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1.
Yonsei Medical Journal ; : 593-602, 2012.
Article in English | WPRIM | ID: wpr-190360

ABSTRACT

PURPOSE: Cockroach (CR) is an important inhalant allergen and can induce allergic asthma. However, the mechanism by which CR induces airway allergic inflammation and the role of endotoxin in CR extract are not clearly understood in regards to the development of airway inflammation. In this study, we evaluated whether endotoxin is essential to the development of CR induced airway allergic inflammation in mice. MATERIALS AND METHODS: Airway allergic inflammation was induced by intranasal administration of either CR extract, CR with additional endotoxin, or endotoxin depleted CR extract, respectively, in BALB/c wild type mice. CR induced inflammation was also evaluated with toll like receptor-4 (TLR-4) mutant (C3H/HeJ) and wild type (C3H/HeN) mice. RESULTS: Intranasal administration of CR extracts significantly induced airway hyperresponsiveness (AHR), eosinophilic and neutrophilic airway inflammation, as well as goblet cell hyperplasia in a dose-dependent manner. The addition of endotoxin along with CR allergen attenuated eosinophilic inflammation, interleukin (IL)-13 level, and goblet cell hyperplasia of respiratory epithelium; however, it did not affect the development of AHR. Endotoxin depletion in CR extract did not attenuate eosinophilic inflammation and lymphocytosis in BAL fluid, AHR and IL-13 expression in the lungs compared to CR alone. The attenuation of AHR, eosinophilic inflammation, and goblet cell hyperplasia induced by CR extract alone was not different between TLR-4 mutant and the wild type mice. In addition, heat inactivated CR extract administration induced attenuated AHR and eosinophilic inflammation. CONCLUSION: Endotoxin in CR extracts may not be essential to the development of airway inflammation.


Subject(s)
Animals , Female , Mice , Allergens/immunology , Asthma/chemically induced , Cockroaches/immunology , Endotoxins/immunology , Enzyme-Linked Immunosorbent Assay , Inflammation/chemically induced , Interferon-gamma/metabolism , Interleukin-13/metabolism , Interleukin-5/metabolism , Mice, Inbred BALB C , Respiratory Hypersensitivity/chemically induced
2.
Braz. oral res ; 19(1): 5-10, Jan.-Mar. 2005. tab
Article in English | LILACS | ID: lil-403727

ABSTRACT

O objetivo desta pesquisa foi avaliar in vitro a capacidade e o tempo necessário para a endotoxina se difundir pelos túbulos dentinários em direção ao cemento. Foram utilizados 30 dentes humanos unirradiculados, que tiveram suas coroas e seus ápices seccionados, padronizando-se o tamanho em 15 mm. Os dentes foram instrumentados até a lima K30 e impermeabilizados externamente com adesivo epóxi, deixando-se 10 mm de raiz exposta (terço médio). Os espécimes foram acondicionados em tubos plásticos e submetidos à radiação gama cobalto 60. Após a radiação, foram divididos em 2 grupos (n = 15): G1) foi inoculada uma solução de endotoxina de Escherichia coli no canal radicular dos espécimes e 1 mL de água apirogênica foi colocado no interior dos tubos; G2 (controle): foi inoculada água apirogênica nos canais radiculares e 1 mL de água apirogência foi colocado em cada tubo. Após 30 min, 2 h, 6 h, 12 h, 24 h, 48 h, 72 h e 7 dias, a água do interior dos tubos foi removida e substituída por outra. A alíquota removida foi testada para se detectar presença de endotoxina através da produção de anticorpos (IgM) em cultura de linfócitos B, pois a endotoxina é um ativador policlonal dessas células. Os resultados foram submetidos à análise estatística ANOVA (5%) e teste de Tukey, em que foi verificado que a água removida dos tubos após 24 h, 48 h, 72 h e 7 dias induziu maior produção de anticorpos em relação aos demais grupos, com diferença significante (p < 0,05). Assim, a endotoxina foi capaz de se difundir pelos túbulos dentinários em direção ao cemento, atingindo a região externa da raiz após 24 h.


Subject(s)
Animals , Humans , Male , Mice , Dentin , Endotoxins/pharmacokinetics , Analysis of Variance , B-Lymphocytes/immunology , Culture Media , Dental Cements , Dentin Permeability , Diffusion , Dental Pulp Cavity/chemistry , Dental Pulp Cavity/microbiology , Dentin/microbiology , Enzyme-Linked Immunosorbent Assay , Endotoxins/immunology , Immunoglobulin G/metabolism , Time Factors
3.
Journal of Korean Medical Science ; : 505-508, 2004.
Article in English | WPRIM | ID: wpr-168454

ABSTRACT

Pillows are known to contain significant levels of indoor allergens and endotoxin, that are of importance to house dust mite sensitized asthmatics. Buckwheat pillows are commonly used in Korea. We studied the levels of the house dust mite allergen, Der f 1, and endotoxin on new synthetic and buckwheat pillows and their accumulation over three months. Endotoxin levels were significantly higher on new buckwheat pillows compared to synthetic pillows; geometric mean levels (95% CI) were 60,950 EU/g (30,270-122,700) and 4,887 EU/g (2,570-9,311) respectively (p<0.001). No Der f 1 was detected on the new pillows. After three months Der f 1 levels were similar on buckwheat and synthetic pillows, geometric mean levels (95% CI) were 1.16 microgram/g (0.02-8.13) and 1.08 microgram/g (0.19-1.68) respectively. These results indicate that buckwheat pillows are a source of very high endotoxin levels that may be of relevance to asthma severity of atopic asthmatics.


Subject(s)
Animals , Humans , Allergens/immunology , Antigens, Dermatophagoides/immunology , Asthma/immunology , Bedding and Linens , Fagopyrum , Dermatophagoides farinae/immunology , Endotoxins/immunology , Korea
5.
Asian Pac J Allergy Immunol ; 1992 Dec; 10(2): 145-50
Article in English | IMSEAR | ID: sea-36670

ABSTRACT

An enzyme-linked immunosorbent assay (ELISA) with endotoxin preparations of P. pseudomallei as antigen was developed for detection of IgG antibodies specific to melioidosis. Forty-seven sera of bacteriologically confirmed melioidosis patients, 55 non-melioidosis sera and 50 sera of healthy blood donors from non-endemic areas were subjected to this assay in comparison with indirect hemagglutination assay (IHA). The data were treated by receiver operating characteristics analysis. The sensitivity, specificity and accuracy in this ELISA were 95.7%, 94.2%, and 94.7%, respectively, with cut-off value of OD = 0.312 at 490 nm. Meanwhile, those in IHA were 81.0%, 91.4%, and 88.1%, respectively, with a cut-off value of > or = 1:160. From these results, the ELISA was judged to be more reliable than IHA as the seroassay for diagnosis of melioidosis.


Subject(s)
Antibodies, Bacterial/analysis , Antigens, Bacterial/immunology , Blood Donors , Burkholderia pseudomallei/immunology , Endotoxins/immunology , Enzyme-Linked Immunosorbent Assay/methods , False Positive Reactions , Humans , Immunoglobulin G/analysis , Melioidosis/diagnosis , Predictive Value of Tests , Reproducibility of Results , Sensitivity and Specificity
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