Esteban-Vazquez Ana, Steiner Martina, Castañeda Elisabet, Andreu-Vazquez Cristina, Thiussard Israel J, Somodevilla Angela, Gracia-Martínez Moisés, Sánchez-Diaz Rosa, García-Yubero Cristina, Paredes-Romero Maria Beatriz, Munoz-Fernández Santiago
Rheumatology Department, Infanta Sofía University Hospital, 28703 Madrid, Spain.
Statistics Deparment, Universidad Europea, 28703 Madrid, Spain.
Vaccines (Basel). 2023 Oct 18;11(10):1610. doi: 10.3390/vaccines11101610.
. The risk of herpes zoster reactivation is increased in immunocompromised patients, especially in those with immune-mediated inflammatory diseases (IMIDs) on Janus kinase inhibitor (JAKi) treatment. The recombinant subunit herpes zoster vaccine (RZV) is a non-live vaccine, recently approved for this subgroup of patients, which shows high rates of vaccine effectiveness, with few adverse effects reported in clinical trials. . The aim of this real-world study was to determine the immunogenicity and safety of RZV in IMID patients on JAKi treatment. . The increase in the concentration of anti-gE antibody for varicella zoster virus post-vaccination, compared to the pre-vaccination concentration, was analyzed to test the humoral immune response. Adverse effects after the first and second vaccine doses were registered. . In total, 49 patients were analyzed, and a fourfold increase in antibody concentration was achieved in almost 40% of subjects, with only one serious local adverse effect. . The resulting immunogenicity was lower than that observed in clinical trials, probably due to the presence of immune disease and immunosuppressive treatment, and to the fact that this was a real-world study. No differences in response according to age, previous virus zoster reactivation, or concomitant treatments were found. . RZV was well tolerated and reached the immune response objective in 40% of patients. These results reinforce the importance of including RZV vaccination for immunosuppressed patients. Real-world studies regarding vaccine effectiveness are still needed in order to gain a full understanding of the response to RZV in this group of patients.
免疫功能低下的患者,尤其是正在接受 Janus 激酶抑制剂(JAKi)治疗的免疫介导性炎症疾病(IMID)患者,带状疱疹再激活的风险会增加。重组亚单位带状疱疹疫苗(RZV)是一种非活疫苗,最近被批准用于这一亚组患者,该疫苗显示出较高的疫苗有效性,临床试验中报告的不良反应较少。 这项真实世界研究的目的是确定 RZV 在接受 JAKi 治疗的 IMID 患者中的免疫原性和安全性。 分析接种疫苗后水痘带状疱疹病毒抗 gE 抗体浓度相对于接种前浓度的增加情况,以测试体液免疫反应。记录第一剂和第二剂疫苗后的不良反应。 总共分析了 49 名患者,近 40% 的受试者抗体浓度增加了四倍,仅出现一例严重的局部不良反应。 由此产生的免疫原性低于临床试验中观察到的情况,这可能是由于存在免疫疾病和免疫抑制治疗,以及这是一项真实世界研究的缘故。未发现根据年龄、既往带状疱疹再激活情况或伴随治疗的反应存在差异。 RZV 耐受性良好,40% 的患者达到了免疫反应目标。这些结果强化了对免疫抑制患者进行 RZV 疫苗接种的重要性。为了全面了解这组患者对 RZV 的反应,仍需要开展关于疫苗有效性的真实世界研究。