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首页> 外文期刊>Clinical and vaccine immunology: CVI >Oral immunization with recombinant Mycobacterium smegmatis expressing the outer membrane protein 26-kilodalton antigen confers prophylactic protection against Helicobacter pylori infection
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Oral immunization with recombinant Mycobacterium smegmatis expressing the outer membrane protein 26-kilodalton antigen confers prophylactic protection against Helicobacter pylori infection

机译:口服免疫与分枝杆菌重组smegmatis表达外膜蛋白26-kilodalton抗原授予预防预防幽门螺杆菌感染

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摘要

Helicobacter pylori infection is prevalent worldwide and results in chronic gastritis, which may lead to gastric mucosa-associated lymphoid tissue lymphoma and gastric cancer. We have previously reported that oral immunization with recombinant Mycobacterium smegmatis expressing the H. pylori outer membrane protein 26-kilodalton (Omp26) antigen affords therapeutic protection against H. pylori infection in mice. In the present study, we investigated the prophylactic effects of this vaccine candidate on H. pylori challenge in mice. We found that oral immunization with recombinant Mycobacterium Omp26 significantly reduced H. pylori colonization in the stomach compared to inoculation with wild-type M. smegmatis in control mice. Six of the recombinant Mycobacterium-immunized mice (60%) were completely protected from H. pylori infection. The severity of H. pylori-associated chronic gastritis assessed histologically was significantly milder in mice vaccinated with recombinant Mycobacterium than in control animals. Mice immunized with recombinant Mycobacterium showed enhanced antigen-specific lymphocyte proliferation and antibody responses. Moreover, immunization with recombinant Mycobacterium resulted in an increased expression of interleukin-2 and gamma interferon in the stomach and spleen, as determined by reverse transcription-PCR analysis. Our results collectively suggest that vaccination with recombinant Mycobacterium Omp26 confers prophylactic protection against H. pylori infection. The inhibition of H. pylori colonization is associated with the induction of antigen-specific humoral and cell-mediated immune responses.
机译:幽门螺杆菌感染是普遍的全球和导致慢性胃炎可能导致胃mucosa-associated淋巴组织淋巴瘤和胃癌。此前报道称,口服免疫接种smegmatis分枝杆菌重组表达幽门螺旋杆菌外膜蛋白26-kilodalton (Omp26)抗原提供治疗预防幽门螺杆菌感染的老鼠。在目前的研究中,我们调查了预防这种候选疫苗的影响幽门螺杆菌挑战在老鼠身上。与重组Omp26分枝杆菌免疫显著降低幽门螺杆菌殖民胃相比,接种野生型m . smegmatis控制老鼠。重组Mycobacterium-immunized老鼠(60%)与幽门螺旋杆菌完全保护感染。慢性胃炎评估组织学检查在小鼠接种明显温和分枝杆菌重组比控制动物。分枝杆菌显示增强抗原淋巴细胞增殖和抗体反应。此外,免疫与重组分枝杆菌导致增加表达式白介素2和γ干扰素胃和脾脏,由逆转一结论分析。集体建议接种分枝杆菌重组Omp26授予预防性保护幽门螺旋杆菌感染。殖民的诱导有关抗原的体液和细胞免疫响应。

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