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National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: I. The 2020 Etiology and Prevention Working Group Report.

Publication ,  Journal Article
Williams, KM; Inamoto, Y; Im, A; Hamilton, B; Koreth, J; Arora, M; Pusic, I; Mays, JW; Carpenter, PA; Luznik, L; Reddy, P; Ritz, J; Pidala, J ...
Published in: Transplant Cell Ther
June 2021

Preventing chronic graft-versus-host disease (GVHD) remains challenging because the unique cellular and molecular pathways that incite chronic GVHD are poorly understood. One major point of intervention for potential prevention of chronic GVHD occurs at the time of transplantation when acute donor anti-recipient immune responses first set the events in motion that result in chronic GVHD. After transplantation, additional insults causing tissue injury can incite aberrant immune responses and loss of tolerance, further contributing to chronic GVHD. Points of intervention are actively being identified so that chronic GVHD initiation pathways can be targeted without affecting immune function. The major objective in the field is to continue basic studies and to translate what is learned about etiopathology to develop targeted prevention strategies that decrease the risk of morbid chronic GVHD without increasing the risks of cancer relapse or infection. Development of strategies to predict the risk of developing debilitating or deadly chronic GVHD is a high research priority. This working group recommends further interrogation into the mechanisms underpinning chronic GVHD development, and we highlight considerations for future trial design in prevention trials.

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Published In

Transplant Cell Ther

DOI

EISSN

2666-6367

Publication Date

June 2021

Volume

27

Issue

6

Start / End Page

452 / 466

Location

United States

Related Subject Headings

  • United States
  • Recurrence
  • National Institutes of Health (U.S.)
  • Immunology
  • Humans
  • Graft vs Host Disease
  • Consensus
  • Chronic Disease
  • 3201 Cardiovascular medicine and haematology
  • 1103 Clinical Sciences
 

Citation

APA
Chicago
ICMJE
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Williams, K. M., Inamoto, Y., Im, A., Hamilton, B., Koreth, J., Arora, M., … Sarantopoulos, S. (2021). National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: I. The 2020 Etiology and Prevention Working Group Report. Transplant Cell Ther, 27(6), 452–466. https://doi.org/10.1016/j.jtct.2021.02.035
Williams, Kirsten M., Yoshihiro Inamoto, Annie Im, Betty Hamilton, John Koreth, Mukta Arora, Iskra Pusic, et al. “National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: I. The 2020 Etiology and Prevention Working Group Report.Transplant Cell Ther 27, no. 6 (June 2021): 452–66. https://doi.org/10.1016/j.jtct.2021.02.035.
Williams, Kirsten M., et al. “National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: I. The 2020 Etiology and Prevention Working Group Report.Transplant Cell Ther, vol. 27, no. 6, June 2021, pp. 452–66. Pubmed, doi:10.1016/j.jtct.2021.02.035.
Williams KM, Inamoto Y, Im A, Hamilton B, Koreth J, Arora M, Pusic I, Mays JW, Carpenter PA, Luznik L, Reddy P, Ritz J, Greinix H, Paczesny S, Blazar BR, Pidala J, Cutler C, Wolff D, Schultz KR, Pavletic SZ, Lee SJ, Martin PJ, Socie G, Sarantopoulos S. National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: I. The 2020 Etiology and Prevention Working Group Report. Transplant Cell Ther. 2021 Jun;27(6):452–466.

Published In

Transplant Cell Ther

DOI

EISSN

2666-6367

Publication Date

June 2021

Volume

27

Issue

6

Start / End Page

452 / 466

Location

United States

Related Subject Headings

  • United States
  • Recurrence
  • National Institutes of Health (U.S.)
  • Immunology
  • Humans
  • Graft vs Host Disease
  • Consensus
  • Chronic Disease
  • 3201 Cardiovascular medicine and haematology
  • 1103 Clinical Sciences