The 'innate' host response protects and damages the infected urinary tract

被引:34
作者
Svanborg, C [1 ]
Bergsten, G [1 ]
Fischer, H [1 ]
Frendéus, B [1 ]
Godaly, G [1 ]
Gustafsson, E [1 ]
Hang, L [1 ]
Hedlund, M [1 ]
Karpman, D [1 ]
Lundstedt, AC [1 ]
Samuelsson, M [1 ]
Samuelsson, P [1 ]
Svensson, M [1 ]
Wullt, B [1 ]
机构
[1] Lund Univ, Dept Microbiol Immunol & Glycobiol, Inst Lab Med, S-22362 Lund, Sweden
关键词
asymptomatic bacteriuria; chemokines; CXCR1; Escherichia coli; epithelial cells; neurophils; TLR4; urinary tract infection;
D O I
10.3109/07853890109002101
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Symptoms of infection and tissue pathology are caused by the host response; not by the microbe per se. The same response is also critical for the defence and is needed to clear infection. It is therefore essential to understand how the host response is activated and to identify the critical effector mechanisms of the defence. We have studied these issues in the urinary tract infection (UTI) model. The symptoms of UTI and the host defence both rely on the so-called 'innate' immune system, making this one of the best characterized human disease models of 'innate immunity,. We discuss the critical molecular events that determine whether the host response will be activated by P-fimbriated uropathogenic Escherichia coli as well as factors determining whether the patient develops acute pyelonephritis or asymptomatic bacteriuria. We will describe the glycoconjugate receptors used by the P-fimbriated bacteria adhering to host tissues, the recruitment of TLR4 co-receptors and the signalling pathways that allow progression to symptomatic disease, and discuss how these mechanisms are altered in asymptomatic carriers, presenting the possible genetic basis for unresponsiveness. We have shown that neutrophils are the critical effectors of the host defence and that neutrophil dysfunctions lead to acute pyelonephritis and renal scarring. Here we discuss the mechanisms of neutrophil-mediated, chemokine receptor (CXCR1)-dependent clearance, and the defect in interleukin-8 receptor homolog knock-out (IL-8Rh KO) mice and describe the data linking low CXCR1 expression to recurrent pyelonephritis in man, as well as the information on the genetic basis for low CXCR1 expression in affected patients. Finally, the mechanisms of renal scarring in IL8Rh KO mice will be discussed in relation to human disease, Our studies hold the promise to provide a molecular and genetic explanation for disease susceptibility in some patients with UTI and to offer more precise tools for the diagnosis and therapy of these infections.
引用
收藏
页码:563 / 570
页数:8
相关论文
共 54 条
[31]  
KUNIN C, 1987, DETECTION MANAGEMENT
[32]   Evidence of ζ protein kinase C involvement in polymorphonuclear neutrophil integrin-dependent adhesion and chemotaxis [J].
Laudanna, C ;
Mochly-Rosen, D ;
Liron, T ;
Constantin, G ;
Butcher, EC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (46) :30306-30315
[33]   GLYCOLIPID RECEPTORS FOR UROPATHOGENIC ESCHERICHIA-COLI ON HUMAN-ERYTHROCYTES AND UROEPITHELIAL CELLS [J].
LEFFLER, H ;
SVANBORGEDEN, C .
INFECTION AND IMMUNITY, 1981, 34 (03) :920-929
[34]   CHEMICAL-IDENTIFICATION OF A GLYCOSPHINGOLIPID RECEPTOR FOR ESCHERICHIA-COLI ATTACHING TO HUMAN URINARY-TRACT EPITHELIAL-CELLS AND AGGLUTINATING HUMAN-ERYTHROCYTES [J].
LEFFLER, H ;
SVANBORGEDEN, C .
FEMS MICROBIOLOGY LETTERS, 1980, 8 (03) :127-134
[35]  
LEFFLER H, 1982, SCAND J INFECT DIS, P46
[36]   THE RECEPTOR REPERTOIRE DEFINES THE HOST RANGE FOR ATTACHING ESCHERICHIA-COLI STRAINS THAT RECOGNIZE GLOBO-A [J].
LINDSTEDT, R ;
LARSON, G ;
FALK, P ;
JODAL, U ;
LEFFLER, H ;
SVANBORG, C .
INFECTION AND IMMUNITY, 1991, 59 (03) :1086-1092
[37]  
LOMBERG H, 1981, LANCET, V1, P551
[38]   INFLUENCE OF BLOOD-GROUP ON THE AVAILABILITY OF RECEPTORS FOR ATTACHMENT OF UROPATHOGENIC ESCHERICHIA-COLI [J].
LOMBERG, H ;
CEDERGREN, B ;
LEFFLER, H ;
NILSSON, B ;
CARLSTROM, AS ;
SVANBORGEDEN, C .
INFECTION AND IMMUNITY, 1986, 51 (03) :919-926
[39]  
ORSKOV I, 1982, SCAND J INFECT DIS, P18
[40]   Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice:: Mutations in Tlr4 gene [J].
Poltorak, A ;
He, XL ;
Smirnova, I ;
Liu, MY ;
Van Huffel, C ;
Du, X ;
Birdwell, D ;
Alejos, E ;
Silva, M ;
Galanos, C ;
Freudenberg, M ;
Ricciardi-Castagnoli, P ;
Layton, B ;
Beutler, B .
SCIENCE, 1998, 282 (5396) :2085-2088