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为鉴定 HIV 感染患者中新型隐球菌病的遗传风险特征。

Toward identification of the genetic risk profile for cryptococcal disease in HIV-infected patients.

机构信息

Department of Medicine and Nijmegen Institute for Infection, Inflammation and Immunity (N4i), Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.

出版信息

mBio. 2013 Oct 15;4(5):e00798-13. doi: 10.1128/mBio.00798-13.

Abstract

Cryptococcus spp. are important fungal pathogens that represent a major cause of morbidity and mortality in both immunocompetent and immunodeficient patients. Although cryptococcal disease is one of the major causes of death in HIV-infected patients, especially in sub-Saharan Africa, not all patients at risk with low CD4 counts develop the disease. It has been thus hypothesized that host genetic variation may represent an important susceptibility risk factor for this infection. In their recent study in mBio, Rohatgi et al. [S. Rohatgi et al., mBio 4(5):e00573-13, 2013, doi:10.1128/mBio.00573-13] present an important piece of evidence to support this hypothesis, by demonstrating that the FCGR3A 158 F/V polymorphism has an important impact on susceptibility to cryptococcal disease in HIV-infected patients. The authors present both genetic evidence and immunological validation for the hypothesis that humoral immunity in general and FCGR3A-mediated uptake and antibody-dependent cellular cytotoxicity (ADCC) in particular play important roles in the pathogenesis of Cryptococcus infection. Their discovery that the 158V allele of this polymorphism can increase the risk of Cryptococcus infections up to 20-fold in homozygous individuals opens the possibility for risk stratification and personalized treatment of HIV-infected patients.

摘要

隐球菌属是重要的真菌病原体,是免疫功能正常和免疫功能低下患者发病和死亡的主要原因。虽然 cryptococcal 病是 HIV 感染患者,尤其是撒哈拉以南非洲地区 HIV 感染患者死亡的主要原因之一,但并非所有 CD4 计数低的高危患者都会发生该病。因此,人们假设宿主遗传变异可能是这种感染的一个重要易感危险因素。在他们最近发表于 mBio 的研究中,Rohatgi 等人[ S. Rohatgi 等人,mBio 4(5):e00573-13, 2013, doi:10.1128/mBio.00573-13]提供了重要证据支持这一假说,表明 FCGR3A 158 F/V 多态性对 HIV 感染患者 cryptococcal 病的易感性有重要影响。作者提出了遗传证据和免疫学验证,支持这样一种假说,即一般的体液免疫和 FCGR3A 介导的摄取和抗体依赖性细胞毒性(ADCC)在隐球菌感染的发病机制中起着重要作用。他们发现该多态性的 158V 等位基因可使纯合子个体的 cryptococcal 感染风险增加 20 倍,这为 HIV 感染患者的风险分层和个体化治疗提供了可能。

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