Papatheodorou Angelos, Stein Adam, Bank Matthew, Sison Cristina P, Gibbs Katie, Davies Peter, Bloom Ona
1 Department of Autoimmune and Musculoskeletal Disorders, North Shore University Hospital , Northwell Health, Manhasset, New York.
2 Department of Physical Medicine and Rehabilitation, North Shore University Hospital , Northwell Health, Manhasset, New York.
J Neurotrauma. 2017 Feb;34(3):746-754. doi: 10.1089/neu.2016.4596. Epub 2016 Oct 26.
Inflammation in traumatic spinal cord injury (SCI) has been proposed to promote damage acutely and oppose functional recovery chronically. However, we do not yet understand the signals that initiate or prolong inflammation in persons with SCI. High-Mobility Group Box 1 (HMGB1) is a potent systemic inflammatory cytokine-or damage-associated molecular pattern molecule (DAMP)-studied in a variety of clinical settings. It is elevated in pre-clinical models of traumatic spinal cord injury (SCI), where it promotes secondary injury, and strategies that block HMGB1 improve functional recovery. To investigate the potential translational relevance of these observations, we measured HMGB1 in plasma from adults with acute (≤ 1 week post-SCI, n = 16) or chronic (≥ 1 year post-SCI, n = 47) SCI. Plasma from uninjured persons (n = 51) served as controls for comparison. In persons with acute SCI, average HMGB1 levels were significantly elevated within 0-3 days post-injury (6.00 ± 1.8 ng/mL, mean ± standard error of the mean [SEM]) or 4-7 (6.26 ± 1.3 ng/mL, mean ± SEM), compared with controls (1.26 ± 0.24 ng/mL, mean ± SEM; p ≤ 0.001 and p ≤ 0.01, respectively). In persons with chronic SCI who were injured for 15 ± 1.5 years (mean ± SEM), HMGB1 also was significantly elevated, compared with uninjured persons (3.7 ± 0.69 vs. 1.26 ± 0.24 ng/mL, mean ± SEM; p ≤ 0.0001). Together, these data suggest that HMGB1 may be a common, early, and persistent danger signal promoting inflammation in individuals with SCI.
创伤性脊髓损伤(SCI)中的炎症被认为在急性期会加剧损伤,而在慢性期则会阻碍功能恢复。然而,我们尚不清楚引发或延长SCI患者炎症反应的信号。高迁移率族蛋白B1(HMGB1)是一种强效的全身性炎症细胞因子或损伤相关分子模式分子(DAMP),已在多种临床环境中进行了研究。在创伤性脊髓损伤(SCI)的临床前模型中,其水平会升高,它会促进继发性损伤,而阻断HMGB1的策略可改善功能恢复。为了研究这些观察结果的潜在转化相关性,我们检测了急性(SCI后≤1周,n = 16)或慢性(SCI后≥1年,n = 47)SCI成年患者血浆中的HMGB1。未受伤者(n = 51)的血浆作为对照进行比较。与对照组相比(1.26±0.24 ng/mL,平均值±平均标准误[SEM]),急性SCI患者在受伤后0 - 3天(6.00±1.8 ng/mL,平均值±SEM)或4 - 7天(6.26±1.3 ng/mL,平均值±SEM)时,HMGB1水平显著升高(分别为p≤0.001和p≤0.01)。在受伤15±1.5年(平均值±SEM)的慢性SCI患者中,与未受伤者相比,HMGB1也显著升高(3.7±0.69 vs. 1.26±0.24 ng/mL,平均值±SEM;p≤0.0001)。总之,这些数据表明HMGB1可能是促进SCI患者炎症反应的常见、早期且持续的危险信号。