毒素特异性抗体对肠外注射大肠杆菌热不稳定毒素诱导的佐剂性和炎症效应的影响

C. Luis, M. Cintra, Denicar Lina Nascimento Fabris Maeda, Camila Mathias-Santos, L. R. Pereira, W. B. Luiz, J. F. Rodrigues
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引用次数: 2

摘要

导言:由产肠毒素大肠杆菌(ETEC)菌株产生的热不稳定毒素(LT),当与经粘膜、经皮或肠外途径递送的抗原混合或结合时,会发挥强大的佐剂作用。关于先前存在的免疫对LT免疫调节特性的影响的信息有限,这在感染ETEC的人群中经常观察到。目的:在本研究中,我们评估了皮下给药后抗LT抗体对LT与特定疫苗抗原混合引发的佐剂和炎症活性的影响。材料和方法/结果:用登革病毒非结构蛋白(NS1)作为模型抗原,在LT特异性抗体存在的情况下与天然LT联合免疫动物。就血清抗ns1 IgG滴度的大小而言,暴露于抗LT抗体并未损害LT的体液佐剂性。此外,抗毒素抗体并没有减少中性粒细胞迁移和s.c.给药后的水肿形成。尽管如此,与抗LT抗体混合给药改变了局部细胞因子的产生情况,并将ns1特异性T细胞反应调节为th1型模式。结论:这些结果表明,预先存在的免疫不影响体液佐剂活性,但可能调节肠外给药LT诱导的先天和适应性免疫反应的不同方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Toxin-Specific Antibodies on the Adjuvanticity and Inflammatory Effects Induced by Parenterally Administered Escherichia coli heat-Labile Toxin
Introduction: Heat-labile toxins (LT), produced by enterotoxigenic Escherichia coli (ETEC) strains, exert potent adjuvant effects when admixed or linked to antigens delivered via mucosal, transcutaneous or parenteral routes. There is limited information regarding the impact of preexisting immunity on the immunomodulatory properties of LT, which is frequently observed among people infected with ETEC. Aims: In the present study, we evaluated the effect of anti-LT antibodies on the adjuvant and inflammatory activities triggered by LT admixed with a specific vaccine antigen following subcutaneous administration to mice. Material and Methods/Results: Animals were immunized with dengue virus nonstructural protein (NS1), as model antigen, in combination with native LT in the presence of LT-specific antibodies. Exposure to anti-LT antibodies did not impair the humoral adjuvanticity of LT regarding to the magnitude of the serum anti-NS1 IgG titers. In addition, anti-toxin antibodies did not reduce neutrophil migration nor edema formation after s.c. administration of LT. Nonetheless, administration of LT admixed with anti-LT antibodies changed the local cytokine production profile and modulated the NS1specific T cell responses to a Th1-type pattern. Conclusion: These results indicate that preexisting immunity does not affect the humoral adjuvant activities but may modulate different aspects of both innate and adaptive immune responses induced by parenterally administered LT.
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