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小鼠口服大肠杆菌提取物后的免疫原性研究。

Studies on the immunogenicity of an Escherichia coli extract after oral application in mice.

作者信息

Baier W, Sedelmeier E A, Bessler W G

机构信息

Institut für Immunobiologie, Universität, Freiburg, Germany.

出版信息

Arzneimittelforschung. 1997 Aug;47(8):980-5.

PMID:9296288
Abstract

A bacterial extract (IBEC, OM-89, Uro-Vaxom), consisting of immunostimulating components derived from 18 Escherichia coli (E. coli) bacterial strains, is used for the treatment of recurrent infections of the urinary tract. Previously it was demonstrated that IBEC constitutes an active immunogen after parenteral administration to mice. Here, the immunogenic properties of IBEC after oral administration to mice are demonstrated. It was shown that, after repeated oral administrations of the extract, an IBEC-specific serum immunoglobulin (Ig), IgA and IgG response was obtained. A weak increase of IBEC-specific faecal IgA was also observed. The sera also bound to the bacterial strains used for the preparation of the extract. Moreover they recognized the bacterial cell wall components muramyl dipeptide (MDP) protein I (porin) and lipopeptide (P3C). In addition to the increase of bacteria-specific Ig, a rise in total serum IgA was demonstrated. Also in supernatants of splenocyte cultures of IBEC-immunized mice an increased level of IgA could be determined. These findings on the immunostimulating properties of IBEC after oral administration, which is also the application route in human patients, might partially explain the therapeutic effect of the extract shown in clinical studies.

摘要

一种细菌提取物(IBEC、OM - 89、Uro - Vaxom),由源自18种大肠杆菌菌株的免疫刺激成分组成,用于治疗复发性尿路感染。此前已证明,将IBEC经肠胃外给药给小鼠后可构成一种活性免疫原。在此,证明了将IBEC经口服给药给小鼠后的免疫原性特性。结果表明,在重复口服该提取物后,获得了针对IBEC的血清免疫球蛋白(Ig)、IgA和IgG应答。还观察到针对IBEC的粪便IgA略有增加。血清也与用于制备提取物的细菌菌株结合。此外,它们识别细菌细胞壁成分胞壁酰二肽(MDP)、蛋白I(孔蛋白)和脂肽(P3C)。除了细菌特异性Ig增加外,还证明了血清总IgA升高。在经IBEC免疫的小鼠的脾细胞培养上清液中也可测定到升高的IgA水平。关于IBEC经口服给药后的免疫刺激特性的这些发现,而口服给药也是人类患者的用药途径,这可能部分解释了临床研究中所示提取物的治疗效果。

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