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The role of soluble CD80 in patients with soft tissue tumors

BACKGROUND: Immune checkpoint protein (ICP), which is a central factor group of the immune system, has been reported to have a correlation between the degree of its expression and the prognosis of patients with malignant tumors, and many inhibitors have appeared as therapeutic targets. On the other...

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Autores principales: Matsuyama, Yumi, Asanuma, Kunihiro, Yoshida, Keisuke, Hagi, Tomohito, Iino, Takahiro, Nakamura, Tomoki, Sudo, Akihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446575/
https://www.ncbi.nlm.nih.gov/pubmed/36064421
http://dx.doi.org/10.1186/s13018-022-03283-2
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author Matsuyama, Yumi
Asanuma, Kunihiro
Yoshida, Keisuke
Hagi, Tomohito
Iino, Takahiro
Nakamura, Tomoki
Sudo, Akihiro
author_facet Matsuyama, Yumi
Asanuma, Kunihiro
Yoshida, Keisuke
Hagi, Tomohito
Iino, Takahiro
Nakamura, Tomoki
Sudo, Akihiro
author_sort Matsuyama, Yumi
collection PubMed
description BACKGROUND: Immune checkpoint protein (ICP), which is a central factor group of the immune system, has been reported to have a correlation between the degree of its expression and the prognosis of patients with malignant tumors, and many inhibitors have appeared as therapeutic targets. On the other hand, a soluble form of ICP in circulating blood induced systemic immunosuppression. In this study, we investigated the relationship between the soluble form of CD80 (sCD80) which is a ligand for the inhibitory system CTLA-4, in blood, and clinicopathological parameters in patients with soft tissue tumors. METHODS: A total of 119 patients with primary soft tissue tumors were enrolled in this study. The sCD80 levels were measured by enzyme immunoassay. RESULTS: There were no significant differences in sCD80 levels between benign (34) and soft tissue sarcoma (STS) patients (85). In STS, the high-sCD80 group had significantly lower metastasis-free survival (MS) and lower overall survival (OS) than the low-sCD80 group at 5 years using the log-rank test (OS: high > 404 pg/mL, low ≤ 404 pg/mL, MS: high > 531 pg/ml, low ≤ 531 pg/ml). On multivariate Cox proportional hazard analysis, the high-sCD80 group had significant differences in 5MS and 5OS compared to the low-sCD80 group. CONCLUSIONS: In conclusion, sCD80 may negatively affect systemic immune circumstances, in STS, and may have potential as a therapeutic target.
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spelling pubmed-94465752022-09-07 The role of soluble CD80 in patients with soft tissue tumors Matsuyama, Yumi Asanuma, Kunihiro Yoshida, Keisuke Hagi, Tomohito Iino, Takahiro Nakamura, Tomoki Sudo, Akihiro J Orthop Surg Res Correspondence BACKGROUND: Immune checkpoint protein (ICP), which is a central factor group of the immune system, has been reported to have a correlation between the degree of its expression and the prognosis of patients with malignant tumors, and many inhibitors have appeared as therapeutic targets. On the other hand, a soluble form of ICP in circulating blood induced systemic immunosuppression. In this study, we investigated the relationship between the soluble form of CD80 (sCD80) which is a ligand for the inhibitory system CTLA-4, in blood, and clinicopathological parameters in patients with soft tissue tumors. METHODS: A total of 119 patients with primary soft tissue tumors were enrolled in this study. The sCD80 levels were measured by enzyme immunoassay. RESULTS: There were no significant differences in sCD80 levels between benign (34) and soft tissue sarcoma (STS) patients (85). In STS, the high-sCD80 group had significantly lower metastasis-free survival (MS) and lower overall survival (OS) than the low-sCD80 group at 5 years using the log-rank test (OS: high > 404 pg/mL, low ≤ 404 pg/mL, MS: high > 531 pg/ml, low ≤ 531 pg/ml). On multivariate Cox proportional hazard analysis, the high-sCD80 group had significant differences in 5MS and 5OS compared to the low-sCD80 group. CONCLUSIONS: In conclusion, sCD80 may negatively affect systemic immune circumstances, in STS, and may have potential as a therapeutic target. BioMed Central 2022-09-05 /pmc/articles/PMC9446575/ /pubmed/36064421 http://dx.doi.org/10.1186/s13018-022-03283-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Correspondence
Matsuyama, Yumi
Asanuma, Kunihiro
Yoshida, Keisuke
Hagi, Tomohito
Iino, Takahiro
Nakamura, Tomoki
Sudo, Akihiro
The role of soluble CD80 in patients with soft tissue tumors
title The role of soluble CD80 in patients with soft tissue tumors
title_full The role of soluble CD80 in patients with soft tissue tumors
title_fullStr The role of soluble CD80 in patients with soft tissue tumors
title_full_unstemmed The role of soluble CD80 in patients with soft tissue tumors
title_short The role of soluble CD80 in patients with soft tissue tumors
title_sort role of soluble cd80 in patients with soft tissue tumors
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9446575/
https://www.ncbi.nlm.nih.gov/pubmed/36064421
http://dx.doi.org/10.1186/s13018-022-03283-2
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