnancy suggest that several research gaps exist. DDIs between ART and anti-TB agents can decrease plasma concentration of ART, with the potential for perinatal transmission of HIV. Current recommendations for the treatment of LTBI, drug-susceptible TB, and multidrug-resistant TB (MDR-TB) are derived from observational studies and case reports in pregnant PLWH. While the use of isoniazid, rifamycins, and ethambutol in pregnancy and their DDIs with various ARTs are well-characterized, there is limited data on the use of pyrazinamide and several new and second-line antitubercular drugs in pregnant PLWH. Further research into treatment outcomes, PK, and safety data for anti-TB agent use during pregnancy and postpartum is urgently needed.
感染 HIV 的孕妇(PLWH)发生潜伏性结核感染(LTBI)向活动性结核病(TB)进展的风险特别高。在 PLWH 孕妇中,并发 TB 会增加子痫前期、胎儿宫内生长受限、低出生体重、早产、围产期 HIV 传播和新生儿重症监护病房收治等并发症的风险。TB 疾病的叠加对 PLWH 产妇发病率和死亡率的严重影响,需要明确的联合治疗指南,以及了解抗结核(anti-TB)药物与妊娠期间抗逆转录病毒治疗(ART)之间的药代动力学(PK)和潜在药物相互作用(DDI)。
本文讨论了目前关于 ART 治疗期间 PLWH 孕妇使用 anti-TB 药物的现有证据。妊娠和产后 anti-TB 药物的 PK 和安全性研究有限,关于在妊娠期间使用二线和新型 anti-TB 药物的数据表明存在几个研究空白。ART 和 anti-TB 药物之间的 DDI 可降低 ART 的血浆浓度,从而增加 HIV 的围产期传播风险。目前针对 LTBI、药物敏感型 TB 和耐多药 TB(MDR-TB)的治疗建议来自于观察性研究和 PLWH 孕妇的病例报告。尽管在妊娠期间使用异烟肼、利福平、乙胺丁醇及其与各种 ART 的 DDI 已得到充分研究,但关于妊娠期间使用吡嗪酰胺和几种新型二线抗结核药物的数据有限。迫切需要进一步研究抗结核药物在妊娠和产后期间的治疗结果、PK 和安全性数据。