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The First Human Epitope Map of the Alphaviral E1 and E2 Proteins Reveals a New E2 Epitope with Significant Virus Neutralizing Activity

机译:甲病毒E1和E2蛋白的第一个人类抗原决定簇图揭示了具有重要病毒中和活​​性的新E2表位

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Background Venezuelan equine encephalitis virus (VEEV) is responsible for VEE epidemics that occur in South and Central America and the U.S. The VEEV envelope contains two glycoproteins E1 (mediates cell membrane fusion) and E2 (binds receptor and elicits virus neutralizing antibodies). Previously we constructed E1 and E2 epitope maps using murine monoclonal antibodies (mMAbs). Six E2 epitopes (E2c,d,e,f,g,h) bound VEEV-neutralizing antibody and mapped to amino acids (aa) 182–207. Nothing is known about the human antibody repertoire to VEEV or epitopes that engage human virus-neutralizing antibodies. There is no specific treatment for VEE; however virus-neutralizing mMAbs are potent protective and therapeutic agents for mice challenged with VEEV by either peripheral or aerosol routes. Therefore, fully human MAbs (hMAbs) with virus-neutralizing activity should be useful for prevention or clinical treatment of human VEE.
机译:背景委内瑞拉马脑炎病毒(VEEV)是南美和中美洲和美国发生的VEE流行的原因.VEEV包膜包含两种糖蛋白E1(介导细胞膜融合)和E2(结合受体并引发病毒中和抗体)。以前,我们使用鼠类单克隆抗体(mMAb)构建了E1和E2表位图。六个E2表位(E2c,d,e,f,g,h)结合VEEV中和抗体,并定位到氨基酸(aa)182-207。关于与人病毒中和抗体结合的VEEV或表位的人抗体库一无所知。 VEE没有特定的治疗方法;但是,病毒中和性mMAb对于通过外周或气溶胶途径受到VEEV攻击的小鼠是有效的保护剂和治疗剂。因此,具有病毒中和活​​性的完全人源单抗(hMAb)对于预防或临床治疗人VEE应该有用。

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