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Published on: February 12, 2022
CD40 expression identifies a prognostically favourable subgroup of diffuse large B-cell lymphoma
Johan Linderoth1, Mats Ehinger, Mats Jerkeman
1Department of Oncology, Institution of Clinical Sciences, Lund University Hospital, Lund, Sweden. johan.linderoth@med.lu.se
Leukemia & Lymphoma
|September 6, 2007
Summary
CD40 expression in diffuse large B-cell lymphoma (DLBCL) is confirmed to improve patient survival. This study found CD40 positivity associated with better outcomes, independent of germinal center phenotype or T-cell infiltration.
Area of Science:
- Oncology
- Immunology
- Pathology
Background:
- Diffuse large B-cell lymphoma (DLBCL) is a heterogeneous non-Hodgkin lymphoma.
- Previous studies suggested prognostic significance of CD23 and CD40 expression in DLBCL.
- Potential associations with germinal center (GC) phenotype and autologous tumor response were hypothesized.
Purpose of the Study:
- To confirm earlier findings on the prognostic effects of CD23 and CD40 expression in de novo DLBCL.
- To investigate the relationship between CD40/CD23 expression, GC phenotype, and tumor-infiltrating T-cells.
Main Methods:
- Immunohistochemical analysis of tumor specimens from 125 de novo DLBCL patients.
- Assessment of CD23, CD40, BCL6, CD10, MUM1, CD4, and CD8 expression.
- Correlation analysis between marker expression, GC phenotype, and overall survival.
Main Results:
- CD40 positivity was observed in 64% of cases and significantly correlated with improved overall survival (p = 0.03).
- A germinal center (GC) phenotype was present in 47% and associated with better survival (p = 0.006), but did not correlate with CD40 expression.
- No correlation was found between CD40 positivity and the amount of tumor-infiltrating T-cells (CD4, CD8). CD23 positivity (10%) did not correlate with prognosis.
Conclusions:
- The positive prognostic effect of CD40 expression in DLBCL is confirmed.
- CD40 expression's prognostic value is independent of the germinal center phenotype and T-cell infiltration.
- CD23 expression did not show a significant correlation with prognosis in this cohort.

