Key result
Severe EV-A71-associated HFMD was associated with lower peripheral monocyte counts, reduced MCP-1 secretion, and higher expression of immune exhaustion markers PD-1 and PD-L1 compared to mild cases.
Why the study?
A minority of enterovirus A71-associated hand, foot and mouth disease cases develop severe neural complications, but whether monocyte-mediated immunity is involved in disease progression remains unknown.
Is monocyte-mediated immunity, specifically MCP-1 secretion and immune exhaustion, associated with disease severity in EV-A71-infected HFMD?
Observational (n=223)
Is monocyte-mediated immunity, specifically MCP-1 secretion and immune exhaustion, associated with disease severity in EV-A71-infected HFMD?
Lower monocyte counts, reduced MCP-1 secretion, and increased immune exhaustion markers (PD-1/PD-L1) are associated with severe disease progression in EV-A71-infected HFMD.
Lower monocyte counts may flag severe EV-A71 HFMD risk; hypothesis-generating for monocyte immunity, pending prospective validation.
A minority of hand, foot and mouth disease (HFMD) caused by enterovirus A71 (EV-A71) results in severe neural complications. However, whether monocyte-mediated immunity is involved in the disease progression of HFMD remains unknown. One hundred and twenty mild and 103 severe HFMD patients were recruited and enzyme-linked immunosorbent assay (ELISA), flow cytometry and Transwell culture were performed in the study. Peripheral monocyte counts were lower in both absolute counts and frequencies in severe cases compared to mild cases. After screening 10 monocyte-related cytokines by ELISA, only monocyte chemoattractant protein-1 (MCP-1) was found at higher levels in sera of mild cases compared to those with severe symptoms. Monocytes purified from mild cases produced more MCP-1 than the cells from severe patients when stimulated in vitro. We observed that immune exhaustion markers programmed death 1 (PD-1) and programmed death ligand 1 (PD-L1) were highly regulated on the surface of monocytes from severe cases compared to mild cases. PD-L1 blockade induced a higher production of MCP-1 in the supernatant of a Transwell system. The production of MCP-1 also increased following PD-L1 blockade of purified monocytes activated by granulocyte-macrophage colony-stimulating factor (GM-CSF) combined with R848 or EV-A71 virus. Our results indicate that absolute count, frequency and levels of MCP-1 secretion of peripheral monocytes, together with their immune status, probably contribute to differential disease prognosis in EV-A71-associated HFMD.
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Pei et al. (2019) conducted an observational in Enterovirus A71-infected hand, foot and mouth disease (n=223). Severe HFMD vs. Mild HFMD was evaluated on Peripheral monocyte counts, MCP-1 levels, and immune exhaustion markers. Severe EV-A71-associated HFMD was associated with lower peripheral monocyte counts, reduced MCP-1 secretion, and higher expression of immune exhaustion markers PD-1 and PD-L1 compared to mild cases.
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