Gloria-Bottini F, Bottini N, Renzetti G, Bottini E
Department of Biopathology and Imaging Diagnostics, University of Rome Tor Vergata, Rome, Italy.
Int Arch Allergy Immunol. 2007;143(3):170-6. doi: 10.1159/000099308. Epub 2007 Feb 5.
Data collected by our group in the past years indicate a relationship between ACP1 genetic polymorphism and susceptibility/resistance to immunological diseases. Recent observations suggest that through modulation of ZAP-70 activity, the enzyme may influence T cell activation. In view of the current interest in gender differences in autoimmune diseases we reviewed our data to enlighten possible effects of gender on the relationship between ACP1 and class of immunological disease.
We studied three samples of subjects with allergic disorders of a total of 299 subjects, 71 subjects with Crohn's disease and 188 children with type 1 diabetes. Three-way contingency tables were analyzed by a log linear model and two-way contingency tables by chi(2) test.
There is an association between ACP1 and allergy (Th2 class) that depends on gender: the presence of the ACP1*A allele seems to make females more susceptible to allergic manifestations as compared to males. ACP1 is also associated with Crohn's disease and type 1 diabetes: the relationship between this class (Th1) of immunological diseases and ACP1 depends on gender. The presence of *A allele seems to make females less susceptible to this class of diseases as compared to males.
The ACP1*A allele which is associated with low ACP1 activity appears responsible for a complex relationship involving gender, ACP1 and Th1/Th2 orientation. Low ACP1 activity influencing ZAP-70 activity and in turn T cell activation seems to have opposite effects on Th1/Th2 orientation depending on gender.
我们小组在过去几年收集的数据表明,ACP1基因多态性与免疫疾病的易感性/抗性之间存在关联。最近的观察结果表明,通过调节ZAP-70的活性,该酶可能影响T细胞的激活。鉴于目前对自身免疫性疾病中性别差异的关注,我们回顾了我们的数据,以阐明性别对ACP1与免疫疾病类别之间关系的可能影响。
我们研究了三组受试者样本,其中共有299名患有过敏性疾病的受试者、71名患有克罗恩病的受试者和188名患有1型糖尿病的儿童。通过对数线性模型分析三维列联表,通过卡方检验分析二维列联表。
ACP1与过敏(Th2类)之间存在关联,且这种关联取决于性别:与男性相比,ACP1*A等位基因的存在似乎使女性更容易出现过敏表现。ACP1也与克罗恩病和1型糖尿病有关:这类(Th1)免疫疾病与ACP1之间的关系取决于性别。与男性相比,*A等位基因的存在似乎使女性对这类疾病的易感性较低。
与低ACP1活性相关的ACP1*A等位基因似乎导致了一种涉及性别、ACP1和Th1/Th2方向的复杂关系。低ACP1活性影响ZAP-70活性,进而影响T细胞激活,这似乎根据性别对Th1/Th2方向产生相反的影响。