2016
DOI: 10.1016/j.cjca.2015.09.022
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Regulating Inflammatory Immune Response to Atherogenic Antigens Prevents Development and Progression of Atherosclerosis in New Zealand White Rabbits

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Cited by 7 publications
(7 citation statements)
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“…Although this therapy may not drastically reduce the plaque development it can induce a more stable plaque. We had earlier reported a reduction in progression of disease in rabbits, wherein at the time of treatment 12% of sinus was covered with plaque 30 , suggesting that immune modulation may still reduce the disease progression if treated at an early stage.…”
Section: Discussionmentioning
confidence: 92%
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“…Although this therapy may not drastically reduce the plaque development it can induce a more stable plaque. We had earlier reported a reduction in progression of disease in rabbits, wherein at the time of treatment 12% of sinus was covered with plaque 30 , suggesting that immune modulation may still reduce the disease progression if treated at an early stage.…”
Section: Discussionmentioning
confidence: 92%
“…We have earlier established that oral treatment with the multi-antigenic construct AHC induces immune tolerance and prevents disease development in both mice and rabbit 18 , 30 . In the present study, we wanted to understand if tolerance can be induced in animals who have already developed the disease and therefore examined the number and functions of Treg cells in treated and control animals in mice with established atherosclerosis.…”
Section: Discussionmentioning
confidence: 99%
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“…In the past three decades, the increasing research data suggest that atherosclerosis is an inflammatory disease [11, 12] and the immune system and inflammatory was gradually recognized to play a pivotal role in the development and progression of atherosclerosis [13, 14]. Atherosclerosis is characterized by the accumulation of monocytes/ macrophages, smooth muscle cells and lymphocytes within the arterial wall.…”
Section: Pathological Process Of Atherosclerosismentioning
confidence: 99%
“…Antigen‐presenting cells (APC) in the gut selectively induce antigen‐specific Treg, which migrate and suppress damaging immune responses. We have earlier shown that oral tolerance to a combination of ApoB and HSP60 peptides and to multiantigenic recombinant molecule expressing a tripeptide derived from ApoB, HSP60, and outer membrane protein from Chlamydia pneumoniae (AHC) in a patented dendroaspin (DSP) scaffold could prevent atherosclerosis development in animal model of atherosclerosis . In this study, we expressed a multiantigenic construct containing three atherogenic peptides in an M. smegmatis secretory vector (pJH154) and explored the use of this recombinant organism in protection against atherosclerosis in ApoE −/− mice in C57/BL6 background.…”
Section: Introductionmentioning
confidence: 99%