Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Jan;29(1):20-34.
doi: 10.1016/j.molmed.2022.09.011. Epub 2022 Oct 22.

Molecular disease mechanisms of human antineuronal monoclonal autoantibodies

Affiliations
Free article
Review

Molecular disease mechanisms of human antineuronal monoclonal autoantibodies

Sophie L Duong et al. Trends Mol Med. 2023 Jan.
Free article

Abstract

Autoantibodies targeting brain antigens can mediate a wide range of neurological symptoms ranging from epileptic seizures to psychosis to dementia. Although earlier experimental work indicated that autoantibodies can be directly pathogenic, detailed studies on disease mechanisms, biophysical autoantibody properties, and target interactions were hampered by the availability of human material and the paucity of monospecific disease-related autoantibodies. The emerging generation of patient-derived monoclonal autoantibodies (mAbs) provides a novel platform for the detailed characterization of immunobiology and autoantibody pathogenicity in vitro and in animal models. This Feature Review focuses on recent advances in mAb generation and discusses their potential as powerful scientific tools for high-resolution imaging, antigenic target identification, atomic-level structural analyses, and the development of antibody-selective immunotherapies.

Keywords: animal models; autoimmune encephalitis; epitope mapping; human monoclonal autoantibody; single-cell cloning; super-resolution microscopy.

PubMed Disclaimer

Conflict of interest statement

Declaration of interests The authors have no interests to declare that are relevant to the content of this Feature Review.

LinkOut - more resources