PMID- 16839409 OWN - NLM STAT- MEDLINE DCOM- 20070222 LR - 20071115 IS - 0954-7894 (Print) IS - 0954-7894 (Linking) VI - 36 IP - 7 DP - 2006 Jul TI - Surfactant protein D inhibits early airway response in Aspergillus fumigatus-sensitized mice. PG - 930-40 AB - BACKGROUND: The surfactant protein SP-D has been reported to reduce bronchial hyper-responsiveness, blood eosinophilia, and T-helper type 2 cytokines in models of allergic asthma. However, little is known about the functional effect of SP-D on the early airway response upon allergen inhalation, which is an important feature of this disease. OBJECTIVE: We investigated whether SP-D is able to reduce the immediate allergen-induced mediator release and the early bronchial obstruction in addition to its effects on airway inflammation and bronchial hyperresponsiveness in an Aspergillus fumigatus mouse asthma model. METHODS: A. fumigatus-sensitized mice were treated with a recombinant fragment of human SP-D or placebo. Lung functions were measured in orotracheally intubated, spontaneously breathing animals using body plethysmography. In addition, passively sensitized precision-cut lung slices (PCLS) were used to determine the effect of SP-D on allergen-induced histamine release. RESULTS: SP-D inhibited the allergen-induced early airway response and reduced airway hyperresponsiveness compared with placebo. Eosinophilia in bronchoalveolar lavage and lung tissue was reduced after SP-D treatment, possibly by reducing eotaxin levels in the lung. Furthermore, SP-D treatment reduced the allergen-induced histamine release from PCLS. CONCLUSION: These data suggest that SP-D not only reduces allergen-induced eosinophilic inflammation and airway hyperresponsiveness but also provides protection against early airway obstruction by inhibition of early mediator release. FAU - Erpenbeck, V J AU - Erpenbeck VJ AD - Fraunhofer Institute of Toxicology and Experimental Medicine, Hannover, Germany. FAU - Ziegert, M AU - Ziegert M FAU - Cavalet-Blanco, D AU - Cavalet-Blanco D FAU - Martin, C AU - Martin C FAU - Baelder, R AU - Baelder R FAU - Glaab, T AU - Glaab T FAU - Braun, A AU - Braun A FAU - Steinhilber, W AU - Steinhilber W FAU - Luettig, B AU - Luettig B FAU - Uhlig, S AU - Uhlig S FAU - Hoymann, H G AU - Hoymann HG FAU - Krug, N AU - Krug N FAU - Hohlfeld, J M AU - Hohlfeld JM LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - England TA - Clin Exp Allergy JT - Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology JID - 8906443 RN - 0 (Allergens) RN - 0 (Antigens, Fungal) RN - 0 (CCL11 protein, human) RN - 0 (Ccl11 protein, mouse) RN - 0 (Chemokine CCL11) RN - 0 (Chemokines, CC) RN - 0 (Interleukin-5) RN - 0 (Pulmonary Surfactant-Associated Protein D) RN - 0 (Recombinant Proteins) RN - 37341-29-0 (Immunoglobulin E) SB - IM MH - Administration, Inhalation MH - Allergens/*immunology MH - Animals MH - Antigens, Fungal/immunology MH - Aspergillus fumigatus/*immunology MH - Asthma/immunology/metabolism/*prevention & control MH - Bronchial Hyperreactivity/immunology/metabolism/prevention & control MH - Bronchoalveolar Lavage Fluid/cytology/immunology MH - Chemokine CCL11 MH - Chemokines, CC/metabolism MH - Disease Models, Animal MH - Drug Evaluation, Preclinical MH - Eosinophilia/prevention & control MH - Female MH - Histamine Release/drug effects MH - Immunoglobulin E/blood MH - Interleukin-5/metabolism MH - Lung/metabolism MH - Lung Compliance MH - Mice MH - Mice, Inbred BALB C MH - Pulmonary Surfactant-Associated Protein D/pharmacokinetics/*therapeutic use MH - Recombinant Proteins/therapeutic use EDAT- 2006/07/15 09:00 MHDA- 2007/02/23 09:00 CRDT- 2006/07/15 09:00 PHST- 2006/07/15 09:00 [pubmed] PHST- 2007/02/23 09:00 [medline] PHST- 2006/07/15 09:00 [entrez] AID - CEA2524 [pii] AID - 10.1111/j.1365-2222.2006.02524.x [doi] PST - ppublish SO - Clin Exp Allergy. 2006 Jul;36(7):930-40. doi: 10.1111/j.1365-2222.2006.02524.x.