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HTNV infection of CD8 + T cells is associated with disease progression in HFRS patients.
- Source :
-
Communications biology [Commun Biol] 2021 Jun 02; Vol. 4 (1), pp. 652. Date of Electronic Publication: 2021 Jun 02. - Publication Year :
- 2021
-
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 <superscript>+</superscript> 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 <superscript>+</superscript> 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 <superscript>+</superscript> T cell numbers in blood were proportional to disease severity. These results demonstrate that viral infected CD8 <superscript>+</superscript> 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.
- Subjects :
- Acute Disease
Adult
CD8-Positive T-Lymphocytes ultrastructure
Cell-Derived Microparticles ultrastructure
Cell-Derived Microparticles virology
Cytokines blood
Disease Progression
Female
Hantaan virus physiology
Hemorrhagic Fever with Renal Syndrome blood
Humans
In Vitro Techniques
Male
Microscopy, Electron, Transmission
Middle Aged
Models, Biological
Virion immunology
Virion pathogenicity
Virus Replication
CD8-Positive T-Lymphocytes immunology
CD8-Positive T-Lymphocytes virology
Hantaan virus immunology
Hantaan virus pathogenicity
Hemorrhagic Fever with Renal Syndrome immunology
Hemorrhagic Fever with Renal Syndrome virology
Subjects
Details
- Language :
- English
- ISSN :
- 2399-3642
- Volume :
- 4
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Communications biology
- Publication Type :
- Academic Journal
- Accession number :
- 34079056
- Full Text :
- https://doi.org/10.1038/s42003-021-02182-2