Zinc supplementation increases resistance to experimental infection by Trypanosoma cruzi

被引:20
作者
Brazao, Vania [1 ]
Caetano, Leony Cristina [1 ]
Filipin, Marina Del Vecchio [1 ]
Alonso Toldo, Miriam Paula [1 ]
Caetano, Luana Naiara [1 ]
do Prado, Jos Clovis, Jr. [1 ]
机构
[1] Univ Sao Paulo, FCFRP, Dept Anal Clin Toxicol & Bromatol, Parasitol Lab, BR-14040903 Ribeirao Preto, SP, Brazil
关键词
Trypanosoma cruzi; zinc; interleukin-12 (IL-12); thymocyte and splenocyte proliferation;
D O I
10.1016/j.vetpar.2008.02.015
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学]; 100103 [病原生物学];
摘要
It is well recognized that zinc is an essential trace element for all organisms, influencing growth and affecting the development and integrity of the immune system. It is also well known that the protective response against Trypanosoma cruzi depends on both innate and acquired immunity and for the control of the parasite load and host survival, the participation of special cells such natural killer (NK), T and B lymphocytes and macrophages are required. So the aims of this study were to evaluate the effects of zinc supplementation on the host's immune response infected with T cruzi. Our data point in the direction that zinc supplementation triggered enhanced thymocyte and splenocyte proliferation as compared to unsupplied group of animals. It is also important to emphasize that interleukin-12 (IL-12) participates in the resistance to several intracellular pathogens including T cruzi. Our findings demonstrate an enhanced production of IL-12 during the acute phase of infection in zinc-supplied groups. So we conclude that zinc supplementation leads to an effective host's immune response by up-modulating the host's immune response, thus contributing in the reduction of blood parasites and the harmful pathogenic effects of the experimental Chagas' disease. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 37
页数:6
相关论文
共 27 条
[1]
Trypanosoma cruzi: IL-10, TNF, IFN-gamma, and IL-12 regulate innate and acquired immunity to infection [J].
Abrahamsohn, IA ;
Coffman, RL .
EXPERIMENTAL PARASITOLOGY, 1996, 84 (02) :231-244
[2]
ABRAHAMSOHN IA, 1995, J IMMUNOL, V155, P3955
[3]
Cytokines in innate and acquired immunity to Trypanosoma cruzi infection [J].
Abrahamsohn, IA .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 1998, 31 (01) :117-121
[4]
Interleukin-12 mediates resistance to Trypanosoma cruzi in mice and is produced by murine macrophages in response to live trypomastigotes [J].
Aliberti, JCS ;
Cardoso, MAG ;
Martins, GA ;
Gazzinelli, RT ;
Vieira, LQ ;
Silva, JS .
INFECTION AND IMMUNITY, 1996, 64 (06) :1961-1967
[5]
BRENER Z., 1962, REV INST MED TROP SAO PAULO, V4, P389
[6]
EXCESSIVE INTAKE OF ZINC IMPAIRS IMMUNE-RESPONSES [J].
CHANDRA, RK .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1984, 252 (11) :1443-1446
[7]
Interleukin-12 stimulation of lymphoproliferative responses in Trypanosoma cruzi infection [J].
Da Silva, APG ;
Abrahamsohn, ID .
IMMUNOLOGY, 2001, 104 (03) :349-354
[8]
Zinc and immune function [J].
Dardenne, M .
EUROPEAN JOURNAL OF CLINICAL NUTRITION, 2002, 56 (Suppl 3) :S20-S23
[9]
TRYPANOSOMA-CRUZI - MAINTENANCE OF PARASITE-SPECIFIC T-CELL RESPONSES IN LYMPH-NODES DURING THE ACUTE PHASE OF THE INFECTION [J].
DELAFAILLE, MAC ;
DEOLIVEIRA, LCB ;
LIMA, GCA ;
ABRAHAMSOHN, IA .
EXPERIMENTAL PARASITOLOGY, 1990, 70 (02) :164-174
[10]
GATELY MK, 1991, J IMMUNOL, V147, P874