Antigen presenting cell function is enhanced in healthy elderly

被引:42
作者
Castle, SC
Uyemura, K
Crawford, W
Wong, W
Makinodan, T
机构
[1] Univ Calif Los Angeles, W Los Angeles Vet Adm Med Ctr, Ctr Geriatr Res Educ & Clin, Multicampus Div Geriatr & Gerontol, Los Angeles, CA 90073 USA
[2] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90073 USA
关键词
D O I
10.1016/S0047-6374(98)00141-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aging is associated with a progressive decline in T cell-mediated immune responses. Little is known about the effect of aging on antigen presenting cells (APC). We have recently reported an age-related decline in proliferative response of peripheral blood mononuclear cells from elderly volunteers to Staphylococcus enterotoxin B (SEB). Since SEE-induced stimulation of T cells is not restricted by major histocompatibility complex, experiments were conducted in which T cells and APC from young and healthy elderly subjects were combined. We initially demonstrated the decreased SEE-induced proliferative capacity of elderly T cell-elderly APC co-cultures when compared with young T cell-young APC co-cultures. Combination of purified T cells from elderly donors with APC from young donors maintained a reduced T cell proliferative response. Age-related decline in T cell function was also established by the reduced proliferative capacity of elderly T cells co-cultured with a reference monocyte cell line. Surprisingly, co-culture of APC from healthy elderly donors with purified T cells from young donors enhanced T cell proliferation. APC from elderly donors also marginally enhanced the proliferative response of an SEE-specific T cell line. (C) 1999 Elsevier Science Ireland Ltd. All rights reserved.
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收藏
页码:137 / 145
页数:9
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