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Published on: September 25, 2018
PD-1/PD-L1 expression in anal squamous intraepithelial lesions
Margot Bucau1, Nathalie Gault2,3, Nanthara Sritharan3
1AP-HP, Département de Pathologie, Hôpital Bichat-Claude Bernard, F-75018 Paris, France.
High-grade anal dysplasia shows more CD8 and PD-1 immune cells than low-grade lesions. This suggests the PD-1/PD-L1 pathway is involved in anal dysplasia progression.
Area of Science:
- Immunology
- Oncology
- Pathology
Background:
- The PD-1/PD-L1 pathway regulates anti-tumor immunity in various cancers.
- PD-1 and PD-L1 expression in anal squamous intra-epithelial lesions (LSIL/HSIL) remains uncharacterized.
Purpose of the Study:
- To investigate the expression and distribution of CD8+ lymphocytes, PD-1+ lymphocytes, and PD-L1+ epithelial cells in anal LSIL and HSIL.
- To compare these immune markers between LSIL and HSIL to understand their role in anal dysplasia progression.
Main Methods:
- Immunohistochemical analysis of CD8, PD-1, and PD-L1 on 78 anal lesion samples (60 HSIL, 18 LSIL).
- Assessment of the presence and distribution of CD8+ lymphocytes, PD-1+ lymphocytes, and PD-L1+ epithelial cells.
- Statistical comparison of immune marker expression between HSIL and LSIL groups.
Main Results:
- CD8+ lymphocytes were significantly more frequent in HSIL compared to LSIL (lamina propria: 90% vs. 60%; intraepithelial: 62% vs. 33%).
- PD-1+ lymphocytes were also significantly more frequent in HSIL than LSIL (41% vs. 11%).
- No significant difference in PD-L1+ epithelial cell expression was observed between HSIL and LSIL.
Conclusions:
- Anal dysplastic lesions feature an inflammatory infiltrate of CD8+ and PD-1+ lymphocytes, which is more pronounced in high-grade lesions.
- The findings indicate the involvement of the PD-1/PD-L1 pathway in the pathogenesis and progression of anal dysplasia.
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