与肿瘤浸润淋巴细胞过继细胞治疗反应相关的外周免疫生物标志物。

IF 3.4 3区 医学 Q3 IMMUNOLOGY
Cecilie Oelvang Madsen, Marta Velasco Santiago, Evelina Martinenaite, Troels Holz Borch, Marco Donia, Inge Marie Svane, Morten Hansen
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引用次数: 0

摘要

体外扩增肿瘤浸润淋巴细胞(TILs, TIL-ACT)的过继细胞疗法(ACT)在很大比例的转移性黑色素瘤患者中显示出临床疗效。为了进一步针对反应性患者靶向TIL-ACT,确定预测性生物标志物和了解更广泛的免疫动力学仍然至关重要。本研究调查了47例接受TIL-ACT治疗的转移性黑色素瘤患者的外周血免疫景观,评估了治疗前后的抗肿瘤反应性和外周血免疫细胞谱。应答者在治疗后循环肿瘤反应细胞的频率增加,激活表达cd57的T细胞的基线水平更高,这是应答的潜在生物标志物。相反,治疗后持续高水平的血清白细胞介素(IL)-6和IL-8,表达cd38的T细胞和调节性T细胞(Tregs)的频率较高,与不利的结果相关。这些发现有助于理解与TIL-ACT反应相关的外周免疫景观,为预测性生物标志物和机制提供有价值的见解,以改善患者选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Peripheral Immune Biomarkers Associated with Response to Adoptive Cell Therapy with Tumor Infiltrating Lymphocytes.

Adoptive cell therapy (ACT) with ex-vivo expanded tumor-infiltrating lymphocytes (TILs, TIL-ACT) has shown clinical efficacy in a significant proportion of patients with metastatic melanoma. To further target TIL-ACT towards responsive patients, identifying predictive biomarkers and understanding broader immune dynamics remain critical. This study investigated the peripheral blood immune landscape in 47 patients with metastatic melanoma undergoing TIL-ACT, assessing antitumor reactivity and peripheral immune cell profiles before and after treatment. Responders displayed increased frequency of circulating tumor-reactive cells post-treatment, and higher baseline levels of activated CD57-expressing T cells, serving as potential biomarkers of response. In contrast, persistent high serum levels of interleukin (IL)-6 and IL-8, higher frequencies of CD38-expressing T cells and regulatory T cells (Tregs) post-treatment, correlated with unfavorable outcomes. These findings contribute to understanding of the peripheral immune landscape associated with response to TIL-ACT, offering valuable insights into predictive biomarkers and mechanisms to improve patient selection.

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来源期刊
CiteScore
8.40
自引率
2.20%
发文量
101
审稿时长
3-8 weeks
期刊介绍: Clinical & Experimental Immunology (established in 1966) is an authoritative international journal publishing high-quality research studies in translational and clinical immunology that have the potential to transform our understanding of the immunopathology of human disease and/or change clinical practice. The journal is focused on translational and clinical immunology and is among the foremost journals in this field, attracting high-quality papers from across the world. Translation is viewed as a process of applying ideas, insights and discoveries generated through scientific studies to the treatment, prevention or diagnosis of human disease. Clinical immunology has evolved as a field to encompass the application of state-of-the-art technologies such as next-generation sequencing, metagenomics and high-dimensional phenotyping to understand mechanisms that govern the outcomes of clinical trials.
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