TNBC衍生的Gal3BP/Gal3复合物通过CD45受体诱导免疫抑制。

IF 7.2 2区 医学 Oncoimmunology Pub Date : 2023-08-14 eCollection Date: 2023-01-01 DOI:10.1080/2162402X.2023.2246322
Annat Raiter, Julia Lipovetsky, Asaf Stenbac, Ido Lubin, Rinat Yerushalmi
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摘要

一项研究侵袭性三阴性癌症(TNBC)免疫疗法策略的初步研究显示,参与细胞外小泡(EV)释放的基因过度表达。EVs表达的蛋白质在肿瘤微环境的重新编程和阻碍免疫疗法的有效反应中发挥作用。半乳糖凝集素3(Gal3)存在于癌症细胞的细胞外空间,下调T细胞受体的表达。Gal3与多种受体结合,包括T细胞受体激活所需的CD45。此前,我们报道了一种新的肿瘤逃逸机制,即TNBC细胞通过CD45细胞内信号抑制免疫细胞。本研究的目的是确定Gal3与TNBC分泌的EVs通过CD45信号通路诱导免疫抑制的潜在关联。EVs从MDA-MB-231细胞和TNBC患者的血浆中分离。质谱分析显示,在分离的小EVs中存在Gal3结合蛋白(Gal3BP),其与TNBC分泌的Gal3相互作用。Gal3BP和Gal3形成复合物,其诱导外周血单核细胞(PBMC)中T调节细胞的显著增加。这种增加与抑制性白介素10和35的显著增加相关。在与肿瘤衍生的EVs培养的PBMC中阻断CD45受体阻碍了Gal3BP/Gal3复合物发挥的免疫抑制作用。这导致IFN-γ的增加以及CD4、CD8和CD56效应细胞的活化。这项研究提出了一种肿瘤逃逸机制,可能有助于开发一种不同的免疫疗法策略,以补充目前用于TNBC的疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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TNBC-derived Gal3BP/Gal3 complex induces immunosuppression through CD45 receptor.

A preliminary study investigating immunotherapy strategies for aggressive triple negative breast cancer (TNBC) revealed an overexpression of genes involved in the release of extracellular vesicles (EVs). Proteins expressed by EVs play a role in reprogramming the tumor microenvironment and impeding effective responses to immunotherapy. Galectin 3 (Gal3), found in the extracellular space of breast cancer cells, downregulates T-cell receptor expression. Gal3 binds to several receptors, including CD45, which is required for T-cell receptor activation. Previously, we reported a novel tumor escape mechanism, whereby TNBC cells suppress immune cells through CD45 intracellular signals. The objective of this study was to determine the potential association of Gal3 with TNBC-secreted EVs induction of immunosuppression via the CD45 signaling pathway. EVs were isolated from MDA-MB-231 cells and the plasma of patients with TNBC. Mass spectrometry revealed the presence of Gal3 binding protein (Gal3BP) in the isolated small EVs, which interacted with TNBC secreted Gal3. Gal3BP and Gal3 form a complex that induces a significant increase in T-regulatory cells in peripheral blood mononuclear cells (PBMCs). This increase correlates with a significant increase in suppressive interleukins 10 and 35. Blocking the CD45 receptor in PBMCs cultured with tumor-derived EVs impeded the immunosuppression exerted by the Gal3BP/Gal3 complex. This led to an increase in IFN-γ and the activation of CD4, CD8 and CD56 effector cells. This study suggests a tumor escape mechanism that may contribute to the development of a different immunotherapy strategy that complements current therapies used for TNBC.

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来源期刊
Oncoimmunology
Oncoimmunology ONCOLOGY-IMMUNOLOGY
CiteScore
12.80
自引率
2.80%
发文量
276
期刊介绍: Tumor immunology explores the natural and therapy-induced recognition of cancers, along with the complex interplay between oncogenesis, inflammation, and immunosurveillance. In response to recent advancements, a new journal, OncoImmunology, is being launched to specifically address tumor immunology. The field has seen significant progress with the clinical demonstration and FDA approval of anticancer immunotherapies. There's also growing evidence suggesting that many current chemotherapeutic agents rely on immune effectors for their efficacy. While oncologists have historically utilized chemotherapeutic and radiotherapeutic regimens successfully, they may have unwittingly leveraged the immune system's ability to recognize tumor-specific antigens and control cancer growth. Consequently, immunological biomarkers are increasingly crucial for cancer prognosis and predicting chemotherapy efficacy. There's strong support for combining conventional anticancer therapies with immunotherapies. OncoImmunology will welcome high-profile submissions spanning fundamental, translational, and clinical aspects of tumor immunology, including solid and hematological cancers, inflammation, and both innate and acquired immune responses.
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