Department of Clinical Pharmacy, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Engineering and Technology Research Center for Pediatric Drug Development, Shandong Medicine and Health Key Laboratory of Clinical Pharmacy, Jinan, China.
Department of Clinical Pharmacy, Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan, China.
Front Immunol. 2022 Oct 24;13:1015409. doi: 10.3389/fimmu.2022.1015409. eCollection 2022.
The incidence and complexity of drug-induced autoimmune diseases (DIAD) have been on the rise in recent years, which may lead to serious or fatal consequences. Besides, many environmental and industrial chemicals can also cause DIAD. However, there are few effective approaches to estimate the DIAD potential of drugs and other chemicals currently, and the structural characteristics and mechanism of action of DIAD compounds have not been clarified. In this study, we developed the models for chemical DIAD prediction and investigated the structural characteristics of DIAD chemicals based on the reliable drug data on human autoimmune diseases. We collected 148 medications which were reported can cause DIAD clinically and 450 medications that clearly do not cause DIAD. Several different machine learning algorithms and molecular fingerprints were combined to develop the models. The best performed model provided the good overall accuracy on validation set with 76.26%. The model was made freely available on the website http://diad.sapredictor.cn/. To further investigate the differences in structural characteristics between DIAD chemicals and non-DIAD chemicals, several key physicochemical properties were analyzed. The results showed that AlogP, molecular polar surface area (MPSA), and the number of hydrogen bond donors (nHDon) were significantly different between the DIAD and non-DIAD structures. They may be related to the DIAD toxicity of chemicals. In addition, 14 structural alerts (SA) for DIAD toxicity were detected from predefined substructures. The SAs may be helpful to explain the mechanism of action of drug induced autoimmune disease, and can used to identify the chemicals with potential DIAD toxicity. The structural alerts have been integrated in a structural alert-based web server SApredictor (http://www.sapredictor.cn). We hope the results could provide useful information for the recognition of DIAD chemicals and the insights of structural characteristics for chemical DIAD toxicity.
近年来,药物诱导的自身免疫性疾病(DIAD)的发病率和复杂性一直在上升,这可能导致严重或致命的后果。此外,许多环境和工业化学品也会引起 DIAD。然而,目前评估药物和其他化学品的 DIAD 潜力的有效方法很少,并且 DIAD 化合物的结构特征和作用机制尚不清楚。在这项研究中,我们基于可靠的人类自身免疫性疾病药物数据,开发了用于化学 DIAD 预测的模型,并研究了 DIAD 化学品的结构特征。我们收集了 148 种临床上报道可引起 DIAD 的药物和 450 种明确不会引起 DIAD 的药物。我们结合了几种不同的机器学习算法和分子指纹,开发了 模型。最佳模型在验证集上的整体准确性达到了 76.26%。该模型已在网站 http://diad.sapredictor.cn/ 上免费提供。为了进一步研究 DIAD 化学品和非 DIAD 化学品之间结构特征的差异,我们分析了几个关键的物理化学性质。结果表明,DIAD 和非 DIAD 结构之间的 AlogP、分子极性表面积(MPSA)和氢键供体数(nHDon)有显著差异。这些性质可能与化学品的 DIAD 毒性有关。此外,我们从预定义的子结构中检测到了 14 种 DIAD 毒性结构警示(SA)。这些警示可能有助于解释药物诱导自身免疫疾病的作用机制,并可用于识别具有潜在 DIAD 毒性的化学品。结构警示已集成到基于结构警示的网络服务器 SAPredictor(http://www.sapredictor.cn)中。我们希望这些结果能为识别 DIAD 化学品和了解化学 DIAD 毒性的结构特征提供有用的信息。