Ki-67 expression reveals strong, transient influenza specific CD4 T cell responses after adult vaccination

被引:14
|
作者
Li, Xi [1 ]
Miao, Hongyu [2 ]
Henn, Alicia [3 ]
Topham, David J. [1 ]
Wu, Hulin [2 ]
Zand, Martin S. [3 ]
Mosmann, Tim R. [1 ]
机构
[1] Univ Rochester, Med Ctr, David H Smith Ctr Vaccine Biol & Immunol, Dept Microbiol & Immunol, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, Div Nephrol, Dept Med, Rochester, NY 14642 USA
[3] Univ Rochester, Med Ctr, Dept Biostat & Computat Biol, Rochester, NY 14642 USA
关键词
Ki-67; Influenza vaccine; CD4 T cell; MEDIATED PROTECTION; MEMORY; VACCINES; ANTIBODY; IMMUNITY;
D O I
10.1016/j.vaccine.2012.04.059
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Although previous studies have found minimal changes in CD4 T cell responses after vaccination of adults with trivalent inactivated influenza vaccine, daily sampling and monitoring of the proliferation marker Ki-67 have now been used to reveal that a substantial fraction of influenza-specific CD4 T cells respond to vaccination. At 4-6 days after vaccination, there is a sharp rise in the numbers of Ki-67-expressing PBMC that produce IFN-gamma, IL-2 and/or TNF alpha in vitro in response to influenza vaccine or peptide. Ki-67(+) cell numbers then decline rapidly, and 10 days after vaccination, both Ki-67(+) and overall influenza-specific cell numbers are similar to pre-vaccination levels. These results provide a tool for assessing the quality and quantity of CD4 T cell responses to different influenza vaccines, and raise the possibility that the anti-influenza T cell memory response may be qualitatively altered by vaccination, even if the overall memory cell numbers do not change significantly. (C) 2012 Published by Elsevier Ltd.
引用
收藏
页码:4581 / 4584
页数:4
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