Twigg Homer L, Weinstock George M, Knox Kenneth S
Department of Medicine, Indiana University, Indianapolis, Ind.
Microbial Genomics, The Jackson Laboratory for Genomic Medicine, Farmington, Conn.
Transl Res. 2017 Jan;179:97-107. doi: 10.1016/j.trsl.2016.07.008. Epub 2016 Jul 18.
The lung microbiome plays a significant role in normal lung function and disease. Because microbial colonization is likely influenced by immunodeficiency, one would speculate that infection with human immunodeficiency virus (HIV) alters the lung microbiome. Furthermore, how this alteration might impact pulmonary complications now seen in HIV-infected patients on antiretroviral therapy (ART), which has shifted from opportunistic infections to diseases associated with chronic inflammation, is not known. There have been limited publications on the lung microbiome in HIV infection, many of them emanating from the Lung HIV Microbiome Project. Current evidence suggests that the lung microbiome in healthy HIV-infected individuals with preserved CD4 counts is similar to uninfected individuals. However, in individuals with more advanced disease, there is an altered alveolar microbiome characterized by a loss of richness and evenness (alpha diversity) within individuals. Furthermore, as a group the taxa making up the HIV-infected and uninfected lung microbiome are different (differences in beta diversity), and the HIV-infected population is more spread out (greater dispersion) than the uninfected population. These differences decline with ART, but even after effective therapy the alveolar microbiome in HIV-infected individuals contains increased amounts of signature bacteria, some of which have previously been associated with chronic lung inflammation. Furthermore, more recent investigations into the lung virome in HIV infection suggest that perturbations in lung viral communities also exist in HIV infection, and that these too are associated with evidence of lung inflammation. Thus, it is likely both microbiome and virome alterations in HIV infection contribute to lung inflammation in these individuals, which has important implications on the changing spectrum of pulmonary complications in patients living with HIV.
肺部微生物群在正常肺功能和疾病中发挥着重要作用。由于微生物定植可能受免疫缺陷影响,因此有人推测,感染人类免疫缺陷病毒(HIV)会改变肺部微生物群。此外,这种改变如何影响目前接受抗逆转录病毒疗法(ART)的HIV感染患者的肺部并发症尚不清楚,这些并发症已从机会性感染转变为与慢性炎症相关的疾病。关于HIV感染中肺部微生物群的出版物有限,其中许多来自肺部HIV微生物群项目。目前的证据表明,CD4计数保持正常的健康HIV感染个体的肺部微生物群与未感染个体相似。然而,在疾病更严重的个体中,肺泡微生物群发生改变,其特征是个体内丰富度和均匀度(α多样性)丧失。此外,作为一个群体,构成HIV感染和未感染肺部微生物群的分类群不同(β多样性差异),且HIV感染人群比未感染人群分布更分散(离散度更大)。这些差异随着ART而减小,但即使在有效治疗后,HIV感染个体的肺泡微生物群中特征性细菌的含量仍会增加,其中一些细菌以前与慢性肺部炎症有关。此外,最近对HIV感染中肺部病毒组的研究表明,HIV感染中肺部病毒群落也存在扰动,且这些扰动也与肺部炎症证据相关。因此,HIV感染中的微生物群和病毒组改变可能都导致了这些个体的肺部炎症,这对HIV感染者肺部并发症谱的变化具有重要意义。