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Single Antibody Detection of T-Cell Receptor αß Clonality by Flow Cytometry Rapidly Identifies Mature T-Cell Neoplasms and Monotypic Small CD8-Positive Subsets of Uncertain Significance.
Shi, Min; Jevremovic, Dragan; Otteson, Gregory E; Timm, Michael M; Olteanu, Horatiu; Horna, Pedro.
Afiliação
  • Shi M; Division of Hematopathology, Mayo Clinic, Rochester, Minnesota.
  • Jevremovic D; Division of Hematopathology, Mayo Clinic, Rochester, Minnesota.
  • Otteson GE; Division of Hematopathology, Mayo Clinic, Rochester, Minnesota.
  • Timm MM; Division of Hematopathology, Mayo Clinic, Rochester, Minnesota.
  • Olteanu H; Division of Hematopathology, Mayo Clinic, Rochester, Minnesota.
  • Horna P; Division of Hematopathology, Mayo Clinic, Rochester, Minnesota.
Cytometry B Clin Cytom ; 98(1): 99-107, 2020 01.
Article em En | MEDLINE | ID: mdl-30972977
ABSTRACT

BACKGROUND:

The diagnosis of T-cell neoplasms is often challenging, due to overlapping features with reactive T-cells and limitations of currently available T-cell clonality assays. The description of an antibody specific for one of two mutually exclusive T-cell receptor (TCR) ß-chain constant regions (TRBC1) provide an opportunity to facilitate the detection of clonal TCRαß T-cells based on TRBC-restriction.

METHODS:

Twenty patients with mature T-cell neoplasms and 44 patients without evidence of T-cell neoplasia were studied. Peripheral blood (51), bone marrow (10), and lymph node (3) specimens were evaluated by 9-color flow cytometry including TRBC1 (CD2/CD3/CD4/CD5/CD7/CD8/CD45/TCRγδ/TRBC1 and/or CD2/CD3/CD4/CD5/CD7/CD8/CD26/CD45/TRBC1). Monophasic TRBC1 expression on any immunophenotypically distinct CD4-positive or CD8-positive/TCRγδ-negative T-cell subset was considered indicative of clonality.

RESULTS:

Monophasic (clonal) TRBC1 expression was identified on immunophenotypically abnormal T-cells from all 20 patients with T-cell malignancies (100% sensitivity), including 17 cases with either >97% or <3% TRBC1-positive events, and three cases with monophasic homogenous TRBC1-dim expression. All immunophenotypically distinct CD4-positive and CD8-positive/TCRγδ-negative T-cell subsets from 44 patients without T-cell malignancies showed the expected mixture of TRBC1-positive and TRBC-1-negative subpopulations (non-clonal), except for seven patients (16%) with very small CD8-positive T-cell subsets exhibiting a monophasic (clonal) pattern.

CONCLUSION:

Inclusion of a single anti-TRBC1 antibody into a diagnostic T-cell flow cytometry panel facilitates the rapid identification of T-cell neoplasms, in addition to small monotypic CD8-positive subsets of uncertain significance. © 2019 International Clinical Cytometry Society.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Antígenos de Linfócitos T alfa-beta / Linfócitos T CD8-Positivos / Linfoma / Anticorpos Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Antígenos de Linfócitos T alfa-beta / Linfócitos T CD8-Positivos / Linfoma / Anticorpos Idioma: En Ano de publicação: 2020 Tipo de documento: Article