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CASPR2 Encephalitis

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wiki page Created: 2026-04-02T07:20:13 By: crosslink-migration Quality: 50% ✓ SciDEX ID: wiki-diseases-caspr2-encephalitis
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CASPR2 Encephalitis

Introduction

Caspr2 Encephalitis is an important component in the neurobiology of neurodegenerative diseases. This page provides detailed information about its structure, function, and role in disease processes.

CASPR2 Encephalitis is an autoimmune neurological disorder caused by antibodies targeting the Contactin-Associated Protein-like 2 (CASPR2), a member of the neurexin family that is crucial for the formation and maintenance of neuronal synapses[@antibodies], [@severe]. [@severe]

Overview

CASPR2 Encephalitis is recognized as one of the major autoimmune encephalitis syndromes[@antibodies]. It exists on a spectrum with Morvan syndrome, with overlapping clinical features. The condition is part of the voltage-gated potassium channel (VGKC) complex antibody spectrum, though the target antigen is actually CASPR2 rather than the potassium channel itself[@severe]. [@morvan]

This disorder provides important insights into synaptic immunology and the role of axonal proteins in autoimmune neurological disease. Recent research indicates that publications on CASPR2 encephalitis have increased substantially, from 2 in 2010 to 54 in 2025, reflecting growing clinical awareness[^9]. [@morvana]

Pathophysiology

Target Antigen

Contactin-Associated Protein-like 2 (CASPR2) is encoded by the [CNTNAP2 gene](/proteins/cntnap2-protein) and is[@antibodies], [@morvan]:

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