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给药可减轻小鼠感染期间的寄生虫血症和炎症。

Administration Diminishes Parasitemia and Inflammation During Infection in Mice.

作者信息

Fitri Loeki Enggar, Sardjono Teguh Wahju, Winaris Nuning, Pawestri Aulia Rahmi, Endharti Agustina Tri, Norahmawati Eviana, Handayani Dian, Kurniawan Shahdevi Nandar, Azizah Syafiatul, Alifia Lustyafa Inassani, Asiyah Rokhmatul, Ayuningtyas Tita Rachma

机构信息

Department of Parasitology, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia.

AIDS, Toxoplasma, Opportunistic Disease, and Malaria (ATOM) Research Group, Faculty of Medicine, Universitas Brawijaya, Malang, Indonesia.

出版信息

J Inflamm Res. 2023 Mar 27;16:1393-1404. doi: 10.2147/JIR.S400782. eCollection 2023.

Abstract

PURPOSE

During () infection, infected erythrocytes are sequestered in gut tissues through microvascular circulation, leading to dysbiosis. This study aimed to investigate the effect of () and () administration on the parasitemia level, gut microbiota composition, expression of cluster of differentiation 103 (CD103) in intestinal dendritic and T regulatory cells (T reg), plasma interferon gamma (IFN-γ) and tumor necrosis factor (TNF-α) levels in infected mice.

METHODS

was inoculated intraperitoneally. Infected mice were randomly divided into 5 groups and treated with either , or the combination of both for 5 days before up to 6 days post-infection (p.i). The control group was treated with phosphate-buffered saline (PBS), while uninfected mice were used as negative control. Levels of CD103 and forkhead box P3 (FoxP3) expression were measured by direct immunofluorescense, while plasma IFN-γ and TNF-α level were determined using enzyme-linked immunosorbent assay (ELISA).

RESULTS

All treated groups showed an increase in parasitemia from day 2 to day 6 p.i, which was significant at day 2 p.i (p = 0.001), with the group receiving displaying the lowest degree of parasitemia. Significant reduction in plasma IFN-γ and TNF-α levels was observed in the group receiving (p = 0.022 and p = 0.026, respectively). The CD103 and FoxP3 expression was highest in the group receiving (p = 0.01 and p = 0.02, respectively).

CONCLUSION

showed the best protective effect against infection by reducing the degree of parasitemia and modulating the gut immunity. This provides a basis for further research involving probiotic supplementation in immunity modulation of infectious diseases.

摘要

目的

在()感染期间,受感染的红细胞通过微血管循环被隔离在肠道组织中,导致生态失调。本研究旨在探讨()和()给药对感染小鼠的寄生虫血症水平、肠道微生物群组成、肠道树突状细胞和调节性T细胞(Treg)中分化簇103(CD103)的表达、血浆干扰素γ(IFN-γ)和肿瘤坏死因子(TNF-α)水平的影响。

方法

腹腔接种()。感染小鼠随机分为5组,在感染后(p.i)长达6天之前,用()、()或两者的组合治疗5天。对照组用磷酸盐缓冲盐水(PBS)治疗,未感染的小鼠用作阴性对照。通过直接免疫荧光法测量CD103和叉头框P3(FoxP3)的表达水平,同时使用酶联免疫吸附测定(ELISA)测定血浆IFN-γ和TNF-α水平。

结果

所有治疗组在感染后第2天至第6天的寄生虫血症均有所增加,在感染后第2天显著增加(p = 0.001),接受()的组寄生虫血症程度最低。在接受()的组中观察到血浆IFN-γ和TNF-α水平显著降低(分别为p = 0.022和p = 0.026)。接受()的组中CD103和FoxP3表达最高(分别为p = 0.01和p = 0.02)。

结论

()通过降低寄生虫血症程度和调节肠道免疫,对()感染显示出最佳的保护作用。这为进一步研究益生菌补充剂在传染病免疫调节中的应用提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9187/10065020/5a647d30c2c4/JIR-16-1393-g0001.jpg

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