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将肽独特性概念应用于抗脊髓灰质炎疫苗接种

Applying the Concept of Peptide Uniqueness to Anti-Polio Vaccination.

作者信息

Kanduc Darja, Fasano Candida, Capone Giovanni, Pesce Delfino Antonella, Calabrò Michele, Polimeno Lorenzo

机构信息

Department of Biosciences, Biotechnologies, and Biopharmaceutics, University of Bari, 70126 Bari, Italy.

Department of Emergency and Organ Transplantation (DETO), University of Bari, 70124 Bari, Italy.

出版信息

J Immunol Res. 2015;2015:541282. doi: 10.1155/2015/541282. Epub 2015 Oct 19.

Abstract

BACKGROUND

Although rare, adverse events may associate with anti-poliovirus vaccination thus possibly hampering global polio eradication worldwide.

OBJECTIVE

To design peptide-based anti-polio vaccines exempt from potential cross-reactivity risks and possibly able to reduce rare potential adverse events such as the postvaccine paralytic poliomyelitis due to the tendency of the poliovirus genome to mutate.

METHODS

Proteins from poliovirus type 1, strain Mahoney, were analyzed for amino acid sequence identity to the human proteome at the pentapeptide level, searching for sequences that (1) have zero percent of identity to human proteins, (2) are potentially endowed with an immunologic potential, and (3) are highly conserved among poliovirus strains.

RESULTS

Sequence analyses produced a set of consensus epitopic peptides potentially able to generate specific anti-polio immune responses exempt from cross-reactivity with the human host.

CONCLUSION

Peptide sequences unique to poliovirus proteins and conserved among polio strains might help formulate a specific and universal anti-polio vaccine able to react with multiple viral strains and exempt from the burden of possible cross-reactions with human proteins. As an additional advantage, using a peptide-based vaccine instead of current anti-polio DNA vaccines would eliminate the rare post-polio poliomyelitis cases and other disabling symptoms that may appear following vaccination.

摘要

背景

尽管罕见,但不良事件可能与抗脊髓灰质炎疫苗相关联,从而可能阻碍全球消灭脊髓灰质炎。

目的

设计基于肽的抗脊髓灰质炎疫苗,以避免潜在的交叉反应风险,并可能减少罕见的潜在不良事件,例如由于脊髓灰质炎病毒基因组突变趋势导致的疫苗接种后麻痹性脊髓灰质炎。

方法

对1型脊髓灰质炎病毒Mahoney株的蛋白质进行分析,以五肽水平确定其与人类蛋白质组的氨基酸序列同一性,寻找符合以下条件的序列:(1)与人类蛋白质的同一性为零;(2)可能具有免疫潜力;(3)在脊髓灰质炎病毒株中高度保守。

结果

序列分析产生了一组共有表位肽,这些肽可能能够产生特异性抗脊髓灰质炎免疫反应,且与人类宿主无交叉反应。

结论

脊髓灰质炎病毒蛋白质特有的且在脊髓灰质炎病毒株中保守的肽序列可能有助于制备一种特异性和通用的抗脊髓灰质炎疫苗,该疫苗能够与多种病毒株反应,且不会带来与人类蛋白质发生交叉反应的负担。另外一个优势是,使用基于肽的疫苗而非目前的抗脊髓灰质炎DNA疫苗,将消除罕见的脊髓灰质炎疫苗接种后脊髓灰质炎病例以及接种后可能出现的其他致残症状。

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本文引用的文献

1
The polio endgame.脊髓灰质炎的终结之战。
Hum Vaccin Immunother. 2014;10(7):2106-8. doi: 10.4161/21645515.2014.981115.
4
The final stages of the global eradication of poliomyelitis.全球消灭脊髓灰质炎的最后阶段。
Philos Trans R Soc Lond B Biol Sci. 2013 Jun 24;368(1623):20120140. doi: 10.1098/rstb.2012.0140. Print 2013 Aug 5.
5
Serological cross-reactivity between human polyomaviruses.人类多瘤病毒之间的血清交叉反应性。
Rev Med Virol. 2013 Jul;23(4):250-64. doi: 10.1002/rmv.1747. Epub 2013 May 6.

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