Intravitreal thalidomide ameliorates inflammation in a model of experimental uveitis induced by BCG

•Intravitreal BCG in sensitized animals induces experimental panuveitis in rabbits.•Treatment with intravitreal thalidomide improves clinical manifestations of uveitis.•Intravitreal thalidomide restores retinal function in uveitis induced by BCG. Uveitis encompasses a heterogeneous and complex group...

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Veröffentlicht in:International immunopharmacology 2020-04, Vol.81, p.106129, Article 106129
Hauptverfasser: Castro, Brenda Fernanda Moreira, Vieira, Lorena Carla, Vasconcelos-Santos, Daniel Vitor, Cenachi, Sarah Pereira de Freitas, Cotta, Oliver Araújo Lacerda, Guerra, Maria Carolina Andrade, Paiva, Mayara Rodrigues Brandão, Silva, Luciana Maria, Silva-Cunha, Armando, Fialho, Sílvia Ligório
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container_title International immunopharmacology
container_volume 81
creator Castro, Brenda Fernanda Moreira
Vieira, Lorena Carla
Vasconcelos-Santos, Daniel Vitor
Cenachi, Sarah Pereira de Freitas
Cotta, Oliver Araújo Lacerda
Guerra, Maria Carolina Andrade
Paiva, Mayara Rodrigues Brandão
Silva, Luciana Maria
Silva-Cunha, Armando
Fialho, Sílvia Ligório
description •Intravitreal BCG in sensitized animals induces experimental panuveitis in rabbits.•Treatment with intravitreal thalidomide improves clinical manifestations of uveitis.•Intravitreal thalidomide restores retinal function in uveitis induced by BCG. Uveitis encompasses a heterogeneous and complex group of conditions characterized by intraocular inflammation, frequently affecting young individuals and representing an important cause of irreversible blindness worldwide. Animal models have been critical to understand etiology and pathogenesis of uveitis, being also employed to assess new therapeutic strategies, preceding human studies. However, there is still a need of developing and studying different models, due to the difficulties in recapitulating all forms of human uveitis effectively. Although corticosteroids are usually the first-line therapy for non-infectious uveitis, their long-term use is limited by potentially serious side effects in all possible delivery routes. Thus, thalidomide, a drug with anti-inflammatory and antiangiogenic properties, was investigated in a novel experimental model of uveitis, induced by Mycobacterium bovis Calmette-Guérin Bacillus (BCG), in rabbits. The experimental protocol consisted of two subcutaneous injections of BCG, followed by two intravitreal injections of the same antigen, inducing panuveitis. Animals were treated with a single intravitreal injection of thalidomide suspension or PBS. Clinical manifestations of uveitis improved after intravitreal thalidomide, involving both anterior and posterior segments. Protein content, N-acetyl-b-glucosaminidase (NAG) and myeloperoxidase (MPO) activities were elevated in ocular tissues after disease induction, further decreasing post-treatment with intravitreal thalidomide. This therapeutic response was also confirmed on ocular electrophysiology, as well as histopathology. This experimental model induced panuveitis in rabbits using a low-cost mycobacterial antigen, with intraocular inflammation subsequently improving after treatment. Intravitreal thalidomide may be a potential alternative to treat intraocular inflammation in corticosteroid-sparing therapies.
doi_str_mv 10.1016/j.intimp.2019.106129
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Uveitis encompasses a heterogeneous and complex group of conditions characterized by intraocular inflammation, frequently affecting young individuals and representing an important cause of irreversible blindness worldwide. Animal models have been critical to understand etiology and pathogenesis of uveitis, being also employed to assess new therapeutic strategies, preceding human studies. However, there is still a need of developing and studying different models, due to the difficulties in recapitulating all forms of human uveitis effectively. Although corticosteroids are usually the first-line therapy for non-infectious uveitis, their long-term use is limited by potentially serious side effects in all possible delivery routes. Thus, thalidomide, a drug with anti-inflammatory and antiangiogenic properties, was investigated in a novel experimental model of uveitis, induced by Mycobacterium bovis Calmette-Guérin Bacillus (BCG), in rabbits. The experimental protocol consisted of two subcutaneous injections of BCG, followed by two intravitreal injections of the same antigen, inducing panuveitis. Animals were treated with a single intravitreal injection of thalidomide suspension or PBS. Clinical manifestations of uveitis improved after intravitreal thalidomide, involving both anterior and posterior segments. Protein content, N-acetyl-b-glucosaminidase (NAG) and myeloperoxidase (MPO) activities were elevated in ocular tissues after disease induction, further decreasing post-treatment with intravitreal thalidomide. This therapeutic response was also confirmed on ocular electrophysiology, as well as histopathology. This experimental model induced panuveitis in rabbits using a low-cost mycobacterial antigen, with intraocular inflammation subsequently improving after treatment. 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Uveitis encompasses a heterogeneous and complex group of conditions characterized by intraocular inflammation, frequently affecting young individuals and representing an important cause of irreversible blindness worldwide. Animal models have been critical to understand etiology and pathogenesis of uveitis, being also employed to assess new therapeutic strategies, preceding human studies. However, there is still a need of developing and studying different models, due to the difficulties in recapitulating all forms of human uveitis effectively. Although corticosteroids are usually the first-line therapy for non-infectious uveitis, their long-term use is limited by potentially serious side effects in all possible delivery routes. Thus, thalidomide, a drug with anti-inflammatory and antiangiogenic properties, was investigated in a novel experimental model of uveitis, induced by Mycobacterium bovis Calmette-Guérin Bacillus (BCG), in rabbits. The experimental protocol consisted of two subcutaneous injections of BCG, followed by two intravitreal injections of the same antigen, inducing panuveitis. Animals were treated with a single intravitreal injection of thalidomide suspension or PBS. Clinical manifestations of uveitis improved after intravitreal thalidomide, involving both anterior and posterior segments. Protein content, N-acetyl-b-glucosaminidase (NAG) and myeloperoxidase (MPO) activities were elevated in ocular tissues after disease induction, further decreasing post-treatment with intravitreal thalidomide. This therapeutic response was also confirmed on ocular electrophysiology, as well as histopathology. This experimental model induced panuveitis in rabbits using a low-cost mycobacterial antigen, with intraocular inflammation subsequently improving after treatment. 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Uveitis encompasses a heterogeneous and complex group of conditions characterized by intraocular inflammation, frequently affecting young individuals and representing an important cause of irreversible blindness worldwide. Animal models have been critical to understand etiology and pathogenesis of uveitis, being also employed to assess new therapeutic strategies, preceding human studies. However, there is still a need of developing and studying different models, due to the difficulties in recapitulating all forms of human uveitis effectively. Although corticosteroids are usually the first-line therapy for non-infectious uveitis, their long-term use is limited by potentially serious side effects in all possible delivery routes. Thus, thalidomide, a drug with anti-inflammatory and antiangiogenic properties, was investigated in a novel experimental model of uveitis, induced by Mycobacterium bovis Calmette-Guérin Bacillus (BCG), in rabbits. The experimental protocol consisted of two subcutaneous injections of BCG, followed by two intravitreal injections of the same antigen, inducing panuveitis. Animals were treated with a single intravitreal injection of thalidomide suspension or PBS. Clinical manifestations of uveitis improved after intravitreal thalidomide, involving both anterior and posterior segments. Protein content, N-acetyl-b-glucosaminidase (NAG) and myeloperoxidase (MPO) activities were elevated in ocular tissues after disease induction, further decreasing post-treatment with intravitreal thalidomide. This therapeutic response was also confirmed on ocular electrophysiology, as well as histopathology. This experimental model induced panuveitis in rabbits using a low-cost mycobacterial antigen, with intraocular inflammation subsequently improving after treatment. Intravitreal thalidomide may be a potential alternative to treat intraocular inflammation in corticosteroid-sparing therapies.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>32018067</pmid><doi>10.1016/j.intimp.2019.106129</doi></addata></record>
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subjects Animal models
Animal-model
Animals
Anti-Inflammatory Agents - therapeutic use
Antiangiogenics
Antigens
Autoimmune Diseases - drug therapy
Bacillus Calmette-Guerin vaccine
BCG
Blindness
Corticoids
Corticosteroids
Drug delivery systems
Electrophysiology
Etiology
Eye
Glucosaminidase
Health services
Histopathology
Humans
Inflammation
Intravitreal Injections
Medical treatment
Models, Animal
Mycobacterium bovis - immunology
Panuveitis - drug therapy
Panuveitis - immunology
Pathogenesis
Peroxidase
Peroxidase - metabolism
Rabbits
Retina - drug effects
Retina - metabolism
Retina - pathology
Side effects
Thalidomide
Thalidomide - therapeutic use
Uveitis
Uveitis - drug therapy
title Intravitreal thalidomide ameliorates inflammation in a model of experimental uveitis induced by BCG
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