INTERLEUKIN-1 - AN IMPORTANT MEDIATOR OF HOST-RESISTANCE AGAINST PNEUMOCYTIS-CARINII

被引:89
作者
CHEN, WX
HAVELL, EA
MOLDAWER, LL
MCINTYRE, KW
CHIZZONITE, RA
HARMSEN, AG
机构
[1] HOFFMANN LA ROCHE INC, DEPT IMMUNOPHARMACOL, NUTLEY, NJ 07110 USA
[2] CORNELL UNIV, MED CTR, COLL MED, DEPT SURG, NEW YORK, NY 10021 USA
[3] HOFFMANN LA ROCHE INC, DEPT MOLEC GENET, NUTLEY, NJ 07110 USA
关键词
D O I
10.1084/jem.176.3.713
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The importance of endogenous interleukin 1 (IL-1) in resistance to Pneumocystis carinii infection was examined in a SCID mouse model. Naturally acquired pulmonary infection of P. carinii in SCID mice was completely cleared by reconstitution of the infected mice with immunocompetent spleen cells. IL-1 activity in the lung homogenate supernatant of these mice increased significantly after reconstitution and returned to baseline level after the clearance of P. carinii. Treatment of reconstituted SCID mice with 35F5, a monoclonal antibody against murine type I IL-1R almost completely inhibited the clearance of P. carinii. In contrast, treatment with control rat immunoglobulin G had no detectable effect. Further study revealed that for the complete clearance of P. carinii, IL-1 must be present at the early stage of immune responses induced by reconstitution, since clearance could be blocked by a single injection of 35F5 into SCID mice at 2 d, but not at either 8 or 13 d postreconstitution. Furthermore, pulmonary recruitment of neutrophils, macrophages, and lymphocytes was significantly inhibited in mice that received 35F5 treatment. These findings strongly suggest that, in reconstituted SCID mice, endogenous IL-1 is important in host resistance to P. carinii infection and that IL-1 may function early in the host response possibly by the recruitment of inflammatory cells into the lungs.
引用
收藏
页码:713 / 718
页数:6
相关论文
共 26 条
[1]
[Anonymous], 1971, STAT PRINCIPLES EXPT
[2]
REDUCTION IN INTENSITY OF PNEUMOCYSTIS-CARINII PNEUMONIA IN MICE BY AEROSOL ADMINISTRATION OF GAMMA-INTERFERON [J].
BECK, JM ;
LIGGITT, HD ;
BRUNETTE, EN ;
FUCHS, HJ ;
SHELLITO, JE ;
DEBS, RJ .
INFECTION AND IMMUNITY, 1991, 59 (11) :3859-3862
[3]
IMPORTANCE OF ENDOGENOUS TUMOR-NECROSIS-FACTOR-ALPHA AND GAMMA-INTERFERON IN HOST-RESISTANCE AGAINST PNEUMOCYSTIS-CARINII INFECTION [J].
CHEN, WX ;
HAVELL, EA ;
HARMSEN, AG .
INFECTION AND IMMUNITY, 1992, 60 (04) :1279-1284
[4]
2 HIGH-AFFINITY INTERLEUKIN-1 RECEPTORS REPRESENT SEPARATE GENE-PRODUCTS [J].
CHIZZONITE, R ;
TRUITT, T ;
KILIAN, PL ;
STERN, AS ;
NUNES, P ;
PARKER, KP ;
KAFFKA, KL ;
CHUA, AO ;
LUGG, DK ;
GUBLER, U .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (20) :8029-8033
[5]
CUSHION MT, 1988, LAB INVEST, V58, P324
[6]
RECOMBINANT MURINE INTERLEUKIN-1-ALPHA ENHANCEMENT OF NONSPECIFIC ANTIBACTERIAL RESISTANCE [J].
CZUPRYNSKI, CJ ;
BROWN, JF .
INFECTION AND IMMUNITY, 1987, 55 (09) :2061-2065
[7]
DINARELLO CA, 1989, ADV IMMUNOL, V44, P153, DOI [10.1016/s0065-2776(08)60642-2, 10.1016/S0065-2776(08)60642-2, DOI 10.1016/S0065-2776(08)60642-2]
[8]
UPTAKE OF PNEUMOCYSTIS-CARINII MEDIATED BY THE MACROPHAGE MANNOSE RECEPTOR [J].
EZEKOWITZ, RAB ;
WILLIAMS, DJ ;
KOZIEL, H ;
ARMSTRONG, MYK ;
WARNER, A ;
RICHARDS, FF ;
ROSE, RM .
NATURE, 1991, 351 (6322) :155-158
[9]
FORTE M, 1991, INT J EXP PATHOL, V72, P589
[10]
INTERLEUKIN-1 RECEPTOR BLOCKADE ATTENUATES THE HOST INFLAMMATORY RESPONSE [J].
GERSHENWALD, JE ;
FONG, Y ;
FAHEY, TJ ;
CALVANO, SE ;
CHIZZONITE, R ;
KILIAN, PL ;
LOWRY, SF ;
MOLDAWER, LL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (13) :4966-4970