Preferential expansion of autoreactive T lymphocytes from the memory T-cell pool by IL-7

被引:56
作者
Bielekova, B
Muraro, PA
Golestaneh, L
Pascal, J
McFarland, HF
Martin, R
机构
[1] NINDS, Cellular Immunol Sect, Neuroimmunol Branch, NIH, Bethesda, MD 20892 USA
[2] Univ G Annunzio, Dept Oncol & Neurosci, Sch Med, I-66013 Chieti, Italy
[3] Multiple Peptide Syst, San Diego, CA 92121 USA
关键词
multiple sclerosis; antigen-specific T cells; interleukin-7; primary proliferation;
D O I
10.1016/S0165-5728(99)00200-3
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 have developed a new technique that allows us to quantify antigen-specific T cells, and to determine their functional phenotype and origin from naive versus memory populations. Using this methodology, we have characterized a total of 286 T-cell lines specific for myelin basic protein (MBP) and influenza hemagglutinin from 16 multiple sclerosis (MS) patients and nine healthy donors. Our data support the notion that MBP-specific T cells undergo in vivo activation in MS patients and indicate a presence of immune dysregulation that renders MS patients prone to develop autoimmunity. Our methodology offers a way to study antigen-specific T-cell characteristics as a surrogate marker in immunotherapy trials. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:115 / 123
页数:9
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