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来自感染肝片吸虫大鼠的腹膜细胞辅助活性的改变

Modification of accessory activity of peritoneal cells from Fasciola hepatica infected rats.

作者信息

Masih D T, Cervi L, Casado J M

机构信息

Departamento de Bioquímica Clinica, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Argentina.

出版信息

Vet Immunol Immunopathol. 1996 Oct;53(3-4):257-68. doi: 10.1016/S0165-2427(96)05611-5.

Abstract

The effect of Fasciola hepatica excretory-secretory antigen (ESA) was studied in the modulation of the accessory functions of peritoneal cells (PC) of rats infected with the parasite. PC rats infected with F. hepatica 7 and 14 days previously showed a marked decrease in phagocytic activity against Candida tropicalis (P < 0.007 and P < 0.004, respectively). The same effect was observed when the assay was carried out with PC from animals injected 7 days before with ESA (P < 0.001) including PC previously treated in vitro with ESA. To investigate the effect of ESA on the antigen presenting ability, PC of animals infected before transfer to syngeneic normal rats were stimulated in vitro with either F. hepatica whole antigen (FhWA), ESA or human serum albumin (HSA). Delayed type hypersensitivity (DTH) response to the different antigens studied over a 35 day period was negative in rats transferred with sensitised PC. When these animals were immunised with the corresponding antigen the DTH response became positive. A similar result was obtained in PC receptors from ESA inoculated rats and in vitro stimulated with FhWA or HSA. These data suggest that the alterations observed in the functions of peritoneal cells may, in part be due to the effect of the F. hepatica ESA.

摘要

研究了肝片吸虫排泄分泌抗原(ESA)对感染该寄生虫的大鼠腹膜细胞(PC)辅助功能的调节作用。感染肝片吸虫7天和14天的大鼠PC对热带念珠菌的吞噬活性显著降低(分别为P < 0.007和P < 0.004)。当用7天前注射ESA的动物的PC进行检测时,包括先前在体外经ESA处理的PC,也观察到了相同的效果(P < 0.001)。为了研究ESA对抗原呈递能力的影响,将感染后转移至同基因正常大鼠的动物的PC在体外分别用肝片吸虫全抗原(FhWA)、ESA或人血清白蛋白(HSA)刺激。在转移致敏PC的大鼠中,在35天期间对所研究的不同抗原的迟发型超敏反应(DTH)为阴性。当用相应抗原免疫这些动物时,DTH反应变为阳性。在用ESA接种的大鼠的PC受体中以及在体外用FhWA或HSA刺激时也获得了类似的结果。这些数据表明,在腹膜细胞功能中观察到的改变可能部分归因于肝片吸虫ESA的作用。

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