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对源自伯氏疏螺旋体外表面蛋白C的合成肽的特异性免疫反应可预测保护性杀螺旋体抗体。

Specific immune response to a synthetic peptide derived from outer surface protein C of Borrelia burgdorferi predicts protective borreliacidal antibodies.

作者信息

Ikushima M, Matsui K, Yamada F, Kawahashi S, Nishikawa S K

机构信息

Division of Clinical Microbiology, Saitama Institute of Public Health, Japan.

出版信息

FEMS Immunol Med Microbiol. 2000 Sep;29(1):15-21. doi: 10.1111/j.1574-695X.2000.tb01499.x.

Abstract

In a previous study, we described the development of a new specific serodiagnostic test for Lyme disease involving enzyme-linked immunosorbent assay and a synthetic peptide, OspC-I. The OspC-I peptide is derived from part of the outer surface protein C (OspC) amino acid sequence of Borrelia burgdorferi and is located in the region conserved among B. burgdorferi sensu stricto or sensu lato isolates. In this study, we demonstrate that sera containing antibodies against OspC-I from patients with early Lyme disease had borreliacidal activity against isolates of three genospecies of Lyme disease spirochete, B. burgdoreferi B31, B. garinii HPI and B. afzelii HT61. However, the borreliacidal activity against B. burgdorferi, which has not been isolated in Japan, was weaker than that against the other species. Vaccination of mice with OspC-I induced the production of anti-OspC-I antibodies in serum with borreliacidal activity. The immune mouse serum had significantly higher levels of borreliacidal activity against HP1 and HT61, than against B31. Neutralization of borreliacidal activity with anti-IgM antibodies showed that the borreliacidal activity of anti-OspC-I antibodies in serum was due to IgM. Furthermore. mice vaccinated with OspC-I were protected against challenge with HPI and HT61. but not fully protected against infection with B31. These results suggest that OspC-I is not only a specific antigen for use in serodiagnostic tests for Lyme disease, but is also a potential candidate for a Lyme disease vaccine in Japan.

摘要

在之前的一项研究中,我们描述了一种用于莱姆病的新型特异性血清诊断检测方法的开发,该方法涉及酶联免疫吸附测定和一种合成肽OspC-I。OspC-I肽源自伯氏疏螺旋体的外表面蛋白C(OspC)氨基酸序列的一部分,位于伯氏疏螺旋体狭义种或广义种分离株中保守的区域。在本研究中,我们证明,来自早期莱姆病患者的含有抗OspC-I抗体的血清对莱姆病螺旋体的三个基因种的分离株,即伯氏疏螺旋体B31、伽氏疏螺旋体HPI和阿氏疏螺旋体HT61,具有杀螺旋体活性。然而,对在日本尚未分离出的伯氏疏螺旋体的杀螺旋体活性比对其他物种的活性弱。用OspC-I对小鼠进行疫苗接种可诱导血清中产生具有杀螺旋体活性的抗OspC-I抗体。免疫小鼠血清对HP1和HT61的杀螺旋体活性水平明显高于对B31的活性水平。用抗IgM抗体中和杀螺旋体活性表明,血清中抗OspC-I抗体的杀螺旋体活性归因于IgM。此外,用OspC-I接种的小鼠受到保护,可抵御HPI和HT61的攻击,但不能完全抵御B31的感染。这些结果表明,OspC-I不仅是用于莱姆病血清诊断检测的特异性抗原,而且在日本还是莱姆病疫苗的潜在候选物。

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