Hodgkin's lymphoma associated T-cells exhibit a transcription factor profile consistent with distinct lymphoid compartments

J Clin Pathol. 2007 Oct;60(10):1092-7. doi: 10.1136/jcp.2006.044222. Epub 2006 Dec 8.

Abstract

Background: Hodgkin's lymphoma (HL) is characterised by an ineffective immune response that is predominantly mediated by CD4+ T-cells.

Aims: To analyse the expression of the key regulatory T-cell transcription factors (TFs) in the T-cells of HL involved tissues in order to assess the nature of the T(H) immune response in HL.

Methods and results: By immunohistochemistry, GATA3 was strongly and T-bet exclusively expressed in a subset of interfollicular lymphocytes in the reactive lymphoid tissues. In classical HL (CHL), which is generally located in the interfollicular zones, a predominance of T-bet+ T-cells and lesser amounts of GATA3+ and c-Maf+ T-cells was found, concordant with the pattern of the normal interfollicular compartment. In reactive lymphoid tissues, c-Maf was observed mostly in T-lymphocytes within the germinal centres (GCs). Nodular lymphocyte predominance type of Hodgkin's lymphoma (NLPHL) and progressively transformed germinal centres cases, showed a majority of c-Maf+ T-cells, consistent with the pattern in normal GCs. NLPHL cases uniformly showed c-Maf+/CD57+ T-cell rosettes around the neoplastic cells; these rosettes were absent in "paragranuloma-type" T-cell/histiocyte rich B-cell lymphoma.

Conclusions: T-cell TF expression profiles of the reactive T-cells in both subtypes of HL are in accordance with the expression profile observed in the distinct lymphoid compartments.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Child
  • Female
  • GABA Plasma Membrane Transport Proteins / metabolism
  • Germinal Center / immunology
  • Hodgkin Disease / immunology*
  • Humans
  • Male
  • Middle Aged
  • Neoplasm Proteins / metabolism
  • Proto-Oncogene Proteins c-maf / metabolism
  • T-Box Domain Proteins / metabolism
  • T-Lymphocyte Subsets / immunology*
  • T-Lymphocytes, Helper-Inducer / immunology
  • Transcription Factors / metabolism*

Substances

  • GABA Plasma Membrane Transport Proteins
  • MAF protein, human
  • Neoplasm Proteins
  • Proto-Oncogene Proteins c-maf
  • SLC6A11 protein, human
  • T-Box Domain Proteins
  • T-box transcription factor TBX21
  • Transcription Factors