Tumor necrosis factor-alpha expression induced by anti-YopB antibodies coincides with protection against Yersinia enterocolitica infection in mice

被引:10
作者
Burdack, S [1 ]
Schmidt, A [1 ]
Knieschies, E [1 ]
Rollinghoff, M [1 ]
Beuscher, HU [1 ]
机构
[1] UNIV ERLANGEN NURNBERG,INST KLIN MIKROBIOL & IMMUNOL,D-91054 ERLANGEN,GERMANY
关键词
Yersinia enterocolitica; YopB; tumor necrosis factor-alpha; anti-YopB antiserum; infection;
D O I
10.1007/s004300050034
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previous studies have suggested that virulence of pathogenic Yersiniae is associated with a suppression of the local cytokine response. In this context, the plasmid-encoded 41-kDa Yersinia outer protein B (YopB) has been implicated with the lack of tumor necrosis factor-alpha (TNF-alpha) expression in Peyer's patches (PP), following oral infection of mice with the enteropathogenic Yersinia enterocolitica. The present study was performed to further evaluate the relationships between YopB-induced suppression of TNF-alpha and bacterial survival in host tissue. Results are presented to show the ability of purified YopB to suppress the release of TNF-alpha by macrophages, the effect of which was neutralized by monospecific anti-YopB antiserum. In mice orally infected with Y. enterocolitica, anti-YopB treatment on days 3 and 5 postinfection, significantly decreased the recovery of live bacteria from PP. This observation correlated with a strong increase in TNF-alpha expression, as determined by reverse transcription-polymerase chain reaction and measuring the levels of TNF activity in homogenates of PP Moreover, treatment of mice with a combination of anti-YopB and anti-TNF-alpha antiserum, completely abrogated the beneficial effect of the anti-YopB antiserum. In controls, expression of other proinflammatory cytokines such as interleukin-1 remained unaffected by either treatment. Therefore, the results indicate that endogenous TNF-alpha is required for eradication of Y. enterocolitica from host tissue, and further imply that YopB significantly contributes to suppression of the local TNF-alpha response in PP.
引用
收藏
页码:223 / 229
页数:7
相关论文
共 27 条
[1]  
AUTENRIETH IB, 1992, MED MICROBIOL IMMUN, V181, P333
[2]  
Beuscher H. Ulrich, 1994, Regional Immunology, V6, P397
[3]   BACTERIAL EVASION OF HOST IMMUNE DEFENSE - YERSINIA-ENTEROCOLITICA ENCODES A SUPPRESSOR FOR TUMOR-NECROSIS-FACTOR-ALPHA EXPRESSION [J].
BEUSCHER, HU ;
RODEL, F ;
FORSBERG, A ;
ROLLINGHOFF, M .
INFECTION AND IMMUNITY, 1995, 63 (04) :1270-1277
[4]   THE YERSINIA TYROSINE PHOSPHATASE - SPECIFICITY OF A BACTERIAL VIRULENCE DETERMINANT FOR PHOSPHOPROTEINS IN THE J774A.1 MACROPHAGE [J].
BLISKA, JB ;
CLEMENS, JC ;
DIXON, JE ;
FALKOW, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (06) :1625-1630
[5]  
CHROMCYNSKI P, 1987, ANAL BIOCHEM, V162, P158
[6]   ESTRADIOL ENHANCES LEUKOCYTE BINDING TO TUMOR-NECROSIS-FACTOR (TNF)-STIMULATED ENDOTHELIAL-CELLS VIA AN INCREASE IN TNF-INDUCED ADHESION MOLECULES E-SELECTIN, INTERCELLULAR-ADHESION MOLECULE TYPE-1, AND VASCULAR CELL-ADHESION MOLECULE TYPE-1 [J].
CID, MC ;
KLEINMAN, HK ;
GRANT, DS ;
SCHNAPER, HW ;
FAUCI, AS ;
HOFFMAN, GS .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (01) :17-25
[7]  
CORNELIS G, 1987, REV INFECT DIS, V9, P64
[8]   A HIGHLY SENSITIVE CELL-LINE, WEHI-164 CLONE 13, FOR MEASURING CYTOTOXIC FACTOR TUMOR-NECROSIS-FACTOR FROM HUMAN-MONOCYTES [J].
ESPEVIK, T ;
NISSENMEYER, J .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 95 (01) :99-105
[9]   EARLY INTERLEUKIN-12 PRODUCTION BY MACROPHAGES IN RESPONSE TO MYCOBACTERIAL INFECTION DEPENDS ON INTERFERON-GAMMA AND TUMOR-NECROSIS-FACTOR-ALPHA [J].
FLESCH, IEA ;
HESS, JH ;
HUANG, S ;
AGUET, M ;
ROTHE, J ;
BLUETHMANN, H ;
KAUFMANN, SHE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (05) :1615-1621
[10]   MOLECULAR-CLONING AND EXPRESSION OF CALCIUM-REGULATED, PLASMID-CODED PROTEINS OF Y-PSEUDOTUBERCULOSIS [J].
FORSBERG, A ;
BOLIN, I ;
NORLANDER, L ;
WOLFWATZ, H .
MICROBIAL PATHOGENESIS, 1987, 2 (02) :123-137