IN-VITRO AND IN-VIVO T-CELL RESPONSES IN MICE DURING BRONCHOPULMONARY INFECTION WITH MUCOID PSEUDOMONAS-AERUGINOSA

被引:45
作者
STEVENSON, MM
KONDRATIEVA, TK
APT, AS
TAM, MF
SKAMENE, E
机构
[1] MCGILL UNIV, MONTREAL, PQ, CANADA
[2] NF GAMALEI INST EPIDEMIOL & MICROBIOL, IMMUNOL TOLERANCE LAB, MOSCOW, RUSSIA
[3] CENT INST TB, EXPTL IMMUNOGENET LAB, MOSCOW, RUSSIA
关键词
T CELLS; PSEUDOMONAS AERUGINOSA; MICE; CYSTIC FIBROSIS;
D O I
10.1111/j.1365-2249.1995.tb03478.x
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 and in vivo T cell responses were determined during the course of bronchopulmonary infection with mucoid Pseudomonas aeruginosa. T cell responses were compared in two inbred mouse strains, namely BALB/c mice, which are resistant to the establishment of chronic bronchopulmonary Ps. aeruginosa infection, and C57B1/6 mice, which have high numbers of bacteria in the lungs through 14 days post-infection. Unseparated lung cells and lung T cells from BALB/c mice exhibited significantly higher in vitro proliferative responses to both heat-killed Ps. aeruginosa and concanavalin A (Con A) than cells from C57B1/6 mice through 20 days post-intratracheal infection with 10(4) colony-forming units (CFU) Ps. aeruginosa. Proliferation of unseparated lung cells but not lung T cells from BALB/c mice infected 6 days previously with 10(5) CFU Ps. aeruginosa was suppressed in response to Con A; these cells were unresponsive to specific antigen. Suppression of lymphocyte proliferation in the lungs of C57B1/6 mice infected with 10(4) CFU Ps. aeruginosa and in BALB/c mice infected with 10(5) CFU was found to be mediated by adherent lung cells via the production of nitric oxide and prostaglandins. Determination of in vivo T cell-mediated responses in infected mice demonstrated that resistant BALB/c mice had high DTH and low Pseudomonas-specific antibody responses, while C57B1/6 mice had low DTH and high antibody levels, in particular, IgG2b and IgM.
引用
收藏
页码:98 / 105
页数:8
相关论文
共 35 条
[11]   CYSTIC-FIBROSIS IN THE MOUSE BY TARGETED INSERTIONAL MUTAGENESIS [J].
DORIN, JR ;
DICKINSON, P ;
ALTON, EWFW ;
SMITH, SN ;
GEDDES, DM ;
STEVENSON, BJ ;
KIMBER, WL ;
FLEMING, S ;
CLARKE, AR ;
HOOPER, ML ;
ANDERSON, L ;
BEDDINGTON, RSP ;
PORTEOUS, DJ .
NATURE, 1992, 359 (6392) :211-215
[12]  
DORING G, 1983, INFECT IMMUN, V42, P197
[13]   ATOPIC CHILDREN WITH CYSTIC-FIBROSIS HAVE INCREASED URINARY LEUKOTRIENE E(4) CONCENTRATIONS AND MORE SEVERE PULMONARY-DISEASE [J].
GREALLY, P ;
COOK, AJ ;
SAMPSON, AP ;
COLEMAN, R ;
CHAMBERS, S ;
PIPER, PJ ;
PRICE, JF .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1994, 93 (01) :100-107
[14]  
Hoiby N., 1977, ACTA PATHOL MIC SC, V262, P3
[15]  
HOLT PG, 1986, CLIN EXP IMMUNOL, V66, P188
[16]   DOWN-REGULATION OF THE ANTIGEN PRESENTING CELL FUNCTION(S) OF PULMONARY DENDRITIC CELLS INVIVO BY RESIDENT ALVEOLAR MACROPHAGES [J].
HOLT, PG ;
OLIVER, J ;
BILYK, N ;
MCMENAMIN, C ;
MCMENAMIN, PG ;
KRAAL, G ;
THEPEN, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (02) :397-407
[17]   ESTABLISHMENT OF MOUSE-CELL LINES WHICH CONSTITUTIVELY SECRETE LARGE QUANTITIES OF INTERLEUKIN-2, INTERLEUKIN-3, INTERLEUKIN-4 OR INTERLEUKIN-5, USING MODIFIED CDNA EXPRESSION VECTORS [J].
KARASUYAMA, H ;
MELCHERS, F .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1988, 18 (01) :97-104
[18]  
KAWABE T, 1992, IMMUNOLOGY, V76, P72
[19]  
KLINGER JD, 1978, J INFECT DIS, V138, P49, DOI 10.1093/infdis/138.1.49
[20]  
LAGACE J, 1989, J CLIN LAB IMMUNOL, V30, P7