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The germline HLA-A02B62 supertype is associated with a PD-L1-positive tumour immune microenvironment and poor prognosis in stage I lung cancer

BACKGROUND: Germline HLA class I molecule supertypes are shown to correlate with response to anti-PD-1 therapy. Here, we investigate the significance of germline HLA-A and HLA-B supertypes in tumour microenvironment of non-small-cell lung cancer. METHODS: Totally 278 NSCLC patients were collected re...

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Autores principales: Lin, Ruijiang, Chen, Xiaohua, Su, Fei, Wang, Hongbin, Han, Biao, Chen, Yanhui, Zhang, Cuixiang, Ma, Minjie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432705/
https://www.ncbi.nlm.nih.gov/pubmed/37600368
http://dx.doi.org/10.1016/j.heliyon.2023.e18948
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author Lin, Ruijiang
Chen, Xiaohua
Su, Fei
Wang, Hongbin
Han, Biao
Chen, Yanhui
Zhang, Cuixiang
Ma, Minjie
author_facet Lin, Ruijiang
Chen, Xiaohua
Su, Fei
Wang, Hongbin
Han, Biao
Chen, Yanhui
Zhang, Cuixiang
Ma, Minjie
author_sort Lin, Ruijiang
collection PubMed
description BACKGROUND: Germline HLA class I molecule supertypes are shown to correlate with response to anti-PD-1 therapy. Here, we investigate the significance of germline HLA-A and HLA-B supertypes in tumour microenvironment of non-small-cell lung cancer. METHODS: Totally 278 NSCLC patients were collected retrospectively. HLA genotyping was conducted using next-generation sequencing. The evaluation of tumour-infiltrating lymphocytes was performed by multiplex immunohistochemistry assay. Correlations among HLA supertypes, tumour infiltrating lymphocytes, and clinicopathological characteristics were assessed. RESULTS: HLA-A03 and HLA-B62 were the supertypes with the highest proportions, at 69.1% and 52.2%, respectively. HLA-A02 or HLA-B62, but not HLA-A03, associated with higher PD-L1(+) tumour and stromal cells levels, CD68(+) cells, and CD68(+)PD-L1(+) cells. Patients with both HLA-A02 and HLA-B62 supertypes displayed significantly higher PD-L1(+) cells, CD68(+) cells, and CD8(+) cells levels than patients with other supertypes (P = 0.0301, P = 0.0479, P = 0.0192). These cells collectively constitute a hot but immunosuppressive tumour microenvironment. Accordingly, patients with both HLA-A02 and HLA-B62 supertypes had short progression-free survival after surgery (HR = 2.27, P = 0.0373). CONCLUSIONS: The HLA-A02B62 supertype could serve as a possible indicator of poor prognosis in early-stage lung cancer. However, it may also act as a favorable prognostic factor for immunotherapy, given its association with a PD-L1-positive tumour microenvironment.
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spelling pubmed-104327052023-08-18 The germline HLA-A02B62 supertype is associated with a PD-L1-positive tumour immune microenvironment and poor prognosis in stage I lung cancer Lin, Ruijiang Chen, Xiaohua Su, Fei Wang, Hongbin Han, Biao Chen, Yanhui Zhang, Cuixiang Ma, Minjie Heliyon Research Article BACKGROUND: Germline HLA class I molecule supertypes are shown to correlate with response to anti-PD-1 therapy. Here, we investigate the significance of germline HLA-A and HLA-B supertypes in tumour microenvironment of non-small-cell lung cancer. METHODS: Totally 278 NSCLC patients were collected retrospectively. HLA genotyping was conducted using next-generation sequencing. The evaluation of tumour-infiltrating lymphocytes was performed by multiplex immunohistochemistry assay. Correlations among HLA supertypes, tumour infiltrating lymphocytes, and clinicopathological characteristics were assessed. RESULTS: HLA-A03 and HLA-B62 were the supertypes with the highest proportions, at 69.1% and 52.2%, respectively. HLA-A02 or HLA-B62, but not HLA-A03, associated with higher PD-L1(+) tumour and stromal cells levels, CD68(+) cells, and CD68(+)PD-L1(+) cells. Patients with both HLA-A02 and HLA-B62 supertypes displayed significantly higher PD-L1(+) cells, CD68(+) cells, and CD8(+) cells levels than patients with other supertypes (P = 0.0301, P = 0.0479, P = 0.0192). These cells collectively constitute a hot but immunosuppressive tumour microenvironment. Accordingly, patients with both HLA-A02 and HLA-B62 supertypes had short progression-free survival after surgery (HR = 2.27, P = 0.0373). CONCLUSIONS: The HLA-A02B62 supertype could serve as a possible indicator of poor prognosis in early-stage lung cancer. However, it may also act as a favorable prognostic factor for immunotherapy, given its association with a PD-L1-positive tumour microenvironment. Elsevier 2023-08-06 /pmc/articles/PMC10432705/ /pubmed/37600368 http://dx.doi.org/10.1016/j.heliyon.2023.e18948 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Lin, Ruijiang
Chen, Xiaohua
Su, Fei
Wang, Hongbin
Han, Biao
Chen, Yanhui
Zhang, Cuixiang
Ma, Minjie
The germline HLA-A02B62 supertype is associated with a PD-L1-positive tumour immune microenvironment and poor prognosis in stage I lung cancer
title The germline HLA-A02B62 supertype is associated with a PD-L1-positive tumour immune microenvironment and poor prognosis in stage I lung cancer
title_full The germline HLA-A02B62 supertype is associated with a PD-L1-positive tumour immune microenvironment and poor prognosis in stage I lung cancer
title_fullStr The germline HLA-A02B62 supertype is associated with a PD-L1-positive tumour immune microenvironment and poor prognosis in stage I lung cancer
title_full_unstemmed The germline HLA-A02B62 supertype is associated with a PD-L1-positive tumour immune microenvironment and poor prognosis in stage I lung cancer
title_short The germline HLA-A02B62 supertype is associated with a PD-L1-positive tumour immune microenvironment and poor prognosis in stage I lung cancer
title_sort germline hla-a02b62 supertype is associated with a pd-l1-positive tumour immune microenvironment and poor prognosis in stage i lung cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10432705/
https://www.ncbi.nlm.nih.gov/pubmed/37600368
http://dx.doi.org/10.1016/j.heliyon.2023.e18948
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