Adenovirus-specific human T cells are pervasive, polyfunctional, and cross-reactive.
Adenovirus-specific human T cells are pervasive, polyfunctional, and cross-reactive.
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DOI:
10.1016/j.vaccine.2009.10.091
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发表时间:
2010-02-23
期刊:
影响因子:
5.5
通讯作者:
Betts, Michael R.
中科院分区:
文献类型:
--
作者:
Hutnick, Natalie A.;Carnathan, Diane;Demers, Korey;Makedonas, George;Ertl, Hildegund C. J.;Betts, Michael R.
Pre-existing immunity to adenovirus (Ad) reduces the efficacy of Ad-based vaccines. The goal of this study was to define the prevalence, magnitude, functionality and phenotype of Ad-specific human T cells directly ex vivo. To study the magnitude of T-cell responses to Ad, we developed a highly reproducible whole Ad vector stimulation assay for use with polychromatic flow cytometry. Ad-specific CD4+ and CD8+ T cell were detected in all 17 human subjects tested and were capable of proliferating upon restimulation. Ad-specific CD4+ T cells were primarily monofunctional CD4+ T cells that produced IL-2, IFN-γ or TNFα and expressed the memory markers CD27 and CD45RO. In contrast, Ad5-specific CD8+ T cells were more polyfunctional, expressing effector-like combinations of IFN-γ, MIP1α and perforin, and generally lacked CD27 and CD45RO expression. Ad-specific CD4+ and CD8+ T cell responses against chimpanzee-derived AdC6 and AdC7 were found in all subjects, indicating the commonality of cross-serotype reactivity of Ad-specific T cells. This cross-reactivity is due in part to extensive CD4+ and CD8+ T cell recognition of hexon regions conserved between multiple Ad serotypes. The prevalence, cross reactivity and effector like functions of Ad-specific T-cells in humans may affect the efficacy of Ad vector-based vaccines by eliminating vector infected cells even when rare serotype Ad vectors are employed.
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影响因子:
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通讯作者:
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影响因子:
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期刊:
HUMAN IMMUNOLOGY: PATIENT-BASED RESEARCH
影响因子:
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通讯作者:
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20.3
作者:
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