CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:The Steroidal Profile Modulates Adaptive Immune Response and Prognosis in Adrenocortical Carcinoma: Analysis of TCR and BCR Repertoires.
The Steroidal Profile Modulates Adaptive Immune Response and Prognosis in Adrenocortical Carcinoma: Analysis of TCR and BCR Repertoires.
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肾上腺皮质癌(ACC)是一种罕见且侵袭性强的恶性肿瘤,治疗选择有限,预后往往较差。深入理解其与免疫系统的相互作用对于推进个体化治疗策略至关重要,尤其是在激素产生的肿瘤异质性背景下。ACC肿瘤可分为高类固醇表型(HSP)和低类固醇表型(LSP)亚型,二者表现出不同的生物学行为和免疫微环境。
然而,这些亚型中T细胞和B细胞受体(TCR和BCR)库的组成及预后意义在很大程度上仍不清楚。在本研究中,我们证明类固醇表型是ACC适应性免疫应答和临床结局的关键决定因素。LSP肿瘤表现出显著更高的淋巴细胞浸润和更大的受体库多样性,反映出更具免疫原性的肿瘤微环境,尽管免疫逃逸和耗竭基因显著表达。这些发现为激素环境如何塑造ACC免疫生物学提供了新见解,揭示了皮质醇产生肿瘤中可能的免疫逃逸机制,并突出了免疫受体库特征的预后相关性。
我们的结果支持将TCR/BCR谱分析与类固醇表型分型相结合,以改善风险分层并为ACC精准免疫治疗策略的设计提供依据。
Adrenocortical carcinoma (ACC) is a rare and aggressive malignant neoplasm with limited therapeutic options and an often poor prognosis. A deeper understanding of its interaction with the immune system is essential for the advancement of personalized treatment strategies, particularly in light of the tumor heterogeneity of hormone production. ACC tumors can be classified into high steroid phenotype (HSP) and low steroid phenotype (LSP) subtypes, which exhibit distinct biological behaviors and immunological microenvironments.
However, the composition and prognostic significance of T-cell and B-cell receptor (TCR and BCR) repertoires in these subtypes remain largely unknown. In this study, we demonstrate that steroid phenotype is a key determinant of the adaptive immune response and clinical outcomes in ACC. LSP tumors exhibit significantly higher lymphocytic infiltration and greater repertoire diversity, reflecting a more immunogenic tumor microenvironment, despite the significant expression of immune evasion and exhaustion genes.
These findings provide new insights into how the hormonal environment shapes the immunobiology of ACC, reveal possible mechanisms of immune escape in cortisol-producing tumors, and highlight the prognostic relevance of immune repertoire characteristics.
Our results support the integration of TCR/BCR profiling with steroid phenotyping to improve risk stratification and inform the design of precision immunotherapeutic strategies for ACC.
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