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疟原虫 knowlesi 疟疾中的中性粒细胞激活、急性肺损伤和疾病严重程度。

Neutrophil activation, acute lung injury and disease severity in Plasmodium knowlesi malaria.

机构信息

Global and Tropical Health Division, Menzies School of Health Research, Charles Darwin University, Darwin, Australia.

Infectious Diseases Society Kota Kinabalu Sabah - Menzies School of Health Research Clinical Research Unit, Kota Kinabalu, Malaysia.

出版信息

PLoS Negl Trop Dis. 2024 Aug 16;18(8):e0012424. doi: 10.1371/journal.pntd.0012424. eCollection 2024 Aug.

Abstract

The risk of severe malaria from the zoonotic parasite Plasmodium knowlesi approximates that from P. falciparum. In severe falciparum malaria, neutrophil activation contributes to inflammatory pathogenesis, including acute lung injury (ALI). The role of neutrophil activation in the pathogenesis of severe knowlesi malaria has not been examined. We evaluated 213 patients with P. knowlesi mono-infection (138 non-severe, 75 severe) and 49 Plasmodium-negative controls from Malaysia. Markers of neutrophil activation (soluble neutrophil elastase [NE], citrullinated histone [CitH3] and circulating neutrophil extracellular traps [NETs]) were quantified in peripheral blood by microscopy and immunoassays. Findings were correlated with malaria severity, ALI clinical criteria, biomarkers of parasite biomass, haemolysis, and endothelial activation. Neutrophil activation increased with disease severity, with median levels higher in severe than non-severe malaria and controls for NE (380[IQR:210-930]ng/mL, 236[139-448]ng/mL, 218[134-307]ng/mL, respectively) and CitH3 (8.72[IQR:3.0-23.1]ng/mL, 4.29[1.46-9.49]ng/mL, 1.53[0.6-2.59]ng/mL, respectively)[all p<0.01]. NETs were higher in severe malaria compared to controls (126/μL[IQR:49-323] vs 51[20-75]/μL, p<0.001). In non-severe malaria, neutrophil activation fell significantly upon discharge from hospital (p<0.03). In severe disease, NETs, NE, and CitH3 were correlated with parasitaemia, cell-free haemoglobin and angiopoietin-2 (all Pearson's r>0.24, p<0.05). Plasma NE and angiopoietin-2 were higher in knowlesi patients with ALI than those without (p<0.008); neutrophilia was associated with an increased risk of ALI (aOR 3.27, p<0.01). In conclusion, neutrophil activation is increased in ALI and in proportion to disease severity in knowlesi malaria, is associated with endothelial activation, and may contribute to disease pathogenesis. Trials of adjunctive therapies to regulate neutrophil activation are warranted in severe knowlesi malaria.

摘要

从动物源性寄生虫疟原虫 knowlesi 感染中罹患严重疟疾的风险与疟原虫 falciparum 感染相当。在严重的恶性疟原虫感染中,中性粒细胞的激活会导致炎症发病机制,包括急性肺损伤(ALI)。中性粒细胞激活在严重 knowlesi 疟疾发病机制中的作用尚未得到检验。我们评估了来自马来西亚的 213 例疟原虫 knowlesi 单一感染患者(138 例非重症,75 例重症)和 49 例疟原虫阴性对照者。通过显微镜和免疫测定法检测外周血中的中性粒细胞激活标志物(可溶性中性粒细胞弹性蛋白酶[NE]、瓜氨酸化组蛋白[CitH3]和循环中性粒细胞胞外诱捕网[NETs])。研究结果与疟疾严重程度、ALI 临床标准、寄生虫生物量、溶血和内皮细胞激活的生物标志物相关联。中性粒细胞的激活随着疾病的严重程度而增加,重症组的 NE(380[IQR:210-930]ng/ml,236[139-448]ng/ml,218[134-307]ng/ml)和 CitH3(8.72[IQR:3.0-23.1]ng/ml,4.29[1.46-9.49]ng/ml,1.53[0.6-2.59]ng/ml)的中位数水平均高于非重症组和对照组(均 p<0.01)。与对照组相比,重症组的 NETs 更高(126/μL[IQR:49-323] vs 51[20-75]/μL,p<0.001)。在非重症疟疾中,中性粒细胞激活在出院时显著下降(p<0.03)。在重症疾病中,NETs、NE 和 CitH3 与寄生虫血症、无细胞血红蛋白和血管生成素-2 相关(均 Pearson's r>0.24,p<0.05)。患有 ALI 的 knowlesi 疟疾患者的血浆 NE 和血管生成素-2 高于无 ALI 者(p<0.008);中性粒细胞增多与 ALI 风险增加相关(优势比 3.27,p<0.01)。总之,中性粒细胞激活在 knowlesi 疟疾的 ALI 中增加,并且与疾病严重程度成比例,与内皮细胞激活相关,可能有助于发病机制。在严重的 knowlesi 疟疾中,有必要进行辅助治疗以调节中性粒细胞激活的试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e21f/11357107/ec2f8f3403f4/pntd.0012424.g001.jpg

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