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HTNV infection of CD8+ T cells is associated with disease progression in HFRS patients.

Abstract
Hantaan viruses (HTNVs) are zoonotic pathogens transmitted mainly by rodents and capable of infecting humans. Increasing knowledge of the human response to HTNV infection can guide the development of new preventative vaccines and therapeutic strategies. Here, we show that HTNV can infect CD8+ T cells in vivo in patients diagnosed with hemorrhagic fever with renal syndrome (HFRS). Electron microscopy-mediated tracking of the life cycle and ultrastructure of HTNV-infected CD8+ T cells in vitro showed an association between notable increases in cytoplasmic multivesicular bodies and virus production. Notably, based on a clinical cohort of 280 patients, we found that circulating HTNV-infected CD8+ T cell numbers in blood were proportional to disease severity. These results demonstrate that viral infected CD8+ T cells may be used as an adjunct marker for monitoring HFRS disease progression and that modulating T cell functions may be explored for new treatment strategies.
AuthorsRongrong Liu, Ruixue Ma, Ziyu Liu, Haifeng Hu, Jiayi Shu, Peizhen Hu, Junjun Kang, Yusi Zhang, Mingwei Han, Xiaoxiao Zhang, Yiting Zheng, Qikang Ying, Shiyuan Hou, Wenqiu Wang, Fang Wang, Ning Cheng, Yan Zhuang, Jianqi Lian, Xia Jin, Xingan Wu
JournalCommunications biology (Commun Biol) Vol. 4 Issue 1 Pg. 652 (06 02 2021) ISSN: 2399-3642 [Electronic] England
PMID34079056 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Cytokines
Topics
  • Acute Disease
  • Adult
  • CD8-Positive T-Lymphocytes (immunology, ultrastructure, virology)
  • Cell-Derived Microparticles (ultrastructure, virology)
  • Cytokines (blood)
  • Disease Progression
  • Female
  • Hantaan virus (immunology, pathogenicity, physiology)
  • Hemorrhagic Fever with Renal Syndrome (blood, immunology, virology)
  • Humans
  • In Vitro Techniques
  • Male
  • Microscopy, Electron, Transmission
  • Middle Aged
  • Models, Biological
  • Virion (immunology, pathogenicity)
  • Virus Replication

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