SFTSV infection is associated with transient overproliferation of monoclonal lambda-type plasma cells
Chuansong Quan1,2, Qinghua Liu3, Lijuan Yu2
1Department of Infectious Disease, The Second Affiliated Hospital of Shandong First Medical University, Taian 271000, China.
Abstract:
The impairment of antibody-mediated immunity is a major factor associated with fatal cases of severe fever with thrombocytopenia syndrome (SFTS). By collating the clinical diagnosis reports of 30 SFTS cases, we discovered the overproliferation of monoclonal plasma cells (MCP cells, CD38+cLambda+cKappa-) in bone marrow, which has only been reported previously in multiple myeloma. The ratio of CD38+cLambda+ versus CD38+cKappa+ in SFTS cases with MCP cells was significantly higher than that in normal cases. MCP cells presented transient expression in the bone marrow, which was distinctly different from multiple myeloma. Moreover, the SFTS patients with MCP cells had higher clinical severity. Further, the overproliferation of MCP cells was also observed in SFTS virus (SFTSV)-infected mice with lethal infectious doses. Together, SFTSV infection induces transient overproliferation of monoclonal lambda-type plasma cells, which have important implications for the study of SFTSV pathogenesis, prognosis, and the rational development of therapeutics.
Insights
Severe fever with thrombocytopenia syndrome (SFTS) involves abnormal antibody immunity. Researchers found monoclonal plasma cells in SFTS patients, indicating a potential new therapeutic target for this severe infectious disease.
Area of Science:
- Immunology
- Virology
- Hematology
Background:
- Antibody-mediated immunity impairment is linked to fatal severe fever with thrombocytopenia syndrome (SFTS).
- Monoclonal plasma cells (MCP cells) are typically associated with multiple myeloma, not infectious diseases.
Purpose of the Study:
- To investigate the presence and characteristics of monoclonal plasma cells in patients with SFTS.
- To explore the potential role of MCP cells in SFTS pathogenesis and clinical severity.
Main Methods:
- Analysis of clinical diagnosis reports from 30 SFTS patients.
- Flow cytometry to identify and quantify plasma cell populations (CD38+cLambda+cKappa-).
- Comparison of MCP cell ratios in SFTS patients versus normal cases and in SFTSV-infected mice.
Main Results:
- Overproliferation of monoclonal plasma cells (MCP cells) was identified in the bone marrow of SFTS patients.
- A significantly higher ratio of CD38+cLambda+ to CD38+cKappa+ cells was observed in SFTS patients with MCP cells compared to normal cases.
- MCP cells exhibited transient expression in SFTS, differing from multiple myeloma, and were associated with higher clinical severity.
- MCP cell overproliferation was also confirmed in SFTS virus (SFTSV)-infected mice.
Conclusions:
- SFTSV infection induces transient overproliferation of monoclonal lambda-type plasma cells.
- These findings have significant implications for understanding SFTSV pathogenesis and prognosis.
- The identification of MCP cells offers potential for developing targeted therapeutics for SFTS.
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