Department of Nephrology, University of Heidelberg, Heidelberg, Germany.
Department of Infectious Diseases, Molecular Virology, University of Heidelberg, Heidelberg, Germany.
Front Immunol. 2022 Mar 4;13:840136. doi: 10.3389/fimmu.2022.840136. eCollection 2022.
Hemodialysis patients are at high risk for severe COVID-19, and impaired seroconversion rates have been demonstrated after COVID-19 vaccination. Humoral immunity wanes over time and variants of concern with immune escape are posing an increasing threat. Little is known about protection against the B.1.617.2 (delta) variant of concern in hemodialysis patients before and after third vaccination. We determined anti-S1 IgG, surrogate neutralizing, and IgG antibodies against different SARS-CoV-2 epitopes in 84 hemodialysis patients directly before and three weeks after a third vaccine dose with BNT162b2. Third vaccination was performed after a median (IQR) of 119 (109-165) days after second vaccination. In addition, neutralizing activity against the B.1.617.2 (delta) variant was assessed in 31 seroconverted hemodialysis patients before and after third vaccination. Triple seropositivity for anti-S1 IgG, surrogate neutralizing, and anti-RBD antibodies increased from 31/84 (37%) dialysis patients after second to 80/84 (95%) after third vaccination. Neutralizing activity against the B.1.617.2 (delta) variant was significantly higher after third vaccination with a median (IQR) ID of 1:320 (1:160-1:1280) compared with 1:20 (0-1:40) before a third vaccine dose (<0.001). The anti-S1 IgG index showed the strongest correlation with the ID against the B.1.617.2 (delta) variant determined by live virus neutralization (r=0.91). We demonstrate low neutralizing activity against the B.1.617.2 (delta) variant in dialysis patients four months after standard two-dose vaccination but a substantial increase after a third vaccine dose. Booster vaccination(s) should be considered earlier than 6 months after the second vaccine dose in immunocompromised individuals.
血液透析患者感染 COVID-19 的风险较高,并且已经证明 COVID-19 疫苗接种后血清转化率受损。随着时间的推移,体液免疫会减弱,具有免疫逃逸能力的关注变体正构成越来越大的威胁。在第三次接种疫苗之前和之后,血液透析患者对 B.1.617.2(德尔塔)关注变体的保护作用知之甚少。我们在 84 名血液透析患者第三次接种 BNT162b2 疫苗前和三周后直接测定了针对 S1 IgG、替代中和和针对不同 SARS-CoV-2 表位的 IgG 抗体。第二次接种后中位数(IQR)119(109-165)天后进行了第三次接种。此外,在第三次接种前后,还评估了 31 名血清转化的血液透析患者对 B.1.617.2(德尔塔)变体的中和活性。第三次接种后,针对 S1 IgG、替代中和和针对 RBD 抗体的三重血清阳性率从第二次接种后的 31/84(37%)增加到第三次接种后的 80/84(95%)。与第三次接种前相比,第三次接种后针对 B.1.617.2(德尔塔)变体的中和活性显着提高,中位数(IQR)ID 为 1:320(1:160-1:1280)比第三次接种前的 1:20(0-1:40)高(<0.001)。抗 S1 IgG 指数与通过活病毒中和测定的针对 B.1.617.2(德尔塔)变体的 ID 相关性最强(r=0.91)。我们证明,在标准两剂疫苗接种后四个月,透析患者对 B.1.617.2(德尔塔)变体的中和活性较低,但在第三次接种疫苗后显着增加。在免疫功能低下的个体中,应考虑在第二次接种疫苗后 6 个月之前进行加强接种。