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Advancing mouse models for transplantation research.
Cravedi, Paolo; Riella, Leonardo V; Ford, Mandy L; Valujskikh, Anna; Menon, Madhav C; Kirk, Allan D; Alegre, Maria-Luisa; Alessandrini, Alessandro; Feng, Sandy; Kehn, Patricia; Najafian, Nader; Hancock, Wayne W; Heeger, Peter S; Maltzman, Jonathan S; Mannon, Roslyn B; Nadig, Satish N; Odim, Jonah; Turnquist, Heth; Shaw, Julia; West, Lori; Luo, Xunrong; Chong, Anita S; Bromberg, Jonathan S.
Afiliación
  • Cravedi P; Icahn School of Medicine at Mount Sinai, New York, New York, USA. Electronic address: paolo.cravedi@mssm.edu.
  • Riella LV; Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Ford ML; Emory University, Atlanta, Georgia, USA.
  • Valujskikh A; Cleveland Clinic, Cleveland, Ohio, USA.
  • Menon MC; Yale University school of Medicine, New Haven, Connecticut, USA.
  • Kirk AD; Duke University, Durham, North Carolina, USA.
  • Alegre ML; University of Chicago, Chicago, Illinois, USA.
  • Alessandrini A; Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Feng S; UC San Francisco, San Francisco, California, USA.
  • Kehn P; Transplantation Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Najafian N; Alexion, AstraZeneca Rare Diseases, Boston, Massachusetts, USA.
  • Hancock WW; University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Heeger PS; Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Maltzman JS; Stanford University School of Medicine, Stanford, California, USA.
  • Mannon RB; Division of Nephrology, Department of Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska.
  • Nadig SN; Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
  • Odim J; Transplantation Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • Turnquist H; Starzl Transplant Institute - University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
  • Shaw J; Transplantation Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.
  • West L; University of Alberta, Alberta, Canada.
  • Luo X; Duke University, Durham, North Carolina, USA.
  • Chong AS; University of Chicago, Chicago, Illinois, USA.
  • Bromberg JS; University of Maryland School of Medicine, Baltimore, Maryland, USA.
Am J Transplant ; 2024 Jan 12.
Article en En | MEDLINE | ID: mdl-38219866
ABSTRACT
Mouse models have been instrumental in understanding mechanisms of transplant rejection and tolerance, but cross-study reproducibility and translation of experimental findings into effective clinical therapies are issues of concern. The Mouse Models in Transplantation symposium gathered scientists and physician-scientists involved in basic and clinical research in transplantation to discuss the strengths and limitations of mouse transplant models and strategies to enhance their utility. Participants recognized that increased procedure standardization, including the use of prespecified, defined endpoints, and statistical power analyses, would benefit the field. They also discussed the generation of new models that incorporate environmental and genetic variables affecting clinical outcomes as potentially important. If implemented, these strategies are expected to improve the reproducibility of mouse studies and increase their translation to clinical trials and, ideally, new Food and Drug Administration-approved drugs.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Am J Transplant Asunto de la revista: TRANSPLANTE Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Am J Transplant Asunto de la revista: TRANSPLANTE Año: 2024 Tipo del documento: Article