Role of T-lymphocytes in the resolution of endotoxin-induced lung injury

被引:33
作者
Morris, PE
Glass, J
Cross, R
Cohen, DA
机构
[1] UNIV KENTUCKY,COLL MED,DEPT MED,LEXINGTON,KY 40536
[2] UNIV KENTUCKY,COLL MED,DEPT MICROBIOL IMMUNOL,LEXINGTON,KY 40536
关键词
Lung Injury; Acute Lung Injury; Bronchoalveolar Lavage; Neutrophilic Infiltration; Total White Blood Cell;
D O I
10.1023/A:1027393715300
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
An acute neutrophilic lung injury was compared in Balb/c normal and nu/nu (nude) mice to assess the role of T lymphocytes in the resolution of acute pulmonary neutrophilic inflammation following the administration of endotoxin. Maximal neutrophilic infiltration occurred on day 1 post-endotoxin treatment and declined to near normal levels by day 5. In contrast, the percentage of lymphocytes in the bronchoalveolar lavage (BAL) fluid increased from 1.8% an day 1 post-endotoxin to greater than 11% on days three and five, during which time neutrophil resolution was occurring. On days 1-5 after endotoxin administration, approximately 40% of the CD4 lymphocytes expressed the cell surface activation marker, CD69. Despite being CD69(+), CD4 cells did not express the high affinity IL-2 receptor chain, CD25, to any significant extent on any of the days studied. To assess the contribution of T cells to the rate of clearance of neutrophils from the BAL, normal and nude Balb/c mice were compared for the percentage of neutrophils following nasal administration of endotoxin. Endotoxin-treated nude mice did not demonstrate significant differences in either the total white blood cell counts or in the clearance of neutrophils from the BAL, as compared to normal Balb/c mice. These data indicate that the influx of activated T cells during the resolution of neutrophilic pneumonitis does not contribute to the rate of neutrophil clearance during acute lung injury.
引用
收藏
页码:269 / 278
页数:10
相关论文
共 11 条
[1]   LYMPHOCYTE RECRUITMENT TO THE LUNG [J].
BERMAN, JS ;
BEER, DJ ;
THEODORE, AC ;
KORNFELD, H ;
BERNARDO, J ;
CENTER, DM .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1990, 142 (01) :238-257
[2]   MACROPHAGE ENGULFMENT OF APOPTOTIC NEUTROPHILS CONTRIBUTES TO THE RESOLUTION OF ACUTE PULMONARY INFLAMMATION IN-VIVO [J].
COX, G ;
CROSSLEY, J ;
XING, Z .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1995, 12 (02) :232-237
[3]  
Druet P, 1995, Clin Exp Immunol, V101 Suppl 1, P9
[4]  
DUKE SS, 1990, LAB INVEST, V62, P355
[5]   ENDOTOXIN ENHANCEMENT OF LYMPHOCYTE ADHERENCE TO CULTURED SHEEP LUNG MICROVASCULAR ENDOTHELIAL-CELLS [J].
JONES, M ;
HOOVER, R ;
MEYRICK, B .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 7 (01) :81-89
[6]   IL-10 and IL-4 synergize with TNF-alpha to induce IL-1ra production by human neutrophils [J].
Marie, C ;
Pitton, C ;
Fitting, C ;
Cavaillon, JM .
CYTOKINE, 1996, 8 (02) :147-151
[7]   BRONCHOALVEOLAR LAVAGE CELLULARITY - THE DISTRIBUTION IN NORMAL VOLUNTEERS [J].
MERCHANT, RK ;
SCHWARTZ, DA ;
HELMERS, RA ;
DAYTON, CS ;
HUNNINGHAKE, GW .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 146 (02) :448-453
[8]  
SHANLEY TP, 1995, J IMMUNOL, V154, P3454
[9]  
Smith WB, 1996, J IMMUNOL, V157, P360
[10]   APOPTOSIS IN LEUKOCYTES [J].
SQUIER, MKT ;
SEHNERT, AJ ;
COHEN, JJ .
JOURNAL OF LEUKOCYTE BIOLOGY, 1995, 57 (01) :2-10