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合成肽引发的针对口蹄疫病毒所有七种血清型的中和抗体。

Neutralizing antibodies to all seven serotypes of foot-and-mouth disease virus elicited by synthetic peptides.

作者信息

Francis M J, Hastings G Z, Clarke B E, Brown A L, Beddell C R, Rowlands D J, Brown F

机构信息

Department of Virology, Wellcome Biotechnology Ltd, Beckenham, Kent, U.K.

出版信息

Immunology. 1990 Feb;69(2):171-6.

PMID:2155177
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1385585/
Abstract

Uncoupled peptides from all seven serotypes of foot-and-mouth disease virus (FMDV) protein VP1 have been used to elicit neutralizing antibody responses in guinea-pigs. The responses were largely serotype specific, although some significant cross-neutralization was observed. Dimeric tandem peptides have also been used to simultaneously elicit neutralizing antibodies to two different FMDV serotypes. The possible existence of structural features common to the B-cell neutralization sites or the guinea-pig helper T-cell sites within all seven peptides are analysed and discussed.

摘要

来自口蹄疫病毒(FMDV)蛋白VP1所有七种血清型的解偶联肽已被用于在豚鼠中引发中和抗体反应。尽管观察到一些显著的交叉中和作用,但这些反应在很大程度上具有血清型特异性。二聚体串联肽也已被用于同时引发针对两种不同FMDV血清型的中和抗体。本文分析并讨论了所有七种肽中B细胞中和位点或豚鼠辅助性T细胞位点可能存在的共同结构特征。

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Neutralizing antibodies to all seven serotypes of foot-and-mouth disease virus elicited by synthetic peptides.合成肽引发的针对口蹄疫病毒所有七种血清型的中和抗体。
Immunology. 1990 Feb;69(2):171-6.
2
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[Antigenic structure of the foot-and-mouth disease virus. III. Immunogenic properties of synthetic peptides of the sequence of the immunodominant region of VP1 proteins of the O1K and A22 strains of foot-and-mouth virus].[口蹄疫病毒的抗原结构。III. 口蹄疫病毒O1K和A22株VP1蛋白免疫显性区序列合成肽的免疫原性]
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本文引用的文献

1
Chemical basis of antigenic variation in foot-and-mouth disease virus.口蹄疫病毒抗原变异的化学基础。
Nature. 1983;306(5944):694-7. doi: 10.1038/306694a0.
2
Antibody response in pig nasal fluid and serum following foot-and-mouth disease infection or vaccination.口蹄疫感染或疫苗接种后猪鼻液和血清中的抗体反应。
J Hyg (Lond). 1983 Oct;91(2):329-34. doi: 10.1017/s0022172400060344.
3
Nucleotide sequence and corresponding amino acid sequence of the gene for the major antigen of foot and mouth disease virus.口蹄疫病毒主要抗原基因的核苷酸序列及相应氨基酸序列。
Nucleic Acids Res. 1981 Apr 24;9(8):1919-31. doi: 10.1093/nar/9.8.1919.
4
Antibodies against a preselected peptide recognize and neutralize foot and mouth disease virus.针对预先选定肽段的抗体可识别并中和口蹄疫病毒。
EMBO J. 1982;1(7):869-74. doi: 10.1002/j.1460-2075.1982.tb01262.x.
5
Synthetic peptide vaccines against foot-and-mouth disease. I. Duration of the immune response and priming in guinea-pigs, rabbits and mice.抗口蹄疫合成肽疫苗。I. 豚鼠、兔子和小鼠免疫反应的持续时间及启动
J Biol Stand. 1987 Jan;15(1):39-51. doi: 10.1016/0092-1157(87)90015-1.
6
Immunological priming with synthetic peptides of foot-and-mouth disease virus.用口蹄疫病毒合成肽进行免疫致敏
J Gen Virol. 1985 Nov;66 ( Pt 11):2347-54. doi: 10.1099/0022-1317-66-11-2347.
7
Qualitative and quantitative differences in the immune response to foot-and-mouth disease virus antigens and synthetic peptides.对口蹄疫病毒抗原和合成肽免疫反应的定性和定量差异。
J Gen Virol. 1988 Oct;69 ( Pt 10):2483-91. doi: 10.1099/0022-1317-69-10-2483.
8
Analysis of neutralizing epitopes on foot-and-mouth disease virus.口蹄疫病毒中和表位分析
J Virol. 1988 Jun;62(6):2033-40. doi: 10.1128/JVI.62.6.2033-2040.1988.
9
Synthetic T and B cell recognition sites: implications for vaccine development.合成的T细胞和B细胞识别位点:对疫苗开发的意义。
Adv Immunol. 1989;45:195-282. doi: 10.1016/s0065-2776(08)60694-x.
10
The cell attachment site on foot-and-mouth disease virus includes the amino acid sequence RGD (arginine-glycine-aspartic acid).口蹄疫病毒上的细胞附着位点包括氨基酸序列RGD(精氨酸-甘氨酸-天冬氨酸)。
J Gen Virol. 1989 Mar;70 ( Pt 3):625-37. doi: 10.1099/0022-1317-70-3-625.