Fernando Kathy, Hu Haitao, Ni Houping, Hoxie James A, Weissman Drew
Division of Infectious Diseases, Department of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Blood. 2007 Mar 15;109(6):2538-44. doi: 10.1182/blood-2006-08-038661. Epub 2006 Dec 7.
The human immunodeficiency virus (HIV) causes impairment of the immune system in part by targeting CD4(+) T cells for infection and dysfunction. HIV envelope (Env) present on free virions and infected cells causes dysfunction of uninfected bystander CD4(+) T cells via interaction with both CD4 and coreceptors. Env is commonly used as part of a cocktail of HIV antigens in current vaccines. In DNA and viral vector vaccine approaches, antigen-presenting cells (APCs) and non-APCs in the vicinity of the vaccine delivery site and draining lymph node express vaccine-derived antigens. The studies here demonstrate that cell-surface expression of Env on APCs and non-APCs as part of the vaccine action causes an inhibition of antigen-induced CD4(+) T-cell activation and proliferation mediated by CD4 binding and suggests a potential mechanism for reduced activity of Env-containing HIV vaccines. Similar studies using a functional Env lacking CD4 binding circumvented suppression, suggesting an alternative and potentially superior approach to HIV vaccine design.
人类免疫缺陷病毒(HIV)部分通过靶向CD4(+) T细胞进行感染并使其功能失调,从而导致免疫系统受损。游离病毒粒子和受感染细胞上存在的HIV包膜(Env)通过与CD4和共受体相互作用,导致未感染的旁观者CD4(+) T细胞功能失调。Env通常作为当前疫苗中HIV抗原混合物的一部分使用。在DNA和病毒载体疫苗方法中,疫苗接种部位和引流淋巴结附近的抗原呈递细胞(APC)和非APC表达疫苗衍生的抗原。此处的研究表明,作为疫苗作用的一部分,APC和非APC上Env的细胞表面表达会抑制由CD4结合介导的抗原诱导的CD4(+) T细胞活化和增殖,并提示含Env的HIV疫苗活性降低的潜在机制。使用缺乏CD4结合功能的功能性Env进行的类似研究避免了抑制作用,这提示了一种替代的、可能更优的HIV疫苗设计方法。