阻止细胞毒性T细胞和肿瘤坏死因子溶解的腺病毒区E3蛋白。

Molecular biology & medicine Pub Date : 1989-10-01
W S Wold, L R Gooding
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引用次数: 0

摘要

人类腺病毒正在为病毒可能采取的逃避免疫监视的策略提供见解。共有47种血清型,分为6组(A至F),具有不同的遗传和生物学特性。腺病毒2型(Ad2)和Ad5是两种C组病毒,在分子生物学方面最常见和最了解,可引起幼儿呼吸道感染,并经常形成持续性感染。感染后,线性双链DNA基因组在两个广泛的阶段表达:“早期”,病毒蛋白发挥作用篡夺细胞;以及“后期”,即病毒DNA和结构蛋白合成以及病毒粒子组装的时候。早期的转录单位之一,E3区,编码两种蛋白质,这两种蛋白质似乎可以抵消宿主抗病毒防御的不同分支。一种名为gp19K的19000 Mr蛋白保护细胞免受腺病毒特异性细胞毒性T淋巴细胞(CTL)的细胞溶解。Gp19K有两个特性对这一功能至关重要:它定位于内质网,它与主要组织相容性复合体(MHC)的I类抗原结合强烈。这两种特性的作用是阻断I类抗原到细胞表面的运输。为了裂解腺病毒感染的细胞,CTL必须识别显示在细胞表面的腺病毒肽抗原与I类主要组织相容性复合体抗原的复合物。由于gp19K阻止了这一点,它使细胞对CTL有效地不可见。第二种抗免疫E3蛋白是14700 Mr的蛋白,称为14.7K。14.7K保护腺病毒感染的细胞免受肿瘤坏死因子(TNF)的细胞溶解。TNF是一种多效性免疫调节蛋白,具有抗病毒特性,被认为可以防御病毒感染。14.7K可能在体内抵消TNF的抗病毒作用。14.7K的作用机制尚不清楚。对gp19K和14.7K的进一步研究将有助于我们对免疫系统和腺病毒发病机制的理解。
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Adenovirus region E3 proteins that prevent cytolysis by cytotoxic T cells and tumor necrosis factor.

Human adenoviruses are providing insights into strategies that viruses may adopt to evade immune surveillance. There are 47 serotypes that form six groups (A to F) with different genetic and biological properties. Adenovirus type 2 (Ad2) and Ad5, two group C types, the most common and best understood in terms of molecular biology, cause respiratory infections in young children and often form persistent infections. Following infection, the linear duplex DNA genome is expressed in two broad phases: "early", when viral proteins function to usurp the cell; and "late", when viral DNA and structural proteins are synthesized and virions are assembled. One of the early transcription units, region E3, encodes two proteins that appear to counteract different branches of the host's anti-viral defenses. A 19,000 Mr protein called gp19K protects cells against cytolysis by adenovirus-specific cytotoxic T lymphocytes (CTL). Gp19K has two properties that are crucial to this function: it is localized in the endoplasmic reticulum, and it binds strongly to class I antigens of the major histocompatibility complex (MHC). The effect of these two properties is to block transport of class I antigens to the cell surface. In order to lyse adenovirus-infected cells, CTL must recognize adenovirus peptide antigens complexed with class I major histocompatability complex antigens displayed on the cell surface. Since gp19K prevents this, it renders the cell effectively invisible to CTL. The second anti-immune E3 protein is a 14,700 Mr protein called 14.7K. The 14.7K protects adenovirus-infected cells against cytolysis by tumor necrosis factor (TNF). TNF is a pleiotropic immunoregulatory protein that has anti-viral properties and is believed to provide a defense against virus infections. The 14.7K presumably counteracts the anti-viral effects of TNF in vivo. The mechanism of action of the 14.7K is unknown. Further studies on gp19K and 14.7K should assist our understanding of the immune system and adenovirus pathogenesis.

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