Editorial Review Treatment targets in renal fibrosis
نویسندگان
چکیده
Renal fibrosis is the principal process underlying the progression of chronic kidney disease (CKD) to endstage renal disease (ESRD). It is a relatively uniform response involving glomerulosclerosis, tubulointerstitial fibrosis and changes in renal vasculature (loss of glomerular and peritubular capillaries) (Figure 1). Of these, tubulointerstitial fibrosis has evolved as the most consistent predictor of an irreversible loss of renal function and progression to ESRD [1]. Mechanisms contributing to tubulointerstitial injury and tubular atrophy include glomerular proteinuria, chronic hypoxia, misdirected glomerular ultrafiltration, tubular protein leakage and direct toxic insults of e.g. drugs (reviewed in detail elsewhere [1–6]) . Direct or indirect tubulointerstitial injury via oxidative stress and various effector molecules trigger cellular responses like (i) tubular epithelial cell (TEC) apoptosis, (ii) activation of fibroblasts and their phenotypic switch to myofibroblasts, (iii) influx and/or proliferation of lymphocytes/macrophages, fibrocytes (the circulating fibroblast precursors), fibroblasts as well as (iv) epithelial-to-mesenchymal transition (EMT) of TECs. Renal fibrosis provides an excellent treatment target, since a large variety of pathophysiologically distinct diseases converge finally into this single process. However, we still do not have effective therapies, nor does such a therapy exist in most other types of organ fibrosis. Why? As part of the vital repair process, the regulation and redundancy in this system must be highly effective. The consequence is an amazingly complicated process that involves many cell types and mediators [1,2,4,5,7]. Not unexpectedly, monotherapeutic approaches, or even a combination of therapies, fail to completely stop the progression of renal fibrosis [8–10]. In addition, not all combination therapies can be additive [11]. When identifying new targets or validating potential therapeutic options, we are confronted with several problems:
منابع مشابه
Editorial Review Inhibitors/antagonists of the TGF-β system in kidney fibrosis
Renal fibrosis is a major hallmark of chronic kidney disease, regardless of the initial causes, and prominent renal fibrosis predicts poor prognosis for renal insufficiency. Transforming growth factor (TGF)-β plays a pivotal role in the progression of renal fibrosis, and therapeutic interventions targeting TGF-β have been successful and well tolerated in animal models. However, these interventi...
متن کاملEditorial Review The renal (myo-)fibroblast: a heterogeneous group of cells
Renal fibrosis is a central pathological process in kidneys of patients with chronic kidney disease (CKD). Identification of effective treatments that halt or reverse fibrosis would be beneficial for most, if not all, CKD patients. Key to this is an understanding of fibrogenesis, including the principal responsible cells, the renal fibroblasts. It is in part due to their inconspicuous appearanc...
متن کاملEditorial Review The role of lymphatics in renal inflammation
Progressive renal diseases are characterized by tubulointerstitial inflammatory cell recruitment, tubular atrophy and fibrosis. Various aspects of the recruitment of leukocytes have been extensively studied, but the exit routes (i. e. the lymphatic vessels and their biology) have only recently found attention. Similar to the recruitment of inflammatory cells, the exit is coordinated by an orche...
متن کاملA Review of Oral Submucousal Fibrosis, Related Factors, Prognosis and New Therapeutic Approaches
Abstract BACKGROUNackground and AIMD & AIM: Oral Submucous Fibrosis (OSF) is an oral premalignant condition with highest premalignant potential among oral precancerous lesions which characterized with inflammation and progressive fibrosis of submucosal oral tissues (cause to significant irreversible rigidity and trismus). During the years, many classification systems have been propo...
متن کاملEditorial: Emerging Molecular Targets for the Treatment of Cystic Fibrosis.
Cystic fibrosis (CF) is a deadly autosomal recessive disease characterized by airway obstruction, infection, inflammation, and eventually end-stage lung failure. It is the most common life-shortening genetic disorder in Caucasians, and caused by mutations in the gene that encodes the CF transmembrane conductance regulator (CFTR). This disease affects approximately 70,000 individuals worldwide a...
متن کامل