Unravelling CD4+ T cell diversity and tissue adaptation of Tregs in abdominal aortic aneurysms through single‐cell sequencing

Author:

Zhai Luna123ORCID,Hu Wangling123,Li Jingyong123,Li Dan123,Xia Ni123,Tang Tingting123,Nie Shaofang123,Zhang Min123,Jiao Jiao123,Lv Bingjie123,Yang Fen123,Lu Yuzhi123,Zha Lingfeng123,Gu Muyang123,Hu Xiajun123,Wen Shuang4,Hu Desheng5,Zhang Li6,Wang Weimin7,Cheng Xiang123ORCID

Affiliation:

1. Department of Cardiology, Union Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China

2. Hubei Key Laboratory of Biological Targeted Therapy, Union Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China

3. Hubei Engineering Research Center for Immunological Diagnosis and Therapy of Cardiovascular Diseases, Union Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China

4. Department of Emergency Medicine, Union Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China

5. Department of Integrated Traditional Chinese and Western Medicine, Union Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China

6. Department of Ultrasound Medicine, Union Hospital, Tongji Medical College Huazhong University of Science and Technology Wuhan China

7. Department of Immunology, School of Basic Medicine, Tongji Medical College Huazhong University of Science and Technology Wuhan China

Abstract

AbstractImmune cell infiltration is a significant pathological process in abdominal aortic aneurysms (AAA). T cells, particularly CD4+ T cells, are essential immune cells responsible for substantial infiltration of the aorta. Regulatory T cells (Tregs) in AAA have been identified as tissue‐specific; however, the time, location, and mechanism of acquiring the tissue‐specific phenotype are still unknown. Using single‐cell RNA sequencing (scRNA‐seq) on CD4+ T cells from the AAA aorta and spleen, we discovered heterogeneity among CD4+ T cells and identified activated, proliferating and developed aorta Tregs. These Tregs originate in the peripheral tissues and acquire the tissue‐specific phenotype in the aorta. The identification of precursors for Tregs in AAA provides new insight into the pathogenesis of AAA.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

Publisher

Wiley

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