Document details

Drug targeting of inflammatory bowel diseases by biomolecules

Author(s): Antunes, Joana Isabel Costa ; Seabra, Catarina Leal ; Domingues, Joana Margarida ; Teixeira, Marta Oliveira ; Nunes, Cláudia ; Costa-Lima, Sofia Antunes ; Homem, Natália Cândido ; Reis, Salette ; Amorim, M. T. Pessoa de ; Felgueiras, Helena Prado

Date: 2021

Persistent ID: https://hdl.handle.net/1822/74156

Origin: RepositóriUM - Universidade do Minho

Subject(s): Biologics; Gut dysbiosis; Infection; Microbiota; Crohn’s disease; Ulcerative colitis; Treatment; Polymeric nanoparticles


Description

Inflammatory bowel disease (IBD) is a group of disabling, destructive and incurable immune-mediated inflammatory diseases comprising Crohn's disease (CD) and ulcerative colitis (UC), disorders that are highly prevalent worldwide and demand a large investment in healthcare. A persistent inflammatory state enables the dysfunction and destruction of healthy tissue, hindering the initiation and endurance of wound healing. Current treatments are ineffective at counteracting disease progression. Further, increased risk of serious side effects, other comorbidities and/or opportunistic infections highlight the need for effective treatment options. Gut microbiota, the key to preserving a healthy state, may, alternatively, increase a patient's susceptibility to IBD onset and development given a relevant bacterial dysbiosis. Hence, the main goal of this review is to showcase the main conventional and emerging therapies for IBD, including microbiota-inspired untargeted and targeted approaches (such as phage therapy) to infection control. Special recognition is given to existing targeted strategies with biologics (via monoclonal antibodies, small molecules and nucleic acids) and stimuli-responsive (pH-, enzyme- and reactive oxygen species-triggered release), polymer-based nanomedicine that is specifically directed towards the regulation of inflammation overload (with some nanosystems additionally functionalized with carbohydrates or peptides directed towards M1-macrophages). The overall goal is to restore gut balance and decrease IBD's societal impact.

Document Type Journal article
Language English
Contributor(s) Universidade do Minho
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