Pharmacy Department, Grenoble Alpes University Hospital and Univ. Grenoble Alpes, Laboratory of Fundamental and Applied Bioenergetic (LBFA), INSERM U1055, Grenoble, France.
Virology Laboratory, Grenoble Alpes University Hospital and Univ. Grenoble Alpes, Institut de Biologie Structurale (IBS), CEA, CNRS, Grenoble, France.
Vaccine. 2022 Oct 19;40(44):6404-6411. doi: 10.1016/j.vaccine.2022.08.065. Epub 2022 Sep 6.
A fourth dose of SARS-CoV-2 vaccine is recommended in solid-organ transplant (SOT) recipients, but the immunogenicity is poorly known.
We conducted a retrospective, observational, monocentric study between the 1st January 2021 and 31st March 2022 of the anti-Spike antibody titers after one to four doses of vaccine in SOT.
825 SOT were included. Median age at first vaccine injection was 61.2 (IQR 50.9-69.3) years; 66.7 % were male; 63.4 % had received four vaccine doses. The proportion of participants with a strong humoral response (>260 BAU/mL) increased with the number of vaccine doses: 10.6 % after the 1st dose (D1), 35.1 % after the 2nd (D2), 48.5 % after the 3rd (D3), and 65.1 % after the 4th (D4) (p < 0.001). Among the tested patients, the proportion with a detectable humoral response was significantly higher after D4 than after D3 (47 % vs 22 %, p = 0.01). Liver transplant recipients had more frequently a strong humoral response after D2, D3 and D4 (OR = 5.3, 3.7 and 6.6 respectively when compared with other organ transplant recipients, p < 0.001). In kidney transplant recipients, belatacept-containing regimen was associated with a lower rate of detectable humoral (9 % vs 40 %, p = 0.025) after D3, but there was no statistical difference after D4.
A fourth dose should be proposed to SOT recipients who did not developed an immune response after 3 doses. Kidney transplant recipients receiving belatacept have a poorer, although frequently detectable response.
建议实体器官移植(SOT)受者接种第四剂 SARS-CoV-2 疫苗,但免疫原性知之甚少。
我们进行了一项回顾性、观察性、单中心研究,纳入了 2021 年 1 月 1 日至 2022 年 3 月 31 日期间接受了一至四剂疫苗后的抗刺突抗体滴度。
共纳入 825 例 SOT。首次接种疫苗时的中位年龄为 61.2(IQR 50.9-69.3)岁;66.7%为男性;63.4%接受了四剂疫苗。随着疫苗接种次数的增加,具有强体液反应(>260 BAU/mL)的参与者比例增加:第 1 剂(D1)为 10.6%,第 2 剂(D2)为 35.1%,第 3 剂(D3)为 48.5%,第 4 剂(D4)为 65.1%(p<0.001)。在检测的患者中,D4 后检测到体液反应的比例明显高于 D3(47%比 22%,p=0.01)。与其他器官移植受者相比,肝移植受者在 D2、D3 和 D4 后更常出现强体液反应(OR=5.3、3.7 和 6.6,当与其他器官移植受者相比,p<0.001)。在肾移植受者中,含贝利尤单抗的方案与 D3 后可检测到的体液反应率较低(9%比 40%,p=0.025)相关,但 D4 后无统计学差异。
对于未在 3 剂后产生免疫反应的 SOT 受者,应建议接种第四剂。接受贝利尤单抗的肾移植受者的反应较差,尽管经常可检测到。