LATE DOMINANCE OF THE INFLAMMATORY PROCESS IN MURINE INFLUENZA BY GAMMA-DELTA+ T-CELLS

被引:211
作者
CARDING, SR
ALLAN, W
KYES, S
HAYDAY, A
BOTTOMLY, K
DOHERTY, PC
机构
[1] YALE UNIV, SCH MED, HOWARD HUGHES MED INST, IMMUNOBIOL SECT, NEW HAVEN, CT 06510 USA
[2] ST JUDE CHILDRENS RES HOSP, DEPT IMMUNOL, MEMPHIS, TN 38101 USA
[3] YALE UNIV, DEPT BIOL, NEW HAVEN, CT 06510 USA
关键词
D O I
10.1084/jem.172.4.1225
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The inflammatory response in the lungs of mice infected with an influenza A virus consists largely of macrophages and CD3+ T cells. Most T lymphocytes recovered before day 7 after infection express mRNA for the T cell receptor α/β (TCR-α/β), while TCR-γ/δ mRNA+ cells are found at much higher frequency over the next 7 d. The predominant surface phenotype for the TCR-γ/δ mRNA+ population is CD3+4−8− TCR-γ/δ−. Some lymphocytes expressing all the known Vγ genes are found in the inflammatory exudate, but Vγ2+/Vγ1+ and Vγ4+ T cells are present at highest frequency. The response is staged, with maximal numbers of Vγ4+ cells occurring on day 10 after infection, while the predominant phenotype on day 13 is Vγ2/Vγ1+. The emerging peak in numbers of Vγ4+ lymphocytes is paralleled by increasing numbers of macrophages expressing hsp mRNA. The later maxima found for the Vγ2+Vγ1+ T cells is consistent with the possibility that at least some of these lymphocytes are responding to the hsp+ cells and are functioning to resolve the inflammatory process. © 1990, Rockefeller University Press., All rights reserved.
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页码:1225 / 1231
页数:7
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