Mishra Reema, Agarwal Preeti, Sharma Anshita, Mittal Meenal, Gulati Pooja, Mohanty Aparajita
Department of Botany, Gargi College, University of Delhi, India.
Department of Microbiology, Maharshi Dayanand University, Rohtak, Haryana, India.
Protein Pept Lett. 2025 Mar 18. doi: 10.2174/0109298665364479250214101422.
The incidences of immune-related disorders have drastically increased in recent years across the world population. Treatment and management of these diseases, especially autoimmune disorders, are complex and challenging. Available synthetic drugs are not completely effective and also pose serious side effects for the patients. Cyclotides are a class of plant-derived cyclic peptides (28-37 amino acids) with three conserved disulfide linkages establishing a cyclic cystine knot (CCK) motif that makes them very stable biomolecules. Their inherent stability, bioavailability and membrane-penetrating capabilities render them attractive potential pharmacological agents. Studies have demonstrated that cyclotides can either enhance or suppress immune responses, making them versatile candidates for treating various immune-related disorders. Of more than 1000 cyclotides discovered to date, only up to 15 native cyclotides (e.g. kalata B1, pase and caripe cyclotides) have been screened to demonstrate their immunomodulatory activity. Of special significance is the chemically synthesised lysine mutant of kalata B1 viz. [T20K], where preclinical studies have shown promise in the treatment of the autoimmune disorder, multiple sclerosis. In vivo studies in mice models have demonstrated that daily administration of 1mg/day of [T20K] led to a significant decrease in the level of cytokine secretion, lesser demyelination (<1%) and very low inflammatory index (<0.5), in the immunized mice. Moreover, when compared with other immunosuppressive drugs (azathioprine, prednisolone, and cyclosporine A) there was a notable drop in mortality and morbidity in mice administered with [T20K]. The cyclotides, kalata B1 and MCoTI-I have also been used as scaffolds to graft bioactive peptides with immunomodulatory activity. Subsequent in vitro and in vivo studies of these grafted cyclotides have demonstrated their therapeutic ability. Keeping in view the therapeutic potential of cyclotides as immunomodulatory peptides, the present review discusses its current research scenario and implications for the future in tackling immune-related disorders.
近年来,免疫相关疾病的发病率在全球人口中急剧上升。这些疾病,尤其是自身免疫性疾病的治疗和管理复杂且具有挑战性。现有的合成药物并不完全有效,而且对患者也有严重的副作用。环肽是一类植物来源的环肽(28 - 37个氨基酸),具有三个保守的二硫键,形成一个环胱氨酸结(CCK)基序,这使它们成为非常稳定的生物分子。它们固有的稳定性、生物利用度和膜穿透能力使它们成为有吸引力的潜在药理剂。研究表明,环肽可以增强或抑制免疫反应,使其成为治疗各种免疫相关疾病的多功能候选药物。在迄今发现的1000多种环肽中,只有多达15种天然环肽(如卡拉塔B1、帕塞环肽和卡里佩环肽)经过筛选以证明其免疫调节活性。特别重要的是卡拉塔B1的化学合成赖氨酸突变体,即[T20K],临床前研究表明它在治疗自身免疫性疾病多发性硬化症方面有前景。在小鼠模型中的体内研究表明,每天给予1mg/天的[T20K]可使免疫小鼠体内细胞因子分泌水平显著降低,脱髓鞘程度较轻(<1%),炎症指数非常低(<0.5)。此外,与其他免疫抑制药物(硫唑嘌呤、泼尼松龙和环孢素A)相比,给予[T20K]的小鼠的死亡率和发病率显著下降。环肽卡拉塔B1和MCoTI - I也被用作支架来嫁接具有免疫调节活性的生物活性肽。随后对这些嫁接环肽的体外和体内研究证明了它们的治疗能力。鉴于环肽作为免疫调节肽的治疗潜力,本综述讨论了其当前的研究情况以及在应对免疫相关疾病方面的未来意义。