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TCRBV23 specificity of two monoclonal antibodies revealed by a panel of human V beta chains expressed in mouse cells.
- Source :
-
Journal of immunological methods [J Immunol Methods] 1995 Oct 26; Vol. 186 (2), pp. 313-22. - Publication Year :
- 1995
-
Abstract
- Two monoclonal antibodies, HUT78#1 and HUT78#7, were made against the T cell receptor of the T leukemia line HUT78. Their specificity was originally determined as TCRBV1S1 (V beta 1), and they have been used as such in repertoire studies (Rebai et al., 1994, Proc. Natl. Acad. Sci. USA 91, 1529). Here, we report their characterization using a large panel of mouse T cell transfectants expressing various human T cell receptor beta chains at their surface. These transfectants revealed that the true specificity of both monoclonal antibodies was for TCRBV23S1 (V beta 23), a result that was confirmed by several other techniques. We show that the original determination as a V beta 1 specificity was due to a crossreactive oligonucleotide used to type the immunizing cell line. The oligonucleotide amplified the V beta 1 as well as the closely related V beta 23 sequence, while the antibodies, by contrast, react exclusively with the beta chain encoded by the V beta 23 subfamily of the T cell receptor. Both antibodies seem to have identical specificities. These antibodies will be useful for the detection of a new subset of human lymphocytes since, to date, no other reagent with reactivity for the V beta 23 chain of the human T cell receptor has been described so far.
- Subjects :
- Amino Acid Sequence
Animals
Antibody Specificity
Base Sequence
Cricetinae
Cross Reactions
DNA, Complementary genetics
Genes
Humans
Leukemia, T-Cell pathology
Mice
Molecular Sequence Data
Polymerase Chain Reaction
Receptors, Antigen, T-Cell, alpha-beta biosynthesis
Receptors, Antigen, T-Cell, alpha-beta genetics
Recombinant Fusion Proteins biosynthesis
Transfection
Tumor Cells, Cultured
Antibodies, Monoclonal immunology
Antibodies, Neoplasm immunology
Receptors, Antigen, T-Cell, alpha-beta immunology
Recombinant Fusion Proteins immunology
Subjects
Details
- Language :
- English
- ISSN :
- 0022-1759
- Volume :
- 186
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of immunological methods
- Publication Type :
- Academic Journal
- Accession number :
- 7594631
- Full Text :
- https://doi.org/10.1016/0022-1759(95)00159-8