广泛靶向的人巨细胞病毒特异性CD4+和CD8+ T细胞在暴露个体的记忆细胞区室中占主导地位。

Broadly targeted human cytomegalovirus-specific CD4+ and CD8+ T cells dominate the memory compartments of exposed subjects.

作者信息

Sylwester Andrew W, Mitchell Bridget L, Edgar John B, Taormina Cara, Pelte Christian, Ruchti Franziska, Sleath Paul R, Grabstein Kenneth H, Hosken Nancy A, Kern Florian, Nelson Jay A, Picker Louis J

机构信息

Vaccine and Gene Therapy Institute, Department of Pathology, Oregon Health & Science University, Beaverton, 97006, USA.

出版信息

J Exp Med. 2005 Sep 5;202(5):673-85. doi: 10.1084/jem.20050882.

Abstract

Human cytomegalovirus (HCMV) infections of immunocompetent hosts are characterized by a dynamic, life-long interaction in which host immune responses, particularly of T cells, restrain viral replication and prevent disease but do not eliminate the virus or preclude transmission. Because HCMV is among the largest and most complex of known viruses, the T cell resources committed to maintaining this balance have never been characterized completely. Here, using cytokine flow cytometry and 13,687 overlapping 15mer peptides comprising 213 HCMV open reading frames (ORFs), we found that 151 HCMV ORFs were immunogenic for CD4(+) and/or CD8(+) T cells, and that ORF immunogenicity was influenced only modestly by ORF expression kinetics and function. We further documented that total HCMV-specific T cell responses in seropositive subjects were enormous, comprising on average approximately 10% of both the CD4(+) and CD8(+) memory compartments in blood, whereas cross-reactive recognition of HCMV proteins in seronegative individuals was limited to CD8(+) T cells and was rare. These data provide the first glimpse of the total human T cell response to a complex infectious agent and will provide insight into the rules governing immunodominance and cross-reactivity in complex viral infections of humans.

摘要

免疫功能正常宿主的人巨细胞病毒(HCMV)感染具有动态、终身相互作用的特点,其中宿主免疫反应,特别是T细胞的免疫反应,可抑制病毒复制并预防疾病,但无法清除病毒或阻止传播。由于HCMV是已知最大且最复杂的病毒之一,致力于维持这种平衡的T细胞资源从未被完全表征。在此,我们使用细胞因子流式细胞术和包含213个HCMV开放阅读框(ORF)的13,687个重叠15聚体肽,发现151个HCMV ORF对CD4(+)和/或CD8(+) T细胞具有免疫原性,并且ORF免疫原性仅受到ORF表达动力学和功能的适度影响。我们进一步证明,血清阳性受试者中总的HCMV特异性T细胞反应非常庞大,平均约占血液中CD4(+)和CD8(+)记忆细胞区室的10%,而血清阴性个体中对HCMV蛋白的交叉反应性识别仅限于CD8(+) T细胞,且很少见。这些数据首次揭示了人类T细胞对一种复杂感染因子的总体反应,并将为了解人类复杂病毒感染中免疫优势和交叉反应性的调控规则提供见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6fe9/2212883/6bfbbddc6c15/20050882f1.jpg

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