Hurdles to the introduction of new therapies for immune-mediated kidney diseases

被引:42
作者
Anders, Hans-Joachim [1 ]
Jayne, David R. W. [2 ]
Rovin, Brad H. [3 ]
机构
[1] Klinikum Univ Munchen, Med Klin & Poliklin 4, Ziemssenstr 1, D-80336 Munich, Germany
[2] Addenbrookes Hosp, Vasculitis & Lupus Clin, Hills Rd, Cambridge CB2 2QQ, England
[3] Ohio State Univ, Wexner Med Ctr, Div Nephrol, 395 West 12 Ave, Columbus, OH 43210 USA
关键词
PROLIFERATIVE LUPUS NEPHRITIS; MEMBRANOUS NEPHROPATHY; MYCOPHENOLATE-MOFETIL; OXFORD CLASSIFICATION; NEPHROTIC SYNDROME; IGA NEPHROPATHY; RENAL-DISEASE; DOUBLE-BLIND; RITUXIMAB; CYCLOPHOSPHAMIDE;
D O I
10.1038/nrneph.2015.206
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
100201 [内科学]; 100221 [泌尿外科学];
摘要
Innovative immunotherapies continue to markedly benefit many disciplines in clinical medicine but disappointingly, these benefits have not translated to the treatment of kidney diseases despite encouraging findings from preclinical models of kidney dysfunction. This lack of progress in nephrology might relate to the unique biology of the kidney. More likely, this lack of progress relates to conceptual hurdles in the application of newer therapies to renal disease. In this Review we discuss seven hurdles that must be addressed in order to appropriately assess and introduce immunologic therapies for immune-mediated kidney disease: the use of appropriate criteria to define disease categories; issues relating to the heterogeneity of kidney diseases and how this heterogeneity affects approaches to treatment; issues related to the rarity of most kidney diseases; the paucity of good animal models of human kidney disease; issues relating to trial design; problems with current approaches to the identification and use of appropriate and feasible study end points; and a lack of adequate biomarkers of intrarenal inflammation and parenchymal injury. We suggest that overcoming these hurdles, in addition to searching for better therapeutic targets, will be necessary to progress the treatment of immune-mediated kidney disease into anew age of drug therapy.
引用
收藏
页码:205 / 216
页数:12
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