In vivo prevention of transplant arteriosclerosis by ex vivo-expanded human regulatory T cells
(2010) In Nature Medicine 16(7). p.809-813- Abstract
Transplant arteriosclerosis is the hallmark of chronic allograft dysfunction (CAD) affecting transplanted organs in the long term. These fibroproliferative lesions lead to neointimal thickening of arteries in all transplanted allografts. Luminal narrowing then leads to graft ischemia and organ demise. To date, there are no known tolerance induction strategies that prevent transplant arteriosclerosis. Therefore, we designed this study to test the hypothesis that human regulatory T cells (T(reg) cells) expanded ex vivo can prevent transplant arteriosclerosis. Here we show the comparative capacity of T(reg) cells, sorted via two separate strategies, to prevent transplant arteriosclerosis in a clinically relevant chimeric humanized mouse... (More)
Transplant arteriosclerosis is the hallmark of chronic allograft dysfunction (CAD) affecting transplanted organs in the long term. These fibroproliferative lesions lead to neointimal thickening of arteries in all transplanted allografts. Luminal narrowing then leads to graft ischemia and organ demise. To date, there are no known tolerance induction strategies that prevent transplant arteriosclerosis. Therefore, we designed this study to test the hypothesis that human regulatory T cells (T(reg) cells) expanded ex vivo can prevent transplant arteriosclerosis. Here we show the comparative capacity of T(reg) cells, sorted via two separate strategies, to prevent transplant arteriosclerosis in a clinically relevant chimeric humanized mouse system. We found that the in vivo development of transplant arteriosclerosis in human arteries was prevented by treatment of ex vivo-expanded human T(reg) cells. Additionally, we show that T(reg) cells sorted on the basis of low expression of CD127 provide a more potent therapy to conventional T(reg) cells. Our results demonstrate that human T(reg) cells can inhibit transplant arteriosclerosis by impairing effector function and graft infiltration. We anticipate our findings to serve as a foundation for the clinical development of therapeutics targeting transplant arteriosclerosis in both allograft transplantation and other immune-mediated causes of vasculopathy.
(Less)
- author
- Nadig, Satish N ; Wieckiewicz, Joanna ; Wu, Douglas C ; Warnecke, Gregor ; Zhang, Wei ; Luo, Shiqiao ; Schiopu, Alexandru LU ; Taggart, David P and Wood, Kathryn J
- publishing date
- 2010
- type
- Contribution to journal
- publication status
- published
- keywords
- Animals, Aorta, Abdominal/surgery, Arteriosclerosis/immunology, CD4-Positive T-Lymphocytes/immunology, Cell Separation, Graft Rejection, Interferon-gamma/metabolism, Interleukin-2 Receptor alpha Subunit/metabolism, Interleukin-7 Receptor alpha Subunit/metabolism, Leukocytes, Mononuclear/transplantation, Mammary Arteries/transplantation, Mice, Mice, Inbred BALB C, T-Lymphocytes, Regulatory/immunology
- in
- Nature Medicine
- volume
- 16
- issue
- 7
- pages
- 809 - 813
- publisher
- Nature Publishing Group
- external identifiers
-
- scopus:77954539326
- pmid:20473306
- ISSN
- 1546-170X
- DOI
- 10.1038/nm.2154
- language
- English
- LU publication?
- no
- id
- 60e7e33b-c5c8-4768-bc14-b6d83201609e
- date added to LUP
- 2023-03-10 12:13:28
- date last changed
- 2024-04-18 19:22:25
@article{60e7e33b-c5c8-4768-bc14-b6d83201609e,
abstract = {{<p>Transplant arteriosclerosis is the hallmark of chronic allograft dysfunction (CAD) affecting transplanted organs in the long term. These fibroproliferative lesions lead to neointimal thickening of arteries in all transplanted allografts. Luminal narrowing then leads to graft ischemia and organ demise. To date, there are no known tolerance induction strategies that prevent transplant arteriosclerosis. Therefore, we designed this study to test the hypothesis that human regulatory T cells (T(reg) cells) expanded ex vivo can prevent transplant arteriosclerosis. Here we show the comparative capacity of T(reg) cells, sorted via two separate strategies, to prevent transplant arteriosclerosis in a clinically relevant chimeric humanized mouse system. We found that the in vivo development of transplant arteriosclerosis in human arteries was prevented by treatment of ex vivo-expanded human T(reg) cells. Additionally, we show that T(reg) cells sorted on the basis of low expression of CD127 provide a more potent therapy to conventional T(reg) cells. Our results demonstrate that human T(reg) cells can inhibit transplant arteriosclerosis by impairing effector function and graft infiltration. We anticipate our findings to serve as a foundation for the clinical development of therapeutics targeting transplant arteriosclerosis in both allograft transplantation and other immune-mediated causes of vasculopathy.</p>}},
author = {{Nadig, Satish N and Wieckiewicz, Joanna and Wu, Douglas C and Warnecke, Gregor and Zhang, Wei and Luo, Shiqiao and Schiopu, Alexandru and Taggart, David P and Wood, Kathryn J}},
issn = {{1546-170X}},
keywords = {{Animals; Aorta, Abdominal/surgery; Arteriosclerosis/immunology; CD4-Positive T-Lymphocytes/immunology; Cell Separation; Graft Rejection; Interferon-gamma/metabolism; Interleukin-2 Receptor alpha Subunit/metabolism; Interleukin-7 Receptor alpha Subunit/metabolism; Leukocytes, Mononuclear/transplantation; Mammary Arteries/transplantation; Mice; Mice, Inbred BALB C; T-Lymphocytes, Regulatory/immunology}},
language = {{eng}},
number = {{7}},
pages = {{809--813}},
publisher = {{Nature Publishing Group}},
series = {{Nature Medicine}},
title = {{In vivo prevention of transplant arteriosclerosis by ex vivo-expanded human regulatory T cells}},
url = {{http://dx.doi.org/10.1038/nm.2154}},
doi = {{10.1038/nm.2154}},
volume = {{16}},
year = {{2010}},
}