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Deficient humoral responses and disrupted B-cell immunity are associated with fatal SFTSV infection

Severe Fever with Thrombocytopenia Syndrome (SFTS), an emerging infectious disease caused by a novel phlebovirus, is associated with high fatality. Therapeutic interventions are lacking and disease pathogenesis is yet to be fully elucidated. The anti-viral immune response has been reported, but humo...

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Detalles Bibliográficos
Autores principales: Song, Peixin, Zheng, Nan, Liu, Yong, Tian, Chen, Wu, Xilin, Ma, Xiaohua, Chen, Deyan, Zou, Xue, Wang, Guiyang, Wang, Huanru, Zhang, Yongyang, Lu, Sufang, Wu, Chao, Wu, Zhiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6102208/
https://www.ncbi.nlm.nih.gov/pubmed/30127439
http://dx.doi.org/10.1038/s41467-018-05746-9
Descripción
Sumario:Severe Fever with Thrombocytopenia Syndrome (SFTS), an emerging infectious disease caused by a novel phlebovirus, is associated with high fatality. Therapeutic interventions are lacking and disease pathogenesis is yet to be fully elucidated. The anti-viral immune response has been reported, but humoral involvement in viral pathogenesis is poorly understood. Here we show defective serological responses to SFTSV is associated with disease fatality and a combination of B-cell and T-cell impairment contribute to disruption of anti-viral immunity. The serological profile in deceased patients is characterized by absence of specific IgG to viral nucleocapsid and glycoprotein due to failure of B-cell class switching. Expansion and impairment of antibody secretion is a signature of fatal SFTSV infection. Apoptosis of monocytes in the early stage of infection diminishes antigen-presentation by dendritic cells, impedes differentiation and function of T follicular helper cells, and contributes to failure of the virus-specific humoral response.