Exploration of immunological responses underpinning severe fever with thrombocytopenia syndrome virus infection reveals IL-6 as a therapeutic target in an immunocompromised mouse model. Issue 1 (10th March 2022)

• Record Type: Journal Article
• Authors: Bryden, Steven R; Dunlop, James I; Clarke, Andrew T; Fares, Mazigh; Pingen, Marieke; Wu, Yan; Willett, Brian J; Patel, Arvind H; Gao, George F; Kohl, Alain; Brennan, Benjamin
• Editors: Levine, Bruce
• Is Part Of: PNAS nexus. Volume 1:Issue 1(2022)
• Publication Date: 2022-03-10
• Subjects: SFTS -- emerging bandavirus -- pathogenesis -- animal model -- therapy; Science -- Periodicals; 505
• DOI: 10.1093/pnasnexus/pgac024
• Languages: English
• ISSNs: 2752-6542

Abstract

Abstract: Dabie bandavirus (previously severe fever with thrombocytopenia syndrome virus; SFTSV), is an emerging tick-borne bunyavirus responsible for severe fever with thrombocytopenia syndrome (SFTS), a disease with high case fatality that is characterized by high fever, thrombocytopenia, and potentially lethal hemorrhagic manifestations. Currently, neither effective therapeutic strategies nor approved vaccines exist for SFTS. Therefore, there remains a pressing need to better understand the pathogenesis of the disease and to identify therapeutic strategies to ameliorate SFTS outcomes. Using a type I interferon (IFN)-deficient mouse model, we investigated the viral tropism, disease kinetics, and the role of the virulence factor nonstructural protein (NSs) in SFTS. Ly6C + MHCII + cells in the lymphatic tissues were identified as an important target cell for SFTSV. Advanced SFTS was characterized by significant migration of inflammatory leukocytes, notably neutrophils, into the lymph node and spleen, however, these cells were not required to orchestrate the disease phenotype. The development of SFTS was associated with significant upregulation of proinflammatory cytokines, including high levels of IFN-γ and IL-6 in the serum, lymph node, and spleen. Humoral immunity generated by inoculation with delNSs SFTSV was 100% protective. Importantly, NSs was critical to the inhibition of the host IFNɣ response or downstream IFN-stimulated gene production and allowed for the establishment of severe disease. Finally, therapeutic but not prophylactic use of anti-IL-6 antibodies significantly increased the survival of mice following SFTSV infection and, therefore, this treatment modality presents a novel therapeutic strategy for treating severe SFTS.