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抗B19微小病毒疫苗设计中的自身与非自身问题

Selfness-nonselfness in designing an anti-B19 erythrovirus vaccine.

作者信息

Fasano Candida, Kanduc Darja

机构信息

Department of Biochemistry and Molecular Biology; University of Bari; Bari, Italy.

出版信息

Self Nonself. 2011 Apr;2(2):114-119. doi: 10.4161/self.2.2.16190. Epub 2011 Apr 1.

Abstract

Although B19 erythrovirus infection may be associated with severe clinical outcomes, especially in early infancy, pregnancy and in immunocompromised or hemolytic subjects, no vaccine is currently available. Using the concept that effective immune responses to an infectious agent may be restricted to the specific peptidome unique to that agent, we analyzed primary amino acid sequence of B19 erythrovirus, searching for peptide motifs to be used in vaccine formulations. Here, we identify and describe a set of unique viral peptides that may guarantee both high efficacy and practically no cross-reactive autoimmune responses in anti-B19 immunotherapeutic approaches.

摘要

尽管B19微小病毒感染可能与严重的临床后果相关,尤其是在婴儿早期、妊娠期间以及免疫功能低下或溶血的患者中,但目前尚无可用的疫苗。利用对感染因子的有效免疫反应可能局限于该因子特有的特定肽组这一概念,我们分析了B19微小病毒的一级氨基酸序列,寻找可用于疫苗制剂的肽基序。在此,我们鉴定并描述了一组独特的病毒肽,它们可能在抗B19免疫治疗方法中保证高效且几乎没有交叉反应性自身免疫反应。

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本文引用的文献

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The self/nonself issue: A confrontation between proteomes.自我/非自我问题:蛋白质组之间的对抗。
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