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TAA/ecdCD40L adenoviral prime-protein boost vaccine for cancer and infectious diseases

机译:用于癌症和传染病的TAA / ecdCD40L腺病毒初蛋白加强疫苗

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摘要

A vaccine platform has been created by attaching the target-associated antigen (TAA) for the vaccine to the extracellular domain (ecd) of the potent immunostimulatory signal CD40 ligand (CD40L). Attachment of the TAA to the CD40L promotes uptake of the TAA into dendritic cells (DCs), binding to Class I as well as Class II MHC leading to presentation of the TAA on the DCs, expansion of the TAA-specific B cell and CD8 effector T-cell lymphocytes, and induction of a memory response. In addition, the TAA/ecdCD40L vaccine can overcome anergy, induce regressions of pre-existing subcutaneous (SC) nodules of cancer cells, and induce high titers of neutralizing antibodies against viral antigens. This vaccine, which can be administered SC as a TAA/ecdCD40L fusion protein, or as expression vectors (viral or plasmid) or as a vector prime-protein boost strategy, is applicable to the development of vaccine for a wide range of cancers and infectious agents.
机译:通过将疫苗的靶标相关抗原(TAA)连接到有效免疫刺激信号CD40配体(CD40L)的胞外域(ecd),创建了一个疫苗平台。将TAA附着到CD40L上可促进TAA被树突状细胞(DC)吸收,与I类和II类MHC结合,导致TAA出现在DC上,TAA特异性B细胞和CD8效应子的扩增。 T细胞淋巴细胞和记忆反应的诱导。此外,TAA / ecdCD40L疫苗可克服无能,诱导癌细胞的皮下(SC)结节消退,并诱导高滴度的抗病毒抗原的中和抗体。这种疫苗可以SC作为TAA / ecdCD40L融合蛋白,也可以作为表达载体(病毒或质粒)或作为载体初免蛋白加强策略进行SC给药,可用于开发针对多种癌症和感染性疫苗代理商。

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