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. 2018 Jun 28;315(4):L485–L501. doi: 10.1152/ajplung.00211.2018

Table 3.

Experimental evidence of OP-induced inflammation and immune modulation

OP Model Exposure Paradigm Key Findings Reference
Multiple Occupationally exposed human serum na ↑Incidence of upper respiratory infections in applicators, ↓serum neutrophil chemotaxis (104)
MAL Mouse Oral; chronic 0.1–100 mg·kg−1·day−1, 14 days acute 450–600 mg/kg ↑Macrophage activity and mast cell degranulation (191, 193)
CPF Rat Oral; 10 or 25 mg/kg Systemic ↑ in TNF-α and core body temperature (198)
Sarin Rat Inhalation; 0.2 or 0.4 mg/m3 for 1 h/day; 1, 5 or 10 days ↑Expression of IL-1β, TNF-α, IL-6 mRNA in brain (103)
CPF Primary human fetal astrocytes 25 µM; 7 days ↑Transcripts of IL-6, GFAP, MAPK (158)
BRP Mouse, dermal challenge and LLNA Dermal sensitization (0.3%); dermal or intrathecal challenge (0.03 or 0.003%); LLNA 0.1–3% ↑Inflammatory cells and IFN-γ (87)
PTH Mouse, LLNA Oral; 0.4–1.2 mg/kg ↑Allergic potential of environmental allergens; ↑TH1 cytokines (86)
PTH Mouse OVA allergic inflammation model Oral; 0.15 or 15 mg·kg−1·day−1, 5 days Exacerbated allergic inflammation; ↑IgE, cytokines, chemokines, and eosinophilia (169)
CPF, methyl-PTH HepG2 cells 2–8 µM, 24–72 h ↓PON1 mRNA and protein, increased inflammatory cytokines (157)
CPF/CPO Human blood in vitro 1–1,000 µg/ml CPO ↑IFN-γ response to LPS (60)

BRP, bromofos; CPF, chlorpyrifos; CPO, chlorpyrifos-oxon; GFAP, glial fibrillary acidic protein; LLNA, local lymph node assay; MAL, malathion; na, not applicable; OP, organophosphorus pesticide; OVA, ovalbumin; PON1, paraoxonase 1; PTH, parathion.