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虹鳟鱼红点综合征:用组织学、免疫组织化学和免疫基因表达分析研究病变中的免疫反应。

Red mark syndrome in rainbow trout Oncorhynchus mykiss: investigation of immune responses in lesions using histology, immunohistochemistry and analysis of immune gene expression.

机构信息

Ellis Building, Marine Scotland Science, Marine Laboratory, 375 Victoria Road, PO Box 101, Aberdeen AB11 9DB, Scotland, UK.

出版信息

Fish Shellfish Immunol. 2013 May;34(5):1119-30. doi: 10.1016/j.fsi.2013.01.019. Epub 2013 Feb 9.

Abstract

Red mark syndrome (RMS) is an economically significant disease which affects farmed rainbow trout in the United Kingdom, in the US and in mainland Europe. From the pattern of incidence, it appears to be transmissable, although no causative agent has yet been identified. RMS presents as a severe lymphocytic infiltration centred on the dermis and an alternative, host-focused approach was taken to understand the disease through investigating immune responses occurring in the lesion. Lesion and non-lesion skin at different stages of lesion development were examined using histochemistry and immunohistochemistry on paraffin sections. Expression of immune-related genes was compared between lesion and non-lesion skin. Investigation of early stage lesions suggested that the initial immune response is targeted at the region of the scale pocket, with lymphocyte infiltration and anti-tumour necrosis factor (TNF)-α staining of the stratum spongiosum, and increased numbers of major histocompatibility complex (MHC) II-positive cells immediately adjacent to the scale pocket. Gene expression analysis suggested a counterbalancing T helper (Th)1 and T regulatory (Treg) - type response is occurring in the lesion, with repression of Th2 and Th17-type responses.

摘要

红斑综合征(RMS)是一种在英国、美国和欧洲大陆养殖虹鳟鱼中具有重要经济意义的疾病。根据发病模式,它似乎具有传染性,尽管尚未确定病原体。RMS 的特征是真皮层以淋巴细胞浸润为主,为了了解这种疾病,我们采取了一种替代的宿主为中心的方法,研究病变中发生的免疫反应。在病变发展的不同阶段,对病变和非病变皮肤进行了石蜡切片的组织化学和免疫组织化学检查。比较了病变和非病变皮肤之间免疫相关基因的表达。对早期病变的研究表明,最初的免疫反应针对鳞片囊区域,表现为淋巴细胞浸润和棘层海绵状 TNF-α 染色,并且紧邻鳞片囊的主要组织相容性复合体(MHC)II 阳性细胞数量增加。基因表达分析表明,病变中发生了一种平衡的辅助性 T 细胞(Th)1 和 T 调节(Treg)型反应,抑制了 Th2 和 Th17 型反应。

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