阐明T细胞受体库在骨髓增生异常肿瘤和急性髓系白血病中的作用。

IF 3 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Diseases (Basel, Switzerland) Pub Date : 2025-01-17 DOI:10.3390/diseases13010019
Georgios Petros Barakos, Vasileios Georgoulis, Epameinondas Koumpis, Eleftheria Hatzimichael
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引用次数: 0

摘要

T细胞作为适应性免疫系统的重要组成部分,通过独特的T细胞受体(tcr)识别多种抗原。为了实现这一点,在T细胞成熟过程中,胸腺产生大量的tcr。这对于了解癌症的进化、进展和免疫疗法的疗效至关重要。骨髓增生异常肿瘤(MDS)和急性髓系白血病(AML)是一种以免疫逃避机制为特征的血液系统肿瘤,迄今为止,免疫治疗仅取得了适度的效果。我们对这些疾病中TCR库动态的回顾揭示了不同的模式:MDS患者随着疾病进展显示TCR克隆性增加,而AML患者根据疾病分期和治疗反应表现出不同的TCR特征。了解这些模式具有重要的临床意义,因为TCR库指标可以作为疾病进展和治疗反应的潜在生物标志物,特别是在免疫治疗和干细胞移植的背景下。这些见解可以指导患者分层和治疗选择,最终改善MDS和AML的治疗效果。
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Elucidating the Role of the T Cell Receptor Repertoire in Myelodysplastic Neoplasms and Acute Myeloid Leukemia.

T cells, as integral components of the adaptive immune system, recognize diverse antigens through unique T cell receptors (TCRs). To achieve this, during T cell maturation, the thymus generates a wide repertoire of TCRs. This is essential for understanding cancer evolution, progression, and the efficacy of immunotherapies. Myelodysplastic neoplasms (MDS) and acute myeloid leukemia (AML) are hematological neoplasms that are characterized by immune evasion mechanisms, with immunotherapy giving only modest results thus far. Our review of TCR repertoire dynamics in these diseases reveals distinct patterns: MDS patients show increased TCR clonality with disease progression, while AML exhibits varied TCR signatures depending on disease stage and treatment response. Understanding these patterns has important clinical implications, as TCR repertoire metrics may serve as potential biomarkers for disease progression and treatment response, particularly in the context of immunotherapy and stem cell transplantation. These insights could guide patient stratification and treatment selection, ultimately improving therapeutic outcomes in MDS and AML.

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