RT Journal Article
SR Electronic
T1 Comparison of two murine models of acute and chronic hypersensitivity pneumonitis due to pigeon serum exposure
JF European Respiratory Journal
JO Eur Respir J
FD European Respiratory Society
SP PA4113
DO 10.1183/13993003.congress-2015.PA4113
VO 46
IS suppl 59
A1 Sánchez-Ortiz, Mónica
A1 Cruz, María-Jesús
A1 Untoria, María-Dolores
A1 Villar, Ana
A1 Morell, Ferran
A1 Ollé-Monge, Marta
A1 Muñoz, Xavier
YR 2015
UL http://erj.ersjournals.com/content/46/suppl_59/PA4113.abstract
AB Introduction: The aim of the study was to compare two murine models of hypersensitivity pneumonitis (HP), one acute and one chronic, with a view to their future use for studying the pathogenesis of this disease.Materials and methods: C57BL/6 mice were used. Two intraperitoneal injections of 100 µL of commercial pigeon serum (200 µg protein/ml) or saline were administered with an interval of 48 h in between. Subsequently, intranasal instillations of 40 µL of pigeon serum (200 µg protein/ml) or saline were performed three days a week, for three weeks in the acute model and for 12 weeks in the chronic model. Lung inflammation in bronchoalveolar lavage (BAL), lung function and values of specific IgG in serum were evaluated 24 hours, 7 days and 14 days after the last exposure.Results: The number of total cells in BAL was significantly higher after 24 hours post-inhalation in the chronic model (mean ± SD (cells x105) = 5.21 ± 2.84) compared to the acute model (mean ± SD (cells x105) = 2.73 ± 1.51), p = 0.006. As regards lung function, a decrease in TLC was observed in both models: it returned to normal levels in the acute model at 14 days but remained unchanged in the chronic model over time (p <0.001). An increase in specific IgG in serum measured in optical density at 450 nm was observed in both models, and was higher in the chronic model (means at 24h = 1.90 and 2.68 in the acute and chronic models respectively; p = 0.003).Conclusions: The chronic model of HP described here presents a higher inflammation and involvement of lung function than the acute HP model. These models may serve as a tool for future studies of the pathogenesis of HP.Study funded by FUCAP and SEPAR.