Saigusa Ryosuke, Roy Payel, Freuchet Antoine, Gulati Rishab, Ghosheh Yanal, Suthahar Sujit Silas Armstrong, Durant Christopher P, Hanna David B, Kiosses William B, Orecchioni Marco, Wen Lai, Wu Runpei, Kuniholm Mark H, Landay Alan L, Anastos Kathryn, Tien Phyllis C, Gange Stephen J, Kassaye Seble, Vallejo Jenifer, Hedrick Catherine C, Kwok William W, Sette Alessandro, Hodis Howard N, Kaplan Robert C, Ley Klaus
La Jolla Institute for Immunology, La Jolla, CA, USA.
Albert Einstein College of Medicine, Department of Epidemiology and Population Health, Bronx, NY, USA.
Nat Cardiovasc Res. 2022 May;1(5):462-475. doi: 10.1038/s44161-022-00063-3. Epub 2022 May 12.
Atherosclerosis is accompanied by a CD4 T cell response to apolipoprotein B (APOB). Major Histocompatibility Complex (MHC)-II tetramers can be used to isolate antigen-specific CD4 T cells by flow sorting. Here, we produce, validate and use an MHC-II tetramer, DRB107:01 APOB-p18, to sort APOB-p18-specific cells from peripheral blood mononuclear cell samples from 8 DRB107:01+ women with and without subclinical cardiovascular disease (sCVD). Single cell RNA sequencing showed that transcriptomes of tetramer+ cells were between regulatory and memory T cells in healthy women and moved closer to memory T cells in women with sCVD. TCR sequencing of tetramer+ cells showed clonal expansion and V and J segment usage similar to those found in regulatory T cells. These findings suggest that APOB-specific regulatory T cells may switch to a more memory-like phenotype in women with atherosclerosis. Mouse studies showed that such switched cells promote atherosclerosis.
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