Nagra Deepak, Bechman Katie, Adas Maryam, Yang Zijing, Alveyn Edward, Subesinghe Sujith, Rutherford Andrew, Allen Victoria, Patel Samir, Russell Mark D, Cope Andrew, Norton Sam, Galloway James
Centre for Rheumatic Disease, King's College London, London WC2R 2LS, UK.
Vaccines (Basel). 2023 Nov 2;11(11):1680. doi: 10.3390/vaccines11111680.
Pneumococcal pneumonia is an important cause of morbidity and mortality amongst patients with inflammatory arthritis. Vaccination is recommended by the National Institute for Health and Care Excellence (NICE) but it remains unclear how vaccine efficacy is impacted by different immunosuppressive agents. Our objective was to compare the chance of a seroconversion following vaccination against pneumococcus in patients with inflammatory arthritis to that in the general population, as well as to compare the chance of seroconversion across different targeted therapies.
We searched MEDLINE, Embase and the Cochrane Library databases from inception until 20 June 2023. We included randomized controlled trials and observational studies. Aggregate data were used to undertake a pairwise meta-analysis. Our primary outcome of interest was vaccine seroconversion. We accepted the definition of serological response reported by the authors of each study.
Twenty studies were identified in the systematic review (2807 patients) with ten reporting sufficient data to be included in the meta-analysis (1443 patients). The chance of seroconversion in patients receiving targeted therapies, relative to the general population, was 0.61 (95% CI 0.35 to 1.08). The reduced odds of response were skewed strongly by the effects of abatacept and rituximab with no difference between patients on TNF inhibitors (TNFis) or IL-6 inhibition and healthy controls. Within different inflammatory arthritis populations the findings remained consistent, with rituximab having the strongest negative impact on vaccine response. TNF inhibition monotherapy was associated with a greater chance of vaccine response compared with methotrexate (2.25 (95% CI 1.28 to 3.96)). JAK inhibitor (JAKi) studies were few in number and did not present comparable vaccine response endpoints to include in the meta-analysis. The information available does not suggest any significant detrimental effects of JAKi on vaccine response.
This updated meta-analysis confirms that, for most patients with inflammatory arthritis, pneumococcal vaccine can be administered with confidence and that it will achieve comparable seroconversion rates to the healthy population. Patients on rituximab were the group least likely to achieve a response and further research is needed to explore the value of multiple-course pneumococcal vaccination schedules in this population.
肺炎球菌肺炎是炎性关节炎患者发病和死亡的重要原因。英国国家卫生与临床优化研究所(NICE)建议进行疫苗接种,但目前尚不清楚不同免疫抑制剂如何影响疫苗效力。我们的目的是比较炎性关节炎患者接种肺炎球菌疫苗后血清转化的几率与普通人群的血清转化几率,并比较不同靶向治疗药物的血清转化几率。
我们检索了MEDLINE、Embase和Cochrane图书馆数据库,检索时间从数据库建立至2023年6月20日。我们纳入了随机对照试验和观察性研究。汇总数据用于进行成对荟萃分析。我们感兴趣的主要结局是疫苗血清转化。我们接受了每项研究作者报告的血清学反应定义。
在系统评价中识别出20项研究(2807例患者),其中10项报告了足够的数据可纳入荟萃分析(1443例患者)。与普通人群相比,接受靶向治疗的患者血清转化几率为0.61(95%CI 0.35至1.08)。阿巴西普和利妥昔单抗的影响使反应几率降低的情况存在严重偏差,使用肿瘤坏死因子抑制剂(TNFis)或IL-6抑制剂的患者与健康对照之间无差异。在不同的炎性关节炎人群中,研究结果保持一致,利妥昔单抗对疫苗反应的负面影响最大。与甲氨蝶呤相比,TNF抑制单药治疗与更高的疫苗反应几率相关(2.25(95%CI 1.28至3.96))。JAK抑制剂(JAKi)的研究数量较少,且未呈现可纳入荟萃分析的可比疫苗反应终点。现有信息未表明JAKi对疫苗反应有任何显著的有害影响。
这项更新的荟萃分析证实,对于大多数炎性关节炎患者,可以放心接种肺炎球菌疫苗,并且其血清转化率与健康人群相当。接受利妥昔单抗治疗的患者是最不可能产生反应的群体,需要进一步研究以探索在该人群中多疗程肺炎球菌疫苗接种方案的价值。