首页> 外文OA文献 >Intranasal Administration of Recombinant Neisseria gonorrhoeae Transferrin Binding Proteins A and B Conjugated to the Cholera Toxin B Subunit Induces Systemic and Vaginal Antibodies in Mice
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Intranasal Administration of Recombinant Neisseria gonorrhoeae Transferrin Binding Proteins A and B Conjugated to the Cholera Toxin B Subunit Induces Systemic and Vaginal Antibodies in Mice

机译:重组淋病奈瑟氏球菌转铁蛋白结合蛋白A和B的鼻内给药与霍乱毒素B亚基结合可诱导小鼠全身和阴道抗体。

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摘要

The transferrin binding proteins (TbpA and TbpB) comprise the gonococcal transferrin receptor and are considered potential antigens for inclusion in a vaccine against Neisseria gonorrhoeae. Intranasal (IN) immunization has shown promise in development of immunity against sexually transmitted disease pathogens, in part due to the induction of antigen-specific genital tract immunoglobulin A (IgA) and IgG. Conjugation of antigens to the highly immunogenic cholera toxin B subunit (Ctb) enhances antibody responses in the serum and mucosal secretions following IN vaccination. In the current study, we characterized the anti-Tbp immune responses following immunization of mice IN with recombinant transferrin binding proteins (rTbpA and rTbpB) conjugated to rCtb. We found that both rTbpA-Ctb and rTbpB-Ctb conjugates administered IN induced antibody responses in the serum and genital tract. IN immunization resulted in both IgA and IgG in the genital tract; however, subcutaneous immunization mainly generated IgG. Surprisingly, rTbpA alone was immunogenic and induced serum and mucosal antibody responses similar to those elicited against the rTbpA-Ctb conjugate. Overall, rTbpB was much more immunogenic than rTbpA, generating serum IgG levels that were greater than those elicited against rTbpA. Bactericidal assays conducted with sera collected from mice immunized IN with TbpA and/or TbpB indicated that both antigens generated antibodies with bactericidal activity. Anti-TbpA antibodies were cross-bactericidal against heterologous gonococcal strains, whereas TbpB-specific antibodies were less cross-reactive. By contrast, antibodies elicited via subcutaneous immunization were not cross-bactericidal against heterologous strains, indicating that IN vaccination could be the preferred route for elicitation of biologically functional antibodies.
机译:转铁蛋白结合蛋白(TbpA和TbpB)包含淋球菌转铁蛋白受体,被认为是包含在淋病奈瑟菌疫苗中的潜在抗原。鼻内(IN)免疫已显示出对性传播疾病病原体免疫的发展前景,部分原因是诱导了抗原特异性生殖道免疫球蛋白A(IgA)和IgG。抗原与高免疫原性霍乱毒素B亚基(Ctb)的结合增强了IN疫苗接种后血清和粘膜分泌物中的抗体反应。在当前的研究中,我们表征了与重组rCtb结合的重组转铁蛋白结合蛋白(rTbpA和rTbpBB)免疫小鼠IN后的抗Tbp免疫应答。我们发现rTbpA-Ctb和rTbpB-Ctb偶联物均在血清和生殖道中IN诱导抗体反应。 IN免疫在生殖道中同时产生IgA和IgG;然而,皮下免疫主要产生IgG。出人意料的是,单独的rTbpA是免疫原性的,并且诱导的血清和粘膜抗体应答类似于针对rTbpA-Ctb偶联物引起的应答。总体而言,rTbpB的免疫原性远高于rTbpA,产生的血清IgG水平高于针对rTbpA的血清IgG水平。用从用TbpA和/或TbpB免疫IN的小鼠收集的血清进行的杀菌试验表明,两种抗原均产生具有杀菌活性的抗体。抗TbpA抗体对异源淋球菌菌株具有交叉杀菌作用,而TbpB特异性抗体的交叉反应较少。相比之下,通过皮下免疫产生的抗体对异源菌株没有交叉杀菌作用,这表明IN疫苗接种可能是引发生物功能抗体的首选途径。

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