van Sleen Yannick, van der Geest Kornelis S M, Buisman Anne-Marie, Sandovici Maria, van Baarle Debbie, Brouwer Elisabeth
University Medical Center Groningen, Groningen, The Netherlands.
National Institute for Public Health and the Environment, Bilthoven, The Netherlands.
Arthritis Care Res (Hoboken). 2024 Jan;76(1):105-110. doi: 10.1002/acr.25173. Epub 2023 Aug 4.
Vaccination remains essential in preventing morbidity of SARS-CoV-2 infections. We previously showed that >10 mg/day of prednisolone and methotrexate was associated with reduced antibody concentrations after primary vaccination in patients with giant cell arteritis (GCA) and polymyalgia rheumatica (PMR). This follow-up study was undertaken to measure the decay of antibody concentrations and the immunogenicity of SARS-CoV-2 booster vaccination.
Patients with GCA/PMR included in the primary vaccination (BNT162b2 [Pfizer-BioNTech] or ChAdOx1 [Oxford/AstraZeneca]) study were asked again to donate blood samples 6 months after primary vaccination (n = 24) and 1 month after booster vaccination (n = 46, BNT162b2 or mRNA1273). Data were compared to those of age-, sex-, and vaccine-matched controls (n = 58 and n = 42, respectively). Multiple linear regression was performed with post-booster antibody concentrations as dependent variable and post-primary vaccination antibodies, prednisolone >10mg/day, and methotrexate use as predicting variables.
Antibody concentrations decreased faster over time in GCA/PMR patients than in controls, which was associated with prednisolone treatment during primary vaccination. Post-booster antibody concentrations were comparable between patients and controls. Antibody concentrations post primary vaccination, but not treatment during booster vaccination, were predictive for antibody concentrations post booster vaccination.
These results indicate that the decay of humoral immunity after primary vaccination is associated with prednisolone treatment, whereas the subsequent increase after booster vaccination, was not. Patients with low antibody concentrations following primary vaccination remained at an immunogenic disadvantage after a single booster vaccination. This longitudinal study in GCA/PMR patients stresses the importance of repeated booster vaccination for patients with poor responses to primary vaccination.
接种疫苗对于预防SARS-CoV-2感染的发病仍然至关重要。我们之前表明,在巨细胞动脉炎(GCA)和风湿性多肌痛(PMR)患者中,每日泼尼松龙和甲氨蝶呤用量>10 mg与初次接种疫苗后抗体浓度降低有关。本随访研究旨在测量抗体浓度的衰减以及SARS-CoV-2加强疫苗接种的免疫原性。
邀请参与初次疫苗接种(BNT162b2[辉瑞-生物科技公司]或ChAdOx1[牛津大学/阿斯利康公司])研究的GCA/PMR患者在初次接种疫苗后6个月(n = 24)和加强疫苗接种后1个月(n = 46,BNT162b2或mRNA1273)再次捐献血样。将数据与年龄、性别和疫苗匹配的对照组(分别为n = 58和n = 42)的数据进行比较。以加强疫苗接种后的抗体浓度为因变量,初次接种疫苗后的抗体、泼尼松龙>10mg/天和甲氨蝶呤的使用作为预测变量进行多元线性回归。
GCA/PMR患者的抗体浓度随时间下降速度比对照组更快,这与初次接种疫苗期间使用泼尼松龙治疗有关。患者和对照组加强疫苗接种后的抗体浓度相当。初次接种疫苗后的抗体浓度,而非加强疫苗接种期间的治疗,可预测加强疫苗接种后的抗体浓度。
这些结果表明,初次接种疫苗后体液免疫的衰减与泼尼松龙治疗有关,而加强疫苗接种后随后的增加则无关。初次接种疫苗后抗体浓度低的患者在单次加强疫苗接种后仍处于免疫原性劣势。这项针对GCA/PMR患者的纵向研究强调了对初次接种疫苗反应不佳的患者重复进行加强疫苗接种的重要性。