Minimal change disease: a dysregulation of the podocyte CD80-CTLA-4 axis?

被引:16
作者
Cara-Fuentes, Gabriel [1 ]
Wasserfall, Clive H. [2 ]
Wang, Heiman [1 ]
Johnson, Richard J. [3 ]
Garin, Eduardo H. [1 ]
机构
[1] Univ Florida, Div Pediat Nephrol, Dept Pediat, Gainesville, FL 32610 USA
[2] Univ Florida, Dept Pathol, Gainesville, FL 32610 USA
[3] Univ Colorado, Dept Med, Div Renal Dis & Hypertens, Denver, CO USA
关键词
CD80; CTLA-4; Minimal Change Disease; Podocyte; URINARY CD80; NEPHROTIC-SYNDROME; EXPRESSION; INCREASES; B7-1;
D O I
10.1007/s00467-014-2874-8
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Minimal Change Disease (MCD) is associated with CD80 expression in podocytes and elevated urinary CD80 excretion during active renal disease. We have evaluated the urinary excretion of CTLA-4 and CD80 during different stages of the nephrotic syndrome in patients with MCD to test the hypothesis that persistent increased urinary CD80 excretion in patients with MCD in relapse is due to an ineffectual CTLA-4 response of the host to curtail the activation of CD80. Thirty-two children with biopsy-proven MCD were studied during relapse and/or remission. Eleven healthy subjects served as controls. Urinary CD80 excretion was significantly increased in MCD patients in relapse relative to that in MCD patients in remission (p < 0.001) and controls (p < 0.001). Although urinary CTLA-4 excretion was higher in MCD patients in relapse than in MCD patients in remission (p = 0.01) and controls (p = 0.03), no significant correlation was observed between urinary CD80 excretion and urinary CTLA-4 level in MCD patients at the time of relapse (p = 0.06). At the time of remission, CD80 had decreased significantly in all patients, but CTLA-4 levels either decreased or remained unchanged in all but five patients, and no correlation was observed between urinary CD80 excretion and CTLA-4 level (p = 0.7). Urinary CTLA-4 levels do not correlate with urinary CD80 excretion, suggesting the possibility that the CTLA4 response may be suboptimal in this disease during relapse.
引用
收藏
页码:2333 / 2340
页数:8
相关论文
共 16 条
[1]   Clinical profile of children with nephrotic syndrome not on glucorticoid therapy, but presenting with infection [J].
Alwadhi, RK ;
Mathew, JL ;
Rath, B .
JOURNAL OF PAEDIATRICS AND CHILD HEALTH, 2004, 40 (1-2) :28-32
[2]  
[Anonymous], 1970, KIDNEY
[3]   A proposed taxonomy for the podocytopathies: A reassessment of the primary nephrotic diseases [J].
Barisoni, Laura ;
Schnaper, H. William ;
Kopp, Jeffrey B. .
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2007, 2 (03) :529-542
[4]  
CHURG J, 1970, LANCET, V1, P1299
[5]  
Feehally J, 2007, COMPREHENSIVE CLIN N, P209
[6]   Urinary CD80 is elevated in minimal change disease but not in focal segmental glomerulosclerosis [J].
Garin, Eduardo H. ;
Mu, Wei ;
Arthur, John M. ;
Rivard, Christopher J. ;
Araya, Carlos E. ;
Shimada, Michiko ;
Johnson, Richard J. .
KIDNEY INTERNATIONAL, 2010, 78 (03) :296-302
[7]   Urinary CD80 Excretion Increases in Idiopathic Minimal-Change Disease [J].
Garin, Eduardo H. ;
Diaz, Leila N. ;
Mu, Wei ;
Wasserfall, Clive ;
Araya, Carlos ;
Segal, Mark ;
Johnson, Richard J. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2009, 20 (02) :260-266
[8]   Toll-like receptor 3 ligand, polyIC, induces proteinuria and glomerular CD80, and increases urinary CD80 in mice [J].
Ishimoto, Takuji ;
Shimada, Michiko ;
Gabriela, Garcia ;
Kosugi, Tomoki ;
Sato, Waichi ;
Lee, Pui Y. ;
Lanaspa, Miguel A. ;
Rivard, Christopher ;
Maruyama, Shoichi ;
Garin, Eduardo H. ;
Johnson, Richard J. .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2013, 28 (06) :1439-1446
[9]   B7-1 (CD80) and B7-2 (CD86) expression in human tubular epithelial cells in vivo and in vitro [J].
Niemann-Masanek, U ;
Mueller, A ;
Yard, BA ;
Waldherr, R ;
van der Woude, FJ .
NEPHRON, 2002, 92 (03) :542-556
[10]   Cutting edge: A soluble form of CTLA-4 in patients with autoimmune thyroid disease [J].
Oaks, MK ;
Hallett, KM .
JOURNAL OF IMMUNOLOGY, 2000, 164 (10) :5015-5018