Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA; WCCT Global, Cypress, CA, USA.
Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA, USA.
Cell Host Microbe. 2021 Dec 8;29(12):1828-1837.e5. doi: 10.1016/j.chom.2021.10.009. Epub 2021 Nov 15.
Developing new influenza vaccines with improved performance and easier administration routes hinges on defining correlates of protection. Vaccine-elicited cellular correlates of protection for influenza in humans have not yet been demonstrated. A phase-2 double-blind randomized placebo and active (inactivated influenza vaccine) controlled study provides evidence that a human-adenovirus-5-based oral influenza vaccine tablet (VXA-A1.1) can protect from H1N1 virus challenge in humans. Mass cytometry characterization of vaccine-elicited cellular immune responses identified shared and vaccine-type-specific responses across B and T cells. For VXA-A1.1, the abundance of hemagglutinin-specific plasmablasts and plasmablasts positive for integrin α4β7, phosphorylated STAT5, or lacking expression of CD62L at day 8 were significantly correlated with protection from developing viral shedding following virus challenge at day 90 and contributed to an effective machine learning model of protection. These findings reveal the characteristics of vaccine-elicited cellular correlates of protection for an oral influenza vaccine.
开发具有更好性能和更便捷给药途径的新型流感疫苗,关键在于确定保护相关因素。尚未证明人类流感疫苗诱导的细胞保护相关因素。一项 2 期双盲随机安慰剂和活性(灭活流感疫苗)对照研究提供了证据,证明基于人腺病毒 5 的口服流感疫苗片剂(VXA-A1.1)可预防人类 H1N1 病毒挑战。疫苗诱导的细胞免疫反应的质谱细胞术特征鉴定了 B 和 T 细胞之间的共享和疫苗类型特异性反应。对于 VXA-A1.1,在第 8 天,针对血凝素的浆母细胞和整合素 α4β7 阳性的浆母细胞、磷酸化 STAT5 或缺乏 CD62L 表达的数量与在第 90 天病毒挑战后防止病毒脱落的保护呈显著相关,并有助于建立有效的保护机器学习模型。这些发现揭示了口服流感疫苗诱导的细胞保护相关因素的特征。