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Differential prognostic impact of CD8(+) T cells based on human leucocyte antigen I and PD-L1 expression in microsatellite-unstable gastric cancer

BACKGROUND: The aim of the study was to determine the human leucocyte antigen class-I (HLA-I), programmed death-ligand 1 (PD-L1) expression and tumour-infiltrating lymphocytes (TILs) of microsatellite instability-high gastric cancer. METHODS: The HLA-I expression type was determined by immunohistoch...

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Autores principales: Kwak, Yoonjin, Koh, Jiwon, Park, Yujun, Hong, Yun Ji, Park, Kyoung Un, Kim, Hyung-Ho, Park, Do Joong, Ahn, Sang-Hoon, Kim, Woo Ho, Lee, Hye Seung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189244/
https://www.ncbi.nlm.nih.gov/pubmed/32203213
http://dx.doi.org/10.1038/s41416-020-0793-y
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author Kwak, Yoonjin
Koh, Jiwon
Park, Yujun
Hong, Yun Ji
Park, Kyoung Un
Kim, Hyung-Ho
Park, Do Joong
Ahn, Sang-Hoon
Kim, Woo Ho
Lee, Hye Seung
author_facet Kwak, Yoonjin
Koh, Jiwon
Park, Yujun
Hong, Yun Ji
Park, Kyoung Un
Kim, Hyung-Ho
Park, Do Joong
Ahn, Sang-Hoon
Kim, Woo Ho
Lee, Hye Seung
author_sort Kwak, Yoonjin
collection PubMed
description BACKGROUND: The aim of the study was to determine the human leucocyte antigen class-I (HLA-I), programmed death-ligand 1 (PD-L1) expression and tumour-infiltrating lymphocytes (TILs) of microsatellite instability-high gastric cancer. METHODS: The HLA-I expression type was determined by immunohistochemistry of HLA-A, HLA-B, HLA-C and β2-microglobulin in the centre of the tumour (CT) and in the invasive margin (IM) of samples from 293 patients (total loss vs. preserved type). PD-L1 expression and TIL density was examined immunohistochemically. HLA-I genotyping was also performed. RESULTS: The expression loss of the HLA-I molecules was significantly associated with low TIL density. According to survival analyses, the HLA-I expression type and PD-L1 positivity were not independent prognostic factors. The TIL density had no prognostic implication when survival analysis was performed for the whole patient group; however, high CD8(+) TIL infiltration was significantly associated with good prognosis in only HLA-I-preserved-type/PD-L1-positive group (p = 0.034). The homozygosity of the HLA-I allele was more frequently observed in the total loss type group. CONCLUSIONS: We confirmed differential prognostic implication of CD8(+) TILs according to the HLA-I and PD-L1 expression. Determination of the HLA-I expression could be helpful to select patients who would benefit from anti-PD-1/PD-L1 therapy.
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spelling pubmed-71892442021-03-17 Differential prognostic impact of CD8(+) T cells based on human leucocyte antigen I and PD-L1 expression in microsatellite-unstable gastric cancer Kwak, Yoonjin Koh, Jiwon Park, Yujun Hong, Yun Ji Park, Kyoung Un Kim, Hyung-Ho Park, Do Joong Ahn, Sang-Hoon Kim, Woo Ho Lee, Hye Seung Br J Cancer Article BACKGROUND: The aim of the study was to determine the human leucocyte antigen class-I (HLA-I), programmed death-ligand 1 (PD-L1) expression and tumour-infiltrating lymphocytes (TILs) of microsatellite instability-high gastric cancer. METHODS: The HLA-I expression type was determined by immunohistochemistry of HLA-A, HLA-B, HLA-C and β2-microglobulin in the centre of the tumour (CT) and in the invasive margin (IM) of samples from 293 patients (total loss vs. preserved type). PD-L1 expression and TIL density was examined immunohistochemically. HLA-I genotyping was also performed. RESULTS: The expression loss of the HLA-I molecules was significantly associated with low TIL density. According to survival analyses, the HLA-I expression type and PD-L1 positivity were not independent prognostic factors. The TIL density had no prognostic implication when survival analysis was performed for the whole patient group; however, high CD8(+) TIL infiltration was significantly associated with good prognosis in only HLA-I-preserved-type/PD-L1-positive group (p = 0.034). The homozygosity of the HLA-I allele was more frequently observed in the total loss type group. CONCLUSIONS: We confirmed differential prognostic implication of CD8(+) TILs according to the HLA-I and PD-L1 expression. Determination of the HLA-I expression could be helpful to select patients who would benefit from anti-PD-1/PD-L1 therapy. Nature Publishing Group UK 2020-03-17 2020-04-28 /pmc/articles/PMC7189244/ /pubmed/32203213 http://dx.doi.org/10.1038/s41416-020-0793-y Text en © The Author(s), under exclusive licence to Cancer Research UK 2020 https://creativecommons.org/licenses/by/4.0/Note This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0).
spellingShingle Article
Kwak, Yoonjin
Koh, Jiwon
Park, Yujun
Hong, Yun Ji
Park, Kyoung Un
Kim, Hyung-Ho
Park, Do Joong
Ahn, Sang-Hoon
Kim, Woo Ho
Lee, Hye Seung
Differential prognostic impact of CD8(+) T cells based on human leucocyte antigen I and PD-L1 expression in microsatellite-unstable gastric cancer
title Differential prognostic impact of CD8(+) T cells based on human leucocyte antigen I and PD-L1 expression in microsatellite-unstable gastric cancer
title_full Differential prognostic impact of CD8(+) T cells based on human leucocyte antigen I and PD-L1 expression in microsatellite-unstable gastric cancer
title_fullStr Differential prognostic impact of CD8(+) T cells based on human leucocyte antigen I and PD-L1 expression in microsatellite-unstable gastric cancer
title_full_unstemmed Differential prognostic impact of CD8(+) T cells based on human leucocyte antigen I and PD-L1 expression in microsatellite-unstable gastric cancer
title_short Differential prognostic impact of CD8(+) T cells based on human leucocyte antigen I and PD-L1 expression in microsatellite-unstable gastric cancer
title_sort differential prognostic impact of cd8(+) t cells based on human leucocyte antigen i and pd-l1 expression in microsatellite-unstable gastric cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189244/
https://www.ncbi.nlm.nih.gov/pubmed/32203213
http://dx.doi.org/10.1038/s41416-020-0793-y
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