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通过缓释配方,可以避免含有 B 细胞表位的合成长肽疫苗引起的 IgG 介导的过敏反应。

IgG-mediated anaphylaxis to a synthetic long peptide vaccine containing a B cell epitope can be avoided by slow-release formulation.

机构信息

Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands;

Department of Human Genetics, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands; and.

出版信息

J Immunol. 2014 Jun 15;192(12):5813-20. doi: 10.4049/jimmunol.1302337. Epub 2014 May 9.

Abstract

Synthetic long peptides (SLP) are a promising vaccine modality to induce therapeutic T cell responses in patients with chronic infections and tumors. We studied different vaccine formulations in mice using SLP derived from carcinoembryonic Ag. We discovered that one of the SLP contains a linear Ab epitope in combination with a CD4 epitope. Repeated vaccination with this carcinoembryonic Ag SLP in mice shows improved T cell responses and simultaneously induced high titers of peptide-specific Abs. These Abs resulted in unexpected anaphylaxis after a third or subsequent vaccinations with the SLP when formulated in saline. Administration of low SLP doses in the slow-release vehicle IFA prevented the anaphylaxis after repeated vaccination. This study underscores both the immunogenicity of SLP vaccination, for inducing T cell as well as B cell responses, and the necessity of safe administration routes.

摘要

合成长肽 (SLP) 是一种很有前途的疫苗模式,可以诱导慢性感染和肿瘤患者产生治疗性 T 细胞反应。我们使用源自癌胚抗原 (CEA) 的 SLP 在小鼠中研究了不同的疫苗配方。我们发现,其中一种 SLP 含有线性 Ab 表位和一个 CD4 表位。在小鼠中重复用这种 CEA SLP 进行免疫接种可提高 T 细胞反应,同时诱导出高水平的肽特异性 Abs。当这些 Abs 在盐水中配制成 SLP 时,在第三次或后续接种后会引发意外的过敏反应。在 IFA 中以缓慢释放载体给予低剂量 SLP 可防止重复接种后的过敏反应。这项研究强调了 SLP 疫苗接种的免疫原性,既能诱导 T 细胞反应,也能诱导 B 细胞反应,同时还强调了安全给药途径的必要性。

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