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Effects of ultrafine particles on the allergic inflammation in the lung of asthmatics: results of a double-blinded randomized cross-over clinical pilot study.
Schaumann, Frank; Frömke, Cornelia; Dijkstra, Dorothea; Alessandrini, Francesca; Windt, Horst; Karg, Erwin; Müller, Meike; Winkler, Carla; Braun, Armin; Koch, Armin; Hohlfeld, Jens Michael; Behrendt, Heidrun; Schmid, Otmar; Koch, Wolfgang; Schulz, Holger; Krug, Norbert.
Afiliação
  • Schaumann F; Fraunhofer Institute for Toxicology and Experimental Medicine, Nikolai-Fuchs-Str. 1a, 30625, Hannover, Germany. Frank.Schaumann@mps-hamburg.com.
  • Frömke C; Hannover Medical School, Hannover, Germany. Cornelia.Froemke@tiho-hannover.de.
  • Dijkstra D; Fraunhofer Institute for Toxicology and Experimental Medicine, Nikolai-Fuchs-Str. 1a, 30625, Hannover, Germany. dijkstra.dorothea@mh-hannover.de.
  • Alessandrini F; Hannover Medical School, Hannover, Germany. dijkstra.dorothea@mh-hannover.de.
  • Windt H; Center of Allergy and Environment (ZAUM), Technische Universität and Helmholtz Zentrum München, Member of the German Center for Lung research (DZL), Munich, Germany, Munich, Germany. franci@helmholtz-muenchen.de.
  • Karg E; Fraunhofer Institute for Toxicology and Experimental Medicine, Nikolai-Fuchs-Str. 1a, 30625, Hannover, Germany. horst.windt@item.fraunhofer.de.
  • Müller M; Cooperationgroup Comprehensive Molecular Analytics (CMA), Joint Mass Spectrometry Centre (JMSC), Helmholtz Zentrum München, Munich, Germany. karg@helmholtz-muenchen.de.
  • Winkler C; Fraunhofer Institute for Toxicology and Experimental Medicine, Nikolai-Fuchs-Str. 1a, 30625, Hannover, Germany. meike.mueller@item.fraunhofer.de.
  • Braun A; Fraunhofer Institute for Toxicology and Experimental Medicine, Nikolai-Fuchs-Str. 1a, 30625, Hannover, Germany. carla.winkler@astrazeneca.com.
  • Koch A; Hannover Medical School, Hannover, Germany. carla.winkler@astrazeneca.com.
  • Hohlfeld JM; Fraunhofer Institute for Toxicology and Experimental Medicine, Nikolai-Fuchs-Str. 1a, 30625, Hannover, Germany. armin.braun@item.fraunhofer.de.
  • Behrendt H; Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), Member of the German Center for Lung Research, Hannover, Germany. armin.braun@item.fraunhofer.de.
  • Schmid O; Hannover Medical School, Hannover, Germany. koch.armin@mh-hannover.de.
  • Koch W; Fraunhofer Institute for Toxicology and Experimental Medicine, Nikolai-Fuchs-Str. 1a, 30625, Hannover, Germany. jens.hohlfeld@item.fraunhofer.de.
  • Schulz H; Hannover Medical School, Hannover, Germany. jens.hohlfeld@item.fraunhofer.de.
  • Krug N; Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), Member of the German Center for Lung Research, Hannover, Germany. jens.hohlfeld@item.fraunhofer.de.
Part Fibre Toxicol ; 11: 39, 2014 Sep 10.
Article em En | MEDLINE | ID: mdl-25204642
ABSTRACT

BACKGROUND:

Epidemiological and experimental studies suggest that exposure to ultrafine particles (UFP) might aggravate the allergic inflammation of the lung in asthmatics.

METHODS:

We exposed 12 allergic asthmatics in two subgroups in a double-blinded randomized cross-over design, first to freshly generated ultrafine carbon particles (64 µg/m³; 6.1 ± 0.4 × 105 particles/cm³ for 2 h) and then to filtered air or vice versa with a 28-day recovery period in-between. Eighteen hours after each exposure, grass pollen was instilled into a lung lobe via bronchoscopy. Another 24 hours later, inflammatory cells were collected by means of bronchoalveolar lavage (BAL). ( TRIAL REGISTRATION NCT00527462)

RESULTS:

For the entire study group, inhalation of UFP by itself had no significant effect on the allergen induced inflammatory response measured with total cell count as compared to exposure with filtered air (p = 0.188). However, the subgroup of subjects, which inhaled UFP during the first exposure, exhibited a significant increase in total BAL cells (p = 0.021), eosinophils (p = 0.031) and monocytes (p = 0.013) after filtered air exposure and subsequent allergen challenge 28 days later. Additionally, the potential of BAL cells to generate oxidant radicals was significantly elevated at that time point. The subgroup that was exposed first to filtered air and 28 days later to UFP did not reveal differences between sessions.

CONCLUSIONS:

Our data demonstrate that pre-allergen exposure to UFP had no acute effect on the allergic inflammation. However, the subgroup analysis lead to the speculation that inhaled UFP particles might have a long-term effect on the inflammatory course in asthmatic patients. This should be reconfirmed in further studies with an appropriate study design and sufficient number of subjects.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia / Hipersensibilidade Respiratória / Asma / Exposição por Inalação / Poluentes Atmosféricos / Material Particulado / Pulmão Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pneumonia / Hipersensibilidade Respiratória / Asma / Exposição por Inalação / Poluentes Atmosféricos / Material Particulado / Pulmão Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2014 Tipo de documento: Article