Evans C A, Gonzalez A E, Gilman R H, Verastegui M, Garcia H H, Chavera A, Pilcher J B, Tsang V C
Department of Medicine, Addenbrooke's Hospital, Cambridge, United Kingdom.
Am J Trop Med Hyg. 1997 Jan;56(1):33-7. doi: 10.4269/ajtmh.1997.56.33.
Taenia solium cysticercosis is an important cause of human disease in many developing countries. Porcine cysticercosis is a vital link in the transmission of this disease and impairs meat production. A treatment for porcine cysticercosis may be an effective way of preventing human disease that would also benefit pig farmers, facilitating control programs in disease-endemic regions. Previous research suggests that reinfection with cysticercosis or immunotherapy with cysticercal antigens may cause degeneration of cysticerci, potentially curing porcine cysticercosis. Therefore, a blinded, randomized, controlled study to assess the efficacy and safety of immunotherapy in 28 naturally parasitized pigs was performed. Four groups of pigs with similar weights were inoculated twice with membrane-enriched cysticercal antigens (MA), saline, aqueous-soluble crude cysticercal antigens (AA) in adjuvant (Freund's complete then incomplete), or adjuvant alone. Immunotherapy was well tolerated but had no consistent effect on the macroscopic appearance of cysticerci or eosinophil count. Histopathologic findings were variable, with both severe and minimal inflammatory reactions seen in adjacent cysticerci in all pigs. Nine (64%) of 14 pigs given immunotherapy developed new antibody bands on electroimmunotransfer blot compared with one (7%) of 14 control pigs (P < 0.01). Treatment with AA in adjuvant caused a significant increase in the proportion of cysticerci that failed to evaginate and were, therefore, not viable for infecting humans (34% for pigs given AA in adjuvant compared with 10% for adjuvant alone; P < 0.04). Although immunotherapy caused a statistically significant decrease in the viability of cysticerci, this immunologic reaction was not great enough to prevent human disease.
猪带绦虫囊尾蚴病是许多发展中国家人类疾病的重要病因。猪囊尾蚴病是该疾病传播的关键环节,并且会影响肉类生产。治疗猪囊尾蚴病可能是预防人类疾病的有效方法,这对养猪户也有益,有助于在疾病流行地区开展防控项目。先前的研究表明,再次感染囊尾蚴病或用囊尾蚴抗原进行免疫治疗可能会导致囊尾蚴退化,有可能治愈猪囊尾蚴病。因此,开展了一项双盲、随机、对照研究,以评估免疫疗法对28头自然感染猪的疗效和安全性。将四组体重相似的猪分别接种两次富含膜的囊尾蚴抗原(MA)、生理盐水、佐剂(先弗氏完全佐剂后弗氏不完全佐剂)中的水溶性粗囊尾蚴抗原(AA)或仅接种佐剂。免疫疗法耐受性良好,但对囊尾蚴的宏观外观或嗜酸性粒细胞计数没有一致的影响。组织病理学结果各不相同,所有猪相邻囊尾蚴中均可见严重和轻微的炎症反应。与14头对照猪中的1头(7%)相比,接受免疫治疗的14头猪中有9头(64%)在电免疫转移印迹上出现了新的抗体条带(P < 0.01)。用佐剂中的AA治疗导致不能外翻从而对人类无感染性的囊尾蚴比例显著增加(接受佐剂中AA治疗的猪为34%,而仅接受佐剂治疗的猪为10%;P < 0.04)。虽然免疫疗法使囊尾蚴的活力在统计学上显著降低,但这种免疫反应不足以预防人类疾病。