Immunohistochemical expression of PD1, LAG3, and CTLA4 in diffuse large B cell lymphoma, clinicopathological correlation, and prognostic value

PD1 and LAG3 are expressed mainly in TILs. PD1 expression (in TILs and tumor cells) is associated with prolonged OS, while LAG3 expression (in tumor cells) is associated with shorter DFS and its expression in TILs tended towards shorter OS. CTLA4 expression is associated with advanced disease stage but not associated with OS. These findings may suggest that immune checkpoint inhibitors targeting LAG3 may offer therapeutic potential in DLBCL by enhancing the antitumor immune response. Additional research is needed to assess the effectiveness of inhibition of these checkpoint molecules in combination with existing treatment modalities.

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Publication Details

Journal
Journal of the Egyptian National Cancer Institute
Published
2025-06-07
DOI
https://doi.org/10.1186/s43046-025-00303-0
Citations
1
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
1.05
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article

Immunohistochemical expression of PD1, LAG3, and CTLA4 in diffuse large B cell lymphoma, clinicopathological correlation, and prognostic value

Dina Tantawy, Mariana M. William, Shaimaa M Yussif, Alyaa R. Elsergany et al.
1 citations
Journal of the Egyptian National Cancer Institute
Cancer Immunotherapy and Biomarkers
1.05
article

Immunohistochemical expression of PD1, LAG3, and CTLA4 in diffuse large B cell lymphoma, clinicopathological correlation, and prognostic value

Dina Tantawy, Mariana M. William, Shaimaa M Yussif, Alyaa R. Elsergany, Amira Kamal El-Hawary
article en
1 citations

Abstract

PD1 and LAG3 are expressed mainly in TILs. PD1 expression (in TILs and tumor cells) is associated with prolonged OS, while LAG3 expression (in tumor cells) is associated with shorter DFS and its expression in TILs tended towards shorter OS. CTLA4 expression is associated with advanced disease stage but not associated with OS. These findings may suggest that immune checkpoint inhibitors targeting LAG3 may offer therapeutic potential in DLBCL by enhancing the antitumor immune response. Additional research is needed to assess the effectiveness of inhibition of these checkpoint molecules in combination with existing treatment modalities.

Journal of the Egyptian National Cancer InstituteVol. 37(1)
Mansoura University (EG)
Good health and well-being
Openalex Percentile: Top 21%
Cancer Immunotherapy and Biomarkers
1.05
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