Changes of peripheral blood immune cells in acute coronary syndrome. (May 2019)
- Record Type:
- Journal Article
- Title:
- Changes of peripheral blood immune cells in acute coronary syndrome. (May 2019)
- Main Title:
- Changes of peripheral blood immune cells in acute coronary syndrome
- Authors:
- Zhang, Chengxin
Liu, Haiyuan
Wang, Huiping
Tao, Qianshan
Lin, Xianhe
Ge, Shenglin
Zhai, Zhimin - Abstract:
- The objective of this study is to explore changes in main immune cells during acute coronary syndrome (ACS), including changes in subsets of monocytes, T cells, and inhibitory myeloid-derived suppressor cells (MDSCs), and to evaluate possible mechanisms. A total of 50 patients suffering from ACS were divided into two subgroups based on attacks of acute infarction, acute myocardial infarction (AMI) with infarction including ST-segment elevation myocardial infarction (STEMI), non-ST-segment elevation myocardial infarction (NSTEMI), and unstable angina (UA). Third, the subgroup of 19 healthy subjects was labeled the normal group (NG). CD14, CD16, and CD45 were used as markers of the subset of monocytes. CD4, CD8, and CD3 were used as markers of the subset of T cells and CD14, human leukocyte antigen—DR isotype (HLA-DR), and CD45 were used as markers of inhibitory MDSCs. Both CD11b + CD206 + and CD11b + CD68 + cells were also assayed. Our data indicated that lymphocytes/karyocytes and monocytes/karyocytes as well as those of CD3 + CD4 + T cells, CD14 + CD16 – monocytes, CD14 + CD16 + monocytes, and CD11b + CD68 + monocytes were significant in all three groups ( P < 0.05). The ratio of T-cell subtypes to total lymphocytes among the three subgroups can be represented as AMI > UA > NG ( P < 0.05). The ratios of CD14 + monocytes to total karyocytes among the three subgroups can be represented as NG > UA > AMI ( P < 0.05). The ratios of CD14 + CD16 – monocytes to total karyocytesThe objective of this study is to explore changes in main immune cells during acute coronary syndrome (ACS), including changes in subsets of monocytes, T cells, and inhibitory myeloid-derived suppressor cells (MDSCs), and to evaluate possible mechanisms. A total of 50 patients suffering from ACS were divided into two subgroups based on attacks of acute infarction, acute myocardial infarction (AMI) with infarction including ST-segment elevation myocardial infarction (STEMI), non-ST-segment elevation myocardial infarction (NSTEMI), and unstable angina (UA). Third, the subgroup of 19 healthy subjects was labeled the normal group (NG). CD14, CD16, and CD45 were used as markers of the subset of monocytes. CD4, CD8, and CD3 were used as markers of the subset of T cells and CD14, human leukocyte antigen—DR isotype (HLA-DR), and CD45 were used as markers of inhibitory MDSCs. Both CD11b + CD206 + and CD11b + CD68 + cells were also assayed. Our data indicated that lymphocytes/karyocytes and monocytes/karyocytes as well as those of CD3 + CD4 + T cells, CD14 + CD16 – monocytes, CD14 + CD16 + monocytes, and CD11b + CD68 + monocytes were significant in all three groups ( P < 0.05). The ratio of T-cell subtypes to total lymphocytes among the three subgroups can be represented as AMI > UA > NG ( P < 0.05). The ratios of CD14 + monocytes to total karyocytes among the three subgroups can be represented as NG > UA > AMI ( P < 0.05). The ratios of CD14 + CD16 – monocytes to total karyocytes among the three subgroups can be represented as NG > UA > AMI ( P < 0.05). The ratios of CD14 + CD16 + monocytes to total karyocytes among the three subgroups can be represented as AMI > UA > NG ( P < 0.05). There were no significant differences in the proportion of MDSCs ( P > 0.05). Certain subsets of monocytes are closely associated with ACS, of which CD14 + CD16 – monocytes present a negative association, while CD14 + CD16 + monocytes show a positive association. In addition, adaptive immunity is associated with unstable plaques of ACS, and CD3 + CD4 + T cells may play a role in early stages of ACS. … (more)
- Is Part Of:
- European journal of inflammation. Volume 17(2019)
- Journal:
- European journal of inflammation
- Issue:
- Volume 17(2019)
- Issue Display:
- Volume 17, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 17
- Issue:
- 2019
- Issue Sort Value:
- 2019-0017-2019-0000
- Page Start:
- Page End:
- Publication Date:
- 2019-05
- Subjects:
- acute coronary syndrome -- immune cells -- subsets of monocytes -- subsets of T cells
Inflammation -- Periodicals
Anti-Inflammatory Agents -- therapeutic use -- Periodicals
Immunotherapy -- Periodicals
Inflammation -- Periodicals
Anti-inflammatory agents -- Periodicals
Immunotherapy -- Periodicals
Anti-inflammatory agents
Immunotherapy
Inflammation
Periodicals
616.0473 - Journal URLs:
- http://eji.sagepub.com/ ↗
http://www.biolifesas.org/blu.htm ↗
http://www.uk.sagepub.com/home.nav ↗ - DOI:
- 10.1177/2058739219851760 ↗
- Languages:
- English
- ISSNs:
- 1721-727X
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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- 12695.xml