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通过裸DNA免疫诱导人巨细胞病毒(HCMV)-糖蛋白B(gB)特异性中和抗体和磷蛋白65(pp65)特异性细胞毒性T淋巴细胞反应。

Induction of human cytomegalovirus (HCMV)-glycoprotein B (gB)-specific neutralizing antibody and phosphoprotein 65 (pp65)-specific cytotoxic T lymphocyte responses by naked DNA immunization.

作者信息

Endresz V, Kari L, Berencsi K, Kari C, Gyulai Z, Jeney C, Pincus S, Rodeck U, Méric C, Plotkin S A, Gönczöl E

机构信息

The Wistar Institute, Philadelphia, PA 19104, USA.

出版信息

Vaccine. 1999 Jan;17(1):50-8. doi: 10.1016/s0264-410x(98)00145-5.

Abstract

Plasmids expressing the human cytomegalovirus (HCMV) glycoprotein B (gB) (UL55) or phosphoprotein 65 (pp65) (UL83) were constructed and evaluated for their ability to induce immune responses in mice. The full-length gB as well as a truncated form expressing amino acids 1-680 of gB, and lacking the fragment encoding amino acids 681 907 including the transmembrane domain of gB (gB680) were evaluated. Immunization of mice with plasmids coding for gB or gB680 induced ELISA and neutralizing antibodies, with the highest titres in mice immunized with the gB680 plasmid. Mice immunized with the gB plasmid predominantly produced IgG2a gB-specific antibody, while the gB680 plasmid raised mostly IgG1 anti-gB antibody. Mice immunized with the pp65 plasmid developed pp65-specific cytotoxic T lymphocytes (CTL) and ELISA antibodies. Immunization with a mixture of both gB and pp65 plasmids raised antibodies to both proteins and pp65-specific CTL, indicating a lack of interference between these two plasmids. These results suggest that DNA immunization is a useful approach for vaccination against HCMV disease.

摘要

构建了表达人巨细胞病毒(HCMV)糖蛋白B(gB)(UL55)或磷蛋白65(pp65)(UL83)的质粒,并评估了它们在小鼠体内诱导免疫反应的能力。对全长gB以及表达gB氨基酸1 - 680且缺少编码包括gB跨膜结构域的氨基酸681 - 907片段的截短形式(gB680)进行了评估。用编码gB或gB680的质粒免疫小鼠可诱导ELISA和中和抗体,其中用gB680质粒免疫的小鼠抗体滴度最高。用gB质粒免疫的小鼠主要产生IgG2a gB特异性抗体,而gB680质粒主要产生IgG1抗gB抗体。用pp65质粒免疫的小鼠产生了pp65特异性细胞毒性T淋巴细胞(CTL)和ELISA抗体。用gB和pp65质粒混合物免疫可产生针对两种蛋白质的抗体和pp65特异性CTL,表明这两种质粒之间不存在干扰。这些结果表明,DNA免疫是预防HCMV疾病的一种有用方法。

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