A TLR7-nanoparticle adjuvant promotes a broad immune response against heterologous strains of influenza and SARS-CoV-2

TLR7纳米颗粒佐剂可促进针对异源流感病毒株和SARS-CoV-2的广泛免疫反应。

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作者:Qian Yin #,Wei Luo #,Vamsee Mallajosyula,Yang Bo,Jing Guo,Jinghang Xie,Meng Sun,Rohit Verma,Chunfeng Li,Christian M Constantz,Lisa E Wagar,Jing Li,Elsa Sola,Neha Gupta,Chunlin Wang,Oliver Kask,Xin Chen,Xue Yuan,Nicholas C Wu,Jianghong Rao,Yueh-Hsiu Chien,Jianjun Cheng,Bali Pulendran ,Mark M Davis

Abstract

The ideal vaccine against viruses such as influenza and SARS-CoV-2 must provide a robust, durable and broad immune protection against multiple viral variants. However, antibody responses to current vaccines often lack robust cross-reactivity. Here we describe a polymeric Toll-like receptor 7 agonist nanoparticle (TLR7-NP) adjuvant, which enhances lymph node targeting, and leads to persistent activation of immune cells and broad immune responses. When mixed with alum-adsorbed antigens, this TLR7-NP adjuvant elicits cross-reactive antibodies for both dominant and subdominant epitopes and antigen-specific CD8+ T-cell responses in mice. This TLR7-NP-adjuvanted influenza subunit vaccine successfully protects mice against viral challenge of a different strain. This strategy also enhances the antibody response to a SARS-CoV-2 subunit vaccine against multiple viral variants that have emerged. Moreover, this TLR7-NP augments antigen-specific responses in human tonsil organoids. Overall, we describe a nanoparticle adjuvant to improve immune responses to viral antigens, with promising implications for developing broadly protective vaccines.

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