Evaluation of Donor Specific Immune Senescence and Exhaustion as Biomarkers of Tolerance Post Liver Transplantation (OPTIMAL)

Principal Investigator

James Markmann, MD, PhD | Massachusettes General Hospital | Boston, MA

Locations

University of California, San Francisco | San Francisco, CA

Northwestern Memorial University | Chicago, IL

Massachusetts General Hospital | Boston, MA

New York Presbyterian/Columbia University Medical Center | New York, NY

University of Pittsburgh Medical Center | Pittsburgh, PA

Baylor University Medical Center | Dallas, TX

Study Code

ITN056ST

Study Status

Active

Abstract

An important goal of transplant research is to allow people with a transplanted organ to live without long-term use of immunosuppression, which has serious side effects including increased risk of infection and malignancy. Previous research suggests that a proportion of liver transplant recipients are able to come off immunosuppressive drugs without experiencing rejection.

The goal of the OPTIMAL study is to gradually reduce anti-rejection medication(s) in liver transplant recipients over a period of time until the medication(s) are stopped. This is called immunosuppression withdrawal. The OPTIMAL Study will enroll 60 adult liver transplant recipients. These recipients will undergo supervised, gradual withdrawal of their immunosuppressive medications to determine how many participants can achieve a state of operational tolerance.

The OPTIMAL investigators also hypothesize that continual exposure to a transplanted organ for a significant period of time may render the immune system “exhausted,” thereby tempering the associated inflammatory response. For this reason, the OPTIMAL study will enroll transplant recipients who have been living with their transplanted liver for at least three years, and will assess whether biomarkers of an exhausted immune system can help predict individuals who can successfully discontinue immunosuppressive medication without experiencing damage to their transplanted organ.

Qualification

Articles

DOI: 

http://dx.doi.org/https://doi.org/10.1016/j.jim.2021.112987

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PMID: 

33556344

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PMCID: 

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PubMed

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