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健康人类志愿者内毒素输注后HLA - DR表达、细胞因子产生及凝血的变化

Changes in HLA-DR expression, cytokine production and coagulation following endotoxin infusion in healthy human volunteers.

作者信息

Mant Timothy G K, Borozdenkova Svetlana, Bradford Daniel B A, Allen Elizabeth, Amin Dipti M, Toothaker Roger D, Collins Robert W M, Hargreaves Roseanna E G, Jurcevic Stipo

机构信息

Guy's Drug Research Unit, London SE1 1YR, United Kingdom.

出版信息

Int Immunopharmacol. 2008 May;8(5):701-7. doi: 10.1016/j.intimp.2008.01.014. Epub 2008 Feb 11.

Abstract

The infusion of a low dose of endotoxin into healthy subjects triggers a complex inflammatory response but the intricacies of which, despite extensive research, are still being unraveled. Nine healthy male volunteers received a dose of 30 Units endotoxin/kg bodyweight as an intravenous bolus. Following endotoxin infusion the concentration of TNF-alpha in their serum rapidly increased within 30 min, peaked after 1-2 h and returned to baseline by 4 h. This corresponded to a similarly rapid increase in anti-inflammatory soluble TNF receptor (sTNFR) levels, which remained elevated for up to 48 h. Increased levels of other cytokines were measured, including IL-6, IL-8, G-CSF, IL-1ra and IL-10. However, these cytokines lagged behind that of TNF-alpha and remained elevated for up to 8 h. Endotoxin injection resulted in complex changes in HLA-DR expression, a marker of monocyte activation state. Initially, following a lag of 2-4 h, HLA-DR expression decreased with a nadir at 8 h, followed by an increase in expression above baseline at 22 h. HLA-DR levels returned to baseline 48 h post-endotoxin challenge. This was in contrast to endotoxin-induced changes in white blood cell (WBC) numbers, which dropped rapidly (at 2-3 h) while HLA-DR levels were stable and then peaked during the nadir in HLA-DR expression (8 h). Furthermore, endotoxin injection caused activation of both fibrinolytic and coagulation pathways. Thus, endotoxin infusion results in complex changes in HLA-DR expression, production of pro- and anti-inflammatory cytokines and activation of coagulation.

摘要

向健康受试者输注低剂量内毒素会引发复杂的炎症反应,尽管进行了广泛研究,但其错综复杂之处仍在不断被揭示。九名健康男性志愿者接受了30单位内毒素/千克体重的静脉推注剂量。内毒素输注后,他们血清中TNF-α的浓度在30分钟内迅速升高,1-2小时后达到峰值,并在4小时后恢复到基线水平。这与抗炎性可溶性TNF受体(sTNFR)水平的类似快速升高相对应,该水平在长达48小时内一直保持升高。还检测到其他细胞因子水平升高,包括IL-6、IL-8、G-CSF、IL-1ra和IL-10。然而,这些细胞因子的变化滞后于TNF-α,并且在长达8小时内一直保持升高。内毒素注射导致HLA-DR表达发生复杂变化,HLA-DR是单核细胞活化状态的标志物。最初,在2-4小时的滞后之后,HLA-DR表达下降,在8小时达到最低点,随后在22小时表达增加至高于基线水平。内毒素激发后48小时,HLA-DR水平恢复到基线。这与内毒素诱导的白细胞(WBC)数量变化形成对比,白细胞数量在HLA-DR水平稳定时迅速下降(在2-3小时),然后在HLA-DR表达的最低点(8小时)达到峰值。此外,内毒素注射导致纤溶和凝血途径的激活。因此,内毒素输注导致HLA-DR表达、促炎和抗炎细胞因子的产生以及凝血激活发生复杂变化。

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