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Airway dendritic cell maturation in children exposed to air pollution.
Whitehouse, Abigail L; Mushtaq, Naseem; Miyashita, Lisa; Barratt, Benjamin; Khan, Ameerah; Kalsi, Harpal; Koh, Lee; Padovan, Michele G; Brugha, Rossa; Balkwill, Frances R; Stagg, Andrew J; Grigg, Jonathan.
Afiliação
  • Whitehouse AL; Centre for Genomics and Child Health, Queen Mary University of London, London, United Kingdom.
  • Mushtaq N; Centre for Genomics and Child Health, Queen Mary University of London, London, United Kingdom.
  • Miyashita L; Centre for Genomics and Child Health, Queen Mary University of London, London, United Kingdom.
  • Barratt B; King's College London, London, United Kingdom.
  • Khan A; Centre of the Cell, Queen Mary University of London, London, United Kingdom.
  • Kalsi H; Centre for Genomics and Child Health, Queen Mary University of London, London, United Kingdom.
  • Koh L; Centre for Genomics and Child Health, Queen Mary University of London, London, United Kingdom.
  • Padovan MG; Centre for Genomics and Child Health, Queen Mary University of London, London, United Kingdom.
  • Brugha R; Centre for Genomics and Child Health, Queen Mary University of London, London, United Kingdom.
  • Balkwill FR; King's College London, London, United Kingdom.
  • Stagg AJ; Barts Cancer Institute, Queen Mary University of London, United Kingdom.
  • Grigg J; Centre for Immunobiology, Queen Mary University of London, London, United Kingdom.
PLoS One ; 15(5): e0232040, 2020.
Article em En | MEDLINE | ID: mdl-32369498
ABSTRACT
Urban particulate matter (PM) enhances airway dendritic cell (DC) maturation in vitro. However, to date, there are no data on the association between exposure to urban PM and DC maturation in vivo. We sought to determine whether exposure of school-age children (8 to 14 y) to PM was associated with expression of CD86, a marker of maturation of airway conventional DCs (cDC). Healthy London school children underwent spirometry and sputum induction. Flow cytometry was used to identify CD86 and CCR7 expression on cDC subsets (CD1c+ cDC2 and CD141+ cDC1). Tertiles of mean annual exposure to PM ≤ 10 microns (PM10) at the school address were determined using the London Air Quality Toolkit model. Tertiles of exposure from the 409 children from 19 schools recruited were; lower (23.1 to 25.6 µg/m3, n = 138), middle (25.6 to 26.8 µg/m3, n = 126), and upper (26.8 to 31.0 µg/m3, n = 145). DC expression was assessed in 164/370 (44%) children who completed sputum induction. The proportion (%) of cDC expressing CD86 in the lower exposure tertile (n = 47) was lower compared with the upper exposure tertile (n = 49); (52% (44 to 70%) vs 66% (51 to 82%), p<0.05). There was a higher percentage of cDC1 cells in the lower tertile of exposure (6.63% (2.48 to 11.64) vs. 2.63% (0.72 to 7.18), p<0.05). Additionally; children in the lower exposure tertile had increased FEV1 compared with children in the upper tertile; (median z-score 0.15 (-0.59 to 0.75) vs. -0.21 (-0.86 to 0.48), p<0.05. Our data reveal that children attending schools in the highest areas of PM exposure in London exhibit increased numbers of "mature" airway cDCs, as evidenced by their expression of the surface marker CD86. This data is supportive of previous in vitro data demonstrating an alteration in the maturation of airway cDCs in response to exposure to pollutants.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células Dendríticas / Poluentes Atmosféricos / Antígeno B7-2 / Material Particulado Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células Dendríticas / Poluentes Atmosféricos / Antígeno B7-2 / Material Particulado Idioma: En Ano de publicação: 2020 Tipo de documento: Article