Modification of Acute and Late-Phase Allergic Responses to Ovalbumin with Lipopolysaccharide
- 1 October 2002
- journal article
- research article
- Published by S. Karger AG in International Archives of Allergy and Immunology
- Vol. 129 (2) , 119-128
- https://doi.org/10.1159/000065881
Abstract
Background: We have previously shown that lipopolysaccharide (LPS) exposure in sensitised animals 18 h after ovalbumin (OVA) challenge inhibits OVA-induced airway hyper-responsiveness (AHR). In the present study, we investigated the effect of LPS on OVA-induced acute and late-phase allergic responses in sensitised rats when challenged with OVA. Methods: Rats were sensitised with OVA and 11 days later challenged with 1% OVA in the presence or absence of LPS (0.5–50 µg/ml) given in the same nebulizer. Acute responses to OVA were measured each minute for 30 min after challenge. In a separate group of animals, late-phase responses to OVA were determined at 24 h. At the end of each study, Evans blue dye was injected and animals sacrificed 30 min later. Bronchoalveolar lavage was obtained to monitor inflammatory cell migration and microvascular leakage. Results: OVA challenge in sensitised animals produced an acute response with changes in lung mechanics peaking 10.0 ± 0.9 min after OVA and returning to baseline within 30 min. This was followed 24 h later by increased responses to methacholine chloride (MCh), inflammatory cell influx and increased Evans blue leakage into the lungs. Presence of 5 or 50 µg/ml LPS in the nebulizer during OVA challenge altered the kinetics of the acute-phase response, with an immediate decrease in lung function (time to peak decreased from 10.3 ± 1.2 to 1.8 ± 0.2 and 2.2 ± 0.3 min, respectively: p < 0.001, n = 6) and a dose-dependent attenuation of late-phase AHR, cellular influx (n = 5, p < 0.001) and Evans blue leakage (n = 5, p < 0.001) at 24 h. Conclusions: In summary, co-administration of OVA with LPS modifies both the acute and late-phase responses to the allergen, inducing an earlier acute change in lung function and a dose-dependent inhibition of late-phase responses to the allergen.Keywords
This publication has 6 references indexed in Scilit:
- Reduced risk of hay fever and asthma among children of farmersClinical and Experimental Allergy, 2000
- Mitochondrial toxicity induced by nucleoside-analogue reverse-transcriptase inhibitors is a key factor in the pathogenesis of antiretroviral-therapy-related lipodystrophyThe Lancet, 1999
- The expanding universe of T-cell subsets: Th1, Th2 and morePublished by Elsevier ,1999
- Effect of mast cell granules on the gene expression of nitric oxide synthase and tumour necrosis factor‐α in macrophagesMediators of Inflammation, 1998
- Interleukin 10 (IL-10) and viral IL-10 strongly reduce antigen-specific human T cell proliferation by diminishing the antigen-presenting capacity of monocytes via downregulation of class II major histocompatibility complex expression.The Journal of Experimental Medicine, 1991
- Interleukin 10: a novel stimulatory factor for mast cells and their progenitors.The Journal of Experimental Medicine, 1991