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Treatment of glomerulonephritis: Will we ever have options other than steroids and cytotoxics|[quest]|

机译:肾小球肾炎的治疗:除类固醇和细胞毒性药物外,我们还会有其他选择| [quest] |

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Treatment of glomerulonephritis: Will we ever have options other than steroids and cytotoxics? Glomerulonephritis refers to a collection of primary renal disorders and those secondary to a systemic disease, all characterized by inflammation within the glomerulus. Given the underlying immunologic nature of these disorders, they are routinely treated with corticosteriods and various cytotoxic agents. Although in many instances such therapies are successful, they are associated with significant morbidity; as such, alternatives are clearly necessary. Our understanding of the pathogenesis of immunologic glomerular diseases has grown remarkably, in large part from the study of rodent disease models. Fundamental to each disorder is the development of an antigen-specific immune response followed by the effector stage of inflammation. To block the immune response, antigen-specific therapy can be used to induce tolerance, such as through the use of double-stranded DNA molecules in lupus nephritis. Since other antigen systems are less well characterized, inducing a more generalized impairment in the immune response by blocking costimulatory molecules CD40-CD154 and CD28-CD80/86 is a growing approach to treat various immunologic disorders and transplantation. To reduce glomerular inflammation, a variety of effector systems have been targeted, including complement, cytokines/chemokines, adhesion molecules, and mediators of cellular proliferation. Of these, antibodies targeting C5 in the complement system, and antibody and receptor antagonists of tumor necrosis factor- (TNF-) have already been used in glomerular disorders with some promise. Less specific blockade of receptor-mediated events stimulated by platelet-derived growth factors and cell cycle proteins may soon be applied to glomerulonephritis. Finally, interruption of fibrosing pathways, which lead to glomerulosclerosis and interstitial fibrosis common to the end-stage of all glomerulonephritis, is the subject of intense effort which may yield effective biologic therapies. In spite of all these advances, we still are dependent on steroids and cytotoxics to treat glomerulonephritis. To get past this, we must devote significant resources to take observations made in basic research laboratories to develop therapeutics and prove their utility in human disease.
机译:肾小球肾炎的治疗:除了类固醇和细胞毒素,我们还能选择吗?肾小球肾炎是指原发性肾脏疾病和继发于全身性疾病的那些疾病的集合,所有这些疾病均以肾小球内的炎症为特征。考虑到这些疾病的潜在免疫学性质,可以常规用皮质类固醇和各种细胞毒剂对其进行治疗。尽管这种疗法在许多情况下都是成功的,但它们与高发病率有关。因此,替代方案显然是必要的。我们对免疫性肾小球疾病发病机理的了解已显着增长,这在很大程度上是基于啮齿动物疾病模型的研究。每种疾病的根本原因是抗原特异性免疫反应的发展,随后是炎症的效应期。为了阻断免疫反应,抗原特异性疗法可用于诱导耐受性,例如通过在狼疮性肾炎中使用双链DNA分子。由于其他抗原系统的特征较差,因此通过阻断共刺激分子CD40-CD154和CD28-CD80 / 86诱导更普遍的免疫反应损害是治疗各种免疫疾病和移植的一种日益发展的方法。为了减少肾小球炎症,已经靶向了多种效应系统,包括补体,细胞因子/趋化因子,粘附分子和细胞增殖的介质。其中,在补体系统中靶向C5的抗体以及肿瘤坏死因子-(TNF-)的抗体和受体拮抗剂已经在肾小球疾病中使用,并具有一定的前景。由血小板衍生的生长因子和细胞周期蛋白刺激的受体介导事件的特异性较低的阻断作用可能很快会应用于肾小球肾炎。最后,费力的工作是中断纤维化途径,导致所有肾小球肾炎终末期常见的肾小球硬化和间质纤维化,这可能会产生有效的生物疗法。尽管取得了所有这些进步,我们仍然依赖类固醇和细胞毒素来治疗肾小球肾炎。为了超越这一点,我们必须投入大量资源来进行基础研究实验室的观察,以开发治疗药物并证明其在人类疾病中的效用。

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