Rapid identification of local T cell expansion in inflammatory organ diseases by flow cytometric T cell receptor Vβ analysis

被引:40
作者
Muraro, PA
Jacobsen, M
Necker, A
Nagle, JW
Gaber, R
Sommer, N
Oertel, WH
Martin, R
Hemmer, B
机构
[1] Univ G DAnnunzio, Med Sch,Neurol Clin, Osped Clin, Dept Oncol & Neurosci, I-66013 Chieti, Italy
[2] NINDS, Neuroimmunol Branch, NIH, Bethesda, MD 20892 USA
[3] Univ Marburg, Dept Neurol, Clin Neuroimmunol Grp, Marburg, Germany
[4] Immunotech, Antibody Dept, Marseille, France
[5] NINDS, DNA Sequencing Facil, NIH, Bethesda, MD 20892 USA
关键词
T cell receptors; flow cytometry; monoclonal antibodies; cerebrospinal fluid; encephalitis;
D O I
10.1016/S0022-1759(00)00309-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Oligoclonal expansion of antigen-specific T cells occurs frequently during inflammatory diseases. These cells may persist for a long time at high frequency in the body and be enriched in the affected tissues. As a screening test for expanded cell T cell populations at sites of inflammation, we developed an optimized methodology for flow-cytometry-based quantification of T cell receptor V beta (TCRBV) expression. We first validated the specificity of a TCRBV-specific monoclonal antibody set by direct comparison with PCR-based analysis of mono- and polyclonal T cell samples. This monoclonal antibody (mAb) panel recognized approximately two thirds of the T cell receptor alpha/beta repertoire in agroup of 64 healthy donors and allowed defining TCR usage in the CD4+ and CD8+ subsets. The reliable detection of expanded V beta gene families in T cell populations was confirmed in experiments on superantigen-stimulated T cells. Through differential TCR analysis on T cell subpopulations in cerebrospinal fluid and blood in patients with acute encephalitis, we were able to identify locally expanded CD8+ T cells. The power of this approach affords not only high-throughput comparative TCR analysis for immunological studies in vitro, but also rapid ex vivo identification of cell populations enriched in organ compartments during inflammatory diseases. (C) 2000 Elsevier Science B.V; All rights reserved.
引用
收藏
页码:131 / 143
页数:13
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