Volume 28, Issue 6 pp. 2121-2125
SHORT COMMUNICATION

CD8+ T-cell predominance in autoimmune glial fibrillary acidic protein astrocytopathy

Zhongmin Yuan

Zhongmin Yuan

Institute of Neuroscience and Department of Neurology, Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, China

Guangdong Province Key Laboratory of Brain Function and Disease, Guangzhou, China

Guangdong-Hong Kong-Macao Greater Bay Area Center for Brain Science and Brain-Inspired Intelligence, Guangzhou, China

Contribution: Writing - original draft (equal)

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Huilu Li

Huilu Li

Institute of Neuroscience and Department of Neurology, Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, China

Department of Neurology, Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China

Contribution: Data curation (equal), ​Investigation (equal), Methodology (equal)

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Lu Huang

Lu Huang

Institute of Neuroscience and Department of Neurology, Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, China

Department of Neurology, Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China

Contribution: Data curation (equal), ​Investigation (equal)

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Congcong Fu

Congcong Fu

Institute of Neuroscience and Department of Neurology, Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, China

Department of Neurology, Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China

Contribution: Data curation (equal), Methodology (equal)

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Yaotang Chen

Yaotang Chen

Department of Radiology, Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China

Contribution: Data curation (equal), Methodology (equal)

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Cheng Zhi

Cheng Zhi

Department of Pathology, Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China

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Wei Qiu

Wei Qiu

Department of Neurology, Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China

Contribution: ​Investigation (equal)

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Youming Long

Corresponding Author

Youming Long

Institute of Neuroscience and Department of Neurology, Second Affiliated Hospital of Guangzhou Medical University, Key Laboratory of Neurogenetics and Channelopathies of Guangdong Province and the Ministry of Education of China, Guangzhou, China

Department of Neurology, Second Affiliated Hospital of Guangzhou Medical University, Guangzhou, China

Correspondence

Youming Long, Department of Neurology, the Second Affiliated Hospital of GuangZhou Medical University, 250 Changgang east Road, GuangZhou, 510260 Guangdong Province, China.

Email: [email protected]

Contribution: Conceptualization (equal), Funding acquisition (equal), ​Investigation (equal), Methodology (equal), Project administration (equal), Writing - review & editing (equal)

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First published: 16 February 2021
Citations: 38

Z. Yuan and H.Li is the co-first author.

Funding information

This study was supported by the National Natural Science Foundation of China (81771302, 81671232); the Science and Technology Program of Guangzhou, China (201803010123); the Natural Science Foundation of Guangdong Province (2019A1515010473) and the Guangdong-Hong Kong-Macao Greater Bay Area Center for Brain Science and Brain-Inspired Intelligence Fund (2019014).

Abstract

Background and objective

We aimed to report the pathological features of T lymphocytes in autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy (GFAP-A).

Methods

A retrospective pathological analysis of patients with GFAP-A was performed.

Results

Eight patients with GFAP-immunoglobulin G (IgG) and pathological data were included. Their biopsy findings were similar, and all showed marked lymphocytic infiltration in the white matter, with perivascular predominance. The lymphocytic infiltration was predominantly composed of CD8+ T lymphocytes rather than CD4+ T lymphocytes, except in one patient who had overlapping positive myelin oligodendrocyte glycoprotein-IgG. Unlike CD4+ T cells, CD8+ T cells were frequently observed adjacent to dystrophic neurons and astrocytes. There was also diffuse infiltration by CD68+ and CD163+ macrophages. CD8+ astrocytes were identified in two samples, but no CD4+ astrocytes were observed.

Conclusions

A predominance of CD8+ T cells may be an important pathological and diagnostic feature in GFAP-A.

CONFLICT OF INTERESTS

None declared.

DATA AVAILABILITY STATEMENT

The data that supports the findings of this study are available in the supplementary material Table S1 of this article.

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