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The role of current and new discriminating markers in the immunodiagnosis of Hodgkin's disease and other phenotypically related lymphomas.

Antonino Carbone, Annunziata Gloghini

Open publisher page 6 citations

Abstract

Recent data have shown that CD40 antigen and its ligand (CD40L), and the CD26 molecule are differentially expressed among Hodgkin's disease (HD) (CD40+, CD26, CD40L), peripheral T-cell (PTCL) (CD40L+/-, CD40, CD26) and CD30 positive anaplastic large cell (ALC) (CD26+, CD40L) lymphomas. Since CD40 molecule is consistently detected on Reed-Sternberg (RS) cells and their morphologic variants with a distinctive staining pattern. CD40 expression provides a new potential tool for the identification of RS cells of HD in fixed and paraffin-embedded material. Furthermore, the combined application of anti-CD40 and anti-CD26 MoAbs may discriminate HD from morphologically and immunophenotypically related ALC lymphomas. In fact a CD26+/CD40 profile is restricted to CD30 positive ALC lymphomas. Finally, the combined application of anti-CD40 and anti-CD40L MoAbs provides additional significant features in differentiating HD from PTCL due to the constant expression of CD40+/CD40L phenotype in HD and its absence in PTCL, which in turn express CD40/CD40L+/- phenotype.

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What this paper is about

Recent data have shown that CD40 antigen and its ligand (CD40L), and the CD26 molecule are differentially expressed among Hodgkin's disease (HD) (CD40+, CD26, CD40L), peripheral T-cell (PTCL) (CD40L+/-, CD40, CD26) and CD30 positive anaplastic large cell (ALC) (CD26+, CD40L) lymphomas. Since CD40 molecule is consistently detected on Reed-Sternberg (RS) cells and their morphologic variants with a distinctive staining pattern. CD40 expression provides a new potential tool for the identification of RS cells of HD in fixed and paraffin-embedded material. Furthermore, the combined application of anti-CD40 and anti-CD26 MoAbs may discriminate HD from morphologically and immunophenotypically related ALC lymphomas. In fact a CD26+/CD40 profile is restricted to CD30 positive ALC lymphomas. Finally, the combined application of anti-CD40 and anti-CD40L MoAbs provides additional significant features in differentiating HD from PTCL due to the constant expression of CD40+/CD40L phenotype in HD and its absence in PTCL, which in turn express CD40/CD40L+/- phenotype.

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Available abstract

Recent data have shown that CD40 antigen and its ligand (CD40L), and the CD26 molecule are differentially expressed among Hodgkin's disease (HD) (CD40+, CD26, CD40L), peripheral T-cell (PTCL) (CD40L+/-, CD40, CD26) and CD30 positive anaplastic large cell (ALC) (CD26+, CD40L) lymphomas. Since CD40 molecule is consistently detected on Reed-Sternberg (RS) cells and their morphologic variants with a distinctive staining pattern. CD40 expression provides a new potential tool for the identification of RS cells of HD in fixed and paraffin-embedded material. Furthermore, the combined application of anti-CD40 and anti-CD26 MoAbs may discriminate HD from morphologically and immunophenotypically related ALC lymphomas. In fact a CD26+/CD40 profile is restricted to CD30 positive ALC lymphomas. Finally, the combined application of anti-CD40 and anti-CD40L MoAbs provides additional significant features in differentiating HD from PTCL due to the constant expression of CD40+/CD40L phenotype in HD and its absence in PTCL, which in turn express CD40/CD40L+/- phenotype.

Key concepts: CD40, CD30, Biology, Phenotype, Lymphoma, Pathology, Immunology, Medicine

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The role of current and new discriminating markers in the immunodiagnosis of Hodgkin's disease and other phenotypically related lymphomas. — Research Paper | ScholarLens