Paraneoplastic Calmodulin Kinase‐Like Vesicle‐Associated Protein (CAMKV) Autoimmune Encephalitis

Author:

Gilligan Michael12,Lesnick Connie E.1,Guo Yong3,Bradshaw Michael J.4ORCID,Ladha Shafeeq S.5,Nowak Mihaela6,Shah Maulik P.7,Wittenborn John R.8,Basal Eati1,Hinson Shannon1,Yang Binxia1,Dubey Divyanshu13ORCID,Mills John R.1,Pittock Sean J.13ORCID,Zekeridou Anastasia13ORCID,McKeon Andrew13ORCID

Affiliation:

1. Department of Laboratory Medicine and Pathology Mayo Clinic Rochester MN USA

2. Department of Neurology University College Dublin, St Vincent's Hospital Elm Park Dublin Ireland

3. Department of Neurology Mayo Clinic Rochester MN USA

4. Department of Neurology University of Washington and Billings Clinic Billings MT USA

5. Department of Neurology Barrow Neurological Institute Phoenix AZ USA

6. Department of Neurology Jefferson Hospital Jefferson Hills PA USA

7. Department of Neurology University of California San Francisco CA USA

8. Department of Neurology Robert Wood Johnson University Hospital New Brunswick NJ USA

Abstract

ObjectivesTo report an autoimmune paraneoplastic encephalitis characterized by immunoglobulin G (IgG) antibody targeting synaptic protein calmodulin kinase‐like vesicle‐associated (CAMKV).MethodsSerum and cerebrospinal fluid (CSF) samples harboring unclassified antibodies on murine brain‐based indirect immunofluorescence assay (IFA) were screened by human protein microarray. In 5 patients with identical cerebral IFA staining, CAMKV was identified as top‐ranking candidate antigen. Western blots, confocal microscopy, immune‐absorption, and mass spectrometry were performed to substantiate CAMKV specificity. Recombinant CAMKV‐specific assays (cell‐based [fixed and live] and Western blot) provided additional confirmation.ResultsOf 5 CAMKV‐IgG positive patients, 3 were women (median symptom‐onset age was 59 years; range, 53–74). Encephalitis‐onset was subacute (4) or acute (1) and manifested with: altered mental status (all), seizures (4), hyperkinetic movements (4), psychiatric features (3), memory loss (2), and insomnia (2). Paraclinical testing revealed CSF lymphocytic pleocytosis (all 4 tested), electrographic seizures (3 of 4 tested), and striking MRI abnormalities in all (mesial temporal lobe T2 hyperintensities [all patients], caudate head T2 hyperintensities [3], and cortical diffusion weighted hyperintensities [2]). None had post‐gadolinium enhancement. Cancers were uterine adenocarcinoma (3 patients: poorly differentiated or neuroendocrine‐differentiated in 2, both demonstrated CAMKV immunoreactivity), bladder urothelial carcinoma (1), and non‐Hodgkin lymphoma (1). Two patients developed encephalitis following immune checkpoint inhibitor cancer therapy (atezolizumab [1], pembrolizumab [1]). All treated patients (4) demonstrated an initial response to immunotherapy (corticosteroids [4], IVIG [2]), though 3 died from cancer.InterpretationCAMKV‐IgG is a biomarker of immunotherapy‐responsive paraneoplastic encephalitis with temporal and extratemporal features and uterine cancer as a prominent oncologic association. ANN NEUROL 2024;96:21–33

Funder

National Institutes of Health

Wellcome Trust

Publisher

Wiley

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1. Autoimmune Neurobeachin Cerebellar Ataxia;Movement Disorders;2024-08-20

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