Shi X J, Zheng P L, Wang Z, Li X, Huang G, Zhou Z G
Department of Metabolism and Endocrinology, the Second Xiangya Hospital, Central South University/National Clinical Research Center for Metabolic Diseases/Key Laboratory of Diabetes Immunology, Ministry of Education, Changsha 410011, China.
Zhonghua Yi Xue Za Zhi. 2021 Jan 26;101(4):243-248. doi: 10.3760/cma.j.cn112137-20200505-01427.
To establish the luciferase immunoprecipitation system assay (LIPS) to test tetraspanin 7 autoantibody (TSPAN7A) and evaluate its value in Chinese type 1 diabetes (T1D) patients. Renilla luciferase-tagged TSPAN7 plasmids were transfected into 293T cells to obtain Renilla luciferase-tagged TSPAN7 fusion protein. The cell lysate was incubated with sera overnight, followed by addition of protein A-agarose and extensive wash. Finally, the substrate of Renilla luciferase was added and luminescence was detected. Sera from 100 T1D patients [64 males and 36 females,with a mean age of (28±16) years], 119 type 2 diabetes (T2D) patients [78 males and 41 females,with a mean age of (47±12) years] and 98 healthy volunteers [55 males and 43 females,with a mean age of (28±12) years] from the Department of Metabolism and Endocrinology of the Second Xiangya Hospital, Central South University from 2014 to 2017, were tested by LIPS to evaluate the frequency of TSPAN7A. Radioligand binding assay (RLA) was used to test glutamic acid decarboxylase autoantibodies (GADA), protein tyrosine phosphatase-2 autoantibodies (IA-2A) and zinc transporter 8 autoantibodies (ZnT8A). The frequencies of GADA, IA-2A, ZnT8A and TSPAN7A in T1D patients were 72.0%, 40.0%, 29.0% and 25.0%, respectively. After Bonferroni correction, the positivity of TSPAN7A was lower than GADA (<0.001), but similar with IA-2A (=0.035) and ZnT8A (=0.630). The positivity of TSPAN7A in T1D patients was significantly higher than that in T2D (0.84%, 0.001) and in healthy controls (1.02%, 0.001). In combination with TSPAN7A, the positivity of islet autoantibodies in T1D patients increased from 82% to 85%. There was no significant difference in clinical characteristics between TSPAN7A-positive T1D and the other three islet autoantibodies-positive patients. This study succeeded in establishing LIPS method to assay TSPAN7A. Moreover, TSPAN7A are valid islet autoantibodies for T1D patients in China.
建立荧光素酶免疫沉淀系统分析(LIPS)以检测四跨膜蛋白7自身抗体(TSPAN7A),并评估其在中国1型糖尿病(T1D)患者中的价值。将海肾荧光素酶标记的TSPAN7质粒转染至293T细胞中,以获得海肾荧光素酶标记的TSPAN7融合蛋白。细胞裂解物与血清孵育过夜,随后加入蛋白A琼脂糖并充分洗涤。最后,加入海肾荧光素酶的底物并检测发光。对2014年至2017年来自中南大学湘雅二医院代谢内分泌科的100例T1D患者[男64例,女36例,平均年龄(28±16)岁]、119例2型糖尿病(T2D)患者[男78例,女41例,平均年龄(47±12)岁]和98例健康志愿者[男55例,女43例,平均年龄(28±12)岁]的血清进行LIPS检测,以评估TSPAN7A的频率。采用放射性配体结合分析(RLA)检测谷氨酸脱羧酶自身抗体(GADA)、蛋白酪氨酸磷酸酶2自身抗体(IA-2A)和锌转运体8自身抗体(ZnT8A)。T1D患者中GADA、IA-2A、ZnT8A和TSPAN7A的频率分别为72.0%、40.0%、29.0%和25.0%。经Bonferroni校正后,TSPAN7A的阳性率低于GADA(<0.001),但与IA-2A(=0.035)和ZnT8A(=0.630)相似。T1D患者中TSPAN7A的阳性率显著高于T2D患者(0.84%,P=0.001)和健康对照者(1.02%,P=0.001)。联合TSPAN7A后,T1D患者中胰岛自身抗体的阳性率从82%提高到85%。TSPAN7A阳性的T1D患者与其他三种胰岛自身抗体阳性患者的临床特征无显著差异。本研究成功建立了检测TSPAN7A的LIPS方法。此外,TSPAN7A是中国T1D患者有效的胰岛自身抗体。