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嵌合抗原受体 T 细胞(CART)治疗后 B 细胞耗竭性淋巴瘤患者对 SARS-CoV-2 及其奥密克戎变异株的疫苗诱导 T 细胞反应。

Vaccine-induced T-cell responses against SARS-CoV-2 and its Omicron variant in patients with B cell-depleted lymphoma after CART therapy.

机构信息

Department of Medicine, University of Maryland School of Medicine, Baltimore, MD.

Transplant and Cellular Therapy Program, University of Maryland Greenebaum Comprehensive Cancer Center, Baltimore, MD.

出版信息

Blood. 2022 Jul 14;140(2):152-156. doi: 10.1182/blood.2022016175.

Abstract

Patients receiving CD19 CAR T-cell therapy for relapsed/refractory lymphoma experience prolonged and profound B-cell aplasia and hypogammaglobulinemia, placing them at a higher risk for severe COVID-19. Independently, Oh et al and Atanackovic et al demonstrate that despite attenuated humoral response to mRNA-based vaccines, patients demonstrate normal or heightened functional T-cell responses, including antiviral T-cell activity against SARS-CoV-2 variants including Omicron. Collectively, these data reinforce the importance of COVID-19 vaccination following CD19 CAR T-cell therapy, despite long-term B-cell aplasia.

摘要

接受针对复发/难治性淋巴瘤的 CD19 CAR T 细胞治疗的患者会经历长期且严重的 B 细胞减少和低丙种球蛋白血症,使他们面临更严重 COVID-19 的风险更高。独立地,Oh 等人和 Atanackovic 等人表明,尽管对基于 mRNA 的疫苗的体液反应减弱,但患者表现出正常或增强的 T 细胞功能反应,包括针对 SARS-CoV-2 变体(包括奥密克戎)的抗病毒 T 细胞活性。总的来说,这些数据强调了尽管存在长期 B 细胞减少,但在接受 CD19 CAR T 细胞治疗后接种 COVID-19 疫苗的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d76/9283964/377e0b099996/bloodBLD2022016175f1.jpg

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