Genetics of innate immunity and UTI susceptibility

被引:99
作者
Ragnarsdottir, Bryndis [1 ]
Lutay, Nataliya [1 ]
Gronberg-Hernandez, Jenny [1 ]
Koves, Bela [1 ]
Svanborg, Catharina [1 ]
机构
[1] Lund Univ, Inst Lab Med, Sect Microbiol Immunol & Glycobiol, S-22362 Lund, Sweden
关键词
URINARY-TRACT-INFECTION; UROPATHOGENIC ESCHERICHIA-COLI; TOLL-LIKE RECEPTOR-4; ANGIOTENSIN-CONVERTING ENZYME; PRIMARY VESICOURETERAL REFLUX; INTRACELLULAR BACTERIAL COMMUNITIES; DEFICIENCY CONFERS SUSCEPTIBILITY; TAMM-HORSFALL GLYCOPROTEIN; ASYMPTOMATIC BACTERIURIA; CYTOKINE RESPONSES;
D O I
10.1038/nrurol.2011.100
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
A functional and well-balanced immune response is required to resist most infections. Slight dysfunctions in innate immunity can turn the 'friendly' host defense into an unpleasant foe and give rise to disease. Beneficial and destructive forces of innate immunity have been discovered in the urinary tract and mechanisms by which they influence the severity of urinary tract infections (UTIs) have been elucidated. By modifying specific aspects of the innate immune response to UTI, genetic variation either exaggerates the severity of acute pyelonephritis to include urosepsis and renal scarring or protects against symptomatic disease by suppressing innate immune signaling, as in asymptomatic bacteriuria (ABU). Different genes are polymorphic in patients prone to acute pyelonephritis or ABU, respectively, and yet discussions of UTI susceptibility in clinical practice still focus mainly on social and behavioral factors or dysfunctional voiding. Is it not time for UTIs to enter the era of molecular medicine? Defining why certain individuals are protected from UTI while others have severe, recurrent infections has long been difficult, but progress is now being made, encouraging new approaches to risk assessment and therapy in this large and important patient group, as well as revealing promising facets of 'good' versus 'bad' inflammation.
引用
收藏
页码:449 / 468
页数:20
相关论文
共 193 条
[41]   Role of fimbriae-mediated adherence for neutrophil migration across Escherichia coli-infected epithelial cell layers [J].
Godaly, G ;
Frendéus, B ;
Proudfoot, A ;
Svensson, M ;
Klemm, P ;
Svanborg, C .
MOLECULAR MICROBIOLOGY, 1998, 30 (04) :725-735
[42]  
Godaly G, 2001, J LEUKOCYTE BIOL, V69, P899
[43]   Genetic control of the circulating concentration of transforming growth factor type β1 [J].
Grainger, DJ ;
Heathcote, K ;
Chiano, M ;
Snieder, H ;
Kemp, PR ;
Metcalfe, JC ;
Carter, ND ;
Spector, TD .
HUMAN MOLECULAR GENETICS, 1999, 8 (01) :93-97
[44]  
GRIO R, 1994, PANMINERVA MED, V36, P198
[45]  
GRIO R, 1994, PANMINERVA MED, V36, P195
[46]   DIFFERENCE IN SUSCEPTIBILITY TO GRAM-NEGATIVE URINARY-TRACT INFECTION BETWEEN C3H-HEJ AND C3H-HEN MICE [J].
HAGBERG, L ;
HULL, R ;
HULL, S ;
MCGHEE, JR ;
MICHALEK, SM ;
EDEN, CS .
INFECTION AND IMMUNITY, 1984, 46 (03) :839-844
[47]  
HAGBERG L, 1985, J IMMUNOL, V134, P4118
[48]   ADHESION, HEMAGGLUTINATION, AND VIRULENCE OF ESCHERICHIA-COLI CAUSING URINARY-TRACT INFECTIONS [J].
HAGBERG, L ;
JODAL, U ;
KORHONEN, TK ;
LIDINJANSON, G ;
LINDBERG, U ;
EDEN, CS .
INFECTION AND IMMUNITY, 1981, 31 (02) :564-570
[49]   Interleukin-8 receptor knockout mice have subepithelial neutrophil entrapment and renal scarring following acute pyelonephritis [J].
Hang, L ;
Frendéus, B ;
Godaly, G ;
Svanborg, C .
JOURNAL OF INFECTIOUS DISEASES, 2000, 182 (06) :1738-1748
[50]   FOLLICULAR CYSTITIS IN GIRLS WITH UNTREATED ASYMPTOMATIC OR COVERT BACTERIURIA [J].
HANSSON, S ;
HANSON, E ;
HJALMAS, K ;
HULTENGREN, M ;
JODAL, U ;
OLLING, S ;
SVANBORGEDEN, C .
JOURNAL OF UROLOGY, 1990, 143 (02) :330-332