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感染性休克患者循环固有免疫细胞中 MerTK 表达增加。

Increased MerTK expression in circulating innate immune cells of patients with septic shock.

机构信息

Laboratoire d'Immunologie, Hôpital E. Herriot, Hospices Civils de Lyon, 5 place d'Arsonval, 69437, Lyon cedex 03, France.

出版信息

Intensive Care Med. 2013 Sep;39(9):1556-64. doi: 10.1007/s00134-013-3006-9. Epub 2013 Jul 9.

Abstract

PURPOSE

A new pathway of three protein tyrosine kinase receptors, namely, the TAM receptor family [Tyro-3, Axl and Mer tyrosine kinase (MerTK)], has recently been described to negatively control immune responses. The objective of this prospective, observational, clinical study was to investigate the expression patterns of TAM receptors in circulating white blood cells collected from patients with septic shock.

METHODS

The expression of TAM receptors was measured by flow cytometry in circulating leukocytes from patients with septic shock sampled on days (D) 1-2 (n = 47) and D3-4 (n = 37) after the onset of shock, severe trauma patients at D1-2 after trauma (n = 51) and healthy individuals (n = 23).

RESULTS

On D1-2 after injury, MerTK was overexpressed in monocytes and neutrophils collected from patients with septic shock in comparison with those collected from healthy volunteers and trauma patients. This phenomenon was also observed for mRNA. Conversely, the expression of Tyro-3 and Axl was higher in monocytes from trauma patients versus healthy volunteers or those in septic shock. MerTK expression between D1-2 and D3-4 remained elevated in patients suffering from septic shock who died or developed an intensive care unit-acquired infection, whereas it decreased in patients who recovered uneventfully. This in vivo observed expression pattern was reproduced ex vivo after the incubation of healthy volunteer cells with plasma from septic shock or trauma patients.

CONCLUSIONS

MerTK expression in circulating innate immune cells is increased in patients with septic shock in comparison with healthy volunteers and trauma patients. Persistent MerTK overexpression after septic shock is associated with adverse outcome. The role of this family of receptors in the pathophysiology of injury-induced immune dysfunctions deserves to be specifically investigated.

摘要

目的

最近描述了一种新的三种蛋白酪氨酸激酶受体途径,即 TAM 受体家族[酪氨酸激酶 3(Tyro-3)、Axl 和 Mer(MerTK)],该途径可负性调控免疫反应。本前瞻性、观察性临床研究的目的是研究循环白细胞中 TAM 受体的表达模式,这些白细胞来自感染性休克患者。

方法

采用流式细胞术检测感染性休克患者休克发作后第 1-2 天(n = 47)和第 3-4 天(n = 37)、严重创伤患者创伤后第 1-2 天(n = 51)和健康个体(n = 23)循环白细胞中 TAM 受体的表达。

结果

与健康志愿者和创伤患者相比,在创伤后第 1-2 天,感染性休克患者的单核细胞和中性粒细胞中 MerTK 表达过度,这种现象在 mRNA 中也有观察到。相反,创伤患者的单核细胞中 Tyro-3 和 Axl 的表达高于健康志愿者或感染性休克患者。在死亡或发生重症监护病房获得性感染的感染性休克患者中,D1-2 至 D3-4 之间 MerTK 表达仍升高,而在恢复良好的患者中表达降低。在体外培养健康志愿者细胞与感染性休克或创伤患者的血浆后,观察到这种体内观察到的表达模式。

结论

与健康志愿者和创伤患者相比,感染性休克患者循环固有免疫细胞中 MerTK 表达增加。感染性休克后 MerTK 持续过度表达与不良预后相关。该受体家族在损伤诱导的免疫功能障碍的病理生理学中的作用值得专门研究。

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