Identification of new HLA-A*0201-restricted cytotoxic T lymphocyte epitopes from LDHC in lung adenocarcinoma
Ruifang Zhong, Xiaohong Guo, Chuncai Wu, Yangyi Guo, Yanli Kang, Jianbin You, Falin Chen, Qianshun Chen, Liangyuan Chen

TL;DR
This study identifies specific peptides from LDHC that can trigger immune responses in lung adenocarcinoma, suggesting their potential use in immunotherapy.
Contribution
The study identifies new HLA-A*0201-restricted cytotoxic T lymphocyte epitopes from LDHC for lung adenocarcinoma immunotherapy.
Findings
Three LDHC-derived peptides showed high affinity for HLA-A2 molecules.
P6 peptide elicited the strongest IFN-γ response and tumor cell lysis.
LDHC may serve as a targetable biomarker for LUAD peptide-based immunotherapy.
Abstract
Lactate dehydrogenase C (LDHC) is a kind of cancer-testis antigen (CTA) that has been reported to be a biomarker for diagnosis, efficacy evaluation, and recurrence monitoring of lung adenocarcinoma (LUAD). This study aims to assess the value of LDHC in peptide-based vaccines for LUAD immunotherapy. The LDHC recombinant protein was purified and its effect on PC9 cells was evaluated by wound healing assay, Transwell invasion, and migration assay. Ten HLA-A2-restricted LDHC-derived peptides were predicted and synthesized, and the affinity for the HLA-A2 molecule was analyzed by T2 binding assay and molecule docking. Enzyme-linked immunospot (ELISpot) and LDH cytotoxicity assay were performed to determine the interferon-γ (IFN-γ) release level and tumor cell lysis ability of peptide-induced specific cytotoxic T lymphocytes (CTLs). The LDHC recombinant protein promoted invasion and…
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Taxonomy
TopicsImmunotherapy and Immune Responses · Cancer Immunotherapy and Biomarkers · Immune Cell Function and Interaction
