Department of Medicine, Westchester Medical Center, Valhalla, New York.
Department of Hematopathology & Microbiology, The Aga Khan University Hospital, Karachi, Pakistan.
Transplant Cell Ther. 2021 Dec;27(12):973-987. doi: 10.1016/j.jtct.2021.09.016. Epub 2021 Sep 27.
Chimeric antigen receptor T cell (CAR-T) therapy has shown unprecedented response rates in patients with relapsed/refractory (R/R) hematologic malignancies. Although CAR-T therapy gives hope to heavily pretreated patients, the rapid commercialization and cumulative immunosuppression of this therapy predispose patients to infections for a prolonged period. CAR-T therapy poses distinctive short- and long-term toxicities and infection risks among patients who receive CAR T-cells after multiple prior treatments, often including hematopoietic cell transplantation. The acute toxicities include cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome. The long-term B cell depletion, hypogammaglobulinemia, and cytopenia further predispose patients to severe infections and abrogate the remission success achieved by the living drug. These on-target-off-tumor toxicities deplete B-cells across the entire lineage and further diminish immune responses to vaccines. Early observational data suggest that patients with hematologic malignancies may not mount adequate humoral and cellular responses to SARS-CoV-2 vaccines. In this review, we summarize the immune compromising factors indigenous to CAR-T recipients. We discuss the immunogenic potential of different SARS-CoV-2 vaccines for CAR-T recipients based on the differences in vaccine manufacturing platforms. Given the lack of data related to the safety and efficacy of SARS-CoV-2 vaccines in this distinctively immunosuppressed cohort, we summarize the infection risks associated with Food and Drug Administration-approved CAR-T constructs and the potential determinants of vaccine responses. The review further highlights the potential need for booster vaccine dosing and the promise for heterologous prime-boosting and other novel vaccine strategies in CAR-T recipients. © 2021 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.
嵌合抗原受体 T 细胞(CAR-T)疗法在复发/难治性(R/R)血液恶性肿瘤患者中显示出前所未有的反应率。尽管 CAR-T 疗法给大量预处理患者带来了希望,但这种疗法的快速商业化和累积免疫抑制使患者在很长一段时间内容易感染。CAR-T 疗法在接受多次先前治疗(通常包括造血细胞移植)后接受 CAR-T 细胞的患者中引起独特的短期和长期毒性和感染风险。急性毒性包括细胞因子释放综合征和免疫效应细胞相关神经毒性综合征。长期 B 细胞耗竭、低丙种球蛋白血症和细胞减少症进一步使患者易发生严重感染,并使活药物治疗获得的缓解成功失败。这些针对肿瘤的脱靶毒性会耗尽整个谱系的 B 细胞,并进一步降低疫苗的免疫反应。早期观察性数据表明,血液恶性肿瘤患者可能无法对 SARS-CoV-2 疫苗产生足够的体液和细胞反应。在这篇综述中,我们总结了 CAR-T 受者特有的免疫抑制因素。我们根据疫苗制造平台的差异,讨论了不同 SARS-CoV-2 疫苗对 CAR-T 受者的免疫原性潜力。鉴于在这个明显免疫抑制的患者群体中缺乏与 SARS-CoV-2 疫苗安全性和有效性相关的数据,我们总结了与经食品和药物管理局批准的 CAR-T 结构相关的感染风险以及疫苗反应的潜在决定因素。该综述进一步强调了在 CAR-T 受者中加强疫苗接种和异源初级-增强以及其他新型疫苗策略的潜在必要性。