ENDOGENOUS TUMOR-NECROSIS-FACTOR-ALPHA IS REQUIRED FOR ENHANCED ANTIMICROBIAL ACTIVITY AGAINST TOXOPLASMA-GONDII AND LISTERIA-MONOCYTOGENES IN RECOMBINANT GAMMA INTERFERON-TREATED MICE

被引:58
作者
LANGERMANS, JAM [1 ]
VANDERHULST, MEB [1 ]
NIBBERING, PH [1 ]
VANFURTH, R [1 ]
机构
[1] UNIV HOSP LEIDEN, DEPT INFECT DIS, BLDG 1 C5P, POB 9600, 2300 RC LEIDEN, NETHERLANDS
关键词
D O I
10.1128/IAI.60.12.5107-5112.1992
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In vitro studies have shown that macrophages stimulated with recombinant gamma interferon (rIFN-gamma) produce tumor necrosis factor alpha (TNF-alpha), which in an autocrine fashion activates these cells. The aim of the present study was to determine whether endogenously formed TNF-alpha also is required for rIFN-gamma-induced macrophage activation and enhanced antimicrobial activity in vivo. After an intraperitoneal injection of rIFN-gamma into CBA/J mice, their peritoneal macrophages released enhanced amounts of NO2- and inhibited the intracellular proliferation of Toxoplasma gondii. Injection of neutralizing antibodies against TNF-alpha simultaneously with the rIFN-gamma completely inhibited both the release of NO2- by macrophages and their toxoplasmastatic activity. Similar results were observed after intraperitoneal injection of a competitive inhibitor of L-arginine, N(G)-monomethyl-L-arginine, together with rIFN-gamma, demonstrating that in vivo L-arginine-derived reactive nitrogen intermediates are essential for the induction of toxoplasmastatic activity. Intravenous injection of rIFN-gamma inhibited the growth of Listeria monocytogenes in the livers and spleens of mice; this effect was abrogated by antibodies against TNF-alpha. Intravenous injection of a large dose of rTNF-alpha resulted in a decrease in the number of bacteria in the liver and spleen, but an injection of rIFN-gamma and rTNF-alpha did not result in enhanced inhibition of the proliferation of L. monocytogenes. Together, the results of the present study are the first to demonstrate that endogenous TNF-alpha is required in vivo for the expression of macrophage activation with respect to the release of reactive nitrogen intermediates and toxoplasmastatic activity and for enhanced listericidal activity in the livers and spleens of mice stimulated with rIFN-gamma.
引用
收藏
页码:5107 / 5112
页数:6
相关论文
共 37 条
[1]  
ADAMS LB, 1991, J IMMUNOL, V147, P1642
[2]  
ADAMS LB, 1990, J IMMUNOL, V144, P2725
[3]  
BELOSEVIC M, 1989, J IMMUNOL, V143, P266
[4]   REQUIREMENT OF ENDOGENOUS INTERFERON-GAMMA PRODUCTION FOR RESOLUTION OF LISTERIA-MONOCYTOGENES INFECTION [J].
BUCHMEIER, NA ;
SCHREIBER, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (21) :7404-7408
[5]   KILLING OF VIRULENT MYCOBACTERIUM-TUBERCULOSIS BY REACTIVE NITROGEN INTERMEDIATES PRODUCED BY ACTIVATED MURINE MACROPHAGES [J].
CHAN, J ;
XING, Y ;
MAGLIOZZO, RS ;
BLOOM, BR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (04) :1111-1122
[6]  
CHANG HR, 1990, IMMUNOLOGY, V69, P33
[7]   HEPATOCYTES PRODUCE NITROGEN-OXIDES FROM L-ARGININE IN RESPONSE TO INFLAMMATORY PRODUCTS OF KUPFFER CELLS [J].
CURRAN, RD ;
BILLIAR, TR ;
STUEHR, DJ ;
HOFMANN, K ;
SIMMONS, RL .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 170 (05) :1769-1774
[8]  
DING AH, 1988, J IMMUNOL, V141, P2407
[9]   INTERFERON-GAMMA AND TUMOR NECROSIS FACTOR INDUCE THE L-ARGININE-DEPENDENT CYTO-TOXIC EFFECTOR MECHANISM IN MURINE MACROPHAGES [J].
DRAPIER, JC ;
WIETZERBIN, J ;
HIBBS, JB .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (10) :1587-1592
[10]   SPECIFIC AMINO-ACID (L-ARGININE) REQUIREMENT FOR THE MICROBIOSTATIC ACTIVITY OF MURINE MACROPHAGES [J].
GRANGER, DL ;
HIBBS, JB ;
PERFECT, JR ;
DURACK, DT .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (04) :1129-1136