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经排泄物-分泌物抗原免疫可减少猪的组织包囊形成。

Immunization with excreted-secreted antigens reduces tissue cyst formation in pigs.

机构信息

State Key Laboratory of Veterinary etiological Biology, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730046, China,

出版信息

Parasitol Res. 2013 Nov;112(11):3835-42. doi: 10.1007/s00436-013-3571-4. Epub 2013 Aug 15.

Abstract

It has been demonstrated that tachyzoite-pooled excreted-secreted antigens (ESAs) of Toxoplasma gondii are highly immunogenic and can be used in vaccine development. However, most of the information regarding protective immunity induced by immunization with ESAs is derived from studies using mouse model systems. These results cannot be extrapolated to pigs due to important differences in the susceptibility and immune response mechanisms between pigs and mice. We show that the immunization of pigs with ESAs emulsified in Freund's adjuvant induced not only a humoral immune response but also a cellular response. The cellular immune response was associated with the production of IFN-γ and IL-4. The humoral immune response was mainly directed against the antigens with molecular masses between 34 and 116 kDa. After intraperitoneal challenge with 10(7) T. gondii of the Gansu Jingtai strain (GJS) of tachyzoites, the immunized pigs remained clinically normal except for a brief low-grade fever (≤40.5 °C), while the control pigs developed clinical signs of toxoplasmosis (cough, anorexia, prostration, and high fever). At necropsy, visible lesions were found at multiple locations (enlarged mesenteric lymph nodes, an enlarged spleen with focal necrosis, and enlarged lungs with miliary or focal necrosis and off-white lesions) in all of the control pigs but not in the pigs that had been immunized. We also found that immunization with ESAs reduced tissue cyst formation in the muscle (P < 0.01). Our data demonstrate that immunization with ESAs can trigger a strong immune response against T. gondii infection in pigs.

摘要

已证实,刚地弓形虫速殖子合并的排泄分泌抗原(ESAs)具有高度免疫原性,可用于疫苗开发。然而,大多数关于用 ESAs 免疫诱导保护免疫的信息是从使用小鼠模型系统的研究中获得的。由于猪和小鼠之间易感性和免疫反应机制的重要差异,这些结果不能外推到猪。我们表明,用弗氏佐剂乳化的 ESAs 免疫猪不仅诱导了体液免疫反应,还诱导了细胞免疫反应。细胞免疫反应与 IFN-γ和 IL-4 的产生有关。体液免疫反应主要针对分子量在 34 和 116 kDa 之间的抗原。用来自甘肃景泰株(GJS)的 10(7) 速殖子腹腔攻击免疫猪后,除短暂的低度发热(≤40.5°C)外,免疫猪仍保持临床正常,而对照猪则出现弓形虫病的临床症状(咳嗽、厌食、虚弱和高热)。剖检时,所有对照猪的多个部位(肠系膜淋巴结肿大、脾脏局灶性坏死肿大、肺脏有粟粒状或局灶性坏死和灰白色病变)都可见明显病变,但免疫猪没有。我们还发现,用 ESAs 免疫可减少肌肉中的组织包囊形成(P<0.01)。我们的数据表明,用 ESAs 免疫可引发猪对弓形虫感染的强烈免疫反应。

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