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T-Cell Receptor Gene Rearrangements as Clinical Markers of Human T-Cell Lymphomas

List of authors.
  • Virginia Bertness, B.S.,
  • Ilan Kirsch, M.D.,
  • Gregory Hollis, Ph.D.,
  • Bruce Johnson, M.D.,
  • and Paul A. Bunn, Jr., M.D.

Abstract

The ability to detect immunoglobulin-gene rearrangements has proved useful in confirming diagnoses of suspected B-cell lymphomas and in establishing their monoclonality. By analogy, we employed a cloned DNA probe for the beta chain of the T-cell receptor gene to determine whether gene rearrangements were present in human T-cell neoplasms representing various stages of T-cell development. Gene rearrangements were present in all cases of T-cell disorders except a single case of T gamma lymphocytosis, a disorder that has not been proved to be a clonal T-cell neoplasm. A germline gene configuration was present in all patients with non-T-cell neoplasms and in normal tissues from patients with T-cell lymphoma. The probe promises to be useful for confirming the pathological and immunologic diagnosis in difficult cases of T-cell disorders and for assessing the extent of disease. (N Engl J Med 1985; 313:534–8.)

Funding and Disclosures

The opinions or assertions in this article are the private views of the authors and are not to be construed as official or as reflecting the views or policies of the Department of the Navy or the Department of Defense, nor does the mention of trade names, commercial products, or organizations imply endorsement by the U.S. government.

We are indebted to John Minna for helpful discussions and critical reading of the manuscript, and to Kathy Wyckoff and Tanya Diggs for help in preparing it.

Author Affiliations

From the NCI—Navy Medical Oncology Branch, National Cancer Institute and Naval Hospital, Bethesda, Md. Address reprint requests to Dr. Bunn or Dr. Kirsch at NCI—Navy Medical Oncology Branch, Bldg. 8, Rm. 5101, Naval Hospital, Bethesda, MD 20814.

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