Detailed analysis of Epstein-Barr virus-specific CD4+ and CD8+ T cell responses during infectious mononucleosis

被引:47
作者
Scherrenburg, J. [1 ]
Piriou, E. R. W. A. N. [2 ]
Nanlohy, N. M. [1 ]
van Baarle, D. [1 ]
机构
[1] Univ Med Ctr Utrecht, Dept Immunol, NL-3584 EA Utrecht, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Sanquin Res & Landsteiner Lab, Dept Clin Viroimmunol, NL-1105 AZ Amsterdam, Netherlands
关键词
EBV; infectious mononucleosis; T cells;
D O I
10.1111/j.1365-2249.2008.03699.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We studied simultaneously Epstein-Barr virus (EBV)-specific CD4(+) and CD8(+) T cell responses during and after infectious mononucleosis (IM), using a previously described 12-day stimulation protocol with EBNA1 or BZLF1 peptide pools. Effector function of EBV-specific T cells was determined after restimulation by measuring intracellular interferon-gamma production. During IM, BZLF1-specifc CD4(+) T cell responses were dominant compared with CD8(+) T cell responses. EBNA1-specific CD4(+) and CD8(+) T cell responses were low and remained similar for 6 months. However, 6 months after IM, BZLF1-specific CD4(+) T cell responses had declined, but CD8(+) T cell responses had increased. At diagnosis, EBV-specific CD8(+) T cells as studied by human leucocyte antigen class I tetramer staining comprised a tetramer(bright)CD8(bright) population consisting mainly of CD27(+) memory T cells and a tetramer(dim)CD8(dim) population consisting primarily of CD27(-) effector T cells. The remaining EBV-specific CD8(+) T cell population 6 months after the diagnosis of IM consisted mainly of tetramer(bright)CD8(bright) CD27(+) T cells, suggesting preferential preservation of memory T cells after contraction of the EBV-specific T cell pool.
引用
收藏
页码:231 / 239
页数:9
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