Interleukin-12p70-dependent interferon-γ production is crucial for resistance in African trypanosomiasis

被引:18
作者
Barkhuizen, Mark
Magez, Stefan
Atkinson, Robert A.
Brombacher, Frank
机构
[1] Univ Cape Town, IIDMM, Div Immunol, Fac Hlth Sci, ZA-7925 Cape Town, South Africa
[2] Vrije Univ Brussels, Univ Ghent VIB, Dept Mol & Cellular Recognit, Cellular & Mol Immunol Lab, Brussels, Belgium
基金
新加坡国家研究基金会; 英国医学研究理事会;
关键词
D O I
10.1086/521681
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
African trypanosomiasis encompasses diseases caused by pathogenic trypanosomes, infecting both humans and animals. In the present article, we dissected the possible role of members of the interleukin ( IL)-12 family during infection with Trypanosoma brucei brucei and Trypanosoma evansi in mice. IL-12p35(-/-) , IL-12p40(-/-) , and IL-12p35(-/-)/p40(-/-) mice were susceptible to both pathogens, as was demonstrated by the increased mortality among these mice, compared with wild-type C57BL/6 mice. The different IL-12p70(-/-) mouse strains showed similar mortality kinetics, suggesting that IL-12p70 - but not the IL-12p80 homodimer or IL-23 plays a crucial role in survival. Although there were similar plasma levels of immunoglobulin (Ig) M and IgG2a in IL-12-deficient mice and wild-type mice, interferon (IFN) - g production, especially during early infection, was severely impaired in all IL-12p70(-/-) mouse strains, demonstrating an IL-12p70 - dependent mechanism for IFN-gamma production. Because IFN-gamma receptor-deficient mice (IFN-gamma R-/(-)) were also highly susceptible to both Trypanosoma species, IL-12p70 - dependent IFN-gamma production seems to be the important mechanism involved in resistance against both pathogens.
引用
收藏
页码:1253 / 1260
页数:8
相关论文
共 38 条
[31]   The VSG expression sites of Trypanosoma brucei:: multipurpose tools for the adaptation of the parasite to mammalian hosts [J].
Pays, E ;
Lips, S ;
Nolan, D ;
Vanhamme, L ;
Pérez-Morga, D .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 2001, 114 (01) :1-16
[32]  
Piccotti JR, 1998, J IMMUNOL, V160, P1132
[33]   Comparative analysis of antibody responses against HSP60, invariant surface glycoprotein 70, and variant surface glycoprotein reveals a complex antigen-specific pattern of immunoglobulin isotype switching during infection by Trypanosoma brucei [J].
Radwanska, M ;
Magez, S ;
Michel, A ;
Stijlemans, B ;
Geuskens, M ;
Pays, E .
INFECTION AND IMMUNITY, 2000, 68 (02) :848-860
[34]   T-CELL-INDEPENDENT AND T-CELL-DEPENDENT B-CELL RESPONSES TO EXPOSED VARIANT SURFACE GLYCOPROTEIN EPITOPES IN TRYPANOSOME-INFECTED MICE [J].
REINITZ, DM ;
MANSFIELD, JM .
INFECTION AND IMMUNITY, 1990, 58 (07) :2337-2342
[35]  
SCHLEIFER KW, 1993, J IMMUNOL, V150, P2910
[36]   Interleukin-4-dependent immunoglobulin G1 isotype switch in the presence of a polarized antigen-specific Th1-cell response to the trypanosome variant surface glycoprotein [J].
Schopf, LR ;
Filutowicz, H ;
Bi, XJ ;
Mansfield, JM .
INFECTION AND IMMUNITY, 1998, 66 (02) :451-461
[37]   PURIFICATION TO HOMOGENEITY AND PARTIAL CHARACTERIZATION OF CYTOTOXIC LYMPHOCYTE MATURATION FACTOR FROM HUMAN B-LYMPHOBLASTOID CELLS [J].
STERN, AS ;
PODLASKI, FJ ;
HULMES, JD ;
PAN, YCE ;
QUINN, PM ;
WOLITZKY, AG ;
FAMILLETTI, PC ;
STREMLO, DL ;
TRUITT, T ;
CHIZZONITE, R ;
GATELY, MK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (17) :6808-6812