Flow cytometric quantitation and characterization of the T-lymphocyte memory response to CMV in healthy donors

被引:18
作者
Hensel, N
Melenhorst, JJ
Bradstock, K
Schwarer, AP
Eniafe, R
Nakamura, R
Barrett, AJ
机构
[1] NHLBI, Hematol Branch, Stem Cell Transplantat Sect, NIH, Bethesda, MD 20892 USA
[2] Westmead Hosp, Dept Haematol, Blood & Marrow Transplant Serv, Westmead, NSW, Australia
[3] Alfred Hosp, Bone Marrow Transplant Programme, Melbourne, Vic, Australia
基金
美国国家卫生研究院;
关键词
cytomegalovirus; CMV; intracellular cytokine; TNF-alpha; interferon-gamma; lymphocyte;
D O I
10.1080/146532402317251509
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background Levels of circulating Of V Ag-specific lymphocytes determine CMV reactivation risk in immunocompromised individuals. Methods Frequencies of T cells producing cytokines after stimulation by CMV Ag were measured in hematopoietic stem-cell donors using flow cytometry. Results In seropositive individuals (n = 75) the mean number of CD8(+) (CD8(bright), CD8(dim)) and CD4(+) cells producing IFN-gamma was respectively 3.1% (12.6 /muL) and 0.38% (3.2/muL), over 10-fold higher than in seronegative subjects (n = 22). CMV stimulation induced tumor necrosis factor-alpha (TNF-alpha) and interferon-gamma (IFN-gamma) in both CD4(+) and CD8(+) cells (usually together), with a shift from memory- to effector-cell phenotype, while only a small proportion of CD4(+) cells produced IL-4. Although the normal range was wide, neither age, sex nor HLA type affected the frequency. Discussion These quantitative studies and the recognition of CD4(+) cells as potential effectors of CMV immunity are of relevance for immunotherapeutic approaches to prevent CMV disease after stem-cell transplantation.
引用
收藏
页码:29 / 40
页数:12
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