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Adv Exp Med Biol ; 703: 151-62, 2010.
Artigo em Inglês | MEDLINE | ID: mdl-20711713

RESUMO

The effect of complement depletion with humanized cobra venom factor (CVF) on retinal lesion development/neovascularization was determined in a mouse model of wet age-related macular degeneration (AMD). Mice were treated with the humanized CVF protein HC3-1496 prior to, and once daily for 28 days after laser coagulation surgery of the retina. CVF transgenic mice exhibiting permanently low levels of serum complement activity and PBS-treated mice served as positive and negative controls, respectively. Fluorescein isothiocyanate (FITC)-dextran funduscopy after laser surgery indicated the presence of lesions in all mice that underwent laser surgery. In HC3-1496-treated mice as well as CVF transgenic mice smaller lesions were seen after 8 days. Measurement of lesion sizes by histopathological examination of eyes after 28 days revealed a significant reduction of lesion area and volume in both HC3-1496-treated animals and CVF transgenic animals compared to PBS-treated control animals. Systemic complement depletion with a complement depletor, such as the humanized CVF protein HC3-1496, represents a promising therapeutic concept for patients with wet AMD.


Assuntos
Inativadores do Complemento/farmacologia , Venenos Elapídicos/farmacologia , Degeneração Macular Exsudativa/tratamento farmacológico , Animais , Complemento C3/genética , Modelos Animais de Doenças , Venenos Elapídicos/genética , Humanos , Camundongos , Camundongos Endogâmicos BALB C , Camundongos Endogâmicos C57BL , Camundongos Transgênicos , Proteínas Recombinantes de Fusão/genética , Degeneração Macular Exsudativa/imunologia , Degeneração Macular Exsudativa/patologia , Degeneração Macular Exsudativa/cirurgia
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