Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Pathology, Molecular and Cell Based Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Nat Commun. 2022 Sep 1;13(1):5135. doi: 10.1038/s41467-022-32389-8.
Immune responses at the respiratory mucosal interface are critical to prevent respiratory infections but it is unclear to what extent antigen specific mucosal secretory IgA (SIgA) antibodies are induced by mRNA vaccination in humans. Here we analyze paired serum and saliva samples from patients with and without prior coronavirus disease 2019 (COVID-19) at multiple time points pre and post severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) mRNA vaccination. Our results suggest mucosal SIgA responses induced by mRNA vaccination are impacted by pre-existing immunity. Indeed, vaccination induced a minimal mucosal SIgA response in individuals without pre-exposure to SARS-CoV-2 while SIgA induction after vaccination was more efficient in patients with a history of COVID-19.
呼吸道黏膜表面的免疫反应对于预防呼吸道感染至关重要,但目前尚不清楚 mRNA 疫苗接种在多大程度上能诱导人类针对抗原的黏膜分泌型免疫球蛋白 A(SIgA)抗体。在此,我们分析了 SARS-CoV-2 mRNA 疫苗接种前后多个时间点患有和未患有既往新型冠状病毒肺炎(COVID-19)的患者的配对血清和唾液样本。结果表明,mRNA 疫苗接种诱导的黏膜 SIgA 反应受固有免疫的影响。事实上,在未接触过 SARS-CoV-2 的个体中,疫苗接种诱导的黏膜 SIgA 反应很小,而在有 COVID-19 病史的患者中,疫苗接种后的 SIgA 诱导更为有效。