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抗HMGB-1中和抗体对疟原虫诱导的疟疾相关急性肺损伤/急性呼吸窘迫综合征模型中肺泡上皮细胞的保护作用

Protective Effect of an Anti-HMGB-1 Neutralizing Antibody on Hemozoin-Induced Alveolar Epithelial Cell in a Model of Malaria Associated ALI/ARDS.

作者信息

Techarang Tachpon, Jariyapong Pitchanee, Viriyavejakul Parnpen, Glaharn Supattra, Srisook Charit, Punsawad Chuchard

机构信息

Department of Medical Sciences, School of Medicine, Walailak University, Nakhon Si Thammarat, Thailand.

Tropical Medicine Research Unit, Research Institute for Health Sciences, Walailak University, Nakhon Si Thammarat, Thailand.

出版信息

Iran J Parasitol. 2021 Jul-Sep;16(3):366-376. doi: 10.18502/ijpa.v16i3.7089.

Abstract

BACKGROUND

We aimed to determine whether neutralizing high mobility group box-1 (HMGB-1) prevents the release of HMGB-1 and proinflammatory cytokines on hemozoin (Hz)-induced alveolar epithelial cell in a model of malaria associated ALI/ARDS.

METHODS

This study was conducted in the Department of Tropical Pathology, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand in 2020. Human pulmonary alveolar epithelial cells (HPAEpiCs) were exposed to medium alone or 20 μM Hz for 24 h and incubated with different concentrations (1, 5, and 10 μg/ml) of anti-HMGB-1 monoclonal antibody (mAb) for various times (0, 4, 12, 24, and 48 h). The levels of HMGB-1, TNF-α and IFN-γ in the supernatants were measured by ELISA. The mRNA expression of RAGE, TLR-2 and TLR-4 were analyzed by real-time PCR.

RESULTS

The HPAEpiCs treated with 10 μg/ml anti-HMGB-1 mAb showed a significant reduction in HMGB-1 release into the supernatant compared with those treated with 1 and 5 μg/ml anti-HMGB-1 mAb. The levels of TNF-α and IFN-γ were significantly decreased in the supernatant of HPAEpiCs treated with 1, 5, and 10 μg/ml anti-HMGB-1 mAb for 4, 12, 24, and 48 h compared with those stimulated with Hz alone. The mRNA expression levels of RAGE, TLR-2, and TLR-4 were significantly decreased after 24 h of anti-HMGB-1 antibody treatment at all concentrations.

CONCLUSION

An anti-HMGB-1 antibody could be an effective agent for inhibiting the release of HMGB-1, TNF-α and IFN-γ. Furthermore, a neutralizing anti-HMGB-1 antibody could be applicable for the treatment of malaria-associated ALI/ARDS.

摘要

背景

我们旨在确定在疟疾相关急性肺损伤/急性呼吸窘迫综合征模型中,中和高迁移率族蛋白B1(HMGB-1)是否能阻止HMGB-1和促炎细胞因子在疟原虫血红素(Hz)诱导的肺泡上皮细胞中的释放。

方法

本研究于2020年在泰国曼谷玛希隆大学热带医学院热带病理系进行。人肺泡上皮细胞(HPAEpiCs)单独暴露于培养基或20 μM Hz中24小时,并与不同浓度(1、5和10 μg/ml)的抗HMGB-1单克隆抗体(mAb)孵育不同时间(0、4、12、24和48小时)。通过酶联免疫吸附测定法(ELISA)测量上清液中HMGB-1、肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)的水平。通过实时聚合酶链反应(PCR)分析晚期糖基化终末产物受体(RAGE)、Toll样受体2(TLR-2)和Toll样受体4(TLR-4)的mRNA表达。

结果

与用1和5 μg/ml抗HMGB-1 mAb处理的细胞相比,用10 μg/ml抗HMGB-1 mAb处理的HPAEpiCs释放到上清液中的HMGB-1显著减少。与仅用Hz刺激的细胞相比,用1、5和10 μg/ml抗HMGB-1 mAb处理4、12、24和48小时的HPAEpiCs上清液中TNF-α和IFN-γ水平显著降低。在所有浓度下,抗HMGB-1抗体处理24小时后,RAGE、TLR-2和TLR-4的mRNA表达水平显著降低。

结论

抗HMGB-1抗体可能是抑制HMGB-1、TNF-α和IFN-γ释放的有效药物。此外,中和性抗HMGB-1抗体可能适用于治疗疟疾相关的急性肺损伤/急性呼吸窘迫综合征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c504/8476737/168b15d40800/IJPA-16-366-g001.jpg

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