Pallister Ian, Topley Nicholas
Department of Trauma & Orthopaedics, Morriston Hospital, Morriston, Swansea, England, United Kingdom.
J Trauma. 2004 Aug;57(2):347-51. doi: 10.1097/01.ta.0000133572.44369.f8.
Neutrophil (PMN) mediated tissue injury is central to the development of post-traumatic ARDS/MOF. Changes in activity caused by PMN isolation may be avoided by studying respiratory burst activity using whole blood chemiluminescence (WBCL).
WBCL and PMNCL were measured in 5 normal laboratory volunteers (NLV) and 9 patients sustaining major trauma, within 2 hours of admission. Receptor mediated (STZ) and independent (PMA) activating agents were used.
PMA activation confirmed significant priming both in WBCL and PMNCL after major trauma. With STZ, priming was confirmed in the WBCL study, but the trauma patient PMNCL showed no difference in response to those of NLV. Although the study population was small, those patients later developing ARDS demonstrated significantly greater STZ activated WBCL, 8 hours after admission.
PMN isolation alters behavior in vitro. This may lead to important differences of in vivo PMN function being obscured when studied in the laboratory setting. Further study of CL response and surface receptor expression is clearly warranted, both in WB and PMN preparations.
中性粒细胞(PMN)介导的组织损伤是创伤后急性呼吸窘迫综合征/多器官功能障碍综合征发生发展的核心。通过全血化学发光法(WBCL)研究呼吸爆发活性可避免因分离PMN导致的活性变化。
在5名正常实验室志愿者(NLV)和9名严重创伤患者入院后2小时内测定WBCL和PMNCL。使用受体介导(STZ)和独立(PMA)激活剂。
PMA激活证实严重创伤后WBCL和PMNCL均有显著预激。对于STZ,在WBCL研究中证实有预激,但创伤患者的PMNCL对NLV的反应无差异。尽管研究人群规模较小,但那些后来发生急性呼吸窘迫综合征的患者在入院8小时后STZ激活的WBCL显著更高。
分离PMN会改变其体外行为。这可能导致在实验室环境中研究时体内PMN功能的重要差异被掩盖。显然有必要对全血和PMN制剂中的化学发光反应及表面受体表达进行进一步研究。