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癌症患者接种疫苗后对 SARS-CoV-2 关注变体的适应性免疫和中和抗体:CAPTURE 研究。

Adaptive immunity and neutralizing antibodies against SARS-CoV-2 variants of concern following vaccination in patients with cancer: The CAPTURE study.

机构信息

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.

出版信息

Nat Cancer. 2021 Dec;2:1321-1337. doi: 10.1038/s43018-021-00274-w. Epub 2021 Oct 27.

DOI:10.1038/s43018-021-00274-w
PMID:34950880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7612125/
Abstract

CAPTURE (NCT03226886) is a prospective cohort study of COVID-19 immunity in patients with cancer. Here we evaluated 585 patients following administration of two doses of BNT162b2 or AZD1222 vaccines, administered 12 weeks apart. Seroconversion rates after two doses were 85% and 59% in patients with solid and hematological malignancies, respectively. A lower proportion of patients had detectable neutralizing antibody titers (NAbT) against SARS-CoV-2 variants of concern (VOCs) vs wildtype (WT). Patients with hematological malignancies were more likely to have undetectable NAbT and had lower median NAbT vs solid cancers against both WT and VOCs. In comparison with individuals without cancer, patients with haematological, but not solid, malignancies had reduced NAb responses. Seroconversion showed poor concordance with NAbT against VOCs. Prior SARS-CoV-2 infection boosted NAb response including against VOCs, and anti-CD20 treatment was associated with undetectable NAbT. Vaccine-induced T-cell responses were detected in 80% of patients, and were comparable between vaccines or cancer types. Our results have implications for the management of cancer patients during the ongoing COVID-19 pandemic.

摘要

CAPTURE(NCT03226886)是一项关于癌症患者 COVID-19 免疫的前瞻性队列研究。在这里,我们评估了在间隔 12 周接受两剂 BNT162b2 或 AZD1222 疫苗接种的 585 例患者。在实体瘤和血液恶性肿瘤患者中,两剂后血清转化率分别为 85%和 59%。与野生型(WT)相比,针对 SARS-CoV-2 关注变异株(VOCs)的可检测中和抗体滴度(NAbT)的患者比例较低。血液恶性肿瘤患者的 NAbT 更难以检测到,并且与 WT 和 VOCs 相比,其 NAbT 的中位数均低于实体瘤。与无癌症的个体相比,血液恶性肿瘤患者的 NAb 反应降低,但实体瘤患者的 NAb 反应没有降低。血清转化率与针对 VOCs 的 NAbT 一致性较差。先前的 SARS-CoV-2 感染增强了 NAb 反应,包括针对 VOCs 的反应,而抗 CD20 治疗与无法检测到的 NAbT 相关。在 80%的患者中检测到疫苗诱导的 T 细胞反应,并且在疫苗或癌症类型之间具有可比性。我们的研究结果对当前 COVID-19 大流行期间癌症患者的管理具有重要意义。

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1
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Nat Commun. 2022 Mar 10;13(1):1251. doi: 10.1038/s41467-022-28898-1.
2
Extended interval BNT162b2 vaccination enhances peak antibody generation.延长间隔接种BNT162b2疫苗可增强抗体峰值生成。
NPJ Vaccines. 2022 Jan 27;7(1):14. doi: 10.1038/s41541-022-00432-w.
3
Patterns of seroconversion for SARS-CoV2-IgG in patients with malignant disease and association with anticancer therapy.恶性肿瘤患者 SARS-CoV2-IgG 血清转化模式及其与抗癌治疗的关系。
免疫预测因子在淋巴瘤和慢性淋巴细胞白血病患者中的疫苗反应。
J Infect Dis. 2024 Jul 25;230(1):15-27. doi: 10.1093/infdis/jiae106.
4
Herpes zoster after the third dose of SARS-CoV-2 mRNA-BNT162b2 vaccine in actively treated cancer patients: a prospective study.在接受积极治疗的癌症患者中,第三剂 SARS-CoV-2 mRNA-BNT162b2 疫苗接种后出现带状疱疹:一项前瞻性研究。
Clin Exp Med. 2024 Jan 20;24(1):13. doi: 10.1007/s10238-023-01263-2.
5
mRNA vaccines against SARS-CoV-2 induce divergent antigen-specific T-cell responses in patients with lung cancer.mRNA 疫苗针对 SARS-CoV-2 可诱导肺癌患者产生不同的抗原特异性 T 细胞反应。
J Immunother Cancer. 2024 Jan 4;12(1):e007922. doi: 10.1136/jitc-2023-007922.
6
COVID-19 in cancer patients: The impact of vaccination on outcomes early in the pandemic.癌症患者中的 COVID-19:大流行早期疫苗接种对结局的影响。
Cancer Med. 2023 Dec;12(24):22006-22022. doi: 10.1002/cam4.6781. Epub 2023 Dec 8.
7
Immune responses and clinical outcomes following the third dose of SARS-CoV-2 mRNA-BNT162b2 vaccine in advanced breast cancer patients receiving targeted therapies: a prospective study.接受靶向治疗的晚期乳腺癌患者接种第三剂严重急性呼吸综合征冠状病毒2(SARS-CoV-2)mRNA-BNT162b2疫苗后的免疫反应和临床结果:一项前瞻性研究
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8
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J Immunother Cancer. 2023 Sep;11(9). doi: 10.1136/jitc-2023-007387.
Nat Cancer. 2021 Apr;2(4):392-399. doi: 10.1038/s43018-021-00191-y. Epub 2021 Mar 22.
4
Adaptive immune determinants of viral clearance and protection in mouse models of SARS-CoV-2.SARS-CoV-2 小鼠模型中病毒清除和保护的适应性免疫决定因素。
Sci Immunol. 2021 Oct 15;6(64):eabl4509. doi: 10.1126/sciimmunol.abl4509. Epub 2021 Sep 2.
5
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Nat Med. 2021 Nov;27(11):1990-2001. doi: 10.1038/s41591-021-01507-2. Epub 2021 Sep 14.
6
Neutralising antibodies after COVID-19 vaccination in UK haemodialysis patients.英国血液透析患者新冠病毒疫苗接种后的中和抗体
Lancet. 2021 Sep 18;398(10305):1038-1041. doi: 10.1016/S0140-6736(21)01854-7. Epub 2021 Aug 13.
7
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N Engl J Med. 2021 Sep 23;385(13):1244-1246. doi: 10.1056/NEJMc2111462. Epub 2021 Aug 11.
8
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9
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Cancer Cell. 2021 Aug 9;39(8):1031-1033. doi: 10.1016/j.ccell.2021.07.012. Epub 2021 Jul 22.
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Blood Cancer J. 2021 Jul 30;11(7):136. doi: 10.1038/s41408-021-00528-x.