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一项前瞻性观察研究,旨在验证在接受维持性血液透析的患者中接种第三剂 mRNA 疫苗的合理性、安全性和有效性。

A prospective observational study for justification, safety, and efficacy of a third dose of mRNA vaccine in patients receiving maintenance hemodialysis.

机构信息

Centre International de Recherche en Infectiologie, Institut National de la Santé et de la Recherche Médicale U1111, Université Claude Bernard Lyon I, Centre National de la Recherche Scientifique Unité Mixte de Recherch 5308, Ecole Normale Supérieure de Lyon, Université Lyon, Lyon, France; Department of Nephrology, Nutrition, and Hemodialysis, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Pierre-Bénite, France.

Centre International de Recherche en Infectiologie, Institut National de la Santé et de la Recherche Médicale U1111, Université Claude Bernard Lyon I, Centre National de la Recherche Scientifique Unité Mixte de Recherch 5308, Ecole Normale Supérieure de Lyon, Université Lyon, Lyon, France.

出版信息

Kidney Int. 2022 Feb;101(2):390-402. doi: 10.1016/j.kint.2021.10.040. Epub 2021 Nov 29.

Abstract

The level of protection achieved by the standard two doses of COVID-19 mRNA vaccines in patients receiving maintenance hemodialysis (MHD) remains unclear. To study this we used the French Renal Epidemiology and Information Network (REIN) Registry to compare the incidence and severity of 1474 cases of COVID-19 diagnosed in patients receiving MHD after none, one or two doses of vaccine. Vaccination significantly reduce COVID-19 incidence and severity, but 11% of patients infected after two doses still died. Lack of vaccinal protection in patients naïve for SARS-CoV-2 could be due to defective Tfh response [38% of patients with negative spike-specific CD4 T-cell interferon gamma release assay] and failure to generate viral neutralizing titers of anti-spike receptor binding domain (RBD) IgGs (63% of patients with titer at or under 997 BAU/ml, defining low/no responders) after two doses of vaccine. To improve protection, a third dose of vaccine was administered to 75 patients [57 low/no responders, 18 high responders after two doses] from the ROMANOV cohort that prospectively enrolled patients receiving MHD vaccinated with BNT162b2 (Pfizer). Tolerance to the third dose was excellent. High responders to two doses did not generate more anti-RBD IgGs after three doses but had more side effects. Importantly, 31 (54%) of low/no responders to two doses reached neutralizing titers of anti-RBD IgGs after three doses. A positive interferon gamma release assay and/or suboptimal titer of anti-RBD IgGs after two doses were the only predictive variables for response to three doses in multivariate analysis. Thus, the standard scheme of vaccination insufficiently protects patients receiving MHD. Anti-RBD IgG and specific CD4 T-cell response after two doses can guide personalized administration of the third dose, which improves the humoral response of SARS-CoV-2-naïve patients receiving MHD.

摘要

标准两剂 COVID-19 mRNA 疫苗在接受维持性血液透析(MHD)患者中的保护水平尚不清楚。为了研究这一点,我们使用法国肾脏流行病学和信息网络(REIN)登记处比较了 1474 例在接受 MHD 治疗后无、一剂或两剂疫苗接种的患者中诊断出的 COVID-19 的发病率和严重程度。疫苗接种显著降低了 COVID-19 的发病率和严重程度,但两剂后仍有 11%的患者感染后死亡。SARS-CoV-2 无疫苗保护的患者可能是由于 Tfh 反应缺陷[阴性棘突特异性 CD4 T 细胞干扰素γ释放试验的患者占 38%]和无法产生针对棘突受体结合域(RBD)IgG 的病毒中和滴度(两剂疫苗后,63%的患者滴度在 997 BAU/ml 或以下,定义为低/无应答者)。为了提高保护水平,对来自前瞻性纳入接受 BNT162b2(辉瑞)疫苗接种的 MHD 患者的 ROMANOV 队列的 75 名患者(57 名低/无应答者,18 名两剂后高应答者)给予了第三剂疫苗。第三剂疫苗的耐受性极好。两剂高应答者在三剂后并未产生更多的抗 RBD IgG,但出现了更多的副作用。重要的是,两剂后低/无应答者中的 31 名(54%)达到了抗 RBD IgG 的中和滴度。干扰素γ释放试验阳性和/或两剂后抗 RBD IgG 滴度不理想是多变量分析中对三剂反应的唯一预测变量。因此,标准的疫苗接种方案不能充分保护接受 MHD 的患者。两剂后抗 RBD IgG 和特异性 CD4 T 细胞反应可以指导三剂个性化给药,从而改善接受 MHD 的 SARS-CoV-2 无疫苗接种史患者的体液反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9703/8628628/01a642319392/fx1_lrg.jpg

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