INVESTIGADORES
RABINOVICH Gabriel Adrian
congresos y reuniones científicas
Título:
CIRCULATING ANTI-GALECTIN-1 ANTIBODIES ARE ASSOCIATED WITH THE SEVERITY OF OCULAR DISEASE IN AUTOIMMUNE AND INFECTIOUS UVEITIS
Autor/es:
C. JUAREZ; M. ROMERO; J.C. MUIÑO; G.A. BIANCO; M. FERRERO; G. RABINOVICH; J.D. LUNA
Lugar:
FLORIDA, USA
Reunión:
Congreso; 2006 ARVO; 2006
Institución organizadora:
ARVO
Resumen:
Circulating AntiGalectin1 Antibodies Are Associated With the Severity of
Ocular Disease in Autoimmune and Infectious Uveitis
C.P. Juarez1, M.D. Romero2, J.C. Muiño3, G.A. Bianco4, M. Ferrero2, G.A.
Rabinovich4 and J.D. Luna5
1 Ophthalmology, Centro, Cordoba, Argentina
2 Laboratory of Immunopathology, LIIDO, Cordoba, Argentina
3 Inmunology, Division Medicina III, Faculty of Medical Sciences, National
University of Córdoba, Cordoba, Argentina
4 Immunogenetics, 1Division of Immunogenetics, Faculty of Medicine, University
of Buenos Aires, Buenos Aires, Argentina
5 Ophthalmology, Fundación Ver, Cordoba, Argentina
Commercial Relationships: C.P. Juarez, None; M.D. Romero, None; J.C. Muiño,
None; G.A. Bianco, None; M. Ferrero, None; G.A. Rabinovich, None; J.D. Luna,
None.
Support: Agencia de Promoción Científica y Tecnológica (PICT 20030513787),
University of Buenos Aires (M091), Wellcome Trust, Fundación Sales, Fundación
Antorchas and Mizutani Foundation for Glycoscience to
Abstract
Purpose: Recent evidence indicates that galectin1 (Gal1), an endogenous lectin
found at sites of immune privilege, plays critical roles on immunoregulation.
Therapeutic administration of Gal1 or its genetic delivery suppresses
inflammation in experimental models of autoimmunity including arthritis and
uveitis. However, the impact of Gal1 in chronic inflammation has not yet been
explored in clinical settings. To investigate the occurrence of circulating
antiGal1 antibodies in patients with autoimmune and infectious uveitis as
potential determinant factors of disease progression.
Methods:IgG, IgE and IgA antiGal1 antibodies were assessed by ELISA and
Western blot in sera from patients with autoimmune (n=47) and infectious (n=15)
uveitis compared to healthy controls (n=30). The frequency of antiGal1
antibodies was examined in patients experiencing progressive or benign
evolution. The ability of antiGal1 antibodies to recognize retinal tissue was
assessed by ELISA, Western blot and immunohistochemistry following elution of
specific antibodies from nitrocellulose filters previously adsorbed with
recombinant Gal1 and further incubated with patient sera.
Results:IgE, IgG and IgA antiGal1 antibodies were increased in sera from
patients with autoimmune uveitis (p<0.001 vs controls), and in toxoplasmic
retinochoroiditis (p< 0.001). The frequency of antiGal1 IgE and IgG antibodies
was associated with progressive disease and poor outcome in autoimmune and
infectious uveitis. Furthermore, antiGal1 antibodies strongly immunoreacted
with retinal cell lysates and recognized several retinal structures mainly
photoreceptors and pigment epithelium in retinal sections.
Conclusions: Antiretinal Gal1 antibodies are associated with the progression
of ocular disease, suggesting their potential use for the followup of patients
with uveitis.
Key Words: uveitis-clinical/animal model uvea autoimmune disease
© 2006, The Association for Research in Vision and Ophthalmology, Inc., all
rights reserved. For permission to reproduce any part of this abstract, contact
the ARVO Office at arvo@arvo.org.