hiv感染者肠道微生物群-宿主稳态的变化——对细菌肠道微生物群的关注

European Journal of Microbiology & Immunology Pub Date : 2017-08-19 eCollection Date: 2017-09-01 DOI:10.1556/1886.2017.00016
Ana Beatriz Dein Terra Mota Ribeiro, Markus M Heimesaat, Stefan Bereswill
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引用次数: 24

摘要

人类免疫缺陷病毒(HIV)感染导致严重的CD4+ T细胞耗竭,导致慢性炎症和免疫激活,屏障功能受损和微生物易位。即使在有效的抗逆转录病毒治疗下,这些过程仍然存在,导致肠道微生物群失调和微生物群-宿主稳态紊乱。本综述旨在分析肠道微生物群与宿主免疫系统在HIV发病过程中的相互影响。应用PubMed数据库进行了在线搜索。总结果数(n = 35)被缩小到5项关注宿主与肠道微生物组相互作用的相关研究,同时采用了严格的排除标准,从而确保没有其他合并症影响研究结果。我们的分析显示,肠道微生物组多样性与CD4+ T细胞计数呈正相关,与微生物易位标记负相关。然而,细菌丰富度的定量变化并不总是与代谢活跃细菌群体的数量相关。尽管有报道称潜在致病菌增加,相反,保护性菌群减少,但肠道微生物群表现出免疫调节特性,因为粘膜炎症后遗症通过减少促炎和加速抗炎细胞因子反应而受到抑制。未来的研究需要进一步阐明这些发现,以更深入地了解宿主-微生物群的相互作用,并制定新的治疗策略。
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Changes of the Intestinal Microbiome-Host Homeostasis in HIV-Infected Individuals - A Focus on the Bacterial Gut Microbiome.

Human immunodeficiency virus (HIV) infections cause severe CD4+ T cell depletion leading to chronic inflammation and immune activation, impaired barrier function, and microbial translocation. Even under effective antiretroviral therapy, these processes persist, leading to gut microbiome dysbiosis and disturbance of microbiome-host homeostasis. This systematic review aims at analyzing how gut microbiome and host immune system influence each other during HIV pathogenesis. An online search applying the PubMed database was conducted. The number of total results (n = 35) was narrowed down to 5 relevant studies focusing on the interaction between the host and gut microbiome, whereas strict exclusion criteria were applied, thereby assuring that no other comorbidities impacted study results. Our analyses revealed that gut microbiome diversity correlated positively with CD4+ T cell counts and negatively with microbial translocation markers. However, quantitative changes in bacterial richness did not consistently correlate with the numbers of metabolically active bacterial populations. Despite the reported increase in potentially pathogenic bacteria and, conversely, decrease in protective populations, the gut microbiota exhibited immune-modulating qualities given that mucosal inflammatory sequelae were dampened by decreasing pro-inflammatory and accelerating anti-inflammatory cytokine responses. Future research is needed to further elucidate these findings, to gain a deeper insight into host-microbiota interactions and to develop novel therapeutic strategies.

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