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Up-regulation of T lymphocyte and antibody production by inflammatory cytokines released by macrophage exposure to multi-walled carbon nanotubes
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References
2011
Year
EngineeringInflammatory Lung DiseaseLung InflammationImmunologyImmune RegulationProliferative ResponseImmunologic MechanismInnate ImmunityImmune SystemImmunotherapyInflammationNanomedicineImmunopathologyCarbon NanotubesInflammatory CytokinesImmune SurveillanceAutoimmunityT Cell ImmunityHumoral ImmunityImmune FunctionMacrophage ExposureInflammatory DiseaseCell BiologyPhagocyteCytokineImmune Cell DevelopmentMedicineMulti-walled Carbon Nanotubes
Our data demonstrate that multi-walled carbon nanotubes (MWCNTs) are internalized by macrophages, subsequently activating them to produce interleukin (IL)-12 (IL-12). This cytokine induced the proliferative response of T lymphocytes to a nonspecific mitogen and to ovalbumin (OVA). This increase in the proliferative response was accompanied by an increase in the expression of pro-inflammatory cytokines, such as interferon-gamma (IFNγ), tumor necrosis factor-alpha (TNFα) and IL-6, in mice inoculated with MWCNTs, whether or not they had been immunized with OVA. A decrease in the expression of transforming growth factor-beta (TGFβ) was observed in the mice treated with MWCNTs, whereas the suppression of the expression of both TGFβ and IL-10 was observed in mice that had been both treated and immunized. The activation of the T lymphocyte response by the pro-inflammatory cytokines leads to an increase in antibody production to OVA, suggesting the important immunostimulatory effect of carbon nanotubes.
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