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嵌合抗原受体T细胞疗法期间细胞因子释放综合征的计算模型。

A Computational Model of Cytokine Release Syndrome during CAR T-cell Therapy.

作者信息

Zhang Zhuoyu, Liu Lunan, Ma Chao, Chen Weiqiang

机构信息

Department of Mechanical and Aerospace Engineering, New York University, Brooklyn, NY 11201, USA.

Department of Biomedical Engineering, New York University, Brooklyn, NY 11201, USA.

出版信息

Adv Ther (Weinh). 2022 Oct;5(10). doi: 10.1002/adtp.202200130. Epub 2022 Aug 4.

Abstract

Cytokine release syndrome (CRS) is a lethal adverse event in chimeric antigen receptor (CAR) T-cell therapy, hindering this promising therapy for cancers, such as B-cell acute lymphoblastic leukemia (B-ALL). Clinical management of CRS requires a better understanding of its underlying mechanisms. In this study, a computational model of CRS during CAR T-cell therapy is built to depict how the cellular interactions among CAR T-cells, B-ALL cells, and bystander monocytes, as well as the accompanying molecular interactions among various inflammatory cytokines, influence the severity of CRS. The model successfully defines the factors related to severe CRS and studied the effects of immunomodulatory therapy on CRS. The use of the model is also demonstrated as a precision medicine tool to optimize the treatment scheme, including personalized choice of CAR T-cell products and control of switchable CAR T-cell activity, for a more efficient and safer immunotherapy. This new computational oncology model can serve as a precision medicine tool to guide the clinical management of CRS during CAR T cell therapy.

摘要

细胞因子释放综合征(CRS)是嵌合抗原受体(CAR)T细胞疗法中的一种致命不良事件,阻碍了这种有前景的癌症治疗方法,如B细胞急性淋巴细胞白血病(B-ALL)。CRS的临床管理需要更好地了解其潜在机制。在本研究中,构建了CAR T细胞疗法期间CRS的计算模型,以描述CAR T细胞、B-ALL细胞和旁观者单核细胞之间的细胞相互作用,以及各种炎性细胞因子之间伴随的分子相互作用如何影响CRS的严重程度。该模型成功定义了与严重CRS相关的因素,并研究了免疫调节疗法对CRS的影响。该模型的应用还被证明是一种精准医学工具,可优化治疗方案,包括个性化选择CAR T细胞产品和控制可切换的CAR T细胞活性,以实现更高效、更安全的免疫治疗。这种新的计算肿瘤学模型可作为一种精准医学工具,指导CAR T细胞疗法期间CRS的临床管理。

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