Bioinformatics pipeline for personalized diagnostics of transplant rejection
- Institution
- DATIRIUM, LLC, OH
- Principal investigator
- Artem Barski
- Funding
- $307K
- Duration
- 2025–2026
Moonbase score
Still being scored
Abstract
Summary Transplantation is the most effective treatment for kidney failure, providing improved survival and quality of life. In the US, ~20,000-25,000 kidney transplants are performed in the US per year. Roughly ~90,000 individuals are waitlisted to receive a kidney allograft with average waiting time ~5 years. Many individuals die before receiving the transplant. Those patients receiving a transplant are required to be on life-long, maintenance immunosuppression (mIS) with calcineurin inhibitors (CNI), such as tacrolimus, to prevent rejection. Unfortunately, rejection still remains the #1 cause of death-censored graft loss. Potential treatment for graft failure is dialysis ($126K/year)1 or another transplant (~$500K) if another compatible kidney is available. Overall, in the US the annual cost of kidney transplant failure is $1.3B with ~ half covered by Medicare2. Thus, even a minor decrease in graft loss carries a potential for enormous human and economic benefit. Our preliminary and published data show that the scRNA/VDJ analysis of kidney biopsies and potentially urine samples can identify the alloreactive expanded cytotoxic T cell clones (CD8exp) that are likely causing rejection. We also showed that the analysis of gene expression in these clones can identify targets for anti- rejection therapy. The aim of the project is to develop a diagnostic test based on scRNA/VDJ analysis that will help physicians select personalized anti-rejection therapy based on the phenotype of the cells causing rejection. In this phase I project, we aim to (i) develop an automated computational pipelines that will process the data and produce a report for treating physician and (ii) to demonstrate the feasibility of completing the test within clinically reasonable time-frame. We will also collect preliminary data that will help justify a larger phase II study that will demonstrate the clinical benefit of the test.
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