Zorzopulos Jorge, Opal Steven M, Hernando-Insúa Andrés, Rodriguez Juan M, Elías Fernanda, Fló Juan, López Ricardo A, Chasseing Norma A, Lux-Lantos Victoria A, Coronel Maria F, Franco Raul, Montaner Alejandro D, Horn David L
Jorge Zorzopulos, Juan Fló, Ricardo A López, Raul Franco, Immunotech S.A., Ciudad de Buenos Aires C1440FFX, Argentina.
World J Stem Cells. 2017 Mar 26;9(3):45-67. doi: 10.4252/wjsc.v9.i3.45.
The immune responses of humans and animals to insults (., infections, traumas, tumoral transformation and radiation) are based on an intricate network of cells and chemical messengers. Abnormally high inflammation immediately after insult or abnormally prolonged pro-inflammatory stimuli bringing about chronic inflammation can lead to life-threatening or severely debilitating diseases. Mesenchymal stem cell (MSC) transplant has proved to be an effective therapy in preclinical studies which evaluated a vast diversity of inflammatory conditions. MSCs lead to resolution of inflammation, preparation for regeneration and actual regeneration, and then ultimate return to normal baseline or homeostasis. However, in clinical trials of transplanted MSCs, the expectations of great medical benefit have not yet been fulfilled. As a practical alternative to MSC transplant, a synthetic drug with the capacity to boost endogenous MSC expansion and/or activation may also be effective. Regarding this, IMT504, the prototype of a major class of immunomodulatory oligonucleotides, induces expansion of MSCs, resulting in a marked improvement in preclinical models of neuropathic pain, osteoporosis, diabetes and sepsis. IMT504 is easily manufactured and has an excellent preclinical safety record. In the small number of patients studied thus far, IMT504 has been well-tolerated, even at very high dosage. Further clinical investigation is necessary to demonstrate the utility of IMT504 for resolution of inflammation and regeneration in a broad array of human diseases that would likely benefit from an immunoprotective/immunoregenerative therapy.
人类和动物对损伤(如感染、创伤、肿瘤转化和辐射)的免疫反应基于一个由细胞和化学信使构成的复杂网络。损伤后立即出现的异常高度炎症或导致慢性炎症的异常延长的促炎刺激可引发危及生命或严重致残的疾病。在评估了多种炎症状况的临床前研究中,间充质干细胞(MSC)移植已被证明是一种有效的治疗方法。间充质干细胞可促使炎症消退、为再生做准备并实现实际再生,最终恢复到正常基线或内稳态。然而,在间充质干细胞移植的临床试验中,尚未实现人们对其巨大医疗益处的期望。作为间充质干细胞移植的一种实际替代方法,一种具有促进内源性间充质干细胞扩增和/或激活能力的合成药物可能也有效。关于这一点,一类主要免疫调节寡核苷酸的原型IMT504可诱导间充质干细胞扩增,在神经性疼痛、骨质疏松症、糖尿病和败血症的临床前模型中产生显著改善。IMT504易于制造,且具有出色的临床前安全记录。在迄今为止研究的少数患者中,即使使用非常高的剂量,IMT504也具有良好的耐受性。有必要进行进一步的临床研究,以证明IMT504在一系列可能受益于免疫保护/免疫再生疗法的人类疾病中解决炎症和促进再生的效用。