Integrin-associated protein (CD47) is a broadly expressed protein that costimulates T cells, facilitates leukocyte migration, and inhibits macrophage scavenger function. To determine the role of CD47 in regulating alloresponses, CD47+/+ or CD47−/− T cells were infused into irradiated or nonconditioned major histocompatibility complex disparate recipients. Graft-versus-host disease lethality was markedly reduced with CD47−/− T cells. Donor CD47−/− T cells failed to engraft in immunodeficient allogeneic recipients. CD47−/− marrow was unable to reconstitute heavily irradiated allogeneic or congenic immune–deficient CD47+/+ recipients. These data suggested that CD47−/− T cells and marrow cells were cleared by the innate immune system. To address this hypothesis, dye-labeled CD47−/− and CD47+/+ lymphocytes or marrow cells were infused in vivo and clearance was followed. Dye-labeled CD47−/− cells were engulfed by splenic dendritic cells and macrophages resulting in the clearance of virtually all CD47−/− lymphohematopoietic cells within 1 day after infusion. Host phagocyte-depleted CD47+/+ recipients partially accepted allogeneic CD47−/− T cells. Thus, dendritic cells and macrophages clear lymphohematopoietic cells that have downregulated CD47 density. CD47 expression may be a critical indicator for determining whether lymphohematopoietic cells will survive or be cleared.
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20 August 2001
Brief Definitive Report|
August 20 2001
Cd47 (Integrin-Associated Protein) Engagement of Dendritic Cell and Macrophage Counterreceptors Is Required to Prevent the Clearance of Donor Lymphohematopoietic Cells
Bruce R. Blazar,
Bruce R. Blazar
aUniversity of Minnesota Cancer Center and Department of Pediatrics, Division of Bone Marrow Transplantation
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Frederik P. Lindberg,
Frederik P. Lindberg
cUniversity of Washington School of Medicine, Department of Medicine, Infectious Diseases Division, Seattle, WA 98195
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Elizabeth Ingulli,
Elizabeth Ingulli
bNephrology Division, Minneapolis, MN 55455
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Angela Panoskaltsis-Mortari,
Angela Panoskaltsis-Mortari
aUniversity of Minnesota Cancer Center and Department of Pediatrics, Division of Bone Marrow Transplantation
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Per-Arne Oldenborg,
Per-Arne Oldenborg
cUniversity of Washington School of Medicine, Department of Medicine, Infectious Diseases Division, Seattle, WA 98195
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Koho Iizuka,
Koho Iizuka
dRheumatology Division and Howard Hughes Medical Institute, St. Louis, MO 63110
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Wayne M. Yokoyama,
Wayne M. Yokoyama
dRheumatology Division and Howard Hughes Medical Institute, St. Louis, MO 63110
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Patricia A. Taylor
Patricia A. Taylor
aUniversity of Minnesota Cancer Center and Department of Pediatrics, Division of Bone Marrow Transplantation
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Bruce R. Blazar
aUniversity of Minnesota Cancer Center and Department of Pediatrics, Division of Bone Marrow Transplantation
Frederik P. Lindberg
cUniversity of Washington School of Medicine, Department of Medicine, Infectious Diseases Division, Seattle, WA 98195
Elizabeth Ingulli
bNephrology Division, Minneapolis, MN 55455
Angela Panoskaltsis-Mortari
aUniversity of Minnesota Cancer Center and Department of Pediatrics, Division of Bone Marrow Transplantation
Per-Arne Oldenborg
cUniversity of Washington School of Medicine, Department of Medicine, Infectious Diseases Division, Seattle, WA 98195
Koho Iizuka
dRheumatology Division and Howard Hughes Medical Institute, St. Louis, MO 63110
Wayne M. Yokoyama
dRheumatology Division and Howard Hughes Medical Institute, St. Louis, MO 63110
Patricia A. Taylor
aUniversity of Minnesota Cancer Center and Department of Pediatrics, Division of Bone Marrow Transplantation
B.R. Blazar and F.P. Lindberg contributed equally to this work.
P.-A. Oldenborg's present address is Department of Integrative Medical Biology, Section for Histology and Cell Biology, Umeå University SE-901 87, Umeå, Sweden.
Received:
December 01 2000
Revision Requested:
June 13 2001
Accepted:
June 28 2001
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 2001 The Rockefeller University Press
2001
The Rockefeller University Press
J Exp Med (2001) 194 (4): 541–550.
Article history
Received:
December 01 2000
Revision Requested:
June 13 2001
Accepted:
June 28 2001
Citation
Bruce R. Blazar, Frederik P. Lindberg, Elizabeth Ingulli, Angela Panoskaltsis-Mortari, Per-Arne Oldenborg, Koho Iizuka, Wayne M. Yokoyama, Patricia A. Taylor; Cd47 (Integrin-Associated Protein) Engagement of Dendritic Cell and Macrophage Counterreceptors Is Required to Prevent the Clearance of Donor Lymphohematopoietic Cells. J Exp Med 20 August 2001; 194 (4): 541–550. doi: https://doi.org/10.1084/jem.194.4.541
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