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Research Article Free access | 10.1172/JCI113453

Comparison of T cell receptor alpha, beta, and gamma gene rearrangement and expression in T cell acute lymphoblastic leukemia.

J Hara, S H Benedict, E Champagne, T W Mak, M Minden, and E W Gelfand

Division of Immunology and Rheumatology, Hospital for Sick Children, Toronto, Ontario, Canada.

Find articles by Hara, J. in: PubMed | Google Scholar

Division of Immunology and Rheumatology, Hospital for Sick Children, Toronto, Ontario, Canada.

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Division of Immunology and Rheumatology, Hospital for Sick Children, Toronto, Ontario, Canada.

Find articles by Champagne, E. in: PubMed | Google Scholar

Division of Immunology and Rheumatology, Hospital for Sick Children, Toronto, Ontario, Canada.

Find articles by Mak, T. in: PubMed | Google Scholar

Division of Immunology and Rheumatology, Hospital for Sick Children, Toronto, Ontario, Canada.

Find articles by Minden, M. in: PubMed | Google Scholar

Division of Immunology and Rheumatology, Hospital for Sick Children, Toronto, Ontario, Canada.

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Published April 1, 1988 - More info

Published in Volume 81, Issue 4 on April 1, 1988
J Clin Invest. 1988;81(4):989–996. https://doi.org/10.1172/JCI113453.
© 1988 The American Society for Clinical Investigation
Published April 1, 1988 - Version history
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Abstract

We have analyzed the configuration of the T cell receptor (TCR) alpha gene using newly developed genomic joining region (J alpha) probes, which cover approximately 80 kb of the J alpha region upstream from the constant region in 19 patients with T cell acute lymphoblastic leukemia (T-ALL) and in three CD3- leukemic T cell lines (HSB2, CEM, and MOLT4). In parallel, transcription of the TCR-alpha, beta, and gamma genes was examined in 11 of these patients and in the T cell lines. All T-ALL and the three T cell lines exhibited both TCR-gamma and beta gene rearrangements. 8 of 10 T-ALL and all T cell lines expressed TCR-gamma transcripts. All samples tested expressed both TCR-beta and CD3-gamma transcripts. TCR alpha transcripts were only observed in CD3+ T-ALL but not in CD3- T-ALL or the CD3- cell lines. Among the CD3+ T-ALL, eight had TCR-alpha gene rearrangements. In addition, TCR-alpha gene rearrangements were detected in one CD3- T-ALL and all three T cell lines. These leukemic cells may represent a transient stage between rearrangement and expression and provide an opportunity for analyzing the mechanism regulating the expression of the TCR-alpha gene.

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