von Ruedorffer U, Fisch R, Peel J, Roosje P, Griot-Wenk M, Welle M
Institut for Animal Pathologie, University of Berne, CH-3012 Berne, Switzerland.
Vet J. 2003 Mar;165(2):149-56. doi: 10.1016/s1090-0233(02)00160-0.
A study was performed to test the effect of sensitization to flea antigen, followed by exposure to fleas on mast cells (MCs), their subtypes, and IgE+ cells. Biopsies were taken from flea-sensitized dogs (n=28) and non-sensitized dogs (n=5) that had been exposed to fleas. Control groups consisted of flea-sensitized (n=12) and non-sensitized dogs (n=9) that were not exposed to fleas. Biopsies, taken before, 24 and 72 h after local flea exposure, were stained with haematoxylin and eosin (H&E), toluidine blue, a double labelling technique for MC chymase and tryptase and anti-IgE. An intradermal test for flea antigen was performed and serum titres of allergen-specific IgE and IgG were measured. Significantly higher numbers (P<0.001) of double labelled MCs compared to toluidine blue stained MCs were detectable in flea-sensitized dogs independent of flea exposure. In contrast, in non-sensitized dogs, the number of toluidine blue stained MCs and the number of double labelled MCs did not differ. In flea-sensitized dogs after flea exposure the percentage of C-MC was significantly increased at day 1 (P<0.001) and day 3 (P<0.001), whereas the percentage of TC-MCs decreased significantly at day 1 (P<0.001) and day 3 (P<0.05). The percentage of T-MCs decreased (P<0.05 day 0 versus day 1; P<0.05 day 0 versus day 3). No significant difference was detectable after toluidine blue staining and staining for IgE+ cells between the groups nor between the MC density and the number of IgE+ cells. All flea-sensitized dogs had positive skin tests to flea antigen and high serum titres of flea-specific serum IgE and IgG antibodies. In non-sensitized dogs, these results were negative. Our data provide strong evidence for an upregulation of MC proteases during the process of sensitization and a generalized selective release of mast cell tryptase after exposure to the antigen.
进行了一项研究,以测试对跳蚤抗原致敏后,再接触跳蚤对肥大细胞(MCs)、其亚型和IgE+细胞的影响。对已接触跳蚤的经跳蚤致敏的犬(n=28)和未致敏的犬(n=5)进行活检。对照组由未接触跳蚤的经跳蚤致敏的犬(n=12)和未致敏的犬(n=9)组成。在局部接触跳蚤前、接触后24小时和72小时采集的活检组织,用苏木精和伊红(H&E)、甲苯胺蓝、一种用于MC糜蛋白酶和类胰蛋白酶的双重标记技术以及抗IgE进行染色。进行了跳蚤抗原的皮内试验,并测量了过敏原特异性IgE和IgG的血清滴度。在经跳蚤致敏的犬中,无论是否接触跳蚤,与甲苯胺蓝染色的MCs相比,可检测到的双重标记MCs数量显著更高(P<0.001)。相比之下,在未致敏的犬中,甲苯胺蓝染色的MCs数量和双重标记的MCs数量没有差异。在经跳蚤致敏的犬接触跳蚤后,第1天(P<0.001)和第3天(P<0.001)C-MC的百分比显著增加,而TC-MCs的百分比在第1天(P<0.001)和第3天(P<0.05)显著下降。T-MCs的百分比下降(第0天与第1天相比P<0.05;第0天与第3天相比P<0.05)。在各组之间以及MC密度和IgE+细胞数量之间,甲苯胺蓝染色和IgE+细胞染色后均未检测到显著差异。所有经跳蚤致敏的犬对跳蚤抗原的皮肤试验均为阳性,且跳蚤特异性血清IgE和IgG抗体的血清滴度较高。在未致敏的犬中,这些结果为阴性。我们的数据为致敏过程中MC蛋白酶的上调以及接触抗原后肥大细胞类胰蛋白酶的普遍选择性释放提供了有力证据。