A*STAR Infectious Diseases Labs, Agency for Science, Technology and Research, Singapore, Singapore.
Singapore Immunology Network, Agency for Science, Technology and Research, Singapore, Singapore.
J Infect Dis. 2024 Aug 16;230(2):e287-e291. doi: 10.1093/infdis/jiad525.
The emergence of rapidly evolving severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants, coupled with waning vaccine-induced immunity, has contributed to the rise of vaccine breakthrough infections. It is crucial to understand how vaccine-induced protection is mediated.
We examined 2 prospective cohorts of mRNA vaccinated and boosted individuals during the Omicron wave of infection in Singapore.
We found that individuals who remain uninfected over the follow-up period had a higher variant-specific IgA, but not IgG, antibody response at 1 month after booster vaccination, compared with individuals who became infected.
We conclude that IgA may have a potential contributory role in protection against Omicron infection. Clinical Trials Registration . NCT05142319.
快速进化的严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)变种的出现,加上疫苗诱导免疫的减弱,导致了疫苗突破性感染的增加。了解疫苗诱导的保护作用是如何介导的至关重要。
我们在新加坡的奥密克戎感染浪潮期间,检查了 2 个接受 mRNA 疫苗接种和加强针的前瞻性队列。
我们发现,与感染的个体相比,在随访期间未感染的个体在加强针接种后 1 个月时具有更高的针对变异株的 IgA,但 IgG 抗体反应较低。
我们的结论是,IgA 可能在预防奥密克戎感染方面具有潜在的作用。临床试验注册. NCT05142319。