ZSCAN1 Autoantibodies Are Associated with Pediatric Paraneoplastic ROHHAD.


Journal

Annals of neurology
ISSN: 1531-8249
Titre abrégé: Ann Neurol
Pays: United States
ID NLM: 7707449

Informations de publication

Date de publication:
08 2022
Historique:
revised: 18 04 2022
received: 22 11 2021
accepted: 21 04 2022
pubmed: 26 4 2022
medline: 28 7 2022
entrez: 25 4 2022
Statut: ppublish

Résumé

Rapid-onset Obesity with Hypothalamic Dysfunction, Hypoventilation and Autonomic Dysregulation (ROHHAD), is a severe pediatric disorder of uncertain etiology resulting in hypothalamic dysfunction and frequent sudden death. Frequent co-occurrence of neuroblastic tumors have fueled suspicion of an autoimmune paraneoplastic neurological syndrome (PNS); however, specific anti-neural autoantibodies, a hallmark of PNS, have not been identified. Our objective is to determine if an autoimmune paraneoplastic etiology underlies ROHHAD. Immunoglobulin G (IgG) from pediatric ROHHAD patients (n = 9), non-inflammatory individuals (n = 100) and relevant pediatric controls (n = 25) was screened using a programmable phage display of the human peptidome (PhIP-Seq). Putative ROHHAD-specific autoantibodies were orthogonally validated using radioactive ligand binding and cell-based assays. Expression of autoantibody targets in ROHHAD tumor and healthy brain tissue was assessed with immunohistochemistry and mass spectrometry, respectively. Autoantibodies to ZSCAN1 were detected in ROHHAD patients by PhIP-Seq and orthogonally validated in 7/9 ROHHAD patients and 0/125 controls using radioactive ligand binding and cell-based assays. Expression of ZSCAN1 in ROHHAD tumor and healthy human brain tissue was confirmed. Our results support the notion that tumor-associated ROHHAD syndrome is a pediatric PNS, potentially initiated by an immune response to peripheral neuroblastic tumor. ZSCAN1 autoantibodies may aid in earlier, accurate diagnosis of ROHHAD syndrome, thus providing a means toward early detection and treatment. This work warrants follow-up studies to test sensitivity and specificity of a novel diagnostic test. Last, given the absence of the ZSCAN1 gene in rodents, our study highlights the value of human-based approaches for detecting novel PNS subtypes. ANN NEUROL 2022;92:279-291.

Identifiants

pubmed: 35466441
doi: 10.1002/ana.26380
pmc: PMC9329235
mid: NIHMS1800950
doi:

Substances chimiques

Autoantibodies 0
Ligands 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

279-291

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH122471
Pays : United States
Organisme : NIAID NIH HHS
ID : T32 AI060537
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM141323
Pays : United States
Organisme : NIA NIH HHS
ID : P30 AG062422
Pays : United States
Organisme : NICHD NIH HHS
ID : P30 HD018655
Pays : United States
Organisme : NIDDK NIH HHS
ID : K23 DK120899
Pays : United States
Organisme : NIDDK NIH HHS
ID : F30 DK123915
Pays : United States
Organisme : NIA NIH HHS
ID : K23 AG031861
Pays : United States
Organisme : NINDS NIH HHS
ID : K99 NS117800
Pays : United States

Informations de copyright

© 2022 The Authors. Annals of Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.

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Auteurs

Caleigh Mandel-Brehm (C)

Department of Biochemistry and Biophysics, University of California, San Francisco, CA, USA.

Leslie A Benson (LA)

Department of Neurology, Harvard Medical School, Boston, MA, USA.

Baouyen Tran (B)

Weill Institute for Neurosciences, Department of Neurology, University of California, San Francisco, CA, USA.

Andrew F Kung (AF)

Department of Biochemistry and Biophysics, University of California, San Francisco, CA, USA.

Sabrina A Mann (SA)

Department of Biochemistry and Biophysics, University of California, San Francisco, CA, USA.

Sara E Vazquez (SE)

Department of Biochemistry and Biophysics, University of California, San Francisco, CA, USA.

Hanna Retallack (H)

Department of Biochemistry and Biophysics, University of California, San Francisco, CA, USA.

Hannah A Sample (HA)

Department of Biochemistry and Biophysics, University of California, San Francisco, CA, USA.

Kelsey C Zorn (KC)

Department of Biochemistry and Biophysics, University of California, San Francisco, CA, USA.

Lillian M Khan (LM)

Department of Biochemistry and Biophysics, University of California, San Francisco, CA, USA.

Lauren M Kerr (LM)

Department of Neurology, Boston Children's Hospital, Boston, MA, USA.

Patrick L McAlpine (PL)

Otolaryngology Head and Neck Surgery Research Division, Stanford University, Stanford, CA, USA.

Lichao Zhang (L)

Chan Zuckerberg Biohub, Stanford, CA, USA.

Frank McCarthy (F)

Chan Zuckerberg Biohub, Stanford, CA, USA.

Joshua E Elias (JE)

Chan Zuckerberg Biohub, Stanford, CA, USA.

Umakanth Katwa (U)

Department of Pulmonary Medicine, Sleep Center, Boston Children's Hospital, Boston, MA, USA.

Christina M Astley (CM)

Division of Endocrinology & Computational Epidemiology, Boston Children's Hospital, Boston, MA, USA.

Stuart Tomko (S)

Department of Neurology, Washington University, St. Louis, MO, USA.

Josep Dalmau (J)

Catalan Institution for Research and Advanced Studies (ICREA), Hospital Clinic-Idibaps, University of Barcelona, Barcelona, Spain.

William W Seeley (WW)

Memory and Aging Center, Department of Neurology, University of California, San Francisco, CA, USA.

Samuel J Pleasure (SJ)

Weill Institute for Neurosciences, Department of Neurology, University of California, San Francisco, CA, USA.

Michael R Wilson (MR)

MAS, Weill Institute for Neurosciences, Department of Neurology, University of California, San Francisco, CA, USA.

Mark P Gorman (MP)

Department of Neurology, Harvard Medical School, Boston, MA, USA.

Joseph L DeRisi (JL)

Chan Zuckerberg Biohub, Department of Biochemistry and Biophysics, University of California, San Francisco, CA, USA.

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Classifications MeSH