Abstract
Atherosclerosis is a chronic, lipid-driven disease of medium sized arteries which causes myocardial infarction and stroke. Recently, an adaptive immune response against the plaque-associated autoantigen Apolipoprotein B100 (ApoB), the structural protein component of low-density lipoprotein, has been implicated in atherogenesis. In healthy individuals, CD4+ T cells responding to ApoB mainly comprised regulatory T cells, which confer immune tolerance and atheroprotection. Mice and patients with atherosclerosis harbor increased numbers of proatherogenic ApoB-reactive T-helper cell subsets. Given the lack of therapies targeting proatherogenic immunity, clarification of the underlying mechanisms is of high clinical relevance. T cells develop in the thymus, where strong autoreactive T cells are eliminated in the process of negative selection. Herein, we investigated whether the transcription factor autoimmune regulator (AIRE), which controls expression of numerous tissue-restricted self-antigens in the thymus, is involved in mediating tolerance to ApoB and whether Aire deficiency might contribute to atherogenesis. Mice deficient for Aire were crossbred to apolipoprotein E-deficient mice to obtain atherosclerosis-prone Aire−/− Apoe−/− mice, which were fed a regular chow diet (CD) or western-type diet (WD). CD4+ T cells responding to the ApoB peptide p6 were analyzed by flow cytometry. We demonstrate that Aire deficiency influences neither generation nor activation of ApoB-reactive T cells and has only minor and overall inconsistent impacts on their phenotype. Furthermore, we show that atherosclerotic plaque size is not affected in Aire−/− Apoe−/− compared to Aire+/+ Apoe−/−, irrespective of diet and gender. In conclusion, our data suggests that AIRE is not involved in regulating thymic expression of ApoB or atherosclerosis. Alternative mechanisms how ApoB-reactive CD4 T cells are selected in the thymus will have to be investigated.
Highlights
Atherosclerosis is a chronic condition of large- and mediumsized arteries that involves formation of leukocyte- and lipid-rich plaques in the arterial wall [1]
Aire deficiency was associated with an increased neutrophil count in female apolipoprotein E (Apoe)−/− mice exposed to a western-type diet (WD) and with an increase in eosinophils and decrease in platelets in chow diet (CD)-fed male Apoe−/− mice
We demonstrate that deficiency of the transcription factor (TF) autoimmune regulator (AIRE), which regulates expression of many tissue-restricted antigens (TRAs), does not affect generation and activation of CD4+ T cells responding to the Apolipoprotein B100 (ApoB) peptide p6 in Apoe−/– mice exposed to a WD
Summary
Atherosclerosis is a chronic condition of large- and mediumsized arteries that involves formation of leukocyte- and lipid-rich plaques in the arterial wall [1]. Atherogenesis is accompanied and modulated by CD4+ T cells responding to plaque-associated autoantigens [2, 3]. One of these autoantigens is Apolipoprotein B (ApoB), the core protein of low-density lipoprotein (LDL) and other lipoprotein particles [2]. ApoB-reactive CD4+ T cells (ApoB+ T cells) can be detected in peripheral blood mononuclear cells (PBMCs) and lymph nodes from healthy and atherosclerotic humans and mice, respectively [4, 5] In healthy individuals these cells are mainly regulatory T cells (Tregs) [4], which confer atheroprotection in mice [6, 7] and predict lower cardiovascular event rates in humans [8]. ApoB+ T cells frequently coexpress TFs typical found in pro-atherogenic T helper 1 (TH1) or T helper 17 (TH17) cells [4]
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