Posttraumatic lymphocyte response: A comparison between peripheral blood T cells and tissue T cells

被引:16
作者
Aguilar, MM
Battistella, FD
Owings, JT
Olson, SA
MacColl, K
机构
[1] Univ Calif Davis, Hlth Syst, Dept Surg, Sacramento, CA 95817 USA
[2] Univ Calif Davis, Hlth Syst, Dept Orthoped, Sacramento, CA 95817 USA
关键词
trauma; T cell; peripheral blood lymphocyte; tissue lymphocyte; lymphatic lymphocyte; CD4; CD8; gamma delta-TcR; L selectin; major histocompatibility complex II; flow cytometry; prefemoral lymph fistula;
D O I
10.1097/00005373-199807000-00003
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: T-cell response to trauma has been assessed primarily by sampling peripheral blood lymphocytes. We hypothesized that lymphocytes residing in tissue and traveling through lymph vessels are more likely to be activated by tissue injury and hemorrhage-induced hypoperfusion.We compared peripheral blood T-cell response with tissue or lymph T-cell response in an ovine model of multiple injury. Methods: Anesthetized adult sheep instrumented with a chronic prefemoral lymph fistula were subjected to lower-extremity fractures, fixed-volume hemorrhage, resuscitation, and fracture stabilization. Peripheral blood and tissue T-cell receptor expression was determined at baseline and after injury. Results: At baseline, we found significant differences in the expression of CD4, CD8, and L selectin between peripheral blood T cells and tissue T cells, After trauma, the percentage of tissue T cells expressing CD8 decreased from 19 +/- 9 to 14 +/- 5 (p < 0.05) and the percentage expressing gamma delta-TcR receptors decreased from 12 +/- 4 to 7 +/- 2 (p < 0.05), T-cell phenotype composition in peripheral blood was not affected by trauma. Conclusion: Peripheral blood T-cell composition differs from tissue T-cell composition before and after trauma. Trauma produced changes in tissue T-cell phenotypes but not in peripheral blood T-cell phenotypes.
引用
收藏
页码:14 / 18
页数:5
相关论文
共 32 条
[1]  
ABRAHAM E, 1992, CLIN EXP IMMUNOL, V90, P497
[2]  
ABRAHAM E, 1989, J IMMUNOL, V142, P899
[3]   THE IMMUNOBIOLOGY OF T-CELLS WITH INVARIANT GAMMA-DELTA ANTIGEN RECEPTORS [J].
ALLISON, JP ;
HAVRAN, WL .
ANNUAL REVIEW OF IMMUNOLOGY, 1991, 9 :679-705
[4]   Immune dysfunction in murine polymicrobial sepsis: Mediators, macrophages, lymphocytes and apoptosis [J].
Ayala, A ;
Chaudry, IH .
SHOCK, 1996, 6 :S27-S38
[5]  
AYALA A, 1990, IMMUNOLOGY, V70, P33
[6]   EPIDEMIOLOGY OF TRAUMA DEATHS [J].
BAKER, CC ;
OPPENHEIMER, L ;
STEPHENS, B ;
LEWIS, FR ;
TRUNKEY, DD .
AMERICAN JOURNAL OF SURGERY, 1980, 140 (01) :144-150
[7]   Interleukin-6 in the injured patient marker of injury or mediator of inflammation? [J].
Biffl, WL ;
Moore, EE ;
Moore, FA ;
Peterson, VM .
ANNALS OF SURGERY, 1996, 224 (05) :647-664
[8]   TOWARD AN EPIDEMIOLOGY AND NATURAL-HISTORY OF SIRS (SYSTEMIC INFLAMMATORY RESPONSE SYNDROME) [J].
BONE, RC .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 268 (24) :3452-3455
[10]   LEUKOCYTE-ENDOTHELIAL CELL RECOGNITION - 3 (OR MORE) STEPS TO SPECIFICITY AND DIVERSITY [J].
BUTCHER, EC .
CELL, 1991, 67 (06) :1033-1036