Department of Clinical Immunology, IML and IdSSC, Hospital Clínico San Carlos, Madrid, Spain.
Department of Innovation and Development, Inmunotek S.L., Alcalá de Henares, Spain.
Front Immunol. 2021 Jun 4;12:675735. doi: 10.3389/fimmu.2021.675735. eCollection 2021.
Conventional or biologic disease-modifying anti-rheumatic drugs (DMARDs) are the mainstay of treatment for systemic autoimmune disease (SAD). Infectious complications are a major concern in their use.
To evaluate the clinical benefit of sublingual mucosal polybacterial vaccines (MV130 and MV140), used to prevent recurrent respiratory and urinary tract infections, in patients with SAD and secondary recurrent infections following conventional or biologic DMARDs.
An observational study in SAD patients with recurrent respiratory tract infections (RRTI) and/or recurrent urinary tract infections (RUTI) was carried out. All patients underwent mucosal (sublingual) vaccination with MV130 for RRTI or with MV140 for RUTI daily for 3 months. Clinical evaluation was assessed during 12 months of follow-up after the first dose, i.e., 3 months under treatment and 9 months once discontinued, and compared with the previous year.
Forty-one out of 55 patients completed 1-year follow-up. All patients were on either conventional or biologic DMARDs. A significant decrease in the frequency of RUTI (p<0.001), lower respiratory tract infections (LRTI) (p=0.009) and upper respiratory tract infections (URTI) (p=0.006) at 12-mo with respect to the previous year was observed. Antibiotic prescriptions and unscheduled medical visits decreased significantly (p<0.020) in all groups. Hospitalization rate also declined in patients with RRTI (p=0.019). The clinical benefit demonstrated was concomitant to a significant increase in both anti- IgA and IgG antibodies following MV130 vaccination.
Sublingual polybacterial vaccines prevent recurrent infections in patients with SAD under treatment with immunosuppressant therapies, supporting a broad non-specific anti-infectious effect in these patients.
传统或生物疾病修正抗风湿药物(DMARDs)是治疗全身性自身免疫性疾病(SAD)的主要方法。其使用存在感染并发症的主要问题。
评估舌下黏膜多细菌疫苗(MV130 和 MV140)在接受传统或生物 DMARDs 治疗后出现复发性呼吸道和尿路感染(RRTI 和/或 RUTI)的 SAD 患者中的临床获益。
对复发性呼吸道感染(RRTI)和/或复发性尿路感染(RUTI)的 SAD 患者进行观察性研究。所有患者接受 MV130 舌下黏膜(舌下)接种治疗 RRTI 或 MV140 每日接种治疗 RUTI,共 3 个月。在第一次接种后进行为期 12 个月的随访,即 3 个月的治疗期和 9 个月的停药后随访,与前一年进行比较。
55 例患者中有 41 例完成了 1 年随访。所有患者均接受传统或生物 DMARDs 治疗。与前一年相比,12 个月时 RUTI(p<0.001)、下呼吸道感染(LRTI)(p=0.009)和上呼吸道感染(URTI)(p=0.006)的频率显著降低。所有组的抗生素处方和非计划就诊次数均显著减少(p<0.020)。RRTI 患者的住院率也下降(p=0.019)。MV130 接种后,IgA 和 IgG 抗体均显著增加,同时显示出临床获益。
舌下多细菌疫苗可预防接受免疫抑制剂治疗的 SAD 患者复发性感染,支持这些患者具有广泛的非特异性抗感染作用。