Diversity of T-cell receptor V(α), V(β), and CDR3 expression by myelin basic protein-specific human T-cell clones

J. R. Richert, E. D. Robinson, K. Camphausen, R. Martin, R. R. Voskuhl, M. A. Faerber, H. F. McFarland, C. K. Hurley

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

We sequenced the cDNAs of alpha and beta T-cell receptors (TCRs), including V, J, and CDR3 regions, expressed by 54 myelin basic protein (MBP)- specific T-cell clones generated from the peripheral blood of 15 multiple sclerosis (MS) patients and three normal controls. Thirteen V(α) gene segments, 18 V(β) gene segments, 23 CDR3(α) sequences, and 30 CDR3(β) sequences were represented among these clones. Some CDR3 motifs were common to several clones that shared epitope specificity, while other motifs were common to clones with diverse epitope specificities. The extensive heterogeneity of TCR gene expression in the human immune response to MBP indicates that therapeutic strategies aimed at blocking a limited number of TCRs are unlikely to fully suppress the T-cell response to MBP in vivo.

Original languageEnglish (US)
Pages (from-to)1919-1922
Number of pages4
JournalNeurology
Volume45
Issue number10
StatePublished - 1995
Externally publishedYes

ASJC Scopus subject areas

  • General Neuroscience
  • Arts and Humanities (miscellaneous)
  • Clinical Neurology

Fingerprint

Dive into the research topics of 'Diversity of T-cell receptor V(α), V(β), and CDR3 expression by myelin basic protein-specific human T-cell clones'. Together they form a unique fingerprint.

Cite this