4.7 Article

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

Journal

EUROPEAN JOURNAL OF NEUROLOGY
Volume 28, Issue 6, Pages 2121-2125

Publisher

WILEY
DOI: 10.1111/ene.14778

Keywords

antibodies; cerebrospinal fluid; glial fibrillary acidic protein; neuroinflammation; T‐ lymphocytes

Funding

  1. National Natural Science Foundation of China [81771302, 81671232]
  2. Science and Technology Program of Guangzhou, China [201803010123]
  3. Natural Science Foundation of Guangdong Province [2019A1515010473]
  4. Guangdong-Hong Kong--Macao Greater Bay Area Center for Brain Science and Brain-Inspired Intelligence Fund [2019014]

Ask authors/readers for more resources

In autoimmune GFAP astrocytopathy (GFAP-A), there is a predominance of CD8(+) T cells with marked lymphocytic infiltration, especially adjacent to dystrophic neurons and astrocytes. Additionally, there is diffuse infiltration by CD68(+) and CD163(+) macrophages. CD8(+) astrocytes were identified in some samples, but no CD4(+) astrocytes were observed.
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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available