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Autoantibodies against the chromosomal passenger protein INCENP found in a patient with Graham Little-Piccardi-Lassueur syndrome.
Rodríguez-Bayona, Beatriz; Ruchaud, Sandrine; Rodríguez, Carmen; Linares, Mario; Astola, Antonio; Ortiz, Manuela; Earnshaw, William C; Valdivia, Manuel M.
Afiliação
  • Rodríguez-Bayona B; Servicio de Inmunología, Hospital Puerta del Mar, 11109 Cádiz, Spain.
  • Ruchaud S; Wellcome Trust Centre for Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3JR, UK.
  • Rodríguez C; Servicio de Inmunología, Hospital Puerta del Mar, 11109 Cádiz, Spain.
  • Linares M; Dermatología, Instituto Social de la Marina, Delegación Provincial de Cádiz, Cádiz, Spain.
  • Astola A; Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, 11510 Puerto Real, Cádiz, Spain.
  • Ortiz M; Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, 11510 Puerto Real, Cádiz, Spain.
  • Earnshaw WC; Wellcome Trust Centre for Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3JR, UK.
  • Valdivia MM; Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, 11510 Puerto Real, Cádiz, Spain.
J Autoimmune Dis ; 4: 1, 2007 Jan 12.
Article em En | MEDLINE | ID: mdl-17222351
ABSTRACT

BACKGROUND:

Graham Little - Piccardi - Lassueur (GLPL) syndrome is a rare dermatosis characterized by scarring alopecia, loss of pubic and axillary hair, and progressive development of variously located follicular papules. We report a first case ever of an autoimmune response in a patient suffering from GLPL syndrome.

METHODS:

Immunofluorescence and immunoblot analysis were used in a variety of cell cultures including human, monkey, hamster, mouse and bovine cells to analyze the presence of autoantibodies in a GLPL patient.

RESULTS:

The autoimmune serum showed a pattern of centromere and spindle microtubule staining resembling that of the chromosomal passenger protein complex. By using a complex of proteins expressed in baculovirus, immunoblot analysis demonstrated that the INCENP protein is a major autoantigen in this patient with GLPL syndrome.

CONCLUSION:

An autoimmune response in GLPL syndrome is reported against the INCENP centromere protein. The occasional development of autoimmunity in GLPL patients could serve as a test in continuing efforts to detect this disease and for a more directed therapy based on the autoantigen response.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Autoimmune Dis Ano de publicação: 2007 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Autoimmune Dis Ano de publicação: 2007 Tipo de documento: Article