Haematologica (Mar 2010)

The inducible T-cell co-stimulator molecule is expressed on subsets of T cells and is a new marker of lymphomas of T follicular helper cell-derivation

  • Teresa Marafioti,
  • Jennifer C. Paterson,
  • Erica Ballabio,
  • Andreas Chott,
  • Yasodha Natkunam,
  • Manuel Rodriguez-Justo,
  • Anne Plonquet,
  • Socorro M. Rodriguez-Pinilla,
  • Wolfram Klapper,
  • Martin-L. Hansmann,
  • Stefano A. Pileri,
  • Peter G. Isaacson,
  • Harald Stein,
  • Miguel A. Piris,
  • David Y. Mason,
  • Philippe Gaulard

DOI
https://doi.org/10.3324/haematol.2009.010991
Journal volume & issue
Vol. 95, no. 3

Abstract

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Background T follicular helper (TFH) cells reside in the light zone of germinal centers and are considered the cell of origin of angioimmunoblastic T-cell lymphoma. Recently, CXCL13, PD-1 and SAP were described as useful markers for TFH cells and angioimmunoblastic T-cell lymphoma but also reported in some peripheral T-cell lymphomas, not otherwise specified.Design and Methods In the present study the expression pattern of ICOS protein was investigated by immunohistochemistry-based techniques in routine sections of normal lymphoid tissues and 633 human lymphomas.Results Cells strongly positive for ICOS were restricted to the light zone of germinal centers and co-expressed TFH-associated molecules. In addition, weak to moderate ICOS expression was observed in a small proportion of FOXP3-positive cells. In lymphomas, ICOS expression was confined to angioimmunoblastic T-cell lymphoma (85/86), peripheral T-cell lymphomas of follicular variant (18/18) and a proportion of peripheral T-cell lymphomas, not otherwise specified (24/56) that also expressed other TFH-associated molecules.Conclusions ICOS is a useful molecule for identifying TFH cells and its restricted expression to angioimmunoblastic T-cell lymphoma and a proportion of peripheral T-cell lymphomas, not otherwise specified (showing a TFH-like profile) suggests its inclusion in the antibody panel for diagnosing TFH-derived lymphomas. Our findings provide further evidence that the histological spectrum of TFH-derived lymphomas is broader than previously assumed.