Perforin expression and cytotoxic activity of sputum CD8+ lymphocytes in patients with COPD

被引:116
作者
Chrysofakis, G
Tzanakis, N
Kyriakoy, D
Tsoumakidou, M
Tsiligianni, I
Klimathianaki, M
Siafakas, NM
机构
[1] Univ Crete, Sch Med, Dept Thorac Med, GR-71110 Iraklion, Crete, Greece
[2] Univ Hosp Heraklion, Dept Thorac Med, Sch Med, Iraklion, Crete, Greece
关键词
CD8(+) cells; COPD; cytotoxicity; perform; smoking;
D O I
10.1378/chest.125.1.71
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Previous studies have shown that the inflammatory response to cigarette smoking differs between smokers who acquire COPD and those who do not, and the CD8(+) T-lymphocytes have been identified as a key player in this response. Objective: To investigate the cytotoxic activity and perforin expression of CD8(+) lymphocytes in the airway lumen of patients with COPD. Methods: Thirty-six male smokers with COPD, 25 male smokers without COPD, and 10 healthy nonsmokers participated in the study. T-lymphocytes of induced sputum samples were labeled with appropriate monoclonal antibodies and measured using flow cytometry. The cytotoxic activity of CD8(+) cells was defined by incubating them with specific target cells (K562). Results: The percentage and the total number of CD8(+) lymphocytes were significantly higher in COPD smokers compared to non-COPD smokers (p = 0.01 and p = 0.005, respectively) or to healthy nonsmokers (p = 0.02 and p = 0.01, respectively). Perforin expression in CD8(+) cells was significantly higher in smokers with COPD compared to the other two groups (p = 0.001). Increased cytotoxic activity of T cells was also observed in induced sputum of patients with COPD in comparison to the other two groups. Conclusion: CD8(+) cells are not only increased in number in sputum samples of smokers with COPD but are highly activated, expressing high levels of perforin. These findings suggest that CD8(+) T-lymphocytes play a significant role in the inflammatory process of COPD.
引用
收藏
页码:71 / 76
页数:6
相关论文
共 31 条
[1]   Increase in perforin-positive peripheral blood lymphocytes in extrinsic and intrinsic asthma [J].
Arnold, V ;
Balkow, S ;
Staats, R ;
Matthys, H ;
Luttmann, W ;
Virchow, JC .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 161 (01) :182-186
[2]   Medical progress: Chronic obstructive pulmonary disease. [J].
Barnes, PJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (04) :269-280
[4]   CYTO-TOXIC T-CELLS CLEAR VIRUS BUT AUGMENT LUNG PATHOLOGY IN MICE INFECTED WITH RESPIRATORY SYNCYTIAL VIRUS [J].
CANNON, MJ ;
OPENSHAW, PJM ;
ASKONAS, BA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 168 (03) :1163-1168
[5]  
CONOVER WJ, 1999, PRACTICAL NONPARAMET, P491
[6]  
DIENER CF, 1975, AM REV RESPIR DIS, V111, P719
[7]   MORTALITY IN RELATION TO SMOKING - 20 YEARS OBSERVATIONS ON MALE BRITISH DOCTORS [J].
DOLL, R ;
PETO, R .
BRITISH MEDICAL JOURNAL, 1976, 2 (6051) :1525-1536
[8]   Structural and functional consequences of alveolar cell recognition by CD8+ T lymphocytes in experimental lung disease [J].
Enelow, RI ;
Mohammed, AZ ;
Stoler, MH ;
Liu, AN ;
Young, JS ;
Lou, YH ;
Braciale, TJ .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (09) :1653-1661
[9]   NATURAL-HISTORY OF CHRONIC AIR-FLOW OBSTRUCTION [J].
FLETCHER, C ;
PETO, R .
BMJ-BRITISH MEDICAL JOURNAL, 1977, 1 (6077) :1645-1648
[10]   Role of latent viral infections in chronic obstructive pulmonary disease and asthma [J].
Hogg, JC .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 164 (10) :S71-S75