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Objectives: Researchers and technicians who use mice in research are exposed to complex mixtures containing mouse allergen, endotoxin and particulates from animals, bedding and feed. The particle characteristics of these different exposures, and whether they are encountered together or separately, are important to better understand their adjuvant and allergic effects. Endotoxin and mouse allergen are derived from the same animal source, but have different physicochemical attributes. It is not known if airborne exposures to these agents are correlated in the laboratory animal workplace.
Methods: Side-by-side personal and area samples for airborne endotoxin (52), mouse allergen (46) and total particulates (43) were obtained in the animal facility and laboratories of a medical research institution. Animal handlers and researchers reported time spent on work tasks with mice, symptoms upon exposure to mice and mouse sensitization was determined by skin test or RAST.
Results: Mean airborne endotoxin exposure was highest during mouse experiments in the animal facility at 960 pg m(-3), peaked at 3125 pg m(-3), and ranged from 46 to 678 pg m(-3) with work in mouse rooms and research labs. Mouse allergen concentrations were highest during direct mouse work and background in research labs (mean 63-68 ng m(-3), range 41-271 ng m(-3)), but were undetectable during mouse research performed under a hood. Endotoxin and mouse allergen concentrations were correlated during direct research with mice and mouse care activities. Particle counts were low, typically < 1 cm(-3), varied widely, and exhibited peaks and valleys during different work tasks. From 80-90% of particles were < 1 microm in aerodynamic diameter during background measurements. The contribution of respirable particles 1-5 microm in size increased to 25-30% during mouse care and mouse research activities, but we found no association between any particle size and endotoxin or mouse allergen concentrations. Animal handlers and researchers in the mouse facility were exposed to the highest daily endotoxin concentrations, whereas researchers working with mice in the mouse facility and in laboratories were exposed to the highest daily mouse allergen concentrations.
Conclusions: These findings suggest that endotoxin and mouse allergen are co-exposures during mouse handling and research, and that control of exposure peaks may be necessary to limit allergic disease in the laboratory animal workplace.
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http://dx.doi.org/10.1093/annhyg/mel019 | DOI Listing |
J Allergy Clin Immunol
September 2025
Pulmonary and Critical Care Medicine, Department of Internal Medicine, Brigham and Women's Hospital and Harvard Medical School; Boston, MA 02115, USA. Electronic address:
Background: Particulate matter (PM) in air pollution is a major health concern. PM includes ultrafine particles (UFPs - PM, particles of ≤ 0.1μm), which can evoke lung inflammation.
View Article and Find Full Text PDFJ Allergy Clin Immunol Glob
November 2025
Department of Entomology, Rutgers-The State University of New Jersey, New Brunswick, NJ.
Background: Recent studies have suggested that the effectiveness of environmental intervention is crucial in reducing levels of the mouse allergen (Mus m 1) in inner-city homes. However, the impact of mouse control alone on mouse allergen reduction has not been studied.
Objective: Our aim was to evaluate the effectiveness of 3 house mouse control programs on mouse allergen reduction.
Clin Exp Otorhinolaryngol
September 2025
Department of Pediatrics, Korea University College of Medicine, Seoul, Republic of Korea.
Objectives: Allergic rhinitis (AR) is a chronic nasal mucosal inflammation triggered by environmental allergens. Although its pathophysiology has been well studied, the effects of environmental aggravating factors-especially combined pollutant exposure-are not fully understood. This study aimed to evaluate the impact of coexposure to PM2.
View Article and Find Full Text PDFInt Arch Allergy Immunol
September 2025
Allergic airway inflammation, including allergic rhinitis and asthma, is a disease characterized by IgE-mediated type I hypersensitivity reactions, with its pathophysiological features being the infiltration and proliferation of inflammatory cells in the airway mucosal epithelial cells. The complexity and heterogeneity of this inflammatory response, as well as the limitations of sampling from patients with allergic airway inflammation, have made animal models play a crucial role in studying the pathophysiological molecular pathways and treatment methods of allergic airway inflammation. Among the many animal models, mouse models are widely used for their diversity of genetic backgrounds, ease of experimental manipulation, and relevance to human diseases.
View Article and Find Full Text PDFMol Nutr Food Res
August 2025
Department of Biotechnology, Faculty of Science and Humanities, SRM Institute of Science and Technology, Kattankulathur, Tamil Nadu, India.
Tropomyosin is a significant allergen found in invertebrates and is recognized as one of the primary triggers of food-induced anaphylaxis. Though many researchers have done the characterization of allergic tropomyosin, a comparative analysis of the allergenicity of vertebrate (porcine) and invertebrate (crab) tropomyosin is still lacking. The present study aims to study the differences in IgE, tropomyosin-specific IgE, and histamine levels between vertebrate (porcine) and invertebrate tropomyosin (crab) using an animal experimental model.
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