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T-cell receptor gamma gene rearrangement analysis of classic Hodgkin lymphoma using a BIOMED-2 assay: a paraffin-embedded tissue analysis of one hundred cases.
Takata, Katsuyoshi; Miyata-Takata, Tomoko; Nishikori, Asami; Haratake, Tomoka; Sato, Yasuharu.
Afiliação
  • Takata K; Department of Cellular and Molecular Pathology, Niigata University Graduate School of Medicine, Niigata, Japan.
  • Miyata-Takata T; Department of Cellular and Molecular Pathology, Niigata University Graduate School of Medicine, Niigata, Japan.
  • Nishikori A; Department of Molecular Hematopathology, Okayama University Graduate School of Health Sciences, Okayama, Japan.
  • Haratake T; Department of Molecular Hematopathology, Okayama University Graduate School of Health Sciences, Okayama, Japan.
  • Sato Y; Department of Molecular Hematopathology, Okayama University Graduate School of Health Sciences, Okayama, Japan.
J Clin Exp Hematop ; 64(2): 138-143, 2024.
Article em En | MEDLINE | ID: mdl-38925974
ABSTRACT
In the new WHO classifications of haematolymphoid tumours (WHO-HAEM5), classic Hodgkin lymphoma (cHL) is categorized into B-cell lymphoid proliferations and lymphomas. Although the majority of Hodgkin Reed-Sternberg (HRS) cells are of germinal center B-cell origin with some defects of B-cell transcription factors, they rarely express T-cell antigens or cytotoxic molecules. Clonality analyses on cHL samples using BIOMED-2 have been reported by several groups; however, those studies were only focused on Ig regions, including IgH, Ig-kappa, and Ig-lambda, and TCR-γ clonality analysis of cHL has not yet been explored. Here, we investigated TCR-γ gene rearrangement for one hundred cases using a PCR-based method. Four of one hundred (4%) cases showed TCR-γ clonal peaks. Of these, three were at an advanced stage and one patient died of the disease. To clarify whether HRS cells showed T-cell clonality or not, we performed PCR analysis using DNAs of microdissected HRS cells. Three samples showed identical clonal peaks with bulk specimens. Our results indicate that cHL is a heterogeneous disease of mainly B-cell and rarely T-cell origin with a special phenotype. Further molecular studies are warranted.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Hodgkin Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Clin Exp Hematop Assunto da revista: HEMATOLOGIA / PATOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Hodgkin Limite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: J Clin Exp Hematop Assunto da revista: HEMATOLOGIA / PATOLOGIA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão