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由肺炎链球菌荚膜多糖和通用辅助性T淋巴细胞表位(PADRE)组成的实验性碳水化合物共轭疫苗的研发

Development of experimental carbohydrate-conjugate vaccines composed of Streptococcus pneumoniae capsular polysaccharides and the universal helper T-lymphocyte epitope (PADRE).

作者信息

Alexander Jeff, del Guercio Marie-France, Frame Barbara, Maewal Ajesh, Sette Alessandro, Nahm Moon H, Newman Mark J

机构信息

Epimmune Inc., 5820 Nancy Ridge Drive, Suite 100, San Diego, CA 92121, USA.

出版信息

Vaccine. 2004 Jun 23;22(19):2362-7. doi: 10.1016/j.vaccine.2003.11.061.

Abstract

Experimental carbohydrate-conjugate vaccines composed of the 13 amino acid universal Pan HLA-DR Epitope (PADRE) and Streptococcus pneumoniae capsular polysaccharides from serotypes 14, 6B and 9V were produced. Simple carbodiimide-mediated condensation chemistry was used to conjugate the PADRE synthetic peptide to the three chemically different capsular polysaccharides in a 1:1 molar ratio. The immunogenicity of the PADRE peptide component of the conjugate vaccines was confirmed by the induction of PADRE-specific CD4+ helper T cell (HTL) responses following immunization of C57BL/6 mice. High titer antibody responses specific for polysaccharides of S. pneumoniae serotypes 14, 6B and 9V were induced using Complete Freund's Adjuvant (CFA) and alhydrogel Al(OH)3 formulations. The HTL, or carrier, effect of the PADRE synthetic peptide was only evident using the PADRE-polysaccharide conjugates; simple mixtures of the PADRE peptide and polysaccharides were essentially nonimmunogenic. The functional or potential protective value of the polysaccharide-specific antibodies was measured as a function of opsonophagocytic activity for the 6B serotype. High titers of opsonophagocytic activity were measured in sera from mice immunized with formulations containing both adjuvants. These data demonstrate that the PADRE synthetic peptide can induce the HTL responses needed to support the development of antibodies specific for bacterial carbohydrates used in conjugate vaccines.

摘要

制备了由13个氨基酸的通用泛HLA - DR表位(PADRE)与14型、6B型和9V型肺炎链球菌荚膜多糖组成的实验性碳水化合物结合疫苗。采用简单的碳二亚胺介导缩合化学方法,以1:1摩尔比将PADRE合成肽与三种化学性质不同的荚膜多糖偶联。通过对C57BL / 6小鼠免疫后诱导PADRE特异性CD4 +辅助性T细胞(HTL)反应,证实了结合疫苗中PADRE肽成分的免疫原性。使用完全弗氏佐剂(CFA)和氢氧化铝凝胶Al(OH)3制剂诱导了针对14型、6B型和9V型肺炎链球菌多糖的高滴度抗体反应。PADRE合成肽的HTL或载体效应仅在使用PADRE - 多糖偶联物时明显;PADRE肽和多糖的简单混合物基本无免疫原性。多糖特异性抗体的功能或潜在保护价值通过对6B血清型的调理吞噬活性来衡量。在用含有两种佐剂制剂免疫的小鼠血清中检测到高滴度的调理吞噬活性。这些数据表明,PADRE合成肽可以诱导支持结合疫苗中用于细菌碳水化合物特异性抗体产生所需的HTL反应。

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