Cargando…

PD-1/PD-L1 expression in anal squamous intraepithelial lesions

Introduction: Studies have shown that the PD-1/PD-L1 immunomodulatory pathway slows down anti-tumor immunity in a number of cancers. The description of the expression of these molecules has never been performed in anal low-grade/high grade squamous intra-epithelial lesions (LSIL/HSIL respectively)....

Descripción completa

Detalles Bibliográficos
Autores principales: Bucau, Margot, Gault, Nathalie, Sritharan, Nanthara, Valette, Emy, Charpentier, Charlotte, Walker, Francine, Couvelard, Anne, Abramowitz, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533075/
https://www.ncbi.nlm.nih.gov/pubmed/33062194
http://dx.doi.org/10.18632/oncotarget.27756
_version_ 1783590059500371968
author Bucau, Margot
Gault, Nathalie
Sritharan, Nanthara
Valette, Emy
Charpentier, Charlotte
Walker, Francine
Couvelard, Anne
Abramowitz, Laurent
author_facet Bucau, Margot
Gault, Nathalie
Sritharan, Nanthara
Valette, Emy
Charpentier, Charlotte
Walker, Francine
Couvelard, Anne
Abramowitz, Laurent
author_sort Bucau, Margot
collection PubMed
description Introduction: Studies have shown that the PD-1/PD-L1 immunomodulatory pathway slows down anti-tumor immunity in a number of cancers. The description of the expression of these molecules has never been performed in anal low-grade/high grade squamous intra-epithelial lesions (LSIL/HSIL respectively). Materials and Methods: Patients followed in the AIN3 cohort were routinely sampled. For each selected sample, an immunohistochemical study was performed with anti-CD8, PD-1, PD-L1 antibodies. The presence and distribution of CD8+ lymphocytes, and the presence of PD-1+ lymphocytes and PD-L1+ epithelial cells were assessed. The comparison of these characteristics was performed between the HSIL and LSIL groups. Results: 33 patients were included and 78 samples selected (60 HSIL and 18 LSIL). CD8+ lymphocytes were observed more frequently in HSIL versus LSIL in the lamina propria or intra epithelial (respectively 90% vs. 60%, p = 0.01; and 62% vs. 33%, p = 0.04). PD-1+ lymphocytes were observed more frequently in HSIL versus LSIL (41% vs 11%, p = 0.03). There was no difference between HSIL and LSIL for PD-L1+ epithelial cells. Conclusions: Anal dysplastic lesions are accompanied by an inflammatory lymphocytic infiltrate expressing CD8 and PD-1, more frequent in high-grade lesions. These results highlight the involvement of the PD-1/PD-L1 pathway in the natural history of anal dysplasia.
format Online
Article
Text
id pubmed-7533075
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-75330752020-10-13 PD-1/PD-L1 expression in anal squamous intraepithelial lesions Bucau, Margot Gault, Nathalie Sritharan, Nanthara Valette, Emy Charpentier, Charlotte Walker, Francine Couvelard, Anne Abramowitz, Laurent Oncotarget Research Paper Introduction: Studies have shown that the PD-1/PD-L1 immunomodulatory pathway slows down anti-tumor immunity in a number of cancers. The description of the expression of these molecules has never been performed in anal low-grade/high grade squamous intra-epithelial lesions (LSIL/HSIL respectively). Materials and Methods: Patients followed in the AIN3 cohort were routinely sampled. For each selected sample, an immunohistochemical study was performed with anti-CD8, PD-1, PD-L1 antibodies. The presence and distribution of CD8+ lymphocytes, and the presence of PD-1+ lymphocytes and PD-L1+ epithelial cells were assessed. The comparison of these characteristics was performed between the HSIL and LSIL groups. Results: 33 patients were included and 78 samples selected (60 HSIL and 18 LSIL). CD8+ lymphocytes were observed more frequently in HSIL versus LSIL in the lamina propria or intra epithelial (respectively 90% vs. 60%, p = 0.01; and 62% vs. 33%, p = 0.04). PD-1+ lymphocytes were observed more frequently in HSIL versus LSIL (41% vs 11%, p = 0.03). There was no difference between HSIL and LSIL for PD-L1+ epithelial cells. Conclusions: Anal dysplastic lesions are accompanied by an inflammatory lymphocytic infiltrate expressing CD8 and PD-1, more frequent in high-grade lesions. These results highlight the involvement of the PD-1/PD-L1 pathway in the natural history of anal dysplasia. Impact Journals LLC 2020-09-29 /pmc/articles/PMC7533075/ /pubmed/33062194 http://dx.doi.org/10.18632/oncotarget.27756 Text en https://creativecommons.org/licenses/by/3.0/ Copyright: © 2020 Bucau et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Bucau, Margot
Gault, Nathalie
Sritharan, Nanthara
Valette, Emy
Charpentier, Charlotte
Walker, Francine
Couvelard, Anne
Abramowitz, Laurent
PD-1/PD-L1 expression in anal squamous intraepithelial lesions
title PD-1/PD-L1 expression in anal squamous intraepithelial lesions
title_full PD-1/PD-L1 expression in anal squamous intraepithelial lesions
title_fullStr PD-1/PD-L1 expression in anal squamous intraepithelial lesions
title_full_unstemmed PD-1/PD-L1 expression in anal squamous intraepithelial lesions
title_short PD-1/PD-L1 expression in anal squamous intraepithelial lesions
title_sort pd-1/pd-l1 expression in anal squamous intraepithelial lesions
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533075/
https://www.ncbi.nlm.nih.gov/pubmed/33062194
http://dx.doi.org/10.18632/oncotarget.27756
work_keys_str_mv AT bucaumargot pd1pdl1expressioninanalsquamousintraepitheliallesions
AT gaultnathalie pd1pdl1expressioninanalsquamousintraepitheliallesions
AT sritharannanthara pd1pdl1expressioninanalsquamousintraepitheliallesions
AT valetteemy pd1pdl1expressioninanalsquamousintraepitheliallesions
AT charpentiercharlotte pd1pdl1expressioninanalsquamousintraepitheliallesions
AT walkerfrancine pd1pdl1expressioninanalsquamousintraepitheliallesions
AT couvelardanne pd1pdl1expressioninanalsquamousintraepitheliallesions
AT abramowitzlaurent pd1pdl1expressioninanalsquamousintraepitheliallesions