Cancer Dynamics Laboratory, The Francis Crick Institute, London NW1 1AT, UK.
Cancer Dynamics Laboratory, The Francis Crick Institute, London NW1 1AT, UK; Skin and Renal Units, The Royal Marsden NHS Foundation Trust, London SW3 6JJ, UK.
Cell Rep Med. 2022 Oct 18;3(10):100781. doi: 10.1016/j.xcrm.2022.100781. Epub 2022 Sep 27.
Patients with blood cancer continue to have a greater risk of inadequate immune responses following three COVID-19 vaccine doses and risk of severe COVID-19 disease. In the context of the CAPTURE study (NCT03226886), we report immune responses in 80 patients with blood cancer who received a fourth dose of BNT162b2. We measured neutralizing antibody titers (NAbTs) using a live virus microneutralization assay against wild-type (WT), Delta, and Omicron BA.1 and BA.2 and T cell responses against WT and Omicron BA.1 using an activation-induced marker (AIM) assay. The proportion of patients with detectable NAb titers and T cell responses after the fourth vaccine dose increased compared with that after the third vaccine dose. Patients who received B cell-depleting therapies within the 12 months before vaccination have the greatest risk of not having detectable NAbT. In addition, we report immune responses in 57 patients with breakthrough infections after vaccination.
血液癌症患者在接种三剂 COVID-19 疫苗后继续存在免疫反应不足和 COVID-19 重症疾病的风险。在 CAPTURE 研究(NCT03226886)中,我们报告了 80 名接受第四剂 BNT162b2 疫苗的血液癌症患者的免疫反应。我们使用针对野生型(WT)、Delta 和 Omicron BA.1 和 BA.2 的活病毒微量中和测定法测量中和抗体滴度(NAbT),并使用激活诱导标记(AIM)测定法测量针对 WT 和 Omicron BA.1 的 T 细胞反应。与第三剂疫苗接种后相比,第四剂疫苗接种后可检测到 NAb 滴度和 T 细胞反应的患者比例增加。在接种疫苗前 12 个月内接受 B 细胞耗竭治疗的患者,无法检测到 NAbT 的风险最高。此外,我们报告了接种疫苗后发生突破性感染的 57 名患者的免疫反应。