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针对痘苗病毒的HLA I类限制性反应可识别多种主要参与毒力和病毒基因调控的蛋白质。

HLA class I-restricted responses to vaccinia recognize a broad array of proteins mainly involved in virulence and viral gene regulation.

作者信息

Oseroff Carla, Kos Ferdynand, Bui Huynh-Hoa, Peters Bjoern, Pasquetto Valerie, Glenn Jean, Palmore Tara, Sidney John, Tscharke David C, Bennink Jack R, Southwood Scott, Grey Howard M, Yewdell Jonathan W, Sette Alessandro

机构信息

La Jolla Institute for Allergy and Immunology, 3030 Bunker Hill Street, Suite 326, San Diego, CA 92109, USA.

出版信息

Proc Natl Acad Sci U S A. 2005 Sep 27;102(39):13980-5. doi: 10.1073/pnas.0506768102. Epub 2005 Sep 19.

Abstract

We have analyzed by ex vivo ELISPOT the anti-vaccinia cytotoxic T lymphocyte responses of peripheral blood mononuclear cells from humans vaccinated with Dryvax vaccine. More than 6,000 peptides from 258 putative vaccinia ORFs predicted to bind the common molecules of the HLA A1, A2, A3, A24, B7, and B44 supertypes were screened with peripheral blood mononuclear cells of 31 vaccinees. A total of 48 epitopes derived from 35 different vaccinia antigens were identified, some of which (B8R, D1R, D5R, C10L, C19L, C7L, F12, and O1L) were recognized by multiple donors and contain multiple epitopes recognized in the context of different HLA types. The antigens recognized tend to be >100 residues in length and are expressed predominantly in the early phases of infection, although some late antigens were also recognized. Viral genome regulation and virulence factor were recognized most frequently, whereas few structural proteins were immunogenic. Finally, most epitopes were highly conserved among vaccinia virus Western Reserve, variola major and modified vaccinia Ankara, supporting their potential use in vaccine and diagnostic applications.

摘要

我们通过体外酶联免疫斑点法(ELISPOT)分析了接种Dryvax疫苗的人类外周血单个核细胞的抗痘苗细胞毒性T淋巴细胞反应。用31名接种者的外周血单个核细胞筛选了来自258个假定痘苗开放阅读框(ORF)的6000多种肽段,这些肽段预计可与HLA A1、A2、A3、A24、B7和B44超型的共同分子结合。共鉴定出35种不同痘苗抗原衍生的48个表位,其中一些(B8R、D1R、D5R、C10L、C19L、C7L、F12和O1L)被多个供体识别,并包含在不同HLA类型背景下识别的多个表位。被识别的抗原长度往往大于100个残基,主要在感染早期表达,不过一些晚期抗原也被识别。病毒基因组调控和毒力因子最常被识别,而很少有结构蛋白具有免疫原性。最后,大多数表位在痘苗病毒西储株、天花病毒和安卡拉改良痘苗病毒中高度保守,支持它们在疫苗和诊断应用中的潜在用途。

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