Long-term influence of lipid nutrition on the induction of CD8+ responses to viral or bacterial antigens

被引:28
作者
Bassaganya-Riera, J [1 ]
Hontecillas, R
Zimmerman, DR
Wannemuehler, MJ
机构
[1] Iowa State Univ, Dept Anim Sci, Ames, IA 50010 USA
[2] Iowa State Univ, Vet Med Res Inst, Ames, IA 50010 USA
关键词
pigs; pseudorabies virus; conjugated linoleic acid;
D O I
10.1016/S0264-410X(01)00465-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Porcine CD8(+) lymphocytes are critical for the development of cellular immune responses to bacterial (i.e. CD8alphaalpha(+)) and viral (i.e. CD8alphabeta(+) lymphocytes) pathogens. Vaccination and challenge modulate the kinetics of appearance of CD8(+) cells in peripheral blood. In addition to antigen-mediated modulation, nutritional modulation can also influence cell-mediated immunity. We had previously observed that diets supplemented with a mixture of conjugated linoleic acid (CLA) isomers expanded porcine CD8(+) peripheral blood mononuclear cells (PBMC). The present study aimed to investigate the influence of prior consumption of a nutraceutical, (i.e. dietary CLA) on phenotypes and effector functions of porcine PBMC following immunization with a bacterin or a modified-live viral vaccine. It was demonstrated that the effects of dietary CLA on immune cell phenotype (i.e. numbers of CD8alphabeta(+) cells) persisted after the compound was withdrawn from the diet (i.e. 67 days), whereas effector functions (i.e. antigen-stimulated proliferation and cytotoxycity) disappeared earlier (i.e. 25 days). Specifically, numbers of CD8alphabeta(+) PBMC in pigs that had been fed diets suplemented with CLA were greater than in pigs fed control (i.e. isoenergetic and unsupplemented) diets, regardless of the vaccination treatment. Furthermore, prior dietary CLA supplementation interacted with viral immunization (i.e. modified-live pseudorabies virus (PRV) vaccine) by enhancing both pseudorabies-specific proliferative responses of CD8alphabeta(+) PBMC and granzyme activities of PBMC. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1435 / 1444
页数:10
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