Elevated chemokine levels in bronchoalveolar lavage fluid of tuberculosis patients

被引:121
作者
Kurashima, K
Mukaida, N
Fujimura, M
Yasui, M
Nakazumi, Y
Matsuda, T
Matsushima, K
机构
[1] KANAZAWA UNIV,SCH MED,DEPT INTERNAL MED 3,KANAZAWA,ISHIKAWA 920,JAPAN
[2] KANAZAWA UNIV,CANC RES INST,DEPT PHARMACOL,KANAZAWA,ISHIKAWA 920,JAPAN
[3] ASANOGAWA GEN HOSP,DEPT INTERNAL MED,KANAZAWA,ISHIKAWA,JAPAN
[4] UNIV TOKYO,GRAD SCH MED,DEPT MOL PREVENT MED,TOKYO,JAPAN
关键词
D O I
10.1164/ajrccm.155.4.9105097
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
In pulmonary tuberculosis, the proportion of lymphocytes, particularly that of CD4(+) T lymphocytes was increased in bronchoalveolar lavage fluid (BALF), reflecting their protective role against mycobacterial infections. In order to elucidate the mechanisms of lymphocyte accumulation in lungs, we measured the levels of chemokines with potent lymphocyte chemotactic activities, including interleukin-8 (IL-8), monocyte chemoattractant protein-1 (MCP-1), and, regulated on activation, normal T-cell expressed and secreted (RANTES) present in BALF from patients with pulmonary tuberculosis in acute (n = 10) and convalescent phases (n = 6), as well as normal subjects (n = 10). During the acute phase of the disease, the proportions of lymphocytes and neutrophils were increased, as reported in previous studies. The levels of IL-8, MCP-1, and RANTES in the acute phase of pulmonary tuberculosis were also markedly elevated as compared with those of normal subjects. MCP-1 and RANTES, but not IL-8 levels present in BALF, decreased in the convalescent phase. Moreover, the concentration of RANTES correlated significantly with the absolute number of CD4(+) cells in BALF. These data suggest that chemotactic cytokines are differentially produced and participate in the host response to Mycobacterium tuberculosis infection.
引用
收藏
页码:1474 / 1477
页数:4
相关论文
共 22 条
  • [11] THE NEUTROPHIL-ACTIVATING PROTEIN (NAP-1) IS ALSO CHEMOTACTIC FOR LYMPHOCYTES-T
    LARSEN, CG
    ANDERSON, AO
    APPELLA, E
    OPPENHEIM, JJ
    MATSUSHIMA, K
    [J]. SCIENCE, 1989, 243 (4897) : 1464 - 1466
  • [12] Increased release of interleukin-1 beta, interleukin-6, and tumor necrosis factor-alpha by bronchoalveolar cells lavaged from involved sites in pulmonary tuberculosis
    Law, K
    Weiden, M
    Harkin, T
    TchouWong, KM
    Chi, CX
    Rom, WN
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (02) : 799 - 804
  • [13] MURRAY CJL, 1992, DISEASE CONTROL PRIO, P50
  • [14] OKAZAKI T, 1992, CHEST, V102, P54
  • [15] EVIDENCE FOR A TH1-LIKE BRONCHOALVEOLAR T-CELL SUBSET AND PREDOMINANCE OF INTERFERON-GAMMA GENE ACTIVATION IN PULMONARY TUBERCULOSIS
    ROBINSON, DS
    YING, S
    TAYLOR, IK
    WANGOO, A
    MITCHELL, DM
    KAY, AB
    HAMID, Q
    SHAW, RJ
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 149 (04) : 989 - 993
  • [16] ROOK GAW, 1985, CLIN EXP IMMUNOL, V59, P414
  • [17] SELECTIVE ATTRACTION OF MONOCYTES AND LYMPHOCYTES-T OF THE MEMORY PHENOTYPE BY CYTOKINE RANTES
    SCHALL, TJ
    BACON, K
    TOY, KJ
    GOEDDEL, DV
    [J]. NATURE, 1990, 347 (6294) : 669 - 671
  • [18] SEMENZATO G, 1985, AM REV RESPIR DIS, V132, P400
  • [19] TAUB DD, 1993, ADV EXP MED BIOL, V351, P139
  • [20] PULMONARY EOSINOPHILIA IN PULMONARY TUBERCULOSIS
    VIJAYAN, VK
    REETHA, AM
    JAWAHAR, MS
    SANKARAN, K
    PRABHAKAR, R
    [J]. CHEST, 1992, 101 (06) : 1708 - 1709