Department of Epidemiology, School of Public Health, Boston University, Boston, MA, USA.
Division of Infection and Immunity, School of Biomedical Sciences, University of Western Australia, Perth, WA, Australia; Division of Medical Microbiology, University of Cape Town, Cape Town, South Africa.
Lancet Glob Health. 2021 Dec;9(12):e1740-e1749. doi: 10.1016/S2214-109X(21)00407-1.
The risk of tuberculosis disease after recent exposure is greatest before age 5 years; however, the mechanisms explaining this increased risk are not well elucidated. Acquisition of viral infections, such as cytomegalovirus, in early life might modulate the immune system. We aimed to evaluate the acquisition of cytomegalovirus infection in infancy and the development of tuberculosis disease in children.
In this prospective, birth cohort study we enrolled pregnant women who were between 20 and 28 weeks of gestation attending antenatal care in Paarl, a periurban setting outside of Cape Town, South Africa. Participants were recruited from two clinics (TC Newman and Mbekweni). Infants were given Bacillus Calmette-Guérin vaccination at birth as per national policy. Nasopharyngeal swabs for cytomegalovirus detection using qPCR were done for infants at birth, age 3 and 6 weeks, and age 3, 6, 12, and 24 months. Children were prospectively followed up for tuberculosis disease until age 9 years using tuberculin skin testing, radiographic examinations, GeneXpert, and sputum testing. Tuberculin skin tests were done at the 6-month visit and then at age 12, 24, 36, 48, and 60 months, and at the time of lower respiratory tract infection. We compared tuberculosis disease incidence after age 1 year or after age 6 months in children with and without cytomegalovirus infection using Cox regression and hazard ratios (HRs) with 95% CIs.
Between March 5, 2012, and March 31, 2015, 1225 pregnant women were recruited and enrolled in the birth cohort. 88 (7%) women were excluded because of loss to antenatal follow-up or pregnancy losses. Of 1143 livebirths, 68 (6%) mother-infant pairs were excluded. In total, 963 children were serially tested for cytomegalovirus (7186 cytomegalovirus measurements taken; median six tests per child, IQR 2-11). The prevalence of congenital cytomegalovirus at age younger than 3 weeks was 2% (18 of 816). Cytomegalovirus positivity increased continuously with age from 3% (27 of 825) by age 6 weeks to 21% (183 of 882) by 3 months, 35% (315 of 909) by 6 months, and 42% (390 of 933) by 12 months. Mother-infant pairs were followed up for a median of 6·9 years (IQR 6·0-7·8). The risk of tuberculosis disease in children after age 1 year was higher in those with cytomegalovirus infection by age 6 weeks (adjusted HR 4·1, 95% CI 1·2-13·8; p=0·022), 3 months (2·8, 1·4-5·8; p=0·0040), 6 months (3·6, 1·7-7·3; p<0·0001), 12 months (3·2, 1·6-6·4; p=0·0010), and 24 months (4·2, 2·0-8·8; p<0·0001). The risk of microbiologically confirmed tuberculosis disease was also higher among children acquiring cytomegalovirus infection before age 3 months (adjusted HR 3·2, 95% CI 1·0-10·6; p=0·048), 6 months (3·9, 1·2-13·0; p=0·027), 12 months (4·4, 1·2-16·3; p=0·027), and 24 months (6·1, 1·3-27·9; p=0·020). In children older than 1 year, the risk of tuberculosis disease was consistently greater in those with high cytomegalovirus loads than in those with low cytomegalovirus loads that were acquired before age 3 months (adjusted HR 2·0 vs 3·7; p=0·0020; both groups compared with cytomegalovirus negative reference) and before age 12 months (2·7 vs 3·7; p=0·0009).
Infants that acquire cytomegalovirus in the first year of life are at high risk of subsequently developing tuberculosis disease. Efforts to prevent tuberculosis in early childhood in high-burden countries might need to deter or delay acquisition of cytomegalovirus perinatally or in the first months of life.
Bill & Melinda Gates Foundation, MRC South Africa, National Research Foundation South Africa, and Wellcome Trust.
最近接触后发生结核病的风险在 5 岁之前最高;然而,解释这种风险增加的机制尚未得到很好的阐明。在生命早期获得巨细胞病毒等病毒感染可能会调节免疫系统。我们旨在评估婴儿期巨细胞病毒感染的获得情况以及儿童结核病的发展情况。
在这项前瞻性出生队列研究中,我们招募了在南非开普敦郊区帕尔尔接受产前护理的 20 至 28 周妊娠的孕妇。参与者来自两个诊所(TC Newman 和 Mbekweni)。根据国家政策,婴儿在出生时接种卡介苗。使用 qPCR 对婴儿在出生时、3 周和 6 周、3 个月、6 个月、12 个月和 24 个月时进行鼻咽拭子检测巨细胞病毒。使用结核菌素皮肤试验、影像学检查、GeneXpert 和痰检对儿童进行前瞻性随访,直至 9 岁,以确定结核病。结核菌素皮肤试验在 6 个月时进行,然后在 12 个月、24 个月、36 个月、48 个月和 60 个月以及下呼吸道感染时进行。我们使用 Cox 回归和危险比(HR)及 95%置信区间(CI)比较了在 1 岁或 6 个月后发生结核病的儿童与巨细胞病毒感染的儿童的发病率。
2012 年 3 月 5 日至 2015 年 3 月 31 日,我们招募了 1225 名孕妇,并纳入了出生队列。由于产前随访丢失或妊娠丢失,88 名(7%)女性被排除在外。在 1143 名活产儿中,有 68 对(6%)母婴对被排除在外。共有 963 名儿童进行了巨细胞病毒的连续检测(共进行了 7186 次巨细胞病毒测量;中位数为每个儿童 6 次,IQR 2-11)。在出生后 3 周内先天性巨细胞病毒的患病率为 2%(816 例中的 18 例)。从 6 周时的 3%(825 例中的 27 例)到 3 个月时的 21%(882 例中的 183 例)、6 个月时的 35%(909 例中的 315 例)和 12 个月时的 42%(933 例中的 390 例),巨细胞病毒阳性率持续增加。母婴对的中位随访时间为 6.9 年(IQR 6.0-7.8)。在 6 周、3 个月、6 个月、12 个月和 24 个月时感染巨细胞病毒的儿童,1 岁后发生结核病的风险更高(调整后的 HR 4.1,95%CI 1.2-13.8;p=0.022)、3 个月(2.8,1.4-5.8;p=0.0040)、6 个月(3.6,1.7-7.3;p<0.0001)、12 个月(3.2,1.6-6.4;p=0.0010)和 24 个月(4.2,2.0-8.8;p<0.0001)。在 3 个月前(调整后的 HR 3.2,95%CI 1.0-10.6;p=0.048)、6 个月(3.9,1.2-13.0;p=0.027)、12 个月(4.4,1.2-16.3;p=0.027)和 24 个月(6.1,1.3-27.9;p=0.020)时感染巨细胞病毒的儿童中,微生物确诊结核病的风险也更高。在年龄大于 1 岁的儿童中,在 3 个月前(调整后的 HR 2.0 vs 3.7;p=0.0020;与巨细胞病毒阴性参考组比较)和 12 个月前(2.7 vs 3.7;p=0.0009)获得高巨细胞病毒负荷的儿童与获得低巨细胞病毒负荷的儿童相比,发生结核病的风险更高。
在生命的第一年中获得巨细胞病毒的婴儿随后患结核病的风险很高。在高负担国家中,为预防儿童早期结核病而采取的措施可能需要阻止或延迟围产期或生命头几个月内获得巨细胞病毒。
比尔和梅琳达·盖茨基金会、南非医学研究理事会、南非国家研究基金会和惠康信托基金会。