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Published on: May 21, 2018
Microplastics dysregulate innate immunity in the SARS-CoV-2 infected lung
Cameron R Bishop1, Kexin Yan1, Wilson Nguyen1
1Inflammation Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Microplastic (MP) beads did not affect SARS-CoV-2 omicron BA.5 viral load in mice. However, MP exposure altered immune responses, suppressing innate immunity early and increasing inflammation later, potentially mimicking cytokine release syndrome in COVID-19.
Area of Science:
- Environmental Health
- Immunology
- Toxicology
Background:
- Microplastic (MP) pollution is a global concern, with increasing evidence of human and animal exposure.
- Potential health impacts of microplastics, particularly in the context of respiratory infections, require further investigation.
Purpose of the Study:
- To investigate the effects of microplastic (MP) beads on the host response to SARS-CoV-2 omicron BA.5 infection in a mouse model.
- To analyze the impact of MPs on viral clearance, innate immunity, and inflammatory signatures during COVID-19.
Main Methods:
- A mouse model of mild COVID-19 was used, co-delivering 1 μm polystyrene MP beads with SARS-CoV-2 omicron BA.5.
- Histopathology and RNA-Seq were employed to analyze host response at 2 and 6 days post-infection (dpi).
Main Results:
- Microplastics did not significantly alter virus titres or RNA levels, despite reduced MP clearance from the lungs post-infection.
- RNA-Seq revealed suppressed innate immune responses at 2 dpi and increased pro-inflammatory signatures at 6 dpi.
- The observed cytokine profile at 6 dpi correlated with the 'cytokine release syndrome' signature in some COVID-19 patients.
Conclusions:
- Microplastic exposure can dysregulate inflammatory processes during viral infections.
- Findings suggest MPs may inhibit phagocytosis and alter immune cell function.
- Further research is needed to understand the long-term health implications of microplastic exposure in disease settings.
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