Mechanism and intervention of murine transfusion-related acute lung injury caused by anti-CD36 antibodies

Anti-CD36 Abs have been suggested to induce transfusion-related acute lung injury (TRALI) upon blood transfusion, particularly in Asian populations. However, little is known about the pathological mechanism of anti-CD36 Ab–mediated TRALI, and potential therapies have not yet been identified. Here, w...

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Main Authors: Da-Wei Chen, Tian Kang, Xiu-Zhang Xu, Wen-Jie Xia, Xin Ye, Yong-Bin Wu, Yao-Ri Xu, Jing Liu, Hui Ren, Jing Deng, Yang-Kai Chen, Hao-Qiang Ding, Muhammad Aslam, Wioleta M. Zelek, B. Paul Morgan, Rick Kapur, Sentot Santoso, Yong-Shui Fu
Format: Article
Language:English
Published: American Society for Clinical investigation 2023-03-01
Series:JCI Insight
Subjects:
Online Access:https://doi.org/10.1172/jci.insight.165142
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author Da-Wei Chen
Tian Kang
Xiu-Zhang Xu
Wen-Jie Xia
Xin Ye
Yong-Bin Wu
Yao-Ri Xu
Jing Liu
Hui Ren
Jing Deng
Yang-Kai Chen
Hao-Qiang Ding
Muhammad Aslam
Wioleta M. Zelek
B. Paul Morgan
Rick Kapur
Sentot Santoso
Yong-Shui Fu
author_facet Da-Wei Chen
Tian Kang
Xiu-Zhang Xu
Wen-Jie Xia
Xin Ye
Yong-Bin Wu
Yao-Ri Xu
Jing Liu
Hui Ren
Jing Deng
Yang-Kai Chen
Hao-Qiang Ding
Muhammad Aslam
Wioleta M. Zelek
B. Paul Morgan
Rick Kapur
Sentot Santoso
Yong-Shui Fu
author_sort Da-Wei Chen
collection DOAJ
description Anti-CD36 Abs have been suggested to induce transfusion-related acute lung injury (TRALI) upon blood transfusion, particularly in Asian populations. However, little is known about the pathological mechanism of anti-CD36 Ab–mediated TRALI, and potential therapies have not yet been identified. Here, we developed a murine model of anti-CD36 Ab–mediated TRALI to address these questions. Administration of mouse mAb against CD36 (mAb GZ1) or human anti-CD36 IgG, but not GZ1 F(ab′)2 fragments, induced severe TRALI in Cd36+/+ male mice. Predepletion of recipient monocytes or complement, but not neutrophils or platelets, prevented the development of murine TRALI. Moreover, plasma C5a levels after TRALI induction by anti-CD36 Abs increased more than 3-fold, implying a critical role of complement C5 activation in the mechanism of Fc-dependent anti-CD36–mediated TRALI. Administration of GZ1 F(ab′)2, antioxidant (N-acetyl cysteine, NAC), or C5 blocker (mAb BB5.1) before TRALI induction completely protected mice from anti-CD36–mediated TRALI. Although no significant amelioration in TRALI was observed when mice were injected with GZ1 F(ab′)2 after TRALI induction, significant improvement was achieved when mice were treated postinduction with NAC or anti-C5. Importantly, anti-C5 treatment completely rescued mice from TRALI, suggesting the potential role of existing anti-C5 drugs in the treatment of patients with TRALI caused by anti-CD36.
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spelling doaj.art-481554b48faf4543965ea71e57c974962023-11-07T16:25:22ZengAmerican Society for Clinical investigationJCI Insight2379-37082023-03-0186Mechanism and intervention of murine transfusion-related acute lung injury caused by anti-CD36 antibodiesDa-Wei ChenTian KangXiu-Zhang XuWen-Jie XiaXin YeYong-Bin WuYao-Ri XuJing LiuHui RenJing DengYang-Kai ChenHao-Qiang DingMuhammad AslamWioleta M. ZelekB. Paul MorganRick KapurSentot SantosoYong-Shui FuAnti-CD36 Abs have been suggested to induce transfusion-related acute lung injury (TRALI) upon blood transfusion, particularly in Asian populations. However, little is known about the pathological mechanism of anti-CD36 Ab–mediated TRALI, and potential therapies have not yet been identified. Here, we developed a murine model of anti-CD36 Ab–mediated TRALI to address these questions. Administration of mouse mAb against CD36 (mAb GZ1) or human anti-CD36 IgG, but not GZ1 F(ab′)2 fragments, induced severe TRALI in Cd36+/+ male mice. Predepletion of recipient monocytes or complement, but not neutrophils or platelets, prevented the development of murine TRALI. Moreover, plasma C5a levels after TRALI induction by anti-CD36 Abs increased more than 3-fold, implying a critical role of complement C5 activation in the mechanism of Fc-dependent anti-CD36–mediated TRALI. Administration of GZ1 F(ab′)2, antioxidant (N-acetyl cysteine, NAC), or C5 blocker (mAb BB5.1) before TRALI induction completely protected mice from anti-CD36–mediated TRALI. Although no significant amelioration in TRALI was observed when mice were injected with GZ1 F(ab′)2 after TRALI induction, significant improvement was achieved when mice were treated postinduction with NAC or anti-C5. Importantly, anti-C5 treatment completely rescued mice from TRALI, suggesting the potential role of existing anti-C5 drugs in the treatment of patients with TRALI caused by anti-CD36.https://doi.org/10.1172/jci.insight.165142ImmunologyPulmonology
spellingShingle Da-Wei Chen
Tian Kang
Xiu-Zhang Xu
Wen-Jie Xia
Xin Ye
Yong-Bin Wu
Yao-Ri Xu
Jing Liu
Hui Ren
Jing Deng
Yang-Kai Chen
Hao-Qiang Ding
Muhammad Aslam
Wioleta M. Zelek
B. Paul Morgan
Rick Kapur
Sentot Santoso
Yong-Shui Fu
Mechanism and intervention of murine transfusion-related acute lung injury caused by anti-CD36 antibodies
JCI Insight
Immunology
Pulmonology
title Mechanism and intervention of murine transfusion-related acute lung injury caused by anti-CD36 antibodies
title_full Mechanism and intervention of murine transfusion-related acute lung injury caused by anti-CD36 antibodies
title_fullStr Mechanism and intervention of murine transfusion-related acute lung injury caused by anti-CD36 antibodies
title_full_unstemmed Mechanism and intervention of murine transfusion-related acute lung injury caused by anti-CD36 antibodies
title_short Mechanism and intervention of murine transfusion-related acute lung injury caused by anti-CD36 antibodies
title_sort mechanism and intervention of murine transfusion related acute lung injury caused by anti cd36 antibodies
topic Immunology
Pulmonology
url https://doi.org/10.1172/jci.insight.165142
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