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腺病毒载体 ChAdOx1 nCoV-19(阿斯利康-牛津)-BNT162b2 mRNA 疫苗异源接种对肺移植受者免疫原性的影响。

Lung Transplant Recipients Immunogenicity after Heterologous ChAdOx1 nCoV-19-BNT162b2 mRNA Vaccination.

机构信息

Department of Laboratory Medicine, CHU UCL Namur, Université Catholique de Louvain, 5530 Yvoir, Belgium.

Department of Laboratory Medicine, Clinique St-Luc Bouge, 5004 Bouge, Belgium.

出版信息

Viruses. 2022 Jul 2;14(7):1470. doi: 10.3390/v14071470.

DOI:10.3390/v14071470
PMID:35891450
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9316698/
Abstract

(1) Background: High immunosuppressive regimen in lung transplant recipients (LTRs) hampers the immune response to vaccination. We prospectively investigated the immunogenicity of heterologous ChAdOx1 nCoV-19-BNT162b2 mRNA vaccination in an LTR cohort. (2) Methods: Forty-nine COVID-19 naïve LTRs received a two-dose regimen ChAdOx1 nCoV-19 vaccine. A subset of 32 patients received a booster dose of BNT162b2 mRNA vaccine 18 weeks after the second dose. (3) Results: Two-doses of ChAdOx1 nCoV-19 induced poor immunogenicity with 7.2% seropositivity at day 180 and low neutralizing capacities. The BNT162b2 mRNA vaccine induced significant increases in IgG titers with means of 197.8 binding antibody units per milliliter (BAU/mL) (95% CI 0-491.4) and neutralizing antibodies, with means of 76.6 AU/mL (95% CI 0-159.6). At day 238, 32.2% of LTRs seroconverted after the booster dose. Seroneutralization capacities against Delta and Omicron variants were found in only 13 and 9 LTRs, respectively. Mycophenolate mofetil and high-dose corticosteroids were associated with a weak serological response. (4) Conclusions: The immunogenicity of a two-dose ChAdOx1 nCoV-19 vaccine regimen was very poor in LTRs, but was significantly enhanced after the booster dose in one-third of LTRs. In immunocompromised individuals, the administration of a fourth dose may be considered to increase the immune response against SARS-CoV-2.

摘要

(1) 背景:肺移植受者(LTRs)中高免疫抑制方案会抑制对疫苗的免疫反应。我们前瞻性地研究了 ChAdOx1 nCoV-19-BNT162b2 mRNA 异源疫苗在 LTR 队列中的免疫原性。(2) 方法:49 名 COVID-19 初治 LTR 接受了两剂 ChAdOx1 nCoV-19 疫苗。32 名患者中的一部分在第二剂后 18 周接受了 BNT162b2 mRNA 疫苗的加强剂量。(3) 结果:两剂 ChAdOx1 nCoV-19 诱导的免疫原性较差,第 180 天血清阳性率为 7.2%,中和能力较低。BNT162b2 mRNA 疫苗诱导 IgG 滴度显著增加,平均为 197.8 单位/毫升(BAU/mL)(95%CI0-491.4)和中和抗体,平均为 76.6 AU/mL(95%CI0-159.6)。在第 238 天,加强剂量后有 32.2%的 LTR 出现血清转化。只有 13 名和 9 名 LTR 对 Delta 和 Omicron 变异体有血清中和能力。霉酚酸酯和高剂量皮质类固醇与弱血清学反应相关。(4) 结论:两剂 ChAdOx1 nCoV-19 疫苗方案在 LTR 中的免疫原性非常差,但在三分之一的 LTR 中,加强剂量后显著增强。在免疫功能低下的个体中,可能考虑给予第四剂以增加对 SARS-CoV-2 的免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc96/9316698/a1d4e6de8fac/viruses-14-01470-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc96/9316698/bce14a6d69f8/viruses-14-01470-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc96/9316698/70b9d76516e2/viruses-14-01470-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc96/9316698/a1d4e6de8fac/viruses-14-01470-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc96/9316698/bce14a6d69f8/viruses-14-01470-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc96/9316698/70b9d76516e2/viruses-14-01470-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc96/9316698/a1d4e6de8fac/viruses-14-01470-g003.jpg

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本文引用的文献

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Bio Protoc. 2022 Apr 5;12(7):e4377. doi: 10.21769/BioProtoc.4377.
2
The T cell immune response against SARS-CoV-2.针对 SARS-CoV-2 的 T 细胞免疫应答。
Nat Immunol. 2022 Feb;23(2):186-193. doi: 10.1038/s41590-021-01122-w. Epub 2022 Feb 1.
3
Impaired Humoral Response to Third Dose of BNT162b2 mRNA COVID-19 Vaccine Despite Detectable Spike Protein-specific T cells in Lung Transplant Recipients.
Susceptibility to SARS-CoV-2 Infection and Immune Responses to COVID-19 Vaccination Among Recipients of Solid Organ Transplants.
实体器官移植受者对 SARS-CoV-2 感染的易感性和对 COVID-19 疫苗接种的免疫反应。
J Infect Dis. 2023 Aug 4;228(Suppl 1):S34-S45. doi: 10.1093/infdis/jiad152.
4
Evaluation of Immunogenicity to Three Doses of the SARS-CoV-2 BNT162b2 mRNA Vaccine in Lung Transplant Patients.肺移植患者中三剂严重急性呼吸综合征冠状病毒2(SARS-CoV-2)BNT162b2 mRNA疫苗免疫原性评估
Vaccines (Basel). 2022 Sep 30;10(10):1642. doi: 10.3390/vaccines10101642.
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5
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6
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7
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8
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9
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10
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J Heart Lung Transplant. 2022 Feb;41(2):148-157. doi: 10.1016/j.healun.2021.08.010. Epub 2021 Aug 28.