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Complexity of T cell receptor recognition sites for defined alloantigens

  • J. Borst
  • , E. de Vries
  • , H. Spits
  • , J. E. de Vries
  • , A. W. Boylston
  • , E. A. Matthews

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Three monoclonal antibodies react with the T cell receptor on the tumor line HPB-ALL and in addition with 3 to 13% of human peripheral blood T cells of normal donors. These antibodies are shown to react with an epitope encoded by the V beta 5 family of T cell receptor beta-chain variable region gene segments. Cells expressing V beta 5 gene segments can have cytotoxic or helper function, be of the T4+ or T8+ phenotype, and have specificity for either class I or class II major histocompatibility complex alloantigens. Seven T cell clones were generated, which express V beta 5 and are specific for the HLA-A2 molecule. With the use of these clones, we illustrate how isoelectric focusing can be used to analyze T cell receptor alpha- and beta-chain structure. The seven clones recognize five distinct conformational determinants on HLA-A2. They procure different binding sites by the use of different alpha-chains, J beta sequences, or both
Original languageEnglish
Pages (from-to)1952-1959
JournalJournal of immunology (Baltimore, Md.
Volume139
Issue number6
Publication statusPublished - 1987

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