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Global burden of atherosclerotic cardiovascular disease in people living with HIV: systematic review and meta-analysis. The changing science of HIV epidemiology in the United States. Cohort profile: the Women’s Interagency HIV Study (WIHS). Two subsets of memory T lymphocytes with distinct homing potentials and effector functions. Sallusto, F., Lenig, D., Förster, R., Lipp, M. High frequency of shared clonotypes in human T cell receptor repertoires. T cell fate and clonality inference from single-cell transcriptomes. Mechanisms for T cell receptor triggering. Adoptive transfer of CD4 + T cells reactive to modified low-density lipoprotein aggravates atherosclerosis. T-cells specific for a self-peptide of ApoB-100 exacerbate aortic atheroma in murine atherosclerosis. Depletion of FOXP3 + regulatory T cells promotes hypercholesterolemia and atherosclerosis. Role of naturally occurring CD4 +CD25 + regulatory T cells in experimental atherosclerosis. Natural regulatory T cells control the development of atherosclerosis in mice. Atherosclerosis: a chronic inflammatory disease with an autoimmune component.
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T cell subsets and functions in atherosclerosis. Pathogenic autoimmunity in atherosclerosis evolves from initially protective apolipoprotein B 100–reactive CD4 + T-regulatory cells. Regulatory CD4 + T cells recognize major histocompatibility complex class II molecule–restricted peptide epitopes of apolipoprotein B. Immunity and inflammation in atherosclerosis. Mouse studies showed that such switched cells promote atherosclerosis.
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These findings suggest that APOB-specific regulatory T cells may switch to a more memory-like phenotype in women with atherosclerosis. T cell receptor sequencing of tetramer-positive cells showed clonal expansion and V and J segment usage similar to those found in regulatory T cells.
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Single-cell RNA sequencing showed that transcriptomes of tetramer-positive cells were between regulatory and memory T cells in healthy women and moved closer to memory T cells in women with sCVD. Here, we produce, validate and use an MHC-II tetramer, DRB1*07:01 APOB-p18, to sort APOB-p18-specific CD4 T cells from peripheral blood mononuclear cell samples from eight DRB1*07:01 + women with and without subclinical cardiovascular disease (sCVD). Major histocompatibility complex class II (MHC-II) tetramers can be used to isolate antigen-specific CD4 T cells by flow sorting. Nature Cardiovascular Research volume 1, pages 462–475 ( 2022) Cite this articleĪtherosclerosis is accompanied by a CD4 T cell response to apolipoprotein B (APOB). Single cell transcriptomics and TCR reconstruction reveal CD4 T cell response to MHC-II-restricted APOB epitope in human cardiovascular disease
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