Suppr超能文献

源自口蹄疫病毒高抗原性VP1区域140至160的序列不能引发牛T细胞针对完整病毒的应答。

Sequences derived from the highly antigenic VP1 region 140 to 160 of foot-and-mouth disease virus do not prime for a bovine T-cell response against intact virus.

作者信息

van Lierop M J, Wagenaar J P, van Noort J M, Hensen E J

机构信息

Department of Immunology, Faculty of Veterinary Medicine, University of Utrecht, The Netherlands.

出版信息

J Virol. 1995 Jul;69(7):4511-4. doi: 10.1128/JVI.69.7.4511-4514.1995.

Abstract

Although VP1 region 140 to 160 of foot-and-mouth disease virus (FMDV) is able to elicit neutralizing antibody in cattle, the protection against virus challenge that is conferred by peptide immunization is often poor. Here, we show that bovine T cells primed with peptides derived from this region generally show no reactivity to intact FMDV. In contrast, T-cell epitope VP4[20-34] is able to prime for a virus-specific response.

摘要

虽然口蹄疫病毒(FMDV)的VP1区域140至160能够在牛体内引发中和抗体,但肽免疫所赋予的针对病毒攻击的保护作用通常较差。在此,我们表明用源自该区域的肽引发的牛T细胞通常对完整的FMDV无反应性。相比之下,T细胞表位VP4[20 - 34]能够引发病毒特异性反应。

相似文献

4
T cell-stimulatory fragments of foot-and-mouth disease virus released by mild treatment with cathepsin D.
J Gen Virol. 1994 Nov;75 ( Pt 11):2937-46. doi: 10.1099/0022-1317-75-11-2937.
5
New virus-specific T-helper epitopes of foot-and-mouth disease viral VP1 protein.
FEBS Lett. 1993 Oct 25;333(1-2):175-8. doi: 10.1016/0014-5793(93)80399-f.
7
Recognition of foot-and-mouth disease virus and its capsid protein VP1 by bovine peripheral T lymphocytes.
J Gen Virol. 1996 Apr;77 ( Pt 4):727-35. doi: 10.1099/0022-1317-77-4-727.

引用本文的文献

2
High-yield production of the VP1 structural protein epitope from serotype O foot-and-mouth disease virus in Escherichia coli.
J Ind Microbiol Biotechnol. 2013 Jul;40(7):705-13. doi: 10.1007/s10295-013-1273-7. Epub 2013 Apr 26.
5
Immune potential of a novel multiple-epitope vaccine to FMDV type Asia 1 in guinea pigs and sheep.
Virol Sin. 2011 Jun;26(3):190-7. doi: 10.1007/s12250-011-3174-0. Epub 2011 Jun 12.
7
Promising multiple-epitope recombinant vaccine against foot-and-mouth disease virus type O in swine.
Clin Vaccine Immunol. 2011 Jan;18(1):143-9. doi: 10.1128/CVI.00236-10. Epub 2010 Nov 17.
8
Recombinant DNA and Protein Vaccines for Foot-and-mouth Disease Induce Humoral and Cellular Immune Responses in Mice.
Immune Netw. 2009 Dec;9(6):265-73. doi: 10.4110/in.2009.9.6.265. Epub 2009 Dec 31.
10
Identification of T-cell epitopes in nonstructural proteins of foot-and-mouth disease virus.
J Virol. 2001 Apr;75(7):3164-74. doi: 10.1128/JVI.75.7.3164-3174.2001.

本文引用的文献

3
T cell-stimulatory fragments of foot-and-mouth disease virus released by mild treatment with cathepsin D.
J Gen Virol. 1994 Nov;75 ( Pt 11):2937-46. doi: 10.1099/0022-1317-75-11-2937.
6
Location and characterization of the antigenic portion of the FMDV immunizing protein.
J Gen Virol. 1982 Apr;59(Pt 2):295-306. doi: 10.1099/0022-1317-59-2-295.
8
Protection of cattle against foot-and-mouth disease by a synthetic peptide.
Science. 1986 May 2;232(4750):639-41. doi: 10.1126/science.3008333.
9
Immunological priming with synthetic peptides of foot-and-mouth disease virus.
J Gen Virol. 1985 Nov;66 ( Pt 11):2347-54. doi: 10.1099/0022-1317-66-11-2347.
10
Biochemically defined polymorphism of bovine MHC class II antigens.
Immunogenetics. 1989;29(3):213-6. doi: 10.1007/BF00373649.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验