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A Rapid Blood Test for Early Detection of Prion Diseases

At a Glance

Researchers at Colorado State University have developed methods for detecting prions directly in blood samples with high sensitivity and specificity. The technology uses an advanced RT-QuIC assay to identify extremely small amounts of disease-associated prion material that traditional diagnostic methods cannot detect. The platform has demonstrated greater than 90% sensitivity with 100% specificity in blood samples from prion-infected deer and hamsters. This approach could support earlier diagnosis, disease surveillance, and improved blood safety monitoring for both human and animal prion diseases.

Background

Prion diseases, including chronic wasting disease (CWD) and variant Creutzfeldt-Jakob disease (vCJD), are fatal neurodegenerative disorders that can spread before symptoms appear. Existing diagnostic methods typically require nervous or lymphoid tissue and are not sensitive enough to reliably detect the very low levels of prions found in blood during early infection. Concerns surrounding asymptomatic carriers and potential blood-borne transmission have increased the need for accurate presymptomatic testing technologies. A sensitive blood-based assay could significantly improve disease monitoring, containment, and public health response efforts.

Overview

This technology improves conventional prion detection methods by adapting and optimizing real-time quaking-induced conversion (RT-QuIC) for use with whole blood samples. The assay amplifies trace amounts of prion-related amyloid material present in blood, allowing researchers to detect infections that would otherwise remain undetectable using standard approaches such as Western blotting or immunohistochemistry. The method enables rapid, reproducible screening while maintaining high analytical performance across multiple animal models and exposure routes.

In published studies, the assay successfully detected blood-borne prions in white-tailed deer, muntjac deer, and Syrian hamsters throughout disease progression, including within minutes of exposure and long before clinical symptoms developed. The platform achieved greater than 90% sensitivity while maintaining 100% specificity, demonstrating reliable detection of very low concentrations of circulating prions. The ability to detect prions directly in blood represents a major advancement for surveillance, diagnostic development, and understanding of how prion diseases spread through the body.

Figure 1. The QuIC blood testing method rapidly and sensitively detects prion-related protein aggregates in infected hamsters within minutes of exposure and throughout the full course of disease progression.

Benefits

  • Detects prions directly from whole blood samples
  • Greater than 90% sensitivity with 100% specificity demonstrated in animal studies
  • Capable of detecting prions during asymptomatic and early-stage infection
  • More sensitive than traditional tissue-based assays for low-level prion detection
  • Rapid and reproducible testing workflow
  • Supports both human and animal disease surveillance efforts
  • Provides insight into blood-borne transmission and disease progression
  • Applicable across multiple prion diseases and exposure routes

Applications

  • Diagnostic testing for chronic wasting disease (CWD) in wildlife
  • Presymptomatic screening for human prion diseases such as vCJD
  • Blood supply safety monitoring and screening
  • Veterinary and agricultural disease surveillance
  • Research tools for studying prion transmission and pathogenesis
  • Public health preparedness and outbreak monitoring
  • Pharmaceutical and therapeutic development support for prion diseases

Publications

C.C. Luk, et al. (2021) Creutzfeldt-Jakob disease in pregnancy: the use of modified RT-QuIC to determine infectivity in placental tissues. Prion. doi: 10.1080/19336896.2021.1933872.PMID: 34132175 

J.M. Tennant, et al. (2020) Shedding and stability of CWD prion seeding activity in cervid feces. PLoS One. doi: 10.1371/journal.pone.0227094. eCollection 2020.PMID: 32126066

E.E. McNulty, et al. (2020) In vitro detection of haematogenous prions in white-tailed deer orally dosed with low concentrations of chronic wasting disease. J Gen Virol. doi: 10.1099/jgv.0.001367. PMID:31846418

A.M. Elder, et al. (2015) Immediate and Ongoing Detection of Prions in the Blood of Hamsters and Deer following Oral, Nasal, or Blood Inoculations. J Virol. doi: 10.1128/JVI.00760-15.

A.M. Elder, et al. (2013) In Vitro Detection of Prionemia in TSE-Infected Cervids and Hamsters. PLOS ONE, Public Library of Science.

D. M. Henderson,et al. (2013) Rapid Antemortem Detection of CWD Prions in Deer Saliva. PloS One, Public Library of Science. www.ncbi.nlm.nih.gov/pubmed/24040235.

N.J. Haley, et al. (2013) Prion-Seeding Activity in Cerebrospinal Fluid of Deer with Chronic Wasting Disease. PloS One, Public Library of Science. www.ncbi.nlm.nih.gov/pubmed/24282599.

Last Updated: May 2026
MRI image of patient with Creutzfeldt-Jakob disease
Opportunity

Available for Exclusive Licensing
TRL: 5

IP Status

​US Patent 10359434
US Patent 11598783

Inventors

Edward A Hoover
Candace K Mathiason

Reference Number
14-012
Licensing Manager

Steve Foster
Steve.Foster@colostate.edu
970-491-7100

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