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Updated: Jan 6, 2026

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Detection of Abnormal Prion Protein by Immunohistochemistry
Published on: May 5, 2023
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Diagnosis of Prion Diseases
Tayyaba Saleem1, Anna-Lisa Fischer1, Sezgi Canaslan1
1Department of Neurology, University Medical Center, Georg-August University, Goettingen, Germany.
Sub-Cellular Biochemistry
|September 26, 2025
Summary
Accurate diagnosis of prion diseases, fatal neurodegenerative disorders, is crucial. New methods like real-time quaking-induced conversion (RT-QuIC) improve early detection, aiding patient management and preventing transmission.
Area of Science:
- Neurology
- Biochemistry
- Pathology
Background:
- Prion diseases are fatal neurodegenerative disorders caused by misfolded prion proteins.
- Early and accurate diagnosis is critical to differentiate prion diseases from treatable dementias and prevent iatrogenic spread.
Purpose of the Study:
- To review advancements in antemortem diagnostic capabilities for prion diseases.
- To highlight the role of new biomarkers and techniques in improving early detection.
Main Methods:
- Review of current diagnostic approaches including clinical evaluation, neuroimaging, electroencephalography, and cerebrospinal fluid biomarkers.
- Emphasis on the development and application of real-time quaking-induced conversion (RT-QuIC) assay for prion protein detection.
Main Results:
- Antemortem diagnostic capabilities have significantly improved beyond traditional postmortem neuropathology.
- Real-time quaking-induced conversion (RT-QuIC) demonstrates high specificity in detecting misfolded prion proteins, complementing existing methods.
Conclusions:
- Despite advancements, challenges in early identification and disease management persist.
- Continued research is vital for enhancing prion disease diagnosis, tracking progression, and understanding pathogenesis.
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