Harnessing Invariant NKT Cells to Improve Influenza Vaccines: A Pig Perspective.

Harnessing Invariant NKT Cells to Improve Influenza Vaccines: A Pig Perspective.
复制标题

DOI:
10.3390/ijms19010068
复制
发表时间:
2017-12-27
影响因子:
5.6
通讯作者:
Driver JP
Driver JP
中科院分区:
生物学2区
文献类型:
--
作者:
Yang G;Richt JA;Driver JP

文献摘要

参考文献

被引文献

相似文献

不变的自然杀伤T(iNKT)细胞是一种“先天性”T细胞谱系,其通过其半不变的T细胞受体识别糖脂而不是肽抗原。由于iNKT细胞可以刺激广泛的免疫应答,因此人们对靶向这些细胞以增强针对各种微生物病原体的人类疫苗非常感兴趣。然而,长期被忽视的是利用iNKT细胞抗原作为表达iNKT细胞-CD 1d系统的家畜物种的疫苗佐剂的潜力。本文综述了猪iNKT细胞作为提高猪流感疫苗免疫效果的一种策略的前景。此外,我们比较了猪iNKT细胞的表型和组织分布。最后,我们讨论了在iNKT细胞激动剂可以考虑用于家畜的兽医用途之前必须克服的挑战。
Invariant natural killer T (iNKT) cells are an “innate-like” T cell lineage that recognize glycolipid rather than peptide antigens by their semi-invariant T cell receptors. Because iNKT cells can stimulate an extensive array of immune responses, there is considerable interest in targeting these cells to enhance human vaccines against a wide range of microbial pathogens. However, long overlooked is the potential to harness iNKT cell antigens as vaccine adjuvants for domestic animal species that express the iNKT cell–CD1d system. In this review, we discuss the prospect of targeting porcine iNKT cells as a strategy to enhance the efficiency of swine influenza vaccines. In addition, we compare the phenotype and tissue distribution of porcine iNKT cells. Finally, we discuss the challenges that must be overcome before iNKT cell agonists can be contemplated for veterinary use in livestock.
DOI: 10.1084/jem.191.11.1895
发表时间: 2000-06-05
影响因子: 15.3
作者:
Benlagha, K;Weiss, A;Beavis, A;Teyton, L;Bendelac, A
通讯作者: Bendelac, A
DOI: 10.1021/acschembio.7b00845
发表时间: 2017-11-01
影响因子: 4
作者:
Anderson, Regan J.;Li, Jasmine;Painter, Gavin F.
通讯作者: Painter, Gavin F.
DOI: 10.1073/pnas.0802968105
发表时间: 2008-06-17
影响因子: 11.1
作者:
Barral, Patricia;Eckl-Dorna, Julia;Batista, Facundo D.
通讯作者: Batista, Facundo D.
DOI: 10.1073/pnas.0700191104
发表时间: 2007-03-06
影响因子: 11.1
作者:
Galli, Grazia;Pittoni, Paola;Abrignani, Sergio
通讯作者: Abrignani, Sergio
DOI: 10.1038/ni.2490
发表时间: 2013-01
期刊: Nature immunology
影响因子: 30.5
作者:
通讯作者: --