Douglas Jasmine, Wang Ziyi, Zumpano Francesca, Satagopan Jaya M, Moye Jack, Arpadi Stephen M, Marsit Carmen J, Barrett Emily S, Shiau Stephanie
Department of Biostatistics and Epidemiology, Rutgers School of Public Health, Piscataway, NJ, USA.
Maternal and Pediatric Infectious Disease Branch, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.
EBioMedicine. 2025 May;115:105696. doi: 10.1016/j.ebiom.2025.105696. Epub 2025 Apr 26.
Epigenetics offers insight into the mechanisms by which early life HIV infection and HIV exposure in utero affects offspring health. However, due to the widespread use of antiretroviral therapy (ART) during pregnancy/infancy, contemporary studies are unable to disentangle effects of HIV from ART exposure on epigenetic profiles.
Using historical specimens collected before widespread use of ART (1985-1991), we compared DNA methylation (DNAm) profiles among infants with perinatally-acquired HIV (PHIV), HIV-exposed but uninfected (HEU), and HIV-unexposed uninfected (HUU). DNAm in peripheral blood mononuclear cells collected at 3 and 12 months of age (36 PHIV, 33 HEU, and 33 HUU) was profiled using the Illumina Infinium MethylationEPIC BeadChip. We tested for differentially methylated (DM) CpG sites between groups at 3 and 12 months, adjusting for sex, race/ethnicity, and cell type proportions. Biological pathway enrichment analyses were conducted.
Comparing PHIV to HEU, there were 2 DM sites at 3 months and 11 at 12 months. Comparing PHIV to HUU, there was 1 DM CpG site at 3 months and 6 at 12 months. Immune-related pathways, including interferon-mediated signalling pathways were enriched. HIV exposure was not associated with any variation in DNA methylation, as no differences were detected between HEU vs. HUU at 3 or 12 months.
HIV infection (in the absence of ART during pregnancy/infancy) was associated with DNA methylation changes at 3 and 12 months of life in infants. Differential methylation in PHIV is related to immune processes and HIV exposure in the absence of infection does not contribute to differential methylation.
This study was supported by funding from the National Institutes of Health (R21HD104558 to SS, K01DA053157 to SS, P30ES019776 to CJM, and P30ES005022 to ESB.
表观遗传学为了解早期生命中感染艾滋病毒以及子宫内接触艾滋病毒影响后代健康的机制提供了线索。然而,由于在怀孕/婴儿期广泛使用抗逆转录病毒疗法(ART),当代研究无法区分艾滋病毒与ART暴露对表观遗传谱的影响。
我们使用在ART广泛使用之前(1985 - 1991年)收集的历史标本,比较了围产期感染艾滋病毒(PHIV)、接触艾滋病毒但未感染(HEU)和未接触艾滋病毒且未感染(HUU)的婴儿的DNA甲基化(DNAm)谱。使用Illumina Infinium MethylationEPIC BeadChip对在3个月和12个月大时采集的外周血单个核细胞中的DNAm进行分析(36例PHIV、33例HEU和33例HUU)。我们在3个月和12个月时测试了组间差异甲基化(DM)的CpG位点,并对性别、种族/民族和细胞类型比例进行了校正。进行了生物途径富集分析。
将PHIV与HEU进行比较,3个月时有2个DM位点,12个月时有11个。将PHIV与HUU进行比较,3个月时有1个DM CpG位点,12个月时有6个。包括干扰素介导的信号通路在内的免疫相关途径得到了富集。艾滋病毒暴露与DNA甲基化的任何变化均无关联,因为在3个月或12个月时,HEU与HUU之间未检测到差异。
艾滋病毒感染(在怀孕/婴儿期未使用ART的情况下)与婴儿3个月和12个月时的DNA甲基化变化有关。PHIV中的差异甲基化与免疫过程有关,未感染情况下的艾滋病毒暴露不会导致差异甲基化。
本研究得到了美国国立卫生研究院的资助(给SS的R21HD104558、给SS的K01DA053157、给CJM的P30ES019776以及给ESB的P30ES005022)。