# Super-sensitive detection of universal markers of allograft rejection

> **NIH NIH R43** · GENETAG TECHNOLOGY, INC. · 2020 · $242,610

## Abstract

Super-sensitive detection of universal markers of allograft rejection Confidential Principal Investigator: Shafer, David A., PhD
PROJECT SUMMARY
 Over 35,000 organ transplants are performed annually in the US, with kidney, liver, heart, and lung
transplants being most common. Transplant recipients are normally prescribed immunosuppressants,
corticosteroids, or other medications to prevent allograft rejection; however, rejection eventually occurs in up to
one third of recipients. Monitoring rejection facilitates timely therapy by switching to a new drug, adding another
drug, or adjusting the dose of the current medications. Tissue biopsies are the gold standard for diagnosing
allograft rejection, although they are invasive, may result in medical complications, and often yield inadequate
specimens. Currently, the AlloMap® test (CareDx) is the only FDA-approved molecular diagnostics test for
identifying the risk of acute cell rejection in transplant recipients. The AlloMap® test does not directly measure
donor-derived cell-free DNA (ddcfDNA), has a low positive-predictive value, and does not detect antibody-
mediated rejection. Thus, a genuine clinical need exists for accurate methods that enable inexpensive, non-
invasive “liquid biopsy” biomarker testing via plasma samples to quickly identify subjects at risk of rejection.
 The overall objective of this project is to develop a real-time PCR SNP profiling test for detecting ddcfDNA
in the plasma of transplant recipients, as an early indicator of rejection. Our primary system, the internal DNA-
Detection Switch (iDDS) probe system, comprises two interacting components: a fluor-labeled probe, and a
quencher-labeled antiprobe that is nearly complementary to the probe. This unique probe system shows superior
single-base discrimination over a much wider annealing-temperature range (10–30ºC) than common methods.
Recently, we merged our iDDS probe technology with our Wild Terminator (WTx) methods that enable detection
of rare mutants (0.1–0.01% frequency) by blocking amplification of the wild-type sequence. The combined
method showed greater sensitivity in detecting circulating EGFR variants from lung cancer patients than the
FDA-approved cobas® EGFR Mutation Test, v2. Our higher sensitivity and specificity will enable development
of platform-independent, liquid biopsy assays. Our Specific Aims are: 1) to develop dual-iDDS probe-based SNP
profiling assays for donor-derived SNPs, and 2) to develop WTx-iDDS probe assays for quantitating SNPs in
ddcfDNA. In Aim 1, we will develop dual-iDDS probe profiling assays for two SNP variants at each of 20 loci, at
sites where the global minor allele frequency is nearly 0.5. Selecting SNPs with nearly equal major/minor allele
frequencies will greatly simplify the process of detecting a spike in ddcfDNA levels in the blood of transplant
recipients before rejection occurs. In Aim 2, we will develop WTx assays that selectively amplify the 20 targeted
SNP alleles, and val...

## Key facts

- **NIH application ID:** 9909410
- **Project number:** 1R43AI150530-01
- **Recipient organization:** GENETAG TECHNOLOGY, INC.
- **Principal Investigator:** James L Murray
- **Activity code:** R43 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $242,610
- **Award type:** 1
- **Project period:** 2020-01-17 → 2020-12-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9909410

## Citation

> US National Institutes of Health, RePORTER application 9909410, Super-sensitive detection of universal markers of allograft rejection (1R43AI150530-01). Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/grant/nih/9909410. Licensed CC0.

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