The intestinal microbiota, a leaky gut, and abnormal immunity in kidney disease

被引:377
作者
Anders, Hans-Joachim [1 ]
Andersen, Kirstin [1 ]
Stecher, Baerbel [2 ]
机构
[1] Klinikum Univ Munchen, Med Klin & Poliklin 4, Nephrol Zentrum, D-80336 Munich, Germany
[2] Univ Munich, Max Von Pettenkofer Inst, Munich, Germany
关键词
C-reactive protein; cytokines; flora; innate immunity; lipopolysaccharide; malnutrition; STAGE RENAL-DISEASE; T-CELL-ACTIVATION; OXIDATIVE STRESS; INNATE IMMUNITY; INFLAMMATION; PATHOGENESIS; RESPONSES; BACTERIA; UREMIA; SUBPOPULATIONS;
D O I
10.1038/ki.2012.440
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
1002 ; 100201 ;
摘要
Chronic kidney disease (CKD) and end-stage renal disease (ESRD) are associated with systemic inflammation and acquired immunodeficiency, which promote cardiovascular disease, body wasting, and infections as leading causes of death. This phenomenon persists despite dialysis-related triggers of immune deregulation having been largely eliminated. Here we propose a potential immunoregulatory role of the intestinal microbiota in CKD/ESRD. We discuss how the metabolic alterations of uremia favor pathogen overgrowth (dysbiosis) in the gut and an increased translocation of living bacteria and bacterial components. This process has the potential to activate innate immunity and systemic inflammation. Persistent innate immune activation involves the induction of immunoregulatory mediators that suppress innate and adaptive immunity, similar to the concept of 'endotoxin tolerance' or 'immune paralysis' in advanced sepsis or chronic infections. Renal science has largely neglected the gut as a source of triggers for CKD/ESRD-related immune derangements and complications and lags behind on the evolving microbiota research. Interdisciplinary research activities at all levels are needed to unravel the pathogenic role of the intestinal microbiota in kidney disease and to evaluate if therapeutic interventions that manipulate the microbiota, such as pre- or probiotics, have a therapeutic potential to correct CKD/ESRD-related immune deregulation and to prevent the associated complications.
引用
收藏
页码:1010 / 1016
页数:7
相关论文
共 66 条
[1]   IMPAIRED PHAGOCYTOSIS IN DIALYSIS PATIENTS - STUDIES ON MECHANISMS [J].
ALEXIEWICZ, JM ;
SMOGORZEWSKI, M ;
FADDA, GZ ;
MASSRY, SG .
AMERICAN JOURNAL OF NEPHROLOGY, 1991, 11 (02) :102-111
[2]   Innate pathogen recognition in the kidney: Toll-like receptors, NOD-like receptors, and RIG-like helicases [J].
Anders, H-J .
KIDNEY INTERNATIONAL, 2007, 72 (09) :1051-1056
[3]   The Inflammasomes in Kidney Disease [J].
Anders, Hans-Joachim ;
Muruve, Daniel A. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2011, 22 (06) :1007-1018
[4]   Colonic Contribution to Uremic Solutes [J].
Aronov, Pavel A. ;
Luo, Frank J. -G. ;
Plummer, Natalie S. ;
Quan, Zhe ;
Holmes, Susan ;
Hostetter, Thomas H. ;
Meyer, Timothy W. .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2011, 22 (09) :1769-1776
[5]   Lethal inflammasome activation by a multidrug- resistant pathobiont upon antibiotic disruption of the microbiota [J].
Ayres, Janelle S. ;
Trinidad, Norver J. ;
Vance, Russell E. .
NATURE MEDICINE, 2012, 18 (05) :799-U201
[6]   T-CELL-INDEPENDENT AND T-CELL-DEPENDENT ANTIBODY-RESPONSES IN PATIENTS WITH CHRONIC RENAL-FAILURE [J].
BEAMAN, M ;
MICHAEL, J ;
MACLENNAN, ICM ;
ADU, D .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1989, 4 (03) :216-221
[7]   Endotoxin tolerance: new mechanisms, molecules and clinical significance [J].
Biswas, Subhra K. ;
Lopez-Collazo, Eduardo .
TRENDS IN IMMUNOLOGY, 2009, 30 (10) :475-487
[8]   Microbial Translocation Across the GI Tract [J].
Brenchley, Jason M. ;
Douek, Daniel C. .
ANNUAL REVIEW OF IMMUNOLOGY, VOL 30, 2012, 30 :149-173
[9]   Inflammation in End-Stage Renal Disease-What Have We Learned in 10 Years? [J].
Carrero, Juan J. ;
Stenvinkel, Peter .
SEMINARS IN DIALYSIS, 2010, 23 (05) :498-509
[10]   The dialog between microbiota and the immune system: Shaping the partners through development and evolution [J].
Cerf-Bensussan, Nadine ;
Eberl, Gerard .
SEMINARS IN IMMUNOLOGY, 2012, 24 (01) :1-2