The age-related resistance of rats to Plasmodium berghei infection is associated with differential cellular and humoral immune responses

被引:23
作者
Adam, E
Pierrot, C
Lafitte, S
Godin, C
Saoudi, A
Capron, M
Khalife, J
机构
[1] Inst Pasteur, INSERM, U547, IFR 17, F-59019 Lille, France
[2] Hop Purpan, INSERM, U563, Toulouse, France
关键词
rat; malaria; age; Plasmodium berghei; cell-mediated immunity; cytokine;
D O I
10.1016/S0020-7519(03)00176-0
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
In this study, we investigated how the age of rats would affect the course of infection of and the immune response to Plasmodium berghei. Both young (4-week-old) and adult rats (8-week-old) can be infected with P. berghei ANKA strain, with significantly higher levels of infected red blood cells in young rats. While 100% of young rats succumbed to infection, adult rats were able to clear blood parasites and no mortality was observed. Analysis of cellular distribution and circulating cytokines demonstrated the persistence of CD4+/CD25+ T cells and high expression of circulating interleukin-10 (IL-10) during the progression of infection in young-susceptible rats, whereas high levels of CD8+ T cells and natural killer T cells are detected in adult-resistant rats. Analysis of antibody isotypes showed that adult rats produced significantly higher levels of interferon-gamma (IFN-gamma)-dependent IgG2c antibodies than young rats during infection. Further evaluation of the role of IL-10, IFN-gamma and of immune cells showed that only the adoptive transfer of spleen cells from adult-resistant rats was able to convert susceptibility of young-susceptible rats to a resistant phenotype. These observations suggest that cell-mediated mechanisms are crucial for the control of a primary infection with P. berghei in Young rats. (C) 2003 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1067 / 1078
页数:12
相关论文
共 67 条
[21]  
ITOH H, 1999, JPN J HOSP PHARM, V25, P162
[22]  
JAYAWARDENA AN, 1978, IMMUNOLOGY, V34, P157
[23]   Analysis of roles of natural killer cells in defense against Plasmodium chabaudi in mice [J].
Kitaguchi, T ;
Nagoya, M ;
Amano, T ;
Suzuki, M ;
Minami, M .
PARASITOLOGY RESEARCH, 1996, 82 (04) :352-357
[24]   Human resistance to Plasmodium falciparum increases during puberty and is predicted by dehydroepiandrosterone sulfate levels [J].
Kurtis, JD ;
Mtalib, R ;
Onyango, FK ;
Duffy, PE .
INFECTION AND IMMUNITY, 2001, 69 (01) :123-128
[25]  
Langhorne J, 2002, CHEM IMMUNOL, V80, P204
[26]   Rodent malarias: the mouse as a model for understanding immune responses and pathology induced by the erythrocytic stages of the parasite [J].
Li, C ;
Seixas, E ;
Langhorne, J .
MEDICAL MICROBIOLOGY AND IMMUNOLOGY, 2001, 189 (03) :115-126
[27]   Interferon-γ responses are associated with resistance to reinfection with Plasmodium falciparum in young African children [J].
Luty, AJF ;
Lell, B ;
Schmidt-Ott, R ;
Lehman, LG ;
Luckner, D ;
Greve, B ;
Matousek, P ;
Herbich, K ;
Schmid, D ;
Migot-Nabias, F ;
Deloron, P ;
Nussenzweig, RS ;
Kremsner, PG .
JOURNAL OF INFECTIOUS DISEASES, 1999, 179 (04) :980-988
[28]   Essential role of extrathymic T cells in protection against malaria [J].
Mannoor, MK ;
Halder, RC ;
Morshed, SRM ;
Ariyasinghe, A ;
Bakir, HY ;
Kawamura, H ;
Watanabe, H ;
Sekikawa, H ;
Abo, T .
JOURNAL OF IMMUNOLOGY, 2002, 169 (01) :301-306
[29]   Resistance to malarial infection is achieved by the cooperation of NK1.1+ and NK1.1- subsets of intermediate TCR cells which are constituents of innate immunity [J].
Mannoor, MK ;
Weerasinghe, A ;
Halder, RC ;
Reza, S ;
Morshed, M ;
Ariyasinghe, A ;
Watanabe, H ;
Sekikawa, H ;
Abo, T .
CELLULAR IMMUNOLOGY, 2001, 211 (02) :96-104
[30]  
MCGOWAN A, 1981, ASPECTS DEV COMP IMM, P307