Looney Mark R, Matthay Michael A
Departments of Medicine and Anesthesia, Cardiovascular Research Institute, University of California-San Francisco, CA, USA.
Crit Care Med. 2006 May;34(5 Suppl):S132-6. doi: 10.1097/01.CCM.0000214287.58444.2D.
To examine the existing animal models of transfusion-related acute lung injury (TRALI) for insight into disease pathogenesis.
The data were taken from published research and from our own experimental results.
Animal models have disproved the microaggregate theory of acute lung injury from blood transfusions. The two major hypotheses of TRALI, passively transfused neutrophil and human leukocyte antigen antibodies and biologically active lipids that accumulate in older, cellular blood products, have been replicated in animal models. The proposed two-hit model of TRALI is also supported by animal studies. A new in vivo mouse model of TRALI based on major histocompatibility complex (MHC) I antibodies has replicated several features of human TRALI, focusing prominently on the role of neutrophils.
Experimental animal models support both the antibody and lipid theories of TRALI. The essential role of neutrophils to producing lung injury is common to all existing models of TRALI. There is a lack of clinically relevant animal models that explain why transfusion of donor antibodies to cognate antigens in the recipient does not always lead to TRALI.
研究现有的输血相关急性肺损伤(TRALI)动物模型,以深入了解疾病发病机制。
数据取自已发表的研究以及我们自己的实验结果。
动物模型已推翻了输血所致急性肺损伤的微聚体理论。TRALI的两个主要假说,即被动输注的中性粒细胞、人类白细胞抗原抗体以及在陈旧的细胞血液制品中积累的生物活性脂质,已在动物模型中得到重现。TRALI的双打击模型也得到了动物研究的支持。一种基于主要组织相容性复合体(MHC)I抗体的新型TRALI体内小鼠模型重现了人类TRALI的几个特征,尤其突出了中性粒细胞的作用。
实验动物模型支持TRALI的抗体和脂质理论。中性粒细胞在产生肺损伤中的关键作用在所有现有的TRALI模型中都是共同的。缺乏能够解释为何将供体抗体输注给受体内的同源抗原并不总是导致TRALI的临床相关动物模型。