Does Lipophilicity Per Se Induce Adjuvant Effects? Methyl Palmitate as Model Substance Does Not Affect Ovalbumin Sensitization

• Published in: Journal of Toxicology and Environmental Health, Part A Vol. 70; no. 2; pp. 128 - 137
• Main Authors: Stilund Hansen, Jitka, Thor Larsen, Søren, Poulsen, Lars K., Damgård Nielsen, Gunnar
• Format: Journal Article
• Language: English
• Published: England Taylor & Francis Group 01-01-2007
• Subjects: Adjuvants, Immunologic - pharmacokinetics; Adjuvants, Immunologic - toxicity; Aerosols; Allergens - administration & dosage; Allergens - immunology; Allergens - pharmacokinetics; Animals; Bronchoalveolar Lavage Fluid - cytology; Female; Gastrointestinal Tract - metabolism; Immunoglobulin E - blood; Immunoglobulin E - immunology; Immunoglobulin G - blood; Immunoglobulin G - immunology; Leukocyte Count; Mice; Mice, Inbred BALB C; Ovalbumin - administration & dosage; Ovalbumin - immunology; Ovalbumin - pharmacokinetics; Palmitates - pharmacokinetics; Palmitates - toxicity; Particle Size; Respiration - drug effects; Respiratory Hypersensitivity - blood; Respiratory Hypersensitivity - chemically induced; Respiratory Hypersensitivity - immunology; Respiratory System - drug effects; Respiratory System - immunology; Respiratory System - metabolism
• ISSN: 1528-7394; 1087-2620
• DOI: 10.1080/15287390600755083

Anthopogenically introduced substances and pollutants are suspected to promote senstitization and development of allergic airway diseases, that is, acting as adjuvants. Lipophilicity may serve as an immunological warning signal, promoting adjuvant effects. Whether the lipophilicity of an inhaled compound induces immunomodulatory effects was investigated in a murine inhalation model with the highly lipophilic methyl palmitate (MP) as model substance. First, studies of acute effects following a 1-h exposure of up to 348 mg/m
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MP showed no effects on cell composition in bronchoalveolar lavage (BAL) or on lung function parameters. Thus, MP did not possess irritant or inflammatory properties, which may be a precursive stimulus for adjuvant effects. Second, mice were exposed to aerosols of MP, 6 or 323 mg/m
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, for 1 h followed by a 20-min low-dose ovalbumin (OVA) inhalation. OVA only and OVA + Al(OH)
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served as control groups. Exposures were performed 5 times/wk for 2 wk followed by a weekly exposure for 10 wk. Finally, the mice were challenged with a high-dose OVA aerosol for 3 consecutive days. Neither OVA-specific immunoglobulin (Ig) G1, IgE, or IgG2a production, nor inflammatory cells in BAL, nor respiratory patterns were significantly affected in the MP groups. The OVA + Al(OH)
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group had a significantly higher IgG1 and IgE production, as well as higher eosinophil infiltration in the BAL fluid. These studies showed that effects of adjuvants not are necessarily due to their lipophilicity; that is, additional structural properties are required.