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A Self-assembled Peptide-based Adjuvant Eliciting Strong Antibody Responses with Minimal Inflammation

机译:基于肽的基于肽的助剂,引起强烈的抗体反应,最小炎症

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OVA-Q11 induced a stronger and more rapid antibody response in mice than Alum-OVA, with modest T cell responses and without inducing local inflammation. The discordance between the minimal inflammatory and T cell responses and the robust T-dependent antibody response suggests that mechanism of OVA-antigen presentation by Q11 is distinct from that of Alum. To identify the mechanism, future work will include using fluorescently-labeled OVA-Q11 or OVA-Alum to identify the sequence of uptake by cells at the injection site and in the draining lymph node. Our observations suggest that Q11-based systems may eventually provide a new route to safe and potent vaccines without undesired inflammation.
机译:OVA-Q11诱导小鼠的较强且更快速的抗体反应,而不是Alum-OVA,具有适度的T细胞应答,并且不诱导局部炎症。最小炎症和T细胞应答与鲁棒T依赖性抗体反应之间的不等调表明,Q11的OVA-抗原呈现的机制与明矾的术语不同。为了识别机制,将来的工作将包括使用荧光标记的OVA-Q11或OVA-ALUM来鉴定注射部位和排水淋巴结的细胞的摄取序列。我们的观察结果表明,基于Q11的系统最终可能提供了在没有不希望的炎症的安全和有效疫苗的新途径。

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