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自身免疫性疾病中的药物。

Drugs in autoimmune diseases.

作者信息

Herrmann D B, Bicker U

机构信息

Boehringer Mannheim GmbH, Research and Development Division Therapeutics, FRG.

出版信息

Klin Wochenschr. 1990;68 Suppl 21:15-25.

PMID:2198387
Abstract

Autoimmune diseases arise when autoimmunity or the loss of self tolerance results in tissue damages. Many mechanisms have been proposed for the origin of autoimmunity, including immunologic, viral, hormonal and genetic factors. All known parts of the immunological network are involved in causing immunopathologic symptoms. Therefore, more or less specific immunosuppressants are widely used in the treatment of autoimmune disorders which range from organ-specific, i.e. Hashimoto's thyroiditis, to non-organ-specific or systemic diseases, i.e. systemic lupus erythematosus. Unspecifically acting cytostatics do not only suppress autoimmune reactions but also create severe side-effects due to the impairment of immune responses against foreign antigens, leading, for example, to an increased risk of infections. Moreover, the genotoxic activity of cytostatics might induce malignancies. Corticosteroids are clinically well known and very active agents for the management of acute symptoms but different side-effects limit their use in the treatment of chronic diseases. Cyclosporin A has been an important step forward to a more specific prevention of organ transplant rejections and to the therapy of some autoimmune disorders. Modern approaches to immunosuppression include monoclonal antibodies directed against a variety of different determinants on immunocompetent cells. Ciamexone and Leflunomide which are in early clinical and preclinical development, respectively, might be interesting new drugs. Future immunopharmacologic drug research and development should lead to more specific, low molecular weight, orally active and chemically defined immunosuppressive compounds with good tolerability under long-term treatment of autoimmune diseases.

摘要

自身免疫性疾病是在自身免疫或自身耐受性丧失导致组织损伤时出现的。关于自身免疫的起源已提出了许多机制,包括免疫、病毒、激素和遗传因素。免疫网络的所有已知部分都参与引发免疫病理症状。因此,或多或少具有特异性的免疫抑制剂被广泛用于治疗自身免疫性疾病,这些疾病范围从器官特异性疾病(如桥本甲状腺炎)到非器官特异性或全身性疾病(如系统性红斑狼疮)。非特异性作用的细胞抑制剂不仅会抑制自身免疫反应,还会因损害针对外来抗原的免疫反应而产生严重的副作用,例如导致感染风险增加。此外,细胞抑制剂的基因毒性活性可能诱发恶性肿瘤。皮质类固醇在临床上是众所周知的,并且是治疗急性症状的非常有效的药物,但不同的副作用限制了它们在慢性病治疗中的应用。环孢素A在更特异性地预防器官移植排斥反应和治疗某些自身免疫性疾病方面是一个重要的进展。现代免疫抑制方法包括针对免疫活性细胞上各种不同决定簇的单克隆抗体。分别处于临床早期和临床前开发阶段的西阿美酮和来氟米特可能是有前景的新药。未来免疫药理学药物的研发应能产生更具特异性、低分子量、口服活性且化学性质明确的免疫抑制化合物,在长期治疗自身免疫性疾病时具有良好的耐受性。

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