Article Text

PDF
Protein kinase Cγ autoimmunity in paraneoplastic cerebellar degeneration and non-small-cell lung cancer
  1. L Sabater1,
  2. L Bataller1,*,
  3. A F Carpentier2,
  4. M L Aguirre-Cruz2,,
  5. A Saiz1,
  6. B Benyahia2,
  7. J Dalmau3,
  8. F Graus1
  1. 1Service of Neurology, Hospital Clinic, and Institut d’ Investigació Biomèdica August Pi i Sunyer (IDIBAPS), Barcelona, Spain
  2. 2Service of Neurology, Hôpital Salpêtrière, Paris, France
  3. 3Department of Neurology, University of Pennsylvania, Philadelphia, PA, USA
  1. Correspondence to:
 F Graus
 Servei de Neurologia, Hospital Clínic, Villarroel 170, Barcelona 08036, Spain; fgraus{at}clinic.ub.es

Abstract

Background: The clinical and immunological profiles of patients with paraneoplastic cerebellar degeneration (PCD) and non-small-cell lung cancer (NSCLC) are not well known.

Objective: To review the clinical and immunological features of patients with PCD, NSCLC and without well-characterised onconeural antibodies.

Methods: The clinical features of nine patients with the diagnosis of classical PCD and NSCLC, included in our archives, were retrospectively reviewed. The presence of antibodies to cerebellar components was determined by immunohistochemistry and immunoblot of rat cerebellum. A cDNA library of human cerebellum was screened with the positive sera to identify the antigen.

Results: Nine patients with PCD and NSCLC were identified. Six patients were men, and the median age at diagnosis of PCD was 63 (range 47–73) years. PCD was completely reversed in two patients, and partially in one, after treatment of the tumour. The serum of one of the patients with PCD showed a unique reactivity with Purkinje cells. The screening of a cerebellar-expression library resulted in the isolation of protein kinase Cγ (PKCγ). PKCγ immunoreactivity was not observed in the serum of 170 patients with non-paraneoplastic neurological syndromes, 27 patients with PCD, no onconeural antibodies and small-cell lung cancer, and 52 patients with NSCLC without paraneoplastic neurological syndromes. The NSCLC from 11 patients without PCD did not express PKCγ at either the RNA or protein level. However, many cells of the NSCLC of the patient with PKCγ antibodies expressed PKCγ.

Conclusion: PCD occurs in patients with NSCLC without typical onconeural antibodies and is associated with immune reactions against key proteins of the Purkinje cells.

  • NSCLC, non-small-cell lung cancer
  • PCD, paraneoplastic cerebellar degeneration
  • PKCγ, protein kinase Cγ
  • SCLC, small-cell lung cancer
  • VGCC, voltage-gated calcium channel

Statistics from Altmetric.com

Footnotes

  • * Present address: Servicio de Neurologia, Hospital “la Fe”, Valencia, Spain

  • Present address: Unidad de Investigación del Sistema Nervioso, Instituto Nacional de Neurología y Neurocirugía, México DF, México

  • Published Online First 26 June 2006

  • See Editorial Commentary, p 1299

  • Funding: This study was supported in part by grants 2001SGR 00387 from Generalitat de Catalunya, PI030028 from Fondo de Investigaciones Sanitarias, Madrid, Spain (to FG), and RO1CA107192 (to JD).

  • Competing interests: None.

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Linked Articles