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分枝杆菌热休克蛋白 65 经口耐受可减少老年小鼠的慢性实验性动脉粥样硬化。

Oral Tolerization with Mycobacterial Heat Shock Protein 65 Reduces Chronic Experimental Atherosclerosis in Aged Mice.

机构信息

Laboratory of Autoimmunity, Division for Experimental Pathophysiology and Immunology, Biocenter, Innsbruck Medical University, Innsbruck, Austria.

出版信息

Gerontology. 2018;64(1):36-48. doi: 10.1159/000480436. Epub 2017 Sep 15.

Abstract

BACKGROUND

Atherosclerosis is a chronic inflammatory disease of the artery wall where both innate and adaptive immunity play important roles. Modulation of the immune response against the stress protein antigen, heat shock protein (HSP) 60, by administration of mycobacterial HSP65 (mbHSP65) orally and/or nasally shows promising therapeutic results in young animals in the sense of less severe experimental atherosclerosis; however, the case of aged animals with already established atherosclerosis has so far never been investigated.

OBJECTIVE

To investigate if mbHSP65 immunization would further accelerate atherosclerotic progression in aged ApoE-/- mice (18 months old) with already long-established atherosclerosis and if these mice could be orally tolerized against mbHSP65.

METHODS

Aged wild-type (WT) and ApoE-/- mice (65 weeks) were immunized and/or orally treated with mbHSP65 and then either kept on normal chow or changed to high-cholesterol diet (HCD). Atherosclerosis was assessed by en face analysis and the number of CD4+CD25+FoxP3+ T regulatory cells (Tregs) was assessed by flow cytometry in lymph node and spleen cells. Total cholesterol and triglyceride levels were determined. Soluble mammalian HSP60 and anti-mouse HSP60 (mHSP60) and anti-mbHSP65 antibodies were detected by enzyme-linked immunosorbent assay.

RESULTS

As expected, aged WT mice had only minor lesions in the aorta, which did not change under HCD for 14 weeks. Aged ApoE-/- mice already had large complicated plaques, which increased in size under HCD. mbHSP65 immunization led to a significant aggravation of atherosclerosis in both WT and ApoE-/- mice irrespective of the nature of their diet. This increase was accompanied by increased titers of both anti-mHSP60 and anti-mbHSP65 antibodies in the circulation. The increased plaque formation could be significantly diminished with oral mbHSP65 tolerization. An increased number of Tregs and lower or unchanged levels of cholesterol and triglycerides were associated with the reduced size of aortal lesions.

CONCLUSION

Oral tolerization against mbHSP65 could be used both to prevent and to treat chronic atherosclerosis in aged individuals.

摘要

背景

动脉粥样硬化是一种动脉壁的慢性炎症性疾病,固有免疫和适应性免疫都起着重要作用。通过口服和/或鼻内给予分枝杆菌 HSP65(mbHSP65)来调节针对应激蛋白抗原 HSP60 的免疫反应,在年轻动物中显示出有希望的治疗效果,即实验性动脉粥样硬化程度较轻;然而,对于已经患有动脉粥样硬化的老年动物,这种情况迄今从未被研究过。

目的

研究 mbHSP65 免疫接种是否会进一步加速已经患有长期动脉粥样硬化的老年 ApoE-/- 小鼠(18 个月大)的动脉粥样硬化进展,以及这些小鼠是否可以对 mbHSP65 进行口服耐受。

方法

给老年野生型(WT)和 ApoE-/- 小鼠(65 周龄)进行免疫接种和/或口服 mbHSP65 治疗,然后继续给予普通饮食或改为高胆固醇饮食(HCD)。通过正面分析评估动脉粥样硬化,通过流式细胞术评估淋巴结和脾脏细胞中 CD4+CD25+FoxP3+T 调节细胞(Tregs)的数量。测定总胆固醇和甘油三酯水平。通过酶联免疫吸附试验检测可溶性哺乳动物 HSP60 和抗小鼠 HSP60(mHSP60)和抗 mbHSP65 抗体。

结果

正如预期的那样,老年 WT 小鼠的主动脉仅存在较小的病变,在 14 周的 HCD 下没有变化。老年 ApoE-/- 小鼠已经有大的复杂斑块,在 HCD 下斑块增大。mbHSP65 免疫接种导致 WT 和 ApoE-/- 小鼠的动脉粥样硬化显著加重,无论其饮食性质如何。这种增加伴随着循环中抗 mHSP60 和抗 mbHSP65 抗体滴度的增加。口服 mbHSP65 耐受可以显著减少斑块形成。Tregs 数量增加,胆固醇和甘油三酯水平降低或不变与主动脉病变的减小相关。

结论

口服 mbHSP65 耐受可用于预防和治疗老年个体的慢性动脉粥样硬化。

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