differential release and phagocytosis of tegument glycoconjugates in neurocysticercosis implications for immune evasion strategies微分释放和吞噬作用的外皮glycoconjugates脑囊尾蚴病的影响免疫逃避策略.pdfVIP

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differential release and phagocytosis of tegument glycoconjugates in neurocysticercosis implications for immune evasion strategies微分释放和吞噬作用的外皮glycoconjugates脑囊尾蚴病的影响免疫逃避策略.pdf

differential release and phagocytosis of tegument glycoconjugates in neurocysticercosis implications for immune evasion strategies微分释放和吞噬作用的外皮glycoconjugates脑囊尾蚴病的影响免疫逃避策略

Differential Release and Phagocytosis of Tegument Glycoconjugates in Neurocysticercosis: Implications for Immune Evasion Strategies 1,2 1 1,2 Jorge I. Alvarez , Jennifer Rivera , Judy M. Teale * 1 Department of Microbiology and Immunology, University of Texas Health Science Center at San Antonio, San Antonio, Texas, United States of America, 2 Department of Biology and South Texas Center for Emerging Infectious Diseases, University of Texas at San Antonio, San Antonio, Texas, United States of America Abstract Neurocysticercosis (NCC) is an infection of the central nervous system (CNS) by the metacestode of the helminth Taenia solium. The severity of the symptoms is associated with the intensity of the immune response. First, there is a long asymptomatic period where host immunity seems incapable of resolving the infection, followed by a chronic hypersensitivity reaction. Since little is known about the initial response to this infection, a murine model using the cestode Mesocestoides corti (syn. Mesocestoides vogae) was employed to analyze morphological changes in the parasite early in the infection. It was found that M. corti material is released from the tegument making close contact with the nervous tissue. These results were confirmed by infecting murine CNS with ex vivo–labeled parasites. Because more than 95% of NCC patients exhibit humoral responses against carbohydrate-based antigens, and the tegument is known to be rich in glycoconjugates (GCs), the expression of these types of molecules was analyzed in human, porcine, and murine NCC specimens. To determine the GCs present in the tegument, fluorochrome-labeled hydrazides as well as fluorochrome- labeled lectins wi

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