| Literature DB >> 31904586 |
Tadaki Suzuki1, Yuko Sato1, Kaori Sano1,2, Takeshi Arashiro1, Harutaka Katano1, Noriko Nakajima1, Masayuki Shimojima3, Michiyo Kataoka1, Kenta Takahashi1, Yuji Wada1, Shigeru Morikawa4, Shuetsu Fukushi3, Tomoki Yoshikawa3, Masayuki Saijo3, Hideki Hasegawa1,2,5.
Abstract
Severe fever with thrombocytopenia syndrome (SFTS) is an emerging hemorrhagic fever caused by a tick-borne banyangvirus and is associated with high fatality. Despite increasing incidence of SFTS and serious public health concerns in East Asia, the pathogenesis of lethal SFTS virus (SFTSV) infection in humans is not fully understood. Numbers of postmortem examinations to determine target cells of the viral infection have so far been limited. Here we showed that B cells differentiating into plasmablasts and macrophages in secondary lymphoid organs were targets for SFTSV at the end stage of lethal infection, and the majority of SFTSV-infected cells were B cell-lineage lymphocytes. In affected individuals, B cell-lineage lymphocytes with SFTSV infection were widely distributed in both lymphoid and nonlymphoid organs, and infiltration of these cells into the capillaries of the organs could be observed occasionally. Moreover, a human plasmablastic lymphoma cell line, PBL-1, was susceptible to SFTSV propagation and had a similar immunophenotype to that of target cells of SFTSV in fatal SFTS. PBL-1 can therefore provide a potential in vitro model for human SFTSV infection. These results extend our understanding of the pathogenesis of human lethal SFTSV infection and can facilitate the development of SFTSV countermeasures.Entities:
Keywords: B cells; Infectious disease; Virology
Mesh:
Year: 2020 PMID: 31904586 PMCID: PMC6994144 DOI: 10.1172/JCI129171
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808