Publications

Neuronal intermediate filament paraneoplastic autoimmunity complicating avelumab therapy of Merkel cell carcinoma  (2022)

Authors:
Dinoto, Alessandro; Mckeon, Andrew; Vattemi, Gaetano; Carta, Sara; Ferrari, Sergio; Mariotto, Sara
Title:
Neuronal intermediate filament paraneoplastic autoimmunity complicating avelumab therapy of Merkel cell carcinoma
Year:
2022
Type of item:
Articolo in Rivista
Tipologia ANVUR:
Articolo su rivista
Language:
Inglese
Format:
Elettronico
Referee:
Name of journal:
Journal of Neuroimmunology
ISSN of journal:
0165-5728
N° Volume:
368
Number or Folder:
577882
Page numbers:
1-3
Keyword:
Avelumab; Immune checkpoint inhibitors; Immune-related adverse events; Neuronal intermediate filament; Paraneoplastic neurological syndromes
Short description of contents:
A 67-years-old woman developed subacute oculomotor nerve palsy and cerebellar gait instability while receiving avelumab as immunotherapy for Merkel cell carcinoma. Brain MRI revealed oculomotor nerve T2/FLAIR hyperintensity and contrast enhancement, CSF cell number and protein concentration were slightly increased. Antibodies against intracellular and surface antigens were excluded through commercial assays, but home-made immunohistochemistry on rat brain sections showed a "neurofilament-like" pattern. Antibodies against neuronal intermediate filament (NIF-IgG) were thus tested and resulted positive in both serum and CSF, confirming the diagnosis of NIF-IgG autoimmunity. Avelumab was discontinued and treatment with steroids and intravenous immunoglobulins led to partial improvement.
Web page:
https://doi.org/10.1016/j.jneuroim.2022.577882
Product ID:
126872
Handle IRIS:
11562/1065104
Last Modified:
June 26, 2024
Bibliographic citation:
Dinoto, Alessandro; Mckeon, Andrew; Vattemi, Gaetano; Carta, Sara; Ferrari, Sergio; Mariotto, Sara, Neuronal intermediate filament paraneoplastic autoimmunity complicating avelumab therapy of Merkel cell carcinoma «Journal of Neuroimmunology» , vol. 368 , n. 5778822022pp. 1-3

Consulta la scheda completa presente nel repository istituzionale della Ricerca di Ateneo IRIS

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