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  • 标题:SARS-CoV-2 and helminth co-infections, and environmental pollution exposure: An epidemiological and immunological perspective
  • 本地全文:下载
  • 作者:Pragalathan Naidoo ; Terisha Ghazi ; Anil A. Chuturgoon
  • 期刊名称:Environment International
  • 印刷版ISSN:0160-4120
  • 电子版ISSN:1873-6750
  • 出版年度:2021
  • 卷号:156
  • 页码:106695
  • DOI:10.1016/j.envint.2021.106695
  • 出版社:Pergamon
  • 摘要:Soil-transmitted helminths infect billions of people globally, particularly those residing in low- and middle-income regions with poor environmental sanitation and high levels of air and water pollution. Helminths display potent immunomodulatory activity by activating T helper type 2 (Th2) anti-inflammatory and Th3 regulatory immune responses. The Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), the virus that causes Coronavirus disease 2019 (COVID-19), can exacerbate Th1/Th17 pro-inflammatory cytokine production in humans, leading to a cytokine storm. Air pollutants (particulate matter, oxygen radicals, hydrocarbons and volatile organic compounds) and water pollutants (metals and organic chemicals) can also intensify Th1/Th17 immune response and could exacerbate SARS-CoV-2 related respiratory distress and failure. The present review focused on the epidemiology of SARS-CoV-2, helminths and fine particulate matter 2.5 µm or less in diameter (PM 2.5 ) air pollution exposure in helminth endemic regions, the possible immunomodulatory activity of helminths against SARS-CoV-2 hyper-inflammatory immune response, and whether air and water pollutants can further exacerbate SARS-CoV-2 related cytokine storm and in the process hinder helminths immunomodulatory functionality. Helminth Th2/Th3 immune response is associated with reductions in lung inflammation and damage, and decreased expression levels of angiotensin-converting enzyme 2 (ACE2) receptors (SARS-CoV-2 uses the ACE2 receptors to infect cells and associated with extensive lung damage). However, air pollutants are associated with overexpression of ACE2 receptors in the epithelial cell surface of the respiratory tract and exhaustion of Th2 immune response. Helminth-induced immunosuppression activity reduces vaccination efficacy, and diminishes vital Th1 cytokine production immune responses that are crucial for combating early stage infections. This could be reversed by continuous air pollution exposure which is known to intensify Th1 pro-inflammatory cytokine production to a point where the immunosuppressive activities of helminths could be hindered. Again, suppressed activities of helminths can also be disadvantageous against SARS-CoV-2 inflammatory response. This “yin and yang” approach seems complex and requires more understanding. Further studies are warranted in a cohort of SARS-CoV-2 infected individuals residing in helminths and air pollution endemic regions to offer more insights, and to impact mass periodic deworming programmes and environmental health policies.
  • 关键词:SARS-CoV-2;COVID-19 ; Environmental pollution ; Th1/Th17-induced pro-inflammatory immune response ; Cytokine storm ; Helminth-induced Th2/Th3 anti-inflammatory immune response ; Immunomodulatory activity of helminths ; ACE2 angiotensin-converting enzyme 2 ; ADCC antibody-dependent cellular cytotoxicity ; AREG amphiregulin ; AT1/AT2 alveolar type 1/2 ; BCG bacillus Calmette–Guérin ; CCL chemokine (C-C motif) ligand ; CO carbon monoxide ; COVID-19 coronavirus disease 2019 ; CXCL chemokine (C-X-C motif) ligand ; EGF epidermal growth factor ; G-CSF granulocyte colony-stimulating factor ; GM-CSF granulocyte-macrophage colony-stimulating factor ; IFN-γ interferon gamma ; IgE immunoglobulin E ; IgG immunoglobulin G ; IL interleukin ; MCP monocyte chemotactic protein ; MIP macrophage inflammatory protein ; NO 2 nitrogen dioxide ; O 3 ozone ; PDGF platelet-derived growth factor ; PM particulate matter ; RANTES regulated upon activation; normal T cell expressed and presumably secreted ; SARS-CoV-2 severe acute respiratory syndrome coronavirus 2 ; sCD40L soluble CD40 ligand ; SDF1 stromal cell-derived factor 1 ; sICAM-1 soluble intercellular adhesion molecule-1 ; SO 2 sulphur dioxide ; sVCAM-1 soluble Vascular Cell Adhesion Molecule-1 ; TGF-β transforming growth factor beta ; Th1/Th17 T helper cell 1/17 ; TMPRSS2 transmembrane protease serine 2 ; TNF-α tumour necrosis factor alpha ; Tregs regulatory T cells ; TSLP thymic stromal lymphopoietin ; VEGF vascular endothelial growth factor
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