Cappuccilli Maria, Bruno Paolo Ferdinando, Spazzoli Alessandra, Righini Matteo, Flachi Marta, Semprini Simona, Grumiro Laura, Marino Maria Michela, Schiavone Pasqua, Fabbri Elisabetta, Fantini Michela, Buscaroli Andrea, Rigotti Angelo, La Manna Gaetano, Sambri Vittorio, Mosconi Giovanni
Nephrology, Dialysis and Renal Transplant Unit, IRCCS-Azienda Ospedaliero-Universitaria di Bologna, Alma Mater Studiorum University of Bologna, 40138 Bologna, Italy.
Nephrology and Dialysis Unit, AUSL Romagna Morgagni-Pierantoni Hospital, 47121 Forlì, Italy.
Pathogens. 2021 Oct 6;10(10):1289. doi: 10.3390/pathogens10101289.
Nephropathic subjects with impaired immune responses show dramatically high infection rates of coronavirus disease 2019 (COVID-19). This work evaluated the ability to acquire and maintain protective antibodies over time in 26 hemodialysis patients and 21 kidney transplant recipients. The subjects were followed-up through quantitative determination of circulating SARS-CoV-2 S1/S2 IgG and neutralizing antibodies in the 6-month period after clinical and laboratory recovery. A group of 143 healthcare workers with no underlying chronic pathologies or renal diseases recovered from COVID was also evaluated. In both dialysis and transplanted patients, antibody titers reached a zenith around the 3rd month, and then a decline occurred on average between the 270th and 300th day. Immunocompromised patients who lost antibodies around the 6th month were more common than non-renal subjects, although the difference was not significant (38.5% vs. 26.6%). Considering the decay of antibody levels below the positivity threshold (15 AU/mL) as "failure", a progressive loss of immunisation was found in the overall population starting 6 months after recovery. A longer overall antibody persistence was observed in severe forms of COVID-19 ( = 0.0183), but within each group, given the small number of patients, the difference was not significant (dialysis: = 0.0702; transplant: = 0.1899). These data suggest that immunocompromised renal patients recovered from COVID-19 have weakened and heterogeneous humoral responses that tend to decay over time. Despite interindividual variability, an association emerged between antibody persistence and clinical severity, similar to the subjects with preserved immune function.
免疫反应受损的肾病患者感染2019冠状病毒病(COVID-19)的几率极高。本研究评估了26名血液透析患者和21名肾移植受者随时间获取和维持保护性抗体的能力。在临床和实验室康复后的6个月内,通过定量测定循环中的SARS-CoV-2 S1/S2 IgG和中和抗体对这些受试者进行随访。还评估了一组143名从COVID中康复且无潜在慢性疾病或肾脏疾病的医护人员。在透析患者和移植患者中,抗体滴度在第3个月左右达到峰值,然后在第270天至第300天之间平均出现下降。在第6个月左右失去抗体的免疫功能低下患者比非肾脏受试者更为常见,尽管差异不显著(38.5%对26.6%)。将抗体水平降至阳性阈值(15 AU/mL)以下视为“失败”,发现在康复6个月后总体人群中免疫逐渐丧失。在COVID-19重症患者中观察到抗体总体持续时间更长(P = 0.0183),但在每组中,由于患者数量较少,差异不显著(透析:P = 0.0702;移植:P = 0.1899)。这些数据表明,从COVID-19中康复的免疫功能低下的肾病患者的体液反应减弱且存在异质性,并且往往会随着时间推移而衰退。尽管存在个体差异,但抗体持续时间与临床严重程度之间仍存在关联,这与免疫功能正常的受试者相似。