Tezuka Hiroyuki, Imai Shinjiro, Hidano Shinya, Tsukidate Setsuko, Fujita Koichiro
Section of Environmental Parasitology, Department of Internation Health Development, Division of Public Health, Graduate School, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8519, Japan.
Infect Immun. 2003 Jul;71(7):3802-11. doi: 10.1128/IAI.71.7.3802-3811.2003.
Dirofilaria immitis polyproteins (DiAgs) are found as 15-kDa monomeric and 30-kDa dimeric forms in excretory-secretory products of the adult worm. We evaluated the ability of various types of recombinant DiAg (rDiAg; V1 and V2 as monomers and V1V2, V2V1, V1V1, and V2V2 as dimers) to influence Th1/Th2 immune responses. V1-, V1Vx- and V2-, V2Vx-driven nonspecific immunoglobulin E (IgE) production peaked at 21 and 14 days after administration, respectively. Dimer-induced IgE response was an interesting biphasic pattern with the second peaks on days 35 (V2Vx) or 42 (V1Vx). Absolute amounts of nonspecific IgE production induced with monomers were larger than those observed with dimers at the first peak. The magnitude of cell expansion and interleukin-10 (IL-10) production in mesenteric lymph node (MLN) B-cell induced with rDiAgs was linked to the levels of the first IgE peak in vivo and IgE produced by rDiAg plus IL-4-stimulated B cells in vitro. All rDiAgs failed to augment IgG2c production. V2 and V2Vx elicited IL-4 production by MLN cells more rapidly than V1 and V1Vx. The inhibitory effect of rDiAg on gamma interferon (IFN-gamma) production was stronger in monomers than in dimers. Neutralization of IL-10 restored IFN-gamma production, whereas the expression of IL-4 and IgE was partly prevented by depletion of IL-10. These results indicate that monomer rather than dimer is an efficient form of DiAg and suggest that the difference of IgE-inducing capacity among these DiAgs is closely associated with the pattern of both B-cell activation and IL-4 production.
犬恶丝虫多聚蛋白(DiAgs)以15 kDa单体和30 kDa二聚体形式存在于成虫的排泄分泌产物中。我们评估了各种类型的重组DiAg(rDiAg;V1和V2为单体,V1V2、V2V1、V1V1和V2V2为二聚体)影响Th1/Th2免疫反应的能力。V1、V1Vx驱动的非特异性免疫球蛋白E(IgE)产生分别在给药后21天和14天达到峰值。V2、V2Vx驱动的非特异性免疫球蛋白E(IgE)产生分别在给药后21天和14天达到峰值。二聚体诱导的IgE反应呈现出有趣的双相模式,在第35天(V2Vx)或第42天(V1Vx)出现第二个峰值。在第一个峰值时,单体诱导产生的非特异性IgE的绝对量大于二聚体。rDiAgs诱导的肠系膜淋巴结(MLN)B细胞中的细胞扩增和白细胞介素-10(IL-10)产生的程度与体内第一个IgE峰值水平以及rDiAg加IL-4刺激的B细胞在体外产生的IgE相关。所有rDiAgs均未能增强IgG2c的产生。V2和V2Vx比V1和V1Vx更快地诱导MLN细胞产生IL-4。rDiAg对γ干扰素(IFN-γ)产生的抑制作用在单体中比在二聚体中更强。IL-10的中和恢复了IFN-γ的产生,而IL-4和IgE的表达则因IL-10的缺失而部分受到抑制。这些结果表明,DiAg的有效形式是单体而非二聚体,并表明这些DiAgs之间IgE诱导能力的差异与B细胞活化和IL-4产生的模式密切相关。