强的松在不能手术的晚期B型胸腺瘤患者中表达CD45RA的T效应记忆细胞的新调节。

IF 4.5 3区 医学 Q1 GENETICS & HEREDITY
Genes and immunity Pub Date : 2025-06-01 Epub Date: 2025-05-06 DOI:10.1038/s41435-025-00329-3
Xin-Tao Yu, Jian Cui, Xing-Guo Yang, Xiang Gao, Lei Yu
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引用次数: 0

摘要

由于胸腺瘤发病隐匿,近30%的患者被诊断为III期或IV期,失去了手术治疗的机会。我们已经启动了强的松治疗难治性胸腺瘤的应用,并探索了生物标志物,以确定可能受益于强的松治疗的潜在病例。在一项涉及96例胸腺瘤患者的研究中,我们证实醋酸泼尼松治疗可显著缩小肿瘤。缩小的胸腺直径比表明B1型和B2型胸腺瘤对醋酸泼尼松的反应最明显,尤其是B2型胸腺瘤。然而,A型、AB型和B3型胸腺瘤的缩小率< 30%。肿瘤组织的免疫荧光和流式细胞术显示,TEMRA (T效应记忆表达CD45RA)细胞主要存在于B型胸腺瘤中。然而,经醋酸泼尼松治疗后,白细胞介素-8 + TEMRA细胞百分比仅在B1和B2胸腺瘤组织中下降。这些发现对III期或IV期B型胸腺瘤患者尤为重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel modulation of T effector memory cells-expressing CD45RA by prednisone in inoperable advanced type B thymoma patients.

Due to the covert onset of thymoma, nearly 30% of patients are diagnosed at stage III or IV, losing the opportunity for surgical treatment. We have initiated the application of prednisone in treating refractory thymoma and explored biomarkers to identify potential cases that might benefit from prednisone treatment. In a study involving 96 patients with thymoma, we confirmed a significant tumor shrinkage with prednisone acetate treatment. A reduced diameter ratio indicated that type B1 and B2 thymomas exhibited the most obvious response to prednisone acetate, especially type B2 thymoma. However, the reduced diameter ratio was < 30% in type A, AB, and B3 thymomas. Immunofluorescence and flow cytometry of tumor tissues indicated that TEMRA (T Effector Memory-Expressing CD45RA) cells primarily exist in type B thymoma. However, the percentage of interleukin-8 + TEMRA cells decreased only in B1 and B2 thymoma tissues after prednisone acetate treatment. These findings are particularly significant for patients with type B thymoma with stage III or IV.

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来源期刊
Genes and immunity
Genes and immunity 医学-免疫学
CiteScore
8.90
自引率
4.00%
发文量
28
审稿时长
6-12 weeks
期刊介绍: Genes & Immunity emphasizes studies investigating how genetic, genomic and functional variations affect immune cells and the immune system, and associated processes in the regulation of health and disease. It further highlights articles on the transcriptional and posttranslational control of gene products involved in signaling pathways regulating immune cells, and protective and destructive immune responses.
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