A vaccine platform targeting lung-resident memory CD4+ T-cells provides protection against heterosubtypic influenza infections in mice and ferrets
Kwang-Wook Ko, Hyun Shik Bae, Jeong Woo Park, Jin-Sun Lee, Somin Park, Jun Heo, Hyunsoo Park, Jaeseok Choi, Eunseo Bae, Woonsung Na, Seong‐Hyun Park, Baik Lin Seong, Seung Hyun Han, Dong-Ho Kim, Seung Bin
Abstract
Lung tissue-resident memory T (TRM) cells induced by influenza vaccination are crucial for heterosubtypic immunity upon re-exposure to the influenza virus, enabling rapid and robust responses upon reactivation. To enhance the efficacy of influenza vaccines, we induce the generation of lung TRM cells following intranasal vaccination with a commercial influenza vaccine adjuvanted with NexaVant (NVT), a TLR3 agonist-based adjuvant. We demonstrate that intranasal immunization with the NVT-adjuvanted vaccine provides improved protection against influenza virus infections by inducing the generation of CD4+ TRM cells in the lungs in a type I interferon-dependent manner. These pulmonary CD4+ TRM cells provide potent mucosal immunity and cross-protection against heterosubtypic infections in both mouse and ferret models. This vaccine platform has the potential to significantly improve conventional intramuscular influenza vaccines by providing broader protection. Lung tissue-resident memory T cells play critical roles in the response to and protection to subsequent re-exposure and infection with influenza viruses. Here the authors explore vaccine induced lung resident memory T cells and their role in protection to heterosubtypic influenza infection in mice and ferrets.