Bronchoalveolar lavage macrophage and lymphocyte phenotypes in lung transplant recipients

被引:31
作者
Ward, C [1 ]
Whitford, H
Snell, G
Bao, H
Zheng, L
Reid, D
Williams, TJ
Walters, EH
机构
[1] Newcastle Univ, William Leech Ctr, Freeman Rd Hosp, Newcastle Upon Tyne NE7 7DN, Tyne & Wear, England
[2] Alfred Hosp, Dept Resp Med, Melbourne, Vic, Australia
[3] Monash Univ, Sch Med, Melbourne, Vic 3004, Australia
[4] Univ Tasmania, Dept Med, Hobart, Tas, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1016/S1053-2498(01)00319-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Recent publications have demonstrated potentially pathologic changes in bronchoalveolar lavage (BAL) from clinically stable lung transplant recipients (SLTRs), but there are few available data on alveolar macrophages (AMs). We formulated the hypothesis that changes in BAL AM and lymphocyte phenotypes would be apparent even in SLTRs. Methods: A cross-sectional study using a standardized 3 x 60 ml BAL, investigating lymphocyte and AM phenotypes in 19 SLTRs, 5 subjects with bronchiolitis obliterans syndrome (BOS) and 18 normal control volunteers. BAL lymphocyte and AM markers were assessed using flow cytometry. Results: We confirmed a significant elevation of neutrophils in all lung transplant recipients with a more marked elevation in the BOS subjects. Flow-cytometric analysis showed increased numbers of natural killer (NK;, CD56/CD16-positive) cells, increased CD11b- and CD11c-positive CD3 lymphocytes, increased CD8-positive lymphocytes and increased HLA-DR expression in CD8 cells from the lung transplant recipients, when compared with normals (p < .005). In contrast, the expression of a number of AM surface markers, associated with a range of host defense functions against bacteria, fungi and viruses (CD11a, CD11b, CD11c, HLA-DR, CD14), was lower in both SLTRs and those with BOS (p < .05). Conclusions: These novel findings are consistent with complex lymphocyte and macrophage changes that may result from clinically silent infection, partially suppressed rejection, or both.
引用
收藏
页码:1064 / 1074
页数:11
相关论文
共 41 条
[1]   EXPRESSION AND FUNCTION OF BETA-2 INTEGRINS ON ALVEOLAR MACROPHAGES FROM HUMAN AND NONHUMAN-PRIMATES [J].
ALBERT, RK ;
EMBREE, LJ ;
MCFEELY, JE ;
HICKSTEIN, DD .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 7 (02) :182-189
[2]   Decreased CD11b expression, phagocytosis, and oxidative burst in urban particulate pollution-exposed human monocytes and alveolar macrophages [J].
Becker, S ;
Soukup, JM .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, 1998, 55 (07) :455-477
[3]   In vitro effect of glucocorticoids on phagocytic function of sheep alveolar macrophages [J].
Belayat, F ;
Meniai, K ;
Michaux, C ;
Kafidi, N ;
Coignoul, F ;
Dewaele, A .
VETERINARY JOURNAL, 1998, 155 (02) :177-181
[4]   Bronchiolitis obliterans after lung transplantation - A review [J].
Boehler, A ;
Kesten, S ;
Weder, W ;
Speich, R .
CHEST, 1998, 114 (05) :1411-1426
[5]   Flow cytometric analysis of lung lymphocytes in lung transplant recipients [J].
Crim, C ;
Keller, CA ;
Dunphy, CH ;
Maluf, HM ;
Ohar, JA .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (03) :1041-1046
[6]  
DiGiovine B, 1996, J IMMUNOL, V157, P4194
[7]  
DUDDRIDGE M, 1993, EUR RESPIR J, V6, P489
[8]  
DUDDRIDGE M, 1990, THORAX, V43
[9]   Fluticasone and budesonide inhibit cytokine release in human lung epithelial cells and alveolar macrophages [J].
Ek, A ;
Larsson, K ;
Siljerud, S ;
Palmberg, L .
ALLERGY, 1999, 54 (07) :691-699
[10]   In stable lung transplant recipients, exhaled nitric oxide levels positively correlate with airway neutrophilia and bronchial epithelial iNOS [J].
Gabbay, E ;
Walters, EH ;
Orsida, B ;
Whitford, H ;
Ward, C ;
Kotsimbos, TC ;
Snell, GI ;
Williams, TJ .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 160 (06) :2093-2099