CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Immunosenescence, inflammaging, and cancer immunotherapy efficacy.
Immunosenescence, inflammaging, and cancer immunotherapy efficacy.
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本综述探讨免疫衰老和炎性衰老对抗癌免疫治疗的潜在影响,以及可对抗免疫衰老的治疗策略。
引言:免疫衰老是免疫功能逐渐重塑的过程,与免疫系统建立有效先天和适应性免疫应答的能力下降有关,同时高度分化T细胞增加、初始T细胞减少。多数癌症的发病率和患病率随年龄增长而增加,部分可由肿瘤逃逸机制和免疫监视减弱解释。衰老还与炎症性衰老相关,这是一种低度促炎状态,特征为炎症介质增加。过去10年,抗癌免疫疗法深刻改变了肿瘤治疗格局。双特异性T细胞连接器、CAR-T 细胞或免疫检查点阻断剂等现代T细胞靶向疗法,理论上可能受到免疫衰老或炎症性衰老影响。综述范围:通过检索PubMed和Embase开展文献回顾,使用的检索词包括“免疫衰老”“免疫治疗”“炎症性衰老”“双特异性抗体”“CAR-T 细胞”“免疫检查点阻断剂”和“老年患者”。专家观点:本文探讨免疫衰老和炎症性衰老对抗癌免疫治疗的潜在影响,以及可对抗免疫衰老的治疗策略。未来临床试验中应更有针对性地研究免疫衰老生物标志物,以开发更有效、更安全的新疗法。
INTRODUCTION: Immunosenescence is a progressive remodeling of immune functions associated with a decreased ability of the immune system to set up an efficient immune response, both innate and adaptive, with an increase of highly differentiated T cells at the expense of naive T cells. The incidence and prevalence of most cancers increase with age, which can partly be explained by tumor escape mechanisms and decreased immunosurveillance. Aging is also associated with inflammaging, a low-grade proinflammatory state characterized by an increase in inflammatory mediators. Anti-cancer immunotherapy has profoundly changed the landscape of oncology therapy in the last 10 years.
Modern T-cell targeted therapies such as bispecific T cell engagers, CAR-T cells, or immune checkpoint blockers may be theoretically affected by immunosenescence or inflammaging. AREAS COVERED: A bibliographic review through PubMed and Embase was carried out using the following search terms: 'immunosenescence,' 'immunotherapy,' 'inflammaging,' 'bispecific antibodies,' 'CAR-T cells,' 'immune checkpoint blockers,' and 'older patients.'
EXPERT OPINION: This review explores the potential impact of immunosenescence and inflammaging on anti-cancer immunotherapy and therapeutic strategies that could counter immune senescence. A more dedicated research on immunosenescence biomarkers in future clinical trials is warranted for the development of new, more effective and safer therapies.
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