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:Nanobody-enhanced chimeric antigen receptor T-cell therapy: overcoming barriers in solid tumors with VHH and VNAR-based constructs.
Nanobody-enhanced chimeric antigen receptor T-cell therapy: overcoming barriers in solid tumors with VHH and VNAR-based constructs.
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CAR-T 细胞是经过基因修饰的T淋巴细胞,其表面表达嵌合抗原受体(CAR)。这些受体使T淋巴细胞能够识别靶细胞上的特定抗原,触发反应,从而导致靶向细胞毒性。尽管CAR-T 疗法已有效治疗多种血液癌症,但在应对实体瘤方面面临重大挑战。这些挑战包括识别精确的肿瘤抗原、克服抗原逃逸,以及增强CAR-T 细胞在肿瘤微环境中的功能。单域抗体作为具有低免疫原性、高稳定性和强亲和力的多功能工具,在提高CAR-T 细胞对抗实体瘤的疗效方面显示出前景。通过应对这些挑战,单域抗体有潜力克服与基于ScFv抗体的CAR-T 疗法相关的局限性。本综述强调了在CAR-T 疗法中利用单域抗体的优势,尤其是在靶向肿瘤抗原方面,并探讨了可推动该领域发展的开发策略。[图片:见正文]
CAR-T cells are genetically modified T lymphocytes that express chimeric antigen receptors (CAR) on their surfaces. These receptors enable T lymphocytes to recognize specific antigens on target cells, triggering a response that leads to targeted cytotoxicity. While CAR-T therapy has effectively treated various blood cancers, it faces significant challenges in addressing solid tumors. These challenges include identifying precise tumor antigens, overcoming antigen evasion, and enhancing the function of CAR-T cells within the tumor microenvironment.
Single domain antibody, versatile tools with low immunogenicity, high stability, and strong affinity, show promise for improving the efficacy of CAR-T cells against solid tumors. By addressing these challenges, single domain antibody has the potential to overcome the limitations associated with ScFv antibody-based CAR-T therapies. This review highlights the benefits of utilizing single domain antibody in CAR-T therapy, particularly in targeting tumor antigens, and explores development strategies that could advance the field. [Image: see text]
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