Jungersen G, Eriksen L, Nansen P, Lind P, Rasmussen T, Meeusen E N
Department of Clinical Studies, Large Animal Medicine, Royal Veterinary and Agricultural University, Frederiksberg C, Copenhagen, Denmark.
Parasite Immunol. 2001 Apr;23(4):185-94. doi: 10.1046/j.1365-3024.2001.00373.x.
The early life-cycle of the pig round worm, Ascaris suum, involves well-defined larval development in the liver, lungs and finally the small intestine. Distinct regional immune responses to larval antigens of A. suum were observed in the draining lymph nodes of immunized and challenged pigs during larval migration. This was reflected in a transient enlargement of the stimulated lymph nodes, due to increases in numbers of B cells and CD4 T cells, and the production of A. suum-specific antibody by antibody secreting cell (ASC) cultures. Larval antigen recognition pattern of antibodies in serum, bile and draining lymph node ASC culture supernatant (ASC-probes) was examined by immunoblotting. This revealed distinct organ-specific recognition patterns of larval-specific antigens by the draining lymph nodes at different times after challenge. In particular, an early larval 42 kDa antigen was recognized specifically by ASC-probes of the liver lymph nodes at 7 but not 14 days postchallenge (pc) which was not detected in other lymph nodes, serum or bile of the same pig. Similarly, a late larval antigen of 34 kDa was uniquely detected by lung and jejunal ASC-probes at 14 days pc. These observations demonstrate how development of distinct regional immune responses in tissues with different antigen stimulation can be monitored with ASC-probes and flow cytometry.
猪蛔虫(猪蛔虫)的早期生命周期包括在肝脏、肺部以及最终在小肠中明确的幼虫发育过程。在幼虫移行期间,在免疫和激发的猪的引流淋巴结中观察到对猪蛔虫幼虫抗原的不同区域免疫反应。这表现为受刺激的淋巴结短暂肿大,这是由于B细胞和CD4 T细胞数量增加以及抗体分泌细胞(ASC)培养物产生猪蛔虫特异性抗体所致。通过免疫印迹法检测血清、胆汁和引流淋巴结ASC培养上清液(ASC探针)中抗体的幼虫抗原识别模式。这揭示了激发后不同时间引流淋巴结对幼虫特异性抗原的不同器官特异性识别模式。特别是,一种早期幼虫42 kDa抗原在激发后7天被肝脏淋巴结的ASC探针特异性识别,但在激发后14天未被识别,且在同一头猪的其他淋巴结、血清或胆汁中未检测到。同样,一种晚期幼虫34 kDa抗原在激发后14天被肺和空肠的ASC探针独特地检测到。这些观察结果表明,如何用ASC探针和流式细胞术监测不同抗原刺激组织中不同区域免疫反应的发展。