Yanamadala Yaswanthi, Muthumula Chandra Mohan Reddy, Gokulan Kuppan, Karn Kumari, Sutherland Vicki, Cunny Helen, Santos Janine H, Khare Sangeeta
Division of Microbiology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR, United States.
Division of Translational Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, NC, United States.
Exp Biol Med (Maywood). 2025 Aug 13;250:10564. doi: 10.3389/ebm.2025.10564. eCollection 2025.
The antiretroviral (ARV) drug combination of abacavir sulfate, dolutegravir, and lamivudine [ABC/DTG/3TC; Tri combination Anti-retroviral therapy (TC-ART)] has revolutionized HIV treatment by effectively targeting different stages of viral replication. Despite its therapeutic efficiency for maintaining low viremia in the mother during pregnancy, there are concerns for long-term liabilities in offspring that are indirectly exposed during vulnerable periods of development. The commensal microbiota plays a crucial role in maintaining overall gut health, and disruption of the microbiome is often linked to various extraintestinal effects such as immune dysregulation and inflammation. We recently reported the effects of this drug combination in altering fecal microbiome composition of aged rats perinatally exposed to ABC/DTG/3TC-ART. The fecal microbiome can provide only a snapshot of the composition of microbial community at the end of the digestive tract, which may not reflect the microbial population interacting with ileal mucosa. Thus, the current work reports the effects of this drug combination in the gut mucosa-associated microbiome of the same animals, which showed significant microbial diversity and species richness in high dose exposed female adult offspring, along with dose-dependent changes in Firmicutes/Bacteroidetes ratio. The high dose exposure also showed an increase in opportunistic bacterial species in male animals. Overall, we found that, similar to the fecal microbiome, perinatal exposure to TC-ART led to sex- and dose-dependent alterations in the gut mucosa-associated microbial population in aged rats, suggesting that early life exposure to these drugs may influence gut mucosa-associated immune responses and intestinal permeability.
硫酸阿巴卡韦、多替拉韦和拉米夫定的抗逆转录病毒(ARV)药物组合[ABC/DTG/3TC;三联抗逆转录病毒疗法(TC-ART)]通过有效靶向病毒复制的不同阶段,彻底改变了HIV治疗。尽管其在孕期能有效维持母亲体内的低病毒血症,但人们担心在发育的脆弱期间接接触该药物的后代会有长期不良影响。共生微生物群在维持肠道整体健康方面起着关键作用,微生物群的破坏通常与各种肠外效应有关,如免疫失调和炎症。我们最近报告了这种药物组合对围产期暴露于ABC/DTG/3TC-ART的老年大鼠粪便微生物群组成的影响。粪便微生物群只能提供消化道末端微生物群落组成的一个快照,可能无法反映与回肠黏膜相互作用的微生物种群。因此,目前的研究报告了这种药物组合对同一动物肠道黏膜相关微生物群的影响,结果显示,高剂量暴露的成年雌性后代具有显著的微生物多样性和物种丰富度,同时厚壁菌门/拟杆菌门的比例也有剂量依赖性变化。高剂量暴露还导致雄性动物中机会性细菌种类增加。总体而言,我们发现,与粪便微生物群类似,围产期暴露于TC-ART会导致老年大鼠肠道黏膜相关微生物种群出现性别和剂量依赖性变化,这表明生命早期接触这些药物可能会影响肠道黏膜相关的免疫反应和肠道通透性。
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