Zhao Jiuzhou, Dong Bing, Wang Zhizhong, Wang Bo, Yan Chi, Li Xiang, Guo Yongjun, Du Ying
Department of Immunology, School of Basic Medical, Zhengzhou University, 450001, Zhengzhou, China.
Department of Molecular Pathology, The Affiliated Cancer Hospital of Zhengzhou, University& Henan Cancer Hospital, 127 Dongming Road, 450003, Zhengzhou, China.
Sci Rep. 2025 Sep 29;15(1):33691. doi: 10.1038/s41598-025-18839-5.
The human leukocyte antigen class I (HLA-I) genotypes have been proven to have an impact on the oncogenic mutational landscape and immunotherapy outcomes in several cancers. However, the HLA-I genotype landscape and its implications for lung cancer remain largely unknown. In this study, whole blood samples from 400 Chinese lung cancer patients were subjected to DNA sequencing for the detection of HLA-I genotypes. RNA sequencing data from 32 SCLC primary tumors were analyzed for immune cell infiltration and activity. Additionally, we collected HLA-I genotype and transcriptome data from 445 LUAD and 430 LUSC patients from The Cancer Genome Atlas (TCGA) database for comparisons. The proportion of HLA supertypes was similar among lung cancer patients with different pathological types but different among patients of different races. Chinese SCLC patients with the B44 supertype had more potent cytolytic activity and increased expression of MHC-II genes, interferon-gamma (IFN-γ), and chemokine signature genes than Chinese patients with other supertypes. Moreover, increased expression levels of immune checkpoint molecules were observed in tumors from B44(+) patients. Most importantly, we analyzed the correlation between the HLA supertype and prognosis and found that the positive effect of the HLA-B44 supertype on PFS verifies the prognostic value of HLA-B44 in SCLC. In conclusion, this study is among the first to depict the landscape of HLA-I genotypes in lung cancer patients. Comprehensive analysis revealed the effect of the B44 supertype on the tumor immune microenvironment and survival outcome of Chinese SCLC patients, providing fresh insight for the treatment of SCLC.
人类白细胞抗原 I 类(HLA-I)基因型已被证明会对多种癌症的致癌突变格局和免疫治疗结果产生影响。然而,HLA-I 基因型格局及其对肺癌的影响在很大程度上仍不清楚。在本研究中,对 400 名中国肺癌患者的全血样本进行 DNA 测序以检测 HLA-I 基因型。分析了 32 个小细胞肺癌(SCLC)原发肿瘤的 RNA 测序数据,以了解免疫细胞浸润和活性情况。此外,我们从癌症基因组图谱(TCGA)数据库收集了 445 名肺腺癌(LUAD)和 430 名肺鳞癌(LUSC)患者的 HLA-I 基因型和转录组数据用于比较。不同病理类型的肺癌患者中 HLA 超级类型的比例相似,但不同种族患者之间存在差异。与其他超级类型的中国患者相比,具有 B44 超级类型的中国 SCLC 患者具有更强的细胞溶解活性,且 MHC-II 基因、干扰素-γ(IFN-γ)和趋化因子特征基因的表达增加。此外,在 B44(+)患者的肿瘤中观察到免疫检查点分子的表达水平升高。最重要的是,我们分析了 HLA 超级类型与预后之间的相关性,发现 HLA-B44 超级类型对无进展生存期(PFS)的积极影响证实了 HLA-B44 在 SCLC 中的预后价值。总之,本研究是最早描绘肺癌患者 HLA-I 基因型格局的研究之一。综合分析揭示了 B44 超级类型对中国 SCLC 患者肿瘤免疫微环境和生存结局的影响,为 SCLC 的治疗提供了新的见解。