首页> 外文期刊>Clinical chemistry and laboratory medicine: CCLM >New sensitive method for the measurement of lysozyme and lactoferrin for the assessment of innate mucosal immunity. part I: time-resolved immunofluorometric assay in serum and mucosal secretions.
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New sensitive method for the measurement of lysozyme and lactoferrin for the assessment of innate mucosal immunity. part I: time-resolved immunofluorometric assay in serum and mucosal secretions.

机译:一种新的灵敏的溶菌酶和乳铁蛋白测定方法,可用于评估先天粘膜免疫力。第一部分:血清和粘膜分泌物的时间分辨免疫荧光测定法。

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Mucous peristalsis, mucus and immunity proteins, such as lysozyme and lactoferrin, are part of humoral innate immunity. The aim of this study was to develop a quantitative method, a time-resolved-immunofluorometric assay, to measure lysozyme and lactoferrin in sera, saliva, stools and cervico-vaginal secretions. This method was validated in 51 healthy subjects. Linearity for lysozyme was between 1.02 and 25 microg/l and for lactoferrin between 1.02 and 100 microg/l. The detection limit was 0.5 microg/l for lysozyme and 1 microg/l for lactoferrin. Albumin and alpha1-antitrypsin were measured by immuno-nephelometry to calculate salivary, intestinal and cervico-vaginal coefficients of excretion. Lysozyme and lactoferrin were present in all types of mucosal surfaces. Very high concentrations of lysozyme and lactoferrin were found in cervico-vaginal fluid (166.2 and 72.7 mg/l, respectively), compared to the concentrations found in the other mucosal fluids. Lysozyme in stools was produced at the rate of 0.42mg/d compared to 0.02 mg/d lactoferrin production. Lysozyme and lactoferrin greatly exceeded the values expected from the molecular weight-affected seepage from plasma, suggesting primarily local synthesis in healthy subjects. Quantitative measurement of lysozyme and lactoferrin can aid in the assessment of the activity of mucus-associated lymphoid tissues in innate immunity, and can help in further understanding of the role of these proteins in mucosal diseases.
机译:粘液蠕动,粘液和免疫蛋白(如溶菌酶和乳铁蛋白)是体液先天免疫的一部​​分。这项研究的目的是开发一种定量方法,一种时间分辨免疫荧光测定法,用于测定血清,唾液,粪便和宫颈阴道分泌物中的溶菌酶和乳铁蛋白。该方法已在51名健康受试者中得到验证。溶菌酶的线性介于1.02至25微克/升之间,乳铁蛋白的线性介于1.02至100微克/升之间。溶菌酶的检出限为0.5微克/升,乳铁蛋白的检出限为1微克/升。通过免疫比浊法测量白蛋白和α1-抗胰蛋白酶,以计算唾液,肠和子宫颈阴道的排泄系数。溶菌酶和乳铁蛋白存在于所有类型的粘膜表面。与其他粘液中发现的浓度相比,宫颈阴道液中发现了很高的溶菌酶和乳铁蛋白浓度(分别为166.2和72.7 mg / l)。粪便中的溶菌酶产生率为0.42mg / d,乳铁蛋白产生率为0.02mg / d。溶菌酶和乳铁蛋白大大超过了血浆中受分子量影响的渗出量所预期的值,这表明在健康受试者中主要是局部合成。溶菌酶和乳铁蛋白的定量测量可以帮助评估与粘液相关的淋巴组织在先天免疫中的活性,并且可以帮助进一步了解这些蛋白在粘膜疾病中的作用。

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