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Inflammation and remodeling in infantile, juvenile, and adult allergic sensitized mice
Author(s) -
Carnieli Denise S.,
Yoshioka Eliane,
Silva Luiz Fernando F.,
Lanças Tatiana,
Arantes Fernanda M.,
Perini Adenir,
Martins Milton A.,
Saldiva Paulo Hilário N.,
Dolhnikoff Marisa,
Mauad Thais
Publication year - 2011
Publication title -
pediatric pulmonology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.866
H-Index - 106
eISSN - 1099-0496
pISSN - 8755-6863
DOI - 10.1002/ppul.21436
Subject(s) - ovalbumin , eosinophil , medicine , mucus , juvenile , inflammation , airway , immunology , pathology , endocrinology , asthma , biology , immune system , anesthesia , ecology , genetics
Background Airway structural changes occur early in childhood asthma, but it is unknown whether the development of airway alterations in children is similar to that of adults. We compared inflammation and remodeling parameters in allergic sensitized infantile, juvenile, and adult mice. Methods Infantile mice (18D) were sensitized with three intraperitoneal injections (i.p.) of ovalbumin (OVA) at days 5 and 7 and challenged with OVA at days 14–16. The 18D1 group received an additional challenge at days 9–11. The juvenile mice (40D) received challenges at days 22–24 and 36–38. Adult mice (100D) were sensitized at days 60–62 and received three inhalations at days 77–79 and 96–98. Animals were submitted to whole body plethysmography. Airway eosinophils, CD3+ T‐lymphocytes, IL‐5+ cells, mucus content, collagen and reticular fibers density, and smooth muscle thickness were quantified. Results All sensitized animals presented with airway hyperresponsiveness, without differences in eosinophil cell density. The density of CD3+ T‐cells was higher in the 100D and 18D1 groups than in the 18D and 40D groups. Infantile sensitized groups demonstrated increased interleukin‐5 expression in the airways. Infantile mice demonstrated more mucus in the bronchiolar epithelium than the 40D and 100D mice. The 18D animals demonstrated less collagen than the 18D1 group. Juvenile and adult mice had increased airway smooth muscle thickness when compared to age‐matched controls, but no differences were observed in the infantile groups. Conclusion We have shown that infantile mice develop inflammatory and structural alterations in the airways that are partially different from those developed in older animals. Pediatr. Pulmonol. 2011; 46:650–665. © 2011 Wiley‐Liss, Inc.