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抗Nak(a)抗体、单核细胞和血小板在输血相关急性肺损伤发生中的作用。

Role of anti-Nak(a) antibody, monocytes and platelets in the development of transfusion-related acute lung injury.

作者信息

Nakajima F, Nishimura M, Hashimoto S, Okazaki H, Tadokoro K

机构信息

Research and Development Department, Central Blood Institute, Japanese Red Cross, Koutou-ku, Tokyo, Japan.

出版信息

Vox Sang. 2008 Nov;95(4):318-23. doi: 10.1111/j.1423-0410.2008.01095.x.

DOI:10.1111/j.1423-0410.2008.01095.x
PMID:19138262
Abstract

BACKGROUND AND OBJECTIVES

Transfusion-related acute lung injury (TRALI) is one of the most serious side-effects of transfusion. We report here the first two cases of TRALI caused by anti-Nak(a) (anti-CD36) antibody from a single blood donor. The aim of this study was to clarify the role of the anti-Nak(a) antibody in TRALI development.

MATERIALS AND METHODS

Human lung microvascular endothelial cells were co-cultured with Nak(a)-positive monocytes and Nak(a)-positive platelets together with serum prepared from blood products of a TRALI-caused anti-Nak(a) antibody-carrying donor. Expressions of leukotriene B(4) (LTB(4)) and tumour necrosis factor alpha (TNF-alpha) in the co-culture supernatants were determined.

RESULTS

The expressions of LTB(4) and TNF-alpha were found to be markedly increased, particularly in the presence of both Nak(a)-positive monocytes and platelets. The expressions of these mediators were almost completed within 4 h after the initiation of co-culture. Monocyte contribution seemed to be stronger than that of platelets. In the absence of human lung microvascular endothelial, no significant LTB(4) or TNF-alpha release was observed.

CONCLUSION

Anti-Nak(a) antibody may be strongly implicated in lung microvascular endothelial dysfunctions that lead to TRALI in a monocyte- and platelet-dependent manner.

摘要

背景与目的

输血相关急性肺损伤(TRALI)是输血最严重的副作用之一。我们在此报告首例由单一献血者的抗Nak(a)(抗CD36)抗体引起的两例TRALI。本研究的目的是阐明抗Nak(a)抗体在TRALI发生中的作用。

材料与方法

将人肺微血管内皮细胞与Nak(a)阳性单核细胞和Nak(a)阳性血小板共同培养,并加入由携带导致TRALI的抗Nak(a)抗体的献血者血液制品制备的血清。测定共培养上清液中白三烯B4(LTB4)和肿瘤坏死因子α(TNF-α)的表达。

结果

发现LTB4和TNF-α的表达显著增加,特别是在同时存在Nak(a)阳性单核细胞和血小板的情况下。这些介质的表达在共培养开始后4小时内几乎完成。单核细胞的作用似乎比血小板更强。在没有人类肺微血管内皮细胞的情况下,未观察到明显的LTB4或TNF-α释放。

结论

抗Nak(a)抗体可能与以单核细胞和血小板依赖方式导致TRALI的肺微血管内皮功能障碍密切相关。

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