Kleinschmidt Sven, Meneses Felix, Nolte Ingo, Hewicker-Trautwein Marion
Department of Pathology, University of Veterinary Medicine Hannover, Bünteweg 17, D-30559 Hannover, Germany.
Vet Immunol Immunopathol. 2007 Dec 15;120(3-4):80-92. doi: 10.1016/j.vetimm.2007.07.006. Epub 2007 Jul 17.
It has been suggested but not proven that hypersensitivity type I reactions are involved in the pathogenesis of canine inflammatory bowel disease (IBD). The main effector cells in type I hypersensitivity reactions are mast cells (MCs). Canine MCs, as human MCs, can be subdivided into three subtypes according to their content of mast cell-specific proteases: tryptase (MCT), chymase (MCC), or tryptase and chymase bearing MCs (MCTC). In this study, numbers and subsets of mast cells were investigated in biopsies from the gastrointestinal tract of dogs with histopathologically confirmed lymphocytic-plasmacytic enteritis (LPE) (n=4), lymphocytic-plasmacytic colitis (LPC) (n=1) and eosinophilic gastroenterocolitis (EGE) (n=11). Paraffin sections of formalin-fixed samples from the stomach, small intestine (duodenum, jejunum, ileum) and colon were stained by using a metachromatic staining method (kresylecht-violet; KEV) and a combined enzyme histochemical and immunohistochemical technique for chymase and tryptase. Additionally, immunohistochemistry with antibodies against T cells (CD3), macrophages (myeloid/histiocyte antigen) and IgA, IgG and IgM bearing cells was conducted. Quantitative evaluation of mast cells and semiquantitative scoring of immunohistochemically stained cells were performed. Between the two histopathologically defined groups clear differences concerning mast cell numbers were detected. In most affected intestinal tissue locations of dogs with LPE/LPC a decrease in metachromatically (kresylecht-violet) stained granule-containing MCs and immunohistochemically stained MCT,C,TC was found. This reduction could be due to mast cell degranulation, a T helper cell 1 dominated reaction pattern or a "thinning out" due to increasing T cells, IgA and IgG bearing cells. Dogs with EGE displayed higher variability in mast cell numbers but most of the affected large and small intestinal locations had increased numbers of MCs. In these cases, T cells, IgA bearing cells and macrophages also increased. Increased numbers of MCs and eosinophils seen in the intestinal mucosa of dogs with EGE could indicate the presence of a type I hypersensitivity reaction (T helper cell 2 pattern) in response to dietary antigens. Changes in cell numbers occurred also in unaffected locations of dogs with LPE/LPC and EGE which showed reduced MCT,C,TC, increased KEV positive cells and partially increased leucocytes and macrophages.
有人提出I型超敏反应参与犬炎性肠病(IBD)的发病机制,但尚未得到证实。I型超敏反应中的主要效应细胞是肥大细胞(MCs)。犬MCs与人MCs一样,根据其肥大细胞特异性蛋白酶的含量可分为三个亚型:类胰蛋白酶(MCT)、糜蛋白酶(MCC)或同时含有类胰蛋白酶和糜蛋白酶的MCs(MCTC)。在本研究中,对组织病理学确诊为淋巴细胞性浆细胞性肠炎(LPE)(n = 4)、淋巴细胞性浆细胞性结肠炎(LPC)(n = 1)和嗜酸性胃肠结肠炎(EGE)(n = 11)的犬胃肠道活检组织中的肥大细胞数量和亚群进行了研究。使用异染性染色方法(结晶紫;KEV)以及针对糜蛋白酶和类胰蛋白酶的联合酶组织化学和免疫组织化学技术,对来自胃、小肠(十二指肠、空肠、回肠)和结肠的福尔马林固定样本的石蜡切片进行染色。此外,还进行了针对T细胞(CD3)、巨噬细胞(髓样/组织细胞抗原)以及含有IgA、IgG和IgM的细胞的免疫组织化学检测。对肥大细胞进行了定量评估,并对免疫组织化学染色细胞进行了半定量评分。在两个组织病理学定义的组之间,检测到肥大细胞数量存在明显差异。在LPE/LPC犬的大多数受影响肠道组织部位,发现异染性(结晶紫)染色的含颗粒MCs以及免疫组织化学染色的MCT、MCC、MCTC减少。这种减少可能是由于肥大细胞脱颗粒、T辅助细胞1主导的反应模式,或者是由于T细胞、含IgA和IgG的细胞增加导致的“稀释”。EGE犬的肥大细胞数量变化较大,但大多数受影响的大肠和小肠部位MCs数量增加。在这些病例中,T细胞、含IgA的细胞和巨噬细胞也增加。EGE犬肠黏膜中MCs和嗜酸性粒细胞数量增加可能表明存在针对饮食抗原的I型超敏反应(T辅助细胞2模式)。LPE/LPC和EGE犬未受影响的部位也出现了细胞数量变化,表现为MCT、MCC、MCTC减少,KEV阳性细胞增加,部分白细胞和巨噬细胞增加。