TY - JOUR
T1 - Miniature swine as a clinically relevant model of graft-versus-host disease
AU - Duran-Struuck, Raimon
AU - Huang, Christene A.
AU - Orf, Katherine
AU - Bronson, Roderick T.
AU - Sachs, David H.
AU - Spitzer, Thomas R.
N1 - Publisher Copyright:
Copyright 2015 by the American Association for Laboratory Animal Science.
PY - 2015/10
Y1 - 2015/10
N2 - Miniature swine provide a preclinical model of hematopoietic cell transplantation (HCT) for studies of graft-versus-host disease. HCT between MHC-matched or -mismatched pigs can be performed to mimic clinical scenarios with outcomes that closely resemble those observed in human HCT recipients. With myeloablative conditioning, HCT across MHC barriers is typically fatal, with pigs developing severe (grade III or IV) GVHD involving the gastrointestinal tract, liver, and skin. Unlike rodent models, miniature swine provide an opportunity to perform extended longitudinal studies on individual animals, because multiple tissue biopsies can be harvested without the need for euthanasia. In addition, we have developed a swine GVHD scoring system that parallels that used in the human clinical setting. Given the similarities of GVHD in pigs and humans, we hope that the use of this scoring system facilitates clinical and scientific discourse between the laboratory and the clinic. We anticipate that results of swine studies will support the development of new strategies to improve the identification and treatment of GVHD in clinical HCT scenarios.
AB - Miniature swine provide a preclinical model of hematopoietic cell transplantation (HCT) for studies of graft-versus-host disease. HCT between MHC-matched or -mismatched pigs can be performed to mimic clinical scenarios with outcomes that closely resemble those observed in human HCT recipients. With myeloablative conditioning, HCT across MHC barriers is typically fatal, with pigs developing severe (grade III or IV) GVHD involving the gastrointestinal tract, liver, and skin. Unlike rodent models, miniature swine provide an opportunity to perform extended longitudinal studies on individual animals, because multiple tissue biopsies can be harvested without the need for euthanasia. In addition, we have developed a swine GVHD scoring system that parallels that used in the human clinical setting. Given the similarities of GVHD in pigs and humans, we hope that the use of this scoring system facilitates clinical and scientific discourse between the laboratory and the clinic. We anticipate that results of swine studies will support the development of new strategies to improve the identification and treatment of GVHD in clinical HCT scenarios.
UR - http://www.scopus.com/inward/record.url?scp=84947759376&partnerID=8YFLogxK
M3 - Review article
C2 - 26473348
AN - SCOPUS:84947759376
SN - 1532-0820
VL - 65
SP - 429
EP - 443
JO - Comparative Medicine
JF - Comparative Medicine
IS - 5
ER -