Johnson Samuel D, Byrareddy Siddappa N
Department of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, United States.
Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, United States.
Clin Transl Discov. 2022 Jun;2(2). doi: 10.1002/ctd2.58. Epub 2022 Apr 28.
The microbiomes of people living with HIV (PLWH) are significantly dysregulated with a loss of bacteria diversity and shifts in composition, including increases in pathogenic and decreases in beneficial species. Because of the microbiome's role in modulating health, the effect of this dysbiosis on immune response in PLWH has been a significant concern, mainly because these shifts can persist even after viral suppression during combination antiretroviral therapy (cART). However, due to limitations on sample availability, few studies have been able to provide insights into these microbiome-immune interactions. Recently, Olivas-Martínez, et al. characterized ileum and caecum mucosa-associated microbiomes of PLWH based on their level of peripheral CD4+ T-cell reconstitution following long-term cART. Their analysis revealed distinct microbiome signatures predictive of recovery. Additionally, differences in markers of gut inflammation and damage between response groups were described, further implicating mucosal disruptions with immune reconstitution. These new data demonstrate an interdependence of microbiome and therapy response, and additional studies were urgently required to fully elucidate this crosstalk and microbiome dynamics from before/after infection and finally, long-term viral suppression with cART.
感染艾滋病毒者(PLWH)的微生物群显著失调,细菌多样性丧失,组成发生变化,包括致病菌种增加和有益菌种减少。由于微生物群在调节健康方面的作用,这种生态失调对PLWH免疫反应的影响一直是一个重大问题,主要是因为即使在联合抗逆转录病毒疗法(cART)期间病毒得到抑制后,这些变化仍可能持续。然而,由于样本可用性的限制,很少有研究能够深入了解这些微生物群与免疫的相互作用。最近,奥利瓦斯 - 马丁内斯等人根据长期cART后外周血CD4 + T细胞的重建水平,对PLWH的回肠和盲肠黏膜相关微生物群进行了特征分析。他们的分析揭示了可预测恢复情况的独特微生物群特征。此外,还描述了反应组之间肠道炎症和损伤标志物的差异,进一步表明黏膜破坏与免疫重建有关。这些新数据证明了微生物群与治疗反应之间的相互依存关系,迫切需要进行更多研究,以全面阐明这种相互作用以及从感染前后到最终通过cART实现长期病毒抑制过程中的微生物群动态变化。