PSEUDOMONAS-AERUGINOSA EXOENZYME-S INDUCES PROLIFERATION OF HUMAN T-LYMPHOCYTES

被引:22
作者
MODY, CH [1 ]
BUSER, DE [1 ]
SYME, RM [1 ]
WOODS, DE [1 ]
机构
[1] UNIV CALGARY,DEPT MICROBIOL & INFECT DIS,CALGARY,AB T2N 4N1,CANADA
关键词
D O I
10.1128/IAI.63.5.1800-1805.1995
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pseudomonas aeruginosa is a gram-negative bacterium that is responsible for devastating acute and chronic infections, which include bronchiectasis in cystic fibrosis, nosocomial pneumonia, and infection of burn wounds. Previous studies have demonstrated that these patients have impaired host responses, including cell-mediated immune responses, which are important in anti-Pseudomonas host defense. The P. aeruginosa exoproduct, exoenzyme S, has a number of characteristics which suggest that it might be important in cell-mediated immunity. To determine whether exoenzyme S activates lymphocytes to proliferate, peripheral blood mononuclear cells (PBMC) from normal volunteers were stimulated with purified exoenzyme S, and the lymphocyte response was assessed by measuring [H-3]thymidine uptake and by counting the number of cells after various times in culture. Ninety-five percent of healthy adult donors had a lymphocyte response to exoenzyme S, The optimal lymphocyte response occurred on day 7, with 4 x 10(5) PBMC per microtiter well when cells were stimulated with 10 mu g exoenzyme S per mi, [H-3]thymidine uptake correlated with an increase in the number of mononuclear cells, indicating that proliferation occurred, In unseparated PBMC, T cells, and to a lesser extent B cells, proliferated. Purified T cells proliferated, while purified B cells proliferated only after the addition of irradiated T cells. Thus, T lymphocytes are necessary and sufficient for the proliferative response to exoenzyme S, We speculate that exoenzyme S from P. aeruginosa is important in T-lymphocyte-mediated host defense to P. aeruginosa, In strategies to enhance impaired cell-mediated immunity, exoenzyme S should be considered as a potential stimulant.
引用
收藏
页码:1800 / 1805
页数:6
相关论文
共 35 条
[1]   MITOGENIC EFFECTS OF PURIFIED OUTER-MEMBRANE PROTEINS FROM PSEUDOMONAS-AERUGINOSA [J].
CHEN, YHU ;
HANCOCK, REW ;
MISHELL, RI .
INFECTION AND IMMUNITY, 1980, 28 (01) :178-184
[2]   ADP-RIBOSYLATION OF P21RAS AND RELATED PROTEINS BY PSEUDOMONAS-AERUGINOSA EXOENZYME-S [J].
COBURN, J ;
GILL, DM .
INFECTION AND IMMUNITY, 1991, 59 (11) :4259-4262
[3]   EFFECT OF ORAL IMMUNIZATION WITH PSEUDOMONAS-AERUGINOSA ON THE DEVELOPMENT OF SPECIFIC ANTIBACTERIAL IMMUNITY IN THE LUNGS [J].
FREIHORST, J ;
MERRICK, JM ;
OGRA, PL .
INFECTION AND IMMUNITY, 1989, 57 (01) :235-238
[4]   HUMAN B-CELL ACTIVATION INVITRO - T-CELL-DEPENDENT POKEWEED MITOGEN-INDUCED DIFFERENTIATION OF BLOOD-B-LYMPHOCYTES [J].
GMELIGMEYLING, F ;
UYTDEHAAG, AGCM ;
BALLIEUX, RE .
CELLULAR IMMUNOLOGY, 1977, 33 (01) :156-169
[5]   SELECTIVE TRIGGERING OF HUMAN T-LYMPHOCYTES AND B-LYMPHOCYTES INVITRO BY POLYCLONAL MITOGENS [J].
GREAVES, M ;
JANOSSY, G ;
DOENHOFF, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1974, 140 (01) :1-18
[6]   INHIBITION OF PSEUDOMONAS-AERUGINOSA EXOENZYME EXPRESSION BY SUBINHIBITORY ANTIBIOTIC CONCENTRATIONS [J].
GRIMWOOD, K ;
TO, M ;
RABIN, HR ;
WOODS, DE .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (01) :41-47
[7]   PSEUDOMONAS-AERUGINOSA EXOENZYME-S - ADENOSINE-DIPHOSPHATE RIBOSYL-TRANSFERASE DISTINCT FROM TOXIN-A [J].
IGLEWSKI, BH ;
SADOFF, J ;
BJORN, MJ ;
MAXWELL, ES .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1978, 75 (07) :3211-3215
[8]   FUNCTIONAL IMMUNOREGULATORY T-CELL ABNORMALITIES IN CYSTIC-FIBROSIS PATIENTS [J].
LAHAT, N ;
RIVLIN, J ;
IANCU, TC .
JOURNAL OF CLINICAL IMMUNOLOGY, 1989, 9 (04) :287-295
[9]   PROSPECTIVE, CONTROLLED-STUDY OF A POLYVALENT PSEUDOMONAS VACCINE IN CYSTIC-FIBROSIS - 3 YEAR RESULTS [J].
LANGFORD, DT ;
HILLER, J .
ARCHIVES OF DISEASE IN CHILDHOOD, 1984, 59 (12) :1131-1134
[10]   THE SUPERANTIGEN PSEUDOMONAS EXOTOXIN-A REQUIRES ADDITIONAL FUNCTIONS FROM ACCESSORY CELLS FOR LYMPHOCYTE-T PROLIFERATION [J].
LEGAARD, PK ;
LEGRAND, RD ;
MISFELDT, ML .
CELLULAR IMMUNOLOGY, 1991, 135 (02) :372-382