Laboratory of Controllable Nanopharmaceuticals, Chinese Academy of Sciences (CAS) Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing, P. R. China.
University of Chinese Academy of Sciences, Beijing, P. R. China.
Nat Biomed Eng. 2023 Sep;7(9):1129-1141. doi: 10.1038/s41551-023-01084-4. Epub 2023 Sep 11.
The infusion of chimaeric antigen receptor (CAR) T cells can trigger the release of life-threatening supraphysiological levels of pro-inflammatory cytokines. However, uncertainty regarding the timing and severity of such cytokine release syndrome (CRS) demands careful monitoring of the conditions required for the administration of neutralizing antibodies. Here we show that a temperature-sensitive hydrogel conjugated with antibodies for the pro-inflammatory cytokine interleukin-6 (IL-6) and subcutaneously injected before the infusion of CAR-T cells substantially reduces the levels of IL-6 during CRS while maintaining the therapy's antitumour efficacy. In immunodeficient mice and in mice with transplanted human haematopoietic stem cells, the subcutaneous IL-6-adsorbing hydrogel largely suppressed CAR-T-cell-induced CRS, substantially improving the animals' survival and alleviating their levels of fever, hypotension and weight loss relative to the administration of free IL-6 antibodies. The implanted hydrogel, which can be easily removed with a syringe following a cooling-induced gel-sol transition, may allow for a shift in the management of CRS, from monitoring to prevention.
嵌合抗原受体 (CAR) T 细胞输注可引发危及生命的超生理水平促炎细胞因子的释放。然而,由于对细胞因子释放综合征 (CRS) 的发生时间和严重程度存在不确定性,因此需要仔细监测中和抗体给药所需的条件。在这里,我们展示了一种与促炎细胞因子白细胞介素 6 (IL-6) 的抗体偶联的温敏水凝胶,在输注 CAR-T 细胞之前皮下注射,可显著降低 CRS 期间的 IL-6 水平,同时保持治疗的抗肿瘤疗效。在免疫缺陷小鼠和移植了人造血干细胞的小鼠中,皮下注射 IL-6 吸附水凝胶可显著抑制 CAR-T 细胞诱导的 CRS,与单独使用游离 IL-6 抗体相比,显著提高了动物的存活率,并降低了它们的发热、低血压和体重减轻水平。可通过冷却诱导的凝胶-溶胶转变用注射器轻松去除的植入水凝胶,可能会改变 CRS 的管理方式,从监测转变为预防。