IL-27-mediated hematopoietic dysregulation exacerbates disease severity in Severe Fever with Thrombocytopenia Syndrome Virus infection 3316

Abstract Description Severe Fever with Thrombocytopenia Syndrome (SFTS) is a life-threatening tick-borne viral infection characterized by high fever, thrombocytopenia, and severe inflammation, with no effective treatments currently available. Through comprehensive analysis of bone marrow and peripheral blood mononuclear cells from SFTS patients, and validation in a mouse model, we identified IL-27 as a key driver of disease progression. Elevated IL-27 levels promote emergency hematopoiesis and impair protective B cell development and antibody production, resulting in worsened inflammation and ineffective viral control. IL-27 induction in monocytes and B cells triggers a vicious inflammatory cycle, exacerbating the severity of SFTS. Neutralizing IL-27 in the mouse model significantly improved survival, reduced viral loads, and restored anti-viral immunity, highlighting IL-27 as a promising therapeutic target for SFTS. Topic Categories Viral Immunology (VIR)

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Publication Details

Journal
The Journal of Immunology
Published
2025-11-01
DOI
https://doi.org/10.1093/jimmun/vkaf283.1132
Primary Topic
Viral Infections and Vectors
Type
article
Field-Weighted Citation Impact
0.00
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article

IL-27-mediated hematopoietic dysregulation exacerbates disease severity in Severe Fever with Thrombocytopenia Syndrome Virus infection 3316

Nam‐Hyuk Cho, Kyeongseok Jeon, Kim Ys, Hyo-Jin Ro
The Journal of Immunology
Viral Infections and Vectors
article

IL-27-mediated hematopoietic dysregulation exacerbates disease severity in Severe Fever with Thrombocytopenia Syndrome Virus infection 3316

Nam‐Hyuk Cho, Kyeongseok Jeon, Kim Ys, Hyo-Jin Ro
article en

Abstract

Abstract Description Severe Fever with Thrombocytopenia Syndrome (SFTS) is a life-threatening tick-borne viral infection characterized by high fever, thrombocytopenia, and severe inflammation, with no effective treatments currently available. Through comprehensive analysis of bone marrow and peripheral blood mononuclear cells from SFTS patients, and validation in a mouse model, we identified IL-27 as a key driver of disease progression. Elevated IL-27 levels promote emergency hematopoiesis and impair protective B cell development and antibody production, resulting in worsened inflammation and ineffective viral control. IL-27 induction in monocytes and B cells triggers a vicious inflammatory cycle, exacerbating the severity of SFTS. Neutralizing IL-27 in the mouse model significantly improved survival, reduced viral loads, and restored anti-viral immunity, highlighting IL-27 as a promising therapeutic target for SFTS. Topic Categories Viral Immunology (VIR)

The Journal of ImmunologyVol. 214(Supplement_1)
Seoul National University (KR), New Generation University College (ET)
Openalex Percentile: Top 58%
Viral Infections and Vectors
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