Goggins Eibhlin, Sharma Binu, Ma Jennie Z, Gautam Jitendra, Bowman Brendan
Division of Nephrology University of Virginia School of Medicine Charlottesville Virginia USA.
Public Health Sciences University of Virginia School of Medicine Charlottesville Virginia USA.
Health Sci Rep. 2024 Feb 13;7(2):e1858. doi: 10.1002/hsr2.1858. eCollection 2024 Feb.
Patients with end stage kidney disease on hemodialysis are vulnerable to SARS-CoV-2 infection. Current guidelines recommend boosters of SARS-CoV-2 mRNA-based vaccines. The long-term humoral response of hemodialysis patients infected with SARS-CoV-2 after receiving a booster of SARS-CoV-2 mRNA-based vaccines has been incompletely characterized. Here, we determined the long-term humoral response of hemodialysis patients to two and three doses of the Pfizer BioNTech (BNT162b2) mRNA SARS-CoV-2 vaccine and investigated the effect of postbooster SARS-CoV-2 infection on antibody levels over time.
Samples were collected on a monthly basis and tested for anti-SARS-CoV-2 antibodies against anti-spike S1 domain. Thirty-five hemodialysis patients were enrolled in the original study and 27 of these received a booster. Patients were followed up to 6 months after the first two doses and an additional 7 months after the third BNT162b2 dose. Results are presented as the internationally harmonized binding antibody units (BAU/mL).
Antibody level significantly increased from prebooster to 2 weeks postbooster, with a median [25th, 75th percentile] rise from 52.72 [28.55, 184.7] to 6216 [3806, 11,730] BAU/mL in the total population. Of patients with a negative or borderline detectable antibody level 6 months after vaccination who received a third dose, 89% developed positive antibody levels 2 weeks postbooster. Postbooster antibody levels declined an average rate of 29% per month in infection-naïve patients. Antibody levels spiked in patients infected with SARS-CoV-2 after receiving a booster but declined rapidly. No patients infected postbooster required hospitalization.
A third dose of BNT162b2 restores antibody levels to high levels in dialysis patients but levels decline over time. A third dose did not necessarily prevent infection, but no patients suffered severe infection or required hospitalization. SARS-CoV-2 recovered patients appear to have a blunted rise in antibody levels after a third dose. Although patients infected with SARS-CoV-2 postbooster had an immediate spike in antibody levels, these declined over time.
接受血液透析的终末期肾病患者易感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2)。当前指南推荐接种SARS-CoV-2信使核糖核酸(mRNA)疫苗加强针。血液透析患者在接种SARS-CoV-2 mRNA疫苗加强针后感染SARS-CoV-2的长期体液免疫反应尚未完全明确。在此,我们确定了血液透析患者对两剂和三剂辉瑞生物科技公司(BNT162b2)mRNA SARS-CoV-2疫苗的长期体液免疫反应,并研究了加强针接种后SARS-CoV-2感染对抗体水平随时间的影响。
每月采集样本,检测针对刺突蛋白S1结构域的抗SARS-CoV-2抗体。35名血液透析患者纳入原研究,其中27名接种了加强针。对患者在前两剂接种后随访6个月,在第三剂BNT162b2接种后再随访7个月。结果以国际统一的结合抗体单位(BAU/mL)表示。
抗体水平从加强针接种前到接种后2周显著升高,总体人群中位数[第25百分位数,第75百分位数]从52.72[28.55,184.7]升至6216[3806,11730]BAU/mL。接种疫苗6个月后抗体水平为阴性或临界可检测水平的患者中,89%在接种加强针后2周抗体水平转为阳性。在未感染过的患者中,加强针接种后抗体水平平均每月下降29%。接种加强针后感染SARS-CoV-2的患者抗体水平飙升,但随后迅速下降。加强针接种后感染的患者均未住院。
第三剂BNT162b2可使透析患者抗体水平恢复到高水平,但随后水平随时间下降。第三剂不一定能预防感染,但无患者发生严重感染或需要住院治疗。SARS-CoV-2康复患者在接种第三剂后抗体水平升高似乎不明显。虽然接种加强针后感染SARS-CoV-2的患者抗体水平立即飙升,但随后随时间下降。