Characterization of age-related changes in bovine CD8+ T-cells

被引:15
|
作者
Hogg, Alison E. [1 ]
Parsons, Keith [1 ]
Taylor, Geraldine [1 ]
Worth, Andrew [2 ]
Beverley, Peter [2 ]
Howard, Christopher J. [1 ]
Villarreal-Ramos, Bernardo [1 ]
机构
[1] Inst Anim Hlth, Newbury RG20 7NN, Berks, England
[2] Edward Jenner Inst Vaccine Res, Newbury RG20 7NN, Berks, England
基金
英国生物技术与生命科学研究理事会;
关键词
Cattle; Age; Memory; CD8(+) T cells; SYNCYTIAL VIRUS-INFECTION; MONOCLONAL-ANTIBODIES; LYMPHOCYTE SUBSETS; IN-VIVO; MEMORY; IDENTIFICATION; CATTLE; ANTIGEN; CD4; GAMMA;
D O I
10.1016/j.vetimm.2010.11.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Evaluation of the changes induced by immunological interventions requires a baseline against which to compare those changes. The age-related changes in the CD8(+) T-cell population of cattle were studied. The results indicate that CD8(+) T-cells could be divided into gamma/delta TCR1(+) and gamma/delta TCR1(-) according to their expression of the gamma/delta T-cell receptor. As a proportion, the CD8(+) gamma/delta TCR1(+) population appears to increase with age. Within the CD8(+)gamma/delta TCR1(-) a population of cells expressing a profile of surface molecules previously associated with effector memory T cells (CD45RO(+), CD62L(-), CD27(-), CD45RA(-) and CD28(-)) increases with age. Furthermore, a parallel increase with age in the proportion of CD8(+)CD45RO(+) T cells that express the cytotoxic granule protein perforin was observed. In peripheral tissues, namely lungs, it was found that the majority of CD8(+) T cells present expressed a phenotype indicative of previously primed T cells (high expression of CD45RO and perforin). In contrast, only a small population of memory CD8(+) T cells was present in lymphoid tissue where most of the CD8(+) T cells expressed a nave phenotype. In conclusion, in cattle, like in human, CDS+ T cells that express a phenotype associated with antigen experience accumulate with age that may play a role in immunocompetence as the individual ages. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:47 / 54
页数:8
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