Related Experiment Video
Updated: Jul 21, 2026

Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
MRI findings in autoimmune encephalitis
T J Hartung1, F Bartels2, J Kuchling1
1Charité - Universitätsmedizin Berlin, Department of Neurology and Experimental Neurology, Berlin, Germany.
Abstract:
Autoimmune encephalitis encompasses a spectrum of conditions characterized by distinct clinical features and magnetic resonance imaging (MRI) findings. Here, we review the literature on acute MRI changes in the most common autoimmune encephalitis variants. In N-methyl-D-aspartate (NMDA) receptor encephalitis, most patients have a normal MRI in the acute stage. When lesions are present in the acute stage, they are typically subtle and non-specific white matter lesions that do not correspond with the clinical syndrome. In some NMDA receptor encephalitis cases, these T2-hyperintense lesions may be indicative of an NMDA receptor encephalitis overlap syndrome with simultaneous co-existence of multiple sclerosis (MS), neuromyelitis optica spectrum disorder (NMOSD) or myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). Encephalitis with leucine-rich glioma-inactivated 1 (LGI1)-, contactin-associated protein-like 2 (CASPR2)- or glutamic acid decarboxylase (GAD)- antibodies typically presents as limbic encephalitis (LE) with unilateral or bilateral T2/fluid attenuated inversion recovery (FLAIR) hyperintensities in the medial temporal lobe that can progress to hippocampal atrophy. Gamma aminobutyric acid-B (GABA-B) receptor encephalitis also often shows such medial temporal hyperintensities but may additionally involve cerebellar lesions and atrophy. Gamma aminobutyric acid-A (GABA-A) receptor encephalitis features multifocal, confluent lesions in cortical and subcortical areas, sometimes leading to generalized atrophy. MRI is unremarkable in most patients with immunoglobulin-like cell adhesion molecule 5 (IgLON5)-disease, while individual case reports identified T2/FLAIR hyperintense lesions, diffusion restriction and atrophy in the brainstem, hippocampus and cerebellum. These findings highlight the need for MRI studies in patients with suspected autoimmune encephalitis to capture disease-specific changes and to exclude alternative diagnoses. Ideally, MRI investigations should be performed using dedicated autoimmune encephalitis imaging protocols. Longitudinal MRI studies play an important role to evaluate potential relapses and to manage long-term complications. Advanced MRI techniques and current research into imaging biomarkers will help to enhance the diagnostic accuracy of MRI investigations and individual patient outcome prediction. This will eventually enable better treatment decisions with improved clinical outcomes.
Insights
Acute MRI findings in autoimmune encephalitis vary by type. While N-methyl-D-aspartate (NMDA) receptor encephalitis often shows normal MRI, other forms like LGI1 or GAD antibody encephalitis present with medial temporal lobe lesions. Recognizing these patterns aids diagnosis.
Area of Science:
- Neurology
- Radiology
- Immunology
Background:
- Autoimmune encephalitis (AE) is a group of neurological disorders caused by immune system attacks on the brain.
- Distinct clinical and neuroimaging features characterize different AE subtypes.
- Magnetic resonance imaging (MRI) plays a crucial role in diagnosing and managing AE.
Purpose of the Study:
- To review and summarize acute MRI findings in common autoimmune encephalitis variants.
- To highlight the diagnostic utility of MRI in differentiating AE subtypes and excluding other conditions.
- To discuss the role of advanced MRI techniques and future research in AE diagnosis and management.
Main Methods:
- Literature review of studies reporting acute MRI findings in autoimmune encephalitis.
- Analysis of MRI characteristics associated with specific AE antibody profiles (e.g., NMDA receptor, LGI1, CASPR2, GAD, GABA-B, GABA-A, IgLON5).
- Synthesis of information on lesion patterns, location, and evolution.
Main Results:
- N-methyl-D-aspartate (NMDA) receptor encephalitis: MRI often normal acutely; subtle white matter lesions may indicate overlap syndromes (MS, NMOSD, MOGAD).
- Limbic encephalitis (LGI1, CASPR2, GAD antibodies): Medial temporal lobe T2/FLAIR hyperintensities, potential hippocampal atrophy.
- GABA-B receptor encephalitis: Similar temporal lobe involvement, possible cerebellar lesions/atrophy. GABA-A receptor encephalitis: Multifocal cortical/subcortical lesions. IgLON5 disease: Mostly unremarkable MRI, rare brainstem/hippocampal lesions.
Conclusions:
- Acute MRI findings in autoimmune encephalitis are diverse and subtype-specific.
- MRI is essential for identifying characteristic lesions, guiding differential diagnosis, and excluding alternative conditions.
- Dedicated MRI protocols and advanced techniques are crucial for improving diagnostic accuracy and patient outcomes in AE.
More Related Videos
Related Concept Videos
Arboviral Encephalitis
Encephalitis l: Introduction
Encephalitis ll: Pathophysiology

