Islam S M Shamsul, Singh Shalini, Keshavarzian Ali, Abdel-Mohsen Mohamed
Northwestern University, 300 E Superior St, Chicago, IL, 60611, USA.
Rush Center for Integrated Microbiome and Chronobiology Research, Rush University Medical Center, Chicago, IL, USA.
Curr HIV/AIDS Rep. 2024 Dec 12;22(1):9. doi: 10.1007/s11904-024-00717-w.
People with HIV (PWH) experience premature aging and an elevated risk of age-related comorbidities, even with viral suppression through antiretroviral therapy (ART). We examine gastrointestinal disruptions, specifically impaired intestinal barrier integrity and microbial dysbiosis, as contributors to these comorbidities.
HIV infection compromises the intestinal epithelial barrier, increasing permeability and microbial translocation, which trigger inflammation and cellular stress. ART does not fully restore gut barrier integrity, leading to persistent inflammation and cellular stress. Additionally, HIV-associated microbial dysbiosis favors pro-inflammatory bacteria, intensifying inflammation and tissue damage, which may contribute to premature aging in PWH. Understanding the interactions between intestinal microbiota, chronic inflammation, cellular stress, and aging is essential to developing therapies aimed at reducing inflammation and slowing age-related diseases in PWH. In this review, we discuss critical knowledge gaps and highlight the therapeutic potential of microbiota-targeted interventions to mitigate inflammation and delay age-associated pathologies in PWH.
即使通过抗逆转录病毒疗法(ART)实现了病毒抑制,感染人类免疫缺陷病毒(HIV)的人群(PWH)仍会经历早衰以及与年龄相关的合并症风险升高。我们研究胃肠道紊乱,特别是肠道屏障完整性受损和微生物群落失调,作为这些合并症的促成因素。
HIV感染会损害肠道上皮屏障,增加通透性和微生物易位,从而引发炎症和细胞应激。ART不能完全恢复肠道屏障完整性,导致持续的炎症和细胞应激。此外,与HIV相关的微生物群落失调有利于促炎细菌生长,加剧炎症和组织损伤,这可能导致PWH早衰。了解肠道微生物群、慢性炎症、细胞应激和衰老之间的相互作用对于开发旨在减轻炎症和减缓PWH与年龄相关疾病的疗法至关重要。在本综述中,我们讨论了关键的知识空白,并强调了以微生物群为靶点的干预措施在减轻PWH炎症和延缓与年龄相关疾病方面的治疗潜力。