IL-4, IL-5 and IL-10 are not required for the control of M-bovis-BCG infection in mice

被引:36
作者
Erb, KJ [1 ]
Kirman, J
Delahunt, B
Chen, WX
Le Gros, G
机构
[1] Malaghan Inst Med Res, Wellington, New Zealand
[2] Wellington Sch Med, Dept Pathol, Wellington, New Zealand
[3] Wakefield Hosp, Wakefield Gastroenterol Res Inst, Wellington, New Zealand
关键词
IL-4; IL-5; IL-10; mycobacteria;
D O I
10.1046/j.1440-1711.1998.00719.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mycobacterial infections in mice are normally characterized by a profound Th1 cell-mediated immune response, in which T cells secrete large amounts of IFN-gamma. Recent evidence suggests that this response also includes a Th2 component. In order to investigate whether production of IL-4, IL-5, or IL-10 influenced the outcome of a Mycobacterium bovis-bacille Calmette-Guerin (BCG) infection, we intranasally infected IL-4, IL-5, and IL-10 gene-deficient and control mice and monitored the resulting immune response and bacterial clearance. IL-4, IL-5, and IL-10 deficient mice cleared the mycobacteria with the same kinetics as control mice. Furthermore, T cells of cytokine deficient and control mice produced similar levels of IFN-gamma following in vitro stimulation with purified protein derivative (PPD) from M. bovis. We conclude that the cytokines IL-4, IL-5 and IL-10 are not essential for and do not negatively influence the protective immune response against M. bovis-BCG in the lung of mice.
引用
收藏
页码:41 / 46
页数:6
相关论文
共 22 条
[1]   INFECTION WITH MYCOBACTERIUM-AVIUM INDUCES PRODUCTION OF INTERLEUKIN-10 (IL-10), AND ADMINISTRATION OF ANTI-IL-10 ANTIBODY IS ASSOCIATED WITH ENHANCED RESISTANCE TO INFECTION IN MICE [J].
BERMUDEZ, LE ;
CHAMPSI, J .
INFECTION AND IMMUNITY, 1993, 61 (07) :3093-3097
[2]   LIVE BUT NOT HEAT-KILLED MYCOBACTERIA CAUSE RAPID CHEMOTAXIS OF LARGE NUMBERS OF EOSINOPHILS INVIVO AND ARE INGESTED BY THE ATTRACTED GRANULOCYTES [J].
CASTRO, AG ;
ESAGUY, N ;
MACEDO, PM ;
AGUAS, AP ;
SILVA, MT .
INFECTION AND IMMUNITY, 1991, 59 (09) :3009-3014
[3]   ANTIBODY TO INTERLEUKIN-5 INHIBITS HELMINTH-INDUCED EOSINOPHILIA IN MICE [J].
COFFMAN, RL ;
SEYMOUR, BWP ;
HUDAK, S ;
JACKSON, J ;
RENNICK, D .
SCIENCE, 1989, 245 (4915) :308-310
[4]  
COOPER AM, 1995, IMMUNOLOGY, V84, P423
[5]  
Dai WJ, 1997, J IMMUNOL, V158, P2259
[6]  
DENIS M, 1993, J IMMUNOL, V151, P5425
[7]   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
[8]   AN ESSENTIAL ROLE FOR INTERFERON-GAMMA IN RESISTANCE TO MYCOBACTERIUM-TUBERCULOSIS INFECTION [J].
FLYNN, JL ;
CHAN, J ;
TRIEBOLD, KJ ;
DALTON, DK ;
STEWART, TA ;
BLOOM, BR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (06) :2249-2254
[9]   PRODUCTION OF INTERFERON-GAMMA, INTERLEUKIN-2, INTERLEUKIN-4, AND INTERLEUKIN-10 BY CD4+ LYMPHOCYTES INVIVO DURING HEALING AND PROGRESSIVE MURINE LEISHMANIASIS [J].
HEINZEL, FP ;
SADICK, MD ;
MUTHA, SS ;
LOCKSLEY, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :7011-7015
[10]   SPLEEN-CELL CYTOKINE SECRETION IN MYCOBACTERIUM-BOVIS BCG-INFECTED MICE [J].
HUYGEN, K ;
ABRAMOWICZ, D ;
VANDENBUSSCHE, P ;
JACOBS, F ;
DEBRUYN, J ;
KENTOS, A ;
DROWART, A ;
VANVOOREN, JP ;
GOLDMAN, M .
INFECTION AND IMMUNITY, 1992, 60 (07) :2880-2886