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靶向Fc2'-3-PE40嵌合蛋白可消除小鼠的被动皮肤过敏反应。

Targeted Fc2'-3-PE40 chimeric protein abolishes passive cutaneous anaphylaxis in mice.

作者信息

Fishman A, Prus D, Belostotsky R, Lorberboum-Galski H

机构信息

Department of Cellular Biochemistry, Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

Clin Exp Immunol. 2000 Mar;119(3):398-403. doi: 10.1046/j.1365-2249.2000.01151.x.

Abstract

The alarming increase in the incidence of allergic diseases in the past decade has led to a clear call for more effective treatment. Recently, we reported on the construction of a chimeric protein for targeted elimination of cells expressing FcepsilonRI receptors. This chimeric protein, designated Fc2'-3-PE40, is composed of a Fc fragment of mouse IgE attached to a truncated form of Pseudomonas exotoxin. The Fc2'-3-PE40 chimeric protein was found to be highly cytotoxic to mouse mast cell lines and primary mouse mast cells. We now demonstrate that Fc2'-3-PE40 successfully prevents the development of passive cutaneous anaphylaxis reaction (PCA) in mice. Treatment with Fc2'-3-PE40 for 7 days prevented the PCA reaction in mice by 80% compared with that in control mice given only PBS. Fc2'-3-PE40M, the mutated, enzymatically inactive analogue of Fc2'-3-PE40, did not display this activity. Fc2'-3-PE40 was also effective when given as a single dose 16 h before antigen exposure, resulting in complete inhibition of the PCA reaction. Moreover, treatment with Fc2'-3-PE40 did not cause mast cell degranulation, as the serum histamine values of mice treated with Fc2'-3-PE40 were within the range obtained for control, untreated mice. Thus, the Fc2'-3-PE40 chimeric protein offers a novel approach to the treatment of allergic disorders.

摘要

在过去十年中,过敏性疾病发病率惊人地上升,这明确呼吁要有更有效的治疗方法。最近,我们报道了一种用于靶向清除表达FcepsilonRI受体细胞的嵌合蛋白的构建。这种嵌合蛋白命名为Fc2'-3-PE40,由连接到铜绿假单胞菌外毒素截短形式的小鼠IgE的Fc片段组成。发现Fc2'-3-PE40嵌合蛋白对小鼠肥大细胞系和原代小鼠肥大细胞具有高度细胞毒性。我们现在证明Fc2'-3-PE40成功地预防了小鼠被动皮肤过敏反应(PCA)的发生。与仅给予PBS的对照小鼠相比,用Fc2'-3-PE40治疗7天可使小鼠的PCA反应降低80%。Fc2'-3-PE40的突变体、无酶活性类似物Fc2'-3-PE40M不显示这种活性。在抗原暴露前16小时单次给予Fc2'-3-PE40也有效,可完全抑制PCA反应。此外,用Fc2'-3-PE40治疗不会引起肥大细胞脱颗粒,因为用Fc2'-3-PE40治疗的小鼠血清组胺值在未治疗的对照小鼠的范围内。因此,Fc2'-3-PE40嵌合蛋白为过敏性疾病的治疗提供了一种新方法。

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