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Autoimmune Encephalitis With Anti-NMDA Receptor Antibodies Following Herpetic Encephalitis

Study of 12 Cases of Autoimmune Encephalitis With Anti-NMDA Receptor Antibodies Following Herpetic Encephalitis and Review of the Literature

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04339127
Acronym
NMDARE-HSE
Enrollment
12
Registered
2020-04-09
Start date
2020-04-01
Completion date
2020-10-01
Last updated
2020-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anti NMDA Receptor Encephalitis, Autoimmune Encephalitis, Herpetic Encephalitis

Brief summary

Herpes Simplex Virus encephalitis is the most common infectious encephalitis, with an estimated annual incidence of 1 / 250,000 to 1 / 500,000 in industrialized countries. Despite a widely used antiviral treatment, the prognosis remains poor with a mortality of 5 to 20% and a considerable morbidity rate. One of the contributing factors of bad prognosis is the development of encephalitis mediated by autoantibodies, most often directed against NMDA receptors, in the weeks following viral encephalitis. The description of this pathology is recent, the pathophysiology of this process remains poorly understood, and the management of these patients is not yet codified.

Interventions

Retrospective, non-interventional study, using clinical, biological, radiological and therapeutic data collected during the initial diagnosis and follow-up.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Clinical autoimmune encephalitis with anti-NMDA antibodies and documented by CBA in the CSF * After a herpetic encephalitis documented by a positive viral PCR for HSV in the CSF * Without age limit

Exclusion criteria

- No respect of inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
Details of clinical, biological, imaging, therapeutic characteristics and patient's evolution.at 6 and 12 monthsRetrospective collection of clinical, diagnostic and therapeutic data, evolution at 6 and 12 months.

Countries

France

Contacts

Primary ContactJérôme Honnorat, PhD
jerome.honnorat@chu-lyon.fr04 72 35 78 06
Backup ContactGéraldine PICARD
geraldine.picard@chu-lyon.fr0472355842

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026