Volume 31, Issue 3 pp. 480-492
Experimental Laboratory Research

MRI characteristics of Japanese macaque encephalomyelitis: Comparison to human diseases

Ian J. Tagge

Corresponding Author

Ian J. Tagge

Advanced Imaging Research Center, Oregon Health & Science University, Portland, Oregon, USA

Montreal Neurological Institute, McGill University, Montréal, Quebec, Canada

Correspondence

Ian J. Tagge, Montreal Neurological Institute, McGill University, 3801 Rue University, WB-321, Montréal, QC H3A 2B4, Canada.

Email: [email protected]

William D. Rooney, Advanced Imaging Research Center, Oregon Health & Science University, (L452), 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA.

Email: [email protected]

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Steven G. Kohama

Steven G. Kohama

Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, Oregon, USA

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Larry S. Sherman

Larry S. Sherman

Division of Neuroscience, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, Oregon, USA

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Dennis N. Bourdette

Dennis N. Bourdette

Neurology, Oregon Health & Science University, Portland, Oregon, USA

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Randall Woltjer

Randall Woltjer

Department of Pathology, Oregon Health & Science University, Portland, Oregon, USA

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Paul Wang

Paul Wang

Department of Radiology, Oregon Health & Science University, Portland, Oregon, USA

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Scott W. Wong

Scott W. Wong

Division of Pathobiology & Immunology, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, Oregon, USA

Vaccine and Gene Therapy Institute, Oregon Health & Science University, Beaverton, Oregon, USA

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William D. Rooney

Corresponding Author

William D. Rooney

Advanced Imaging Research Center, Oregon Health & Science University, Portland, Oregon, USA

Neurology, Oregon Health & Science University, Portland, Oregon, USA

Correspondence

Ian J. Tagge, Montreal Neurological Institute, McGill University, 3801 Rue University, WB-321, Montréal, QC H3A 2B4, Canada.

Email: [email protected]

William D. Rooney, Advanced Imaging Research Center, Oregon Health & Science University, (L452), 3181 SW Sam Jackson Park Road, Portland, OR 97239, USA.

Email: [email protected]

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First published: 30 April 2021
Citations: 1

Abstract

Background and Purpose

To describe MRI findings in Japanese macaque encephalomyelitis (JME) with emphasis on lesion characteristics, lesion evolution, normal-appearing brain tissue, and similarities to human demyelinating disease.

Methods

MRI data were obtained from 114 Japanese macaques, 30 presenting neurological signs of JME. All animals were screened for presence of T2-weighted white matter signal hyperintensities; animals with behavioral signs of JME were additionally screened for contrast-enhancing lesions. Whole-brain quantitative T1 maps were collected, and histogram analysis was performed with regression across age to evaluate microstructural changes in normal appearing brain tissue in JME and neurologically normal animals. Quantitative estimates of blood-brain-barrier (BBB) permeability to gadolinium-based-contrast agent (GBCA) were obtained in acute, GBCA-enhancing lesions. Longitudinal imaging data were acquired for 15 JME animals.

Results

One hundred and seventy-three focal GBCA-enhancing lesions were identified in 30 animals demonstrating behavioral signs of neurological dysfunction. JME GBCA-enhancing lesions were typically focal and ovoid, demonstrating highest BBB GBCA permeability in the lesion core, similar to acute, focal multiple sclerosis lesions. New GBCA-enhancing lesions arose rapidly from normal-appearing tissue, and BBB permeability remained elevated for weeks. T1 values in normal-appearing tissue were significantly associated with age, but not with sex or disease.

Conclusions

Intense, focal neuroinflammation is a key MRI finding in JME. Several features of JME compare directly to human inflammatory demyelinating diseases. Investigation of JME combined with the development and validation of noninvasive imaging biomarkers offers substantial potential to improve diagnostic specificity and contribute to the understanding of human demyelinating diseases.

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