# Chronic wasting disease as a model for human prion therapy

**Authors:** Michael Bordonaro

PMC · DOI: 10.1080/19336896.2025.2510665 · Prion · 2025-05-24

## TL;DR

The paper suggests using chronic wasting disease in cervids as a model to test therapies for human prion diseases, due to its natural occurrence and potential future transmission risks.

## Contribution

The novelty lies in proposing CWD as a natural model for testing human prion therapies in real-world settings.

## Key findings

- CWD occurs naturally in free-ranging cervids, making it a unique model for prion disease research.
- Testing therapies on CWD could reduce animal suffering and prevent potential future transmission to humans.
- Current therapies include prion expression knockdown and overexpression of dominant negative prion forms.

## Abstract

Prion diseases, also known as transmissible spongiform encephalopathies (TSEs), are fatal neurodegenerative disorders that result from abnormally folded prion proteins. These disorders can be sporadic, acquired, or genetic. Acquired TSEs can be found in a number of animal species including sheep (scrapie), cows (bovine spongiform encephalopathy), and cervids (chronic wasting disease). Chronic wasting disease (CWD) is unusual in that it is found in free ranging animals in their natural environment. There has been heretofore no reported cases of CWD being transmitted to humans; however, the possibility of future adaption for human transmission exists. Several novel approaches for the prevention and treatment of prion disease in humans are under development, including knockdown of endogenous prion expression or overexpression of dominant negative prion forms. Here, I propose that CWD, as a naturally occurring prion disease, should be considered an important testing target for such therapies, which can demonstrate efficacy outside of controlled laboratory environments. Further, from the ethical standpoint of reducing animal suffering, decreasing the CWD burden in cervid populations is highly desirable. Finally, lowering CWD incidence can reduce future possibilities of transmission to humans or to other animal species.

## Linked entities

- **Diseases:** chronic wasting disease (MONDO:0002680), scrapie (MONDO:0006961), bovine spongiform encephalopathy (MONDO:0025149)

## Full-text entities

- **Diseases:** neurodegenerative disorders (MESH:D019636), CWD (MESH:D034081), scrapie (MESH:D012608), Prion diseases (MESH:D017096)
- **Species:** Homo sapiens (human, species) [taxon 9606], Ovis aries (domestic sheep, species) [taxon 9940], Bos taurus (bovine, species) [taxon 9913]

## Full text

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## Figures

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12118434/full.md

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Source: https://tomesphere.com/paper/PMC12118434