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棘球蚴抗原免疫治疗后皮炎芽生菌病患者巨噬细胞功能特征及 Th1/Th2 平衡的变化。

Functional characterization of macrophages and change of Th1/Th2 balance in patients with pythiosis after Pythium insidiosum antigen immunotherapy.

机构信息

Department of Transfusion Medicine and Clinical Microbiology, Faculty of Allied Health Sciences, Chulalongkorn University, Phayathai Road, Pathumwan, Bangkok, 10330, Thailand.

Research Unit of Medical Mycology Diagnosis, Chulalongkorn University, Bangkok, Thailand.

出版信息

Sci Rep. 2024 Nov 9;14(1):27363. doi: 10.1038/s41598-024-78756-x.

Abstract

There has been limited research into the role of the Pythium insidiosum antigen (PIA) in modulating immune response in patients with pythiosis. This study investigated the balance of T helper type 2 (Th2) and T helper type 1 (Th1) responses after receiving PIA immunotherapy in patients with pythiosis. Next, the phagocytic activity and phagocytic index of IFN-γ primed PIA-treated macrophages were examined. Furthermore, the phagocytosis of infective P. insidiosum zoospores by macrophages was investigated. This work showed that the PIA vaccine induced Th1 response and M1 macrophages in patients with vascular pythiosis who survived and those with localized pythiosis. Phagocytic activity and phagocytic index were increased considerably in localized pythiosis patients compared to vascular pythiosis patients with hematological diseases. IFN-γ priming of PIA-treated macrophages against P. insidiosum zoospores enhanced the phagocytic activity and phagocytic index in vascular and localized pythiosis patients. Macrophages engulfed P. insidiosum zoospores, but the zoospores continued germination, resulting in macrophage death. Overall, our results suggest that PIA can modulate the immune responses, contributing to higher levels of Th1-type cytokine and potentially improving the survival of patients with vascular pythiosis. This study is the first to uncover that P. insidiosum zoospores can survive within macrophages.

摘要

对于瓶霉抗原(PIA)在调节棘球蚴病患者免疫反应中的作用,研究还很有限。本研究调查了棘球蚴病患者接受 PIA 免疫治疗后辅助性 T 细胞 2(Th2)和辅助性 T 细胞 1(Th1)反应的平衡。接下来,检查了 IFN-γ 预处理 PIA 处理的巨噬细胞的吞噬活性和吞噬指数。此外,还研究了感染性瓶霉游动孢子被巨噬细胞吞噬的情况。这项工作表明,PIA 疫苗可诱导血管性棘球蚴病和局限性棘球蚴病存活患者以及局限性棘球蚴病患者产生 Th1 反应和 M1 巨噬细胞。与患有血液病的血管性棘球蚴病患者相比,局限性棘球蚴病患者的吞噬活性和吞噬指数明显增加。IFN-γ 预处理的 PIA 处理的巨噬细胞对瓶霉游动孢子的吞噬活性和吞噬指数在血管性和局限性棘球蚴病患者中均有显著提高。巨噬细胞吞噬瓶霉游动孢子,但游动孢子继续发芽,导致巨噬细胞死亡。总的来说,我们的研究结果表明,PIA 可以调节免疫反应,导致 Th1 型细胞因子水平升高,并可能提高血管性棘球蚴病患者的生存率。这项研究首次揭示了瓶霉游动孢子可以在巨噬细胞内存活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/70ef/11550834/3d01eb868b5c/41598_2024_78756_Fig1_HTML.jpg

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