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Research Article Free access | 10.1172/JCI114634

T cell antigen receptor V gene usage. Increases in V beta 8+ T cells in Crohn's disease.

D N Posnett, I Schmelkin, D A Burton, A August, H McGrath, and L F Mayer

Department of Medicine, Cornell University Medical College, New York 10021.

Find articles by Posnett, D. in: PubMed | Google Scholar

Department of Medicine, Cornell University Medical College, New York 10021.

Find articles by Schmelkin, I. in: PubMed | Google Scholar

Department of Medicine, Cornell University Medical College, New York 10021.

Find articles by Burton, D. in: PubMed | Google Scholar

Department of Medicine, Cornell University Medical College, New York 10021.

Find articles by August, A. in: PubMed | Google Scholar

Department of Medicine, Cornell University Medical College, New York 10021.

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Department of Medicine, Cornell University Medical College, New York 10021.

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Published June 1, 1990 - More info

Published in Volume 85, Issue 6 on June 1, 1990
J Clin Invest. 1990;85(6):1770–1776. https://doi.org/10.1172/JCI114634.
© 1990 The American Society for Clinical Investigation
Published June 1, 1990 - Version history
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Abstract

Crohn's disease represents part of a spectrum of inflammatory bowel diseases characterized by immune regulatory defects and genetic predisposition. T cell antigen receptor V gene usage by T lymphocytes was investigated using four MAbs specific for various V gene products. One MAb (Ti3a), reactive with V beta 8 gene products, detected increased numbers of T cells in a subset of Crohn's disease patients as compared with normal controls and ulcerative colitis patients. In family studies there was no apparent inherited predisposition to the use of V beta 8 genes, and there was no association between a restriction fragment length polymorphism of the V beta 8.1 gene and Crohn's disease. The V beta 8+ T cells were concentrated in the mesenteric lymph nodes draining the inflammatory lesions and belonged to both the CD4+ and CD8+ T cell subsets. In contrast, lamina propria and intraepithelial T cells were not enriched in V beta 8+ T cells, suggesting that these cells were participating in the afferent limb of a gut-associated immune response. The expanded V beta 8+ T cells in Crohn's disease appear to result from an immune response to an as yet unknown antigen.

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