Role of donor macrophages after heart and lung transplantation.

basic (laboratory) research/science heart (allograft) function/dysfunction heart disease: immune/inflammatory heart transplantation/cardiology immunosuppressant immunosuppression/immune modulation lung (allograft) function/dysfunction lung disease: immune/inflammatory translational research/science

Journal

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
ISSN: 1600-6143
Titre abrégé: Am J Transplant
Pays: United States
ID NLM: 100968638

Informations de publication

Date de publication:
05 2020
Historique:
received: 18 10 2019
revised: 06 12 2019
accepted: 08 12 2019
pubmed: 19 12 2019
medline: 22 6 2021
entrez: 19 12 2019
Statut: ppublish

Résumé

Since the 1960s, heart and lung transplantation has remained the optimal therapy for patients with end-stage disease, extending and improving quality of life for thousands of individuals annually. Expanding donor organ availability and immunologic compatibility is a priority to help meet the clinical demand for organ transplant. While effective, current immunosuppression is imperfect as it lacks specificity and imposes unintended adverse effects such as opportunistic infections and malignancy that limit the health and longevity of transplant recipients. In this review, we focus on donor macrophages as a new target to achieve allograft tolerance. Donor organ-directed therapies have the potential to improve allograft survival while minimizing patient harm related to global suppression of recipient immune responses. Topics highlighted include the role of ontogenically distinct donor macrophage populations in ischemia-reperfusion injury and rejection, including their interaction with allograft-infiltrating recipient immune cells and potential therapeutic approaches. Ultimately, a better understanding of how donor intrinsic immunity influences allograft acceptance and survival will provide new opportunities to improve the outcomes of transplant recipients.

Identifiants

pubmed: 31850651
doi: 10.1111/ajt.15751
pmc: PMC7202685
mid: NIHMS1583733
pii: S1600-6135(22)22308-9
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

1225-1235

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL138466
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL139714
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL151078
Pays : United States

Informations de copyright

© 2019 The American Society of Transplantation and the American Society of Transplant Surgeons.

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Auteurs

Benjamin J Kopecky (BJ)

Department of Medicine, Washington University, Saint Louis, Missouri, USA.

Christian Frye (C)

Department of Surgery, Washington University, Saint Louis, Missouri, USA.

Yuriko Terada (Y)

Department of Surgery, Washington University, Saint Louis, Missouri, USA.

Keki R Balsara (KR)

Department of Surgery, Vanderbilt University, Nashville, Tennessee, USA.

Daniel Kreisel (D)

Department of Surgery, Washington University, Saint Louis, Missouri, USA.
Department of Pathology and Immunology, Washington University, Saint Louis, Missouri, USA.

Kory J Lavine (KJ)

Department of Medicine, Washington University, Saint Louis, Missouri, USA.
Department of Pathology and Immunology, Washington University, Saint Louis, Missouri, USA.
Department of Developmental Biology, Washington University, Saint Louis, Missouri, USA.

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