» Articles » PMID: 10642595

Stable Mixed Chimerism and Tolerance Using a Nonmyeloablative Preparative Regimen in a Large-animal Model

Overview
Journal J Clin Invest
Specialty General Medicine
Date 2000 Jan 22
PMID 10642595
Citations 54
Authors
Affiliations
Soon will be listed here.
Abstract

Bone marrow transplantation (BMT) has considerable potential for the treatment of malignancies, hemoglobinopathies, and autoimmune diseases, as well as the induction of transplantation allograft tolerance. Toxicities associated with standard preparative regimens for bone marrow transplantation, however, make this approach unacceptable for all but the most severe of these clinical situations. Here, we demonstrate that stable mixed hematopoietic cell chimerism and donor-specific tolerance can be established in miniature swine, using a relatively mild, non-myeloablative preparative regimen. We conditioned recipient swine with whole-body and thymic irradiation, and we depleted their T-cells by CD3 immunotoxin-treatment. Infusion of either bone marrow cells or cytokine-mobilized peripheral blood stem cells from leukocyte antigen-matched animals resulted in stable mixed chimerism, as detected by flow cytometry in the peripheral blood, thymus, and bone marrow, without any clinical evidence of graft-versus-host disease (GvHD). Long-term acceptance of donor skin and consistent rejection of third-party skin indicated that the recipients had developed donor-specific tolerance.

Citing Articles

Animal models for transplant immunology: bridging bench to bedside.

Kang M, Park H, Kim K, Choi D Clin Transplant Res. 2024; 38(4):354-376.

PMID: 39233453 PMC: 11732767. DOI: 10.4285/ctr.24.0029.


Tolerance in intestinal transplantation.

Sykes M Hum Immunol. 2024; 85(3):110793.

PMID: 38580539 PMC: 11144570. DOI: 10.1016/j.humimm.2024.110793.


CD3e-immunotoxin spares CD62L Tregs and reshapes organ-specific T-cell composition by preferentially depleting CD3e T cells.

Kim S, Shukla R, Yu H, Baek A, Cressman S, Golconda S Front Immunol. 2022; 13:1011190.

PMID: 36389741 PMC: 9643874. DOI: 10.3389/fimmu.2022.1011190.


Transplant Tolerance, Not Only Clonal Deletion.

Hall B, Verma N, Tran G, Hodgkinson S Front Immunol. 2022; 13:810798.

PMID: 35529847 PMC: 9069565. DOI: 10.3389/fimmu.2022.810798.


Establishment of Chimerism and Organ Transplant Tolerance in Laboratory Animals: Safety and Efficacy of Adaptation to Humans.

Lowsky R, Strober S Front Immunol. 2022; 13:805177.

PMID: 35222384 PMC: 8866443. DOI: 10.3389/fimmu.2022.805177.


References
1.
Boyse E, Lance E, CARSWELL E, Cooper S, Old L . Rejection of skin allografts by radiation chimaeras: selective gene action in the specification of cell surface structure. Nature. 1970; 227(5261):901-3. DOI: 10.1038/227901a0. View

2.
Huang C, Yamada K, Murphy M, Shimizu A, Colvin R, Neville Jr D . In vivo T cell depletion in miniature swine using the swine CD3 immunotoxin, pCD3-CRM9. Transplantation. 1999; 68(6):855-60. DOI: 10.1097/00007890-199909270-00019. View

3.
Steinmuller D, Lofgreen J . Differential survival of skin and heart allografts in radiation chimaeras provides further evidence for Sk histocompatibility antigen. Nature. 1974; 248(5451):796-7. DOI: 10.1038/248796a0. View

4.
Sachs D, Leight G, Cone J, Schwarz S, Stuart L, Rosenberg S . Transplantation in miniature swine. I. Fixation of the major histocompatibility complex. Transplantation. 1976; 22(6):559-67. DOI: 10.1097/00007890-197612000-00004. View

5.
Leight G, Kirkman R, Rasmusen B, Rosenberg S, Sachs D, Terrill R . Transplantation in miniature swine. III: effects of MSLA and A-O blood group matching on skin allograft survival. Tissue Antigens. 1978; 12(2):65-74. DOI: 10.1111/j.1399-0039.1978.tb01301.x. View