Memory inflation during chronic viral infection is maintained by continuous production of short-lived, functional T cells.

Memory inflation during chronic viral infection is maintained by continuous production of short-lived, functional T cells.
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DOI:
10.1016/j.immuni.2008.07.017
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发表时间:
2008-10-17
期刊:
影响因子:
32.4
通讯作者:
Hill, Ann B.
Hill, Ann B.
中科院分区:
医学1区
文献类型:
--
作者:
Snyder, Christopher M.;Cho, Kathy S.;Bonnett, Elizabeth L.;van Dommelen, Serani;Shellam, Geoffrey R.;Hill, Ann B.

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During persistent murine cytomegalovirus (MCMV) infection the T cell response is maintained at extremely high levels for the life of the host. These cells closely resemble human CMV-specific cells which comprise a major component of the peripheral T cell compartment in most people. Despite a phenotype that suggests extensive antigen-driven differentiation, MCMV-specific T cells remain functional and respond vigorously to viral challenge. We hypothesized that a low rate of antigen-driven proliferation would account for the maintenance of this population. Instead, we found that most of these cells divide only sporadically in chronically infected hosts and have a short half-life in circulation. The overall population is supported, at least in part, by memory cells primed early in infection as well as recruitment of naïve T cells at late times. These data show that memory inflation is maintained by a continuous replacement of short-lived, functional cells during chronic MCMV infection.
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