Expression and clinical significance of VISTA, B7-H3, and PD-L1 in glioma

Copyright © 2022. Published by Elsevier Inc.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 245(2022) vom: 10. Dez., Seite 109178
1. Verfasser: Wang, Li-Chong (VerfasserIn)
Weitere Verfasser: Wang, Yue-Long, He, Bin, Zheng, Yan-Jiang, Yu, Hong-Chi, Liu, Zhi-Yong, Fan, Rang-Rang, Zan, Xin, Liang, Rui-Chao, Wu, Ze-Pei, Tang, Xin, Wang, Guo-Qing, Xu, Jian-Guo, Zhou, Liang-Xue
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2022
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, Non-U.S. Gov't B7-H3 Glioma PD-L1 VISTA mIF B7-H1 Antigen B7 Antigens Biomarkers, Tumor
Beschreibung
Zusammenfassung:Copyright © 2022. Published by Elsevier Inc.
Immune checkpoint (IC) therapy has led to a breakthrough in cancer treatment. However, the interaction of ICs is controversial in glioma. We detected features of ICs using transcriptome data and a multicolor immunofluorescence assay. We discovered that B7-H3 increased with grade and age and predicted worse overall survival (OS) at the transcriptional and proteomic levels. VISTA and PD-L1 were associated with OS and grade at the RNA level. At the protein level, VISTA was primarily expressed in tumor cells and TAMs. B7-H3 and VISTA were positively correlated with PD-L1. There was a strong correlation between PD-L1 and CD3 and between VISTA and IBA-1. PD-L1 was coexpressed with T cells. VISTA was coexpressed with TAMs. In T cells, we found a strong correlation in ICs, which worsened in TAMs and tumor cells. In conclusion, B7-H3 is a vital prognostic target for immunotherapy. We provided a potential mechanism for the immunosuppressive microenvironment in glioma
Beschreibung:Date Completed 25.11.2022
Date Revised 26.12.2022
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2022.109178