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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Novel chimeric antigen receptor T cell-based immunotherapy: a perspective for triple-negative breast cancer.
Novel chimeric antigen receptor T cell-based immunotherapy: a perspective for triple-negative breast cancer.
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三阴性乳腺癌(TNBC)具有高度侵袭性,不表达雌激素受体(ER)、孕激素受体(PR)和人表皮生长因子受体2(HER2)。其预后较差,传统内分泌治疗和抗HER2靶向治疗对其疗效较低。相比之下,手术、放疗和/或全身化疗在控制TNBC方面相对有效。TNBC对当前可用临床治疗的耐药性对其治疗结果产生了显著的负面影响。
因此,迫切需要新的治疗选择。CAR-T 细胞疗法是一种整合了抗体的抗原特异性和T细胞的肿瘤杀伤效应的免疫疗法。CAR-T 疗法已在血液系统恶性肿瘤中展现出优异的临床疗效。
然而,其对TNBC等实体瘤的疗效不足。本综述旨在探讨CAR-T 作为TNBC治疗的各个方面。我们总结了在TNBC的临床前研究和临床试验中发现的CAR-T 潜在治疗靶点。
我们讨论了使用CAR-T 治疗TNBC特别是实体瘤的局限性,并探讨了克服这些障碍的关键策略。最后,我们全面审视了CAR-T 免疫疗法的进展以及可提高其作为TNBC治疗疗效和改善此类癌症患者预后的对策。
Triple-negative breast cancer (TNBC) is highly aggressive and does not express estrogen receptor (ER), progesterone (PR), or human epidermal growth factor receptor 2 (HER2). It has a poor prognosis, and traditional endocrine and anti-HER2 targeted therapies have low efficacy against it. In contrast, surgery, radiotherapy, and/or systemic chemotherapy are relatively effective at controlling TNBC.
The resistance of TNBC to currently available clinical therapies has had a significantly negative impact on its treatment outcomes. Hence, new therapeutic options are urgently required. Chimeric antigen receptor T cell (CAR-T) therapy is a type of immunotherapy that integrates the antigen specificity of antibodies and the tumor-killing effect of T cells. CAR-T therapy has demonstrated excellent clinical efficacy against hematological cancers.
However, its efficacy against solid tumors such as TNBC is inadequate. The present review aimed to investigate various aspects of CAR-T administration as TNBC therapy.
We summarized the potential therapeutic targets of CAR-T that were identified in preclinical studies and clinical trials on TNBC.
We addressed the limitations of using CAR-T in the treatment of TNBC in particular and solid tumors in general and explored key strategies to overcome these impediments.
Finally, we comprehensively examined the advancement of CAR-T immunotherapy as well as countermeasures that could improve its efficacy as a TNBC treatment and the prognosis of patients with this type of cancer.
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