Apuzzo M L, Sheikh K M, Heiden J S, Weiss M H, Kurze T
J Neurosurg. 1979 Sep;51(3):317-22. doi: 10.3171/jns.1979.51.3.0317.
Cellular immune responses to brain antigens in patients with head injury were studied by applying the leukocyte adherence inhibition (LAI) assay. The investigation was conducted in three phases. 1) In the initial phase, evaluation of a series of 22 test and 25 control cases obtained at random during a 2- to 6-week time frame following a traumatic event indicated significant non-adherence of leukocytes (NAL) in 77% of the test group and 20% of the control group in the presence of brain antigen. 2) In a second phase, larger test population was divided into four groups of different posttraumatic intervals. This study measured NAL in the presence of normal heart of normal brain antigen. Assays revealed an initial significant NAL in the presence of both antigens; however, after the first week following injury the majority of cases manifested significant NAL only with brain antigen. These values of NAL persisted over a 6- to 8-week period. 3) As a final phase of investigation, analysis of a sequential series of assays in 12 patients over a 90-day period indicated significant NAL in the presence of brain antigen within the first week of injury, this was followed by a drop in NAL in most of the cases. Studies at 7 to 60 days posttrauma demonstrated significant NAL with brain antigen alone, with a subsequent drop by 90 days. These observations are interpreted to represent sensitization of leukocyte subgroups to brain proteins that are immunologically recognized following the traumatic event.
通过应用白细胞黏附抑制(LAI)试验,研究了头部受伤患者对脑抗原的细胞免疫反应。该研究分三个阶段进行。1)在初始阶段,对在创伤事件后2至6周时间内随机获取的22例测试病例和25例对照病例进行评估,结果表明在存在脑抗原的情况下,测试组77%的病例和对照组20%的病例出现了白细胞显著非黏附(NAL)现象。2)在第二阶段,将更大的测试人群分为四组不同创伤后间隔的人群。本研究在存在正常心脏或正常脑抗原的情况下测量NAL。检测显示在两种抗原存在时最初均出现显著的NAL;然而,在受伤后的第一周后,大多数病例仅在脑抗原存在时表现出显著的NAL。这些NAL值在6至8周的时间内持续存在。3)作为研究的最后阶段,对12例患者在90天内进行的一系列连续检测分析表明,在受伤后的第一周内,在脑抗原存在时出现显著的NAL,随后大多数病例的NAL下降。创伤后7至60天的研究表明仅在脑抗原存在时出现显著的NAL,随后到90天时下降。这些观察结果被解释为代表白细胞亚群对创伤事件后被免疫识别的脑蛋白产生了致敏作用。