TABLE 3

Immune responses and potential effects induced by particulate matter with a diameter ≤2.5 μm (PM2.5) on viral infections

Experimental platformPM2.5 exposure time#PathogenImmune responseReference
Immune responses/effects enhanced by PM2.5 on virus infection
 BALB/c miceShort-termCoxsackievirus B3PM2.5 enhances Treg cell and IL-6, TNF-α and TGF-β[99]
 Murine modelShort-termInfluenza A virusPM2.5 increases secreted IL-6, IL-1β and IFN-β in the lungs[100]
 C57BL/6long-termSARS-CoV-2PM2.5 increases TNF-α, TGF-β1 and IL-6 in the lungs[118]
 BABL/c miceLong-term
(>1 week)
Influenza A virusPM2.5 drives influenza A virus deep into the lower respiratory tract and distant organs[119]
Immune responses reduced by PM2.5 on virus infection
 Macrophage isolated from  C57BL/6 miceShort-termInfluenza A virusPM2.5 decreases IL-1β and IFN-β production[72]
 A549 cellsShort-termVesicular stomatitis virusPM2.5 degrades p-IRF3 via ubiquitination, resulting in decreased IFN-β levels and promoting viral replication[111]
 C57BL/6 miceLong-term
(3 days)
Influenza A virusPM2.5 decreases IL-1β and IFN-β production[72]
 Murine modelLong-term
(2 weeks)
Influenza A virusPM2.5 suppresses influenza A-induced secreted IL-6, IL-1β and IFN-β in the lungs[100]

#: Short-term exposure: exposure to PM2.5 within 24 h; long-term exposure: exposure to PM2.5 for more than 24 h. IFN-β: interferon-β; IL: interleukin; p-IRF3: phosphorylated interferon regulatory factor 3; SARS-CoV-2: severe acute respiratory syndrome coronavirus 2; TGF: transforming growth factor; TNF-α: tumour necrosis factor-α; Treg: regulatory T-cell.