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dc.date.accessioned 2020-10-28T16:11:56Z
dc.date.available 2020-10-28T16:11:56Z
dc.date.issued 2020
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/107870
dc.description.abstract Purpose: Proteases play an essential role in the pathophysiology of inflammatory bowel disease (IBD), contributing to the intestinal mucosal lesions through the degradation of the extracellular matrix and alteration of the barrier function. Ulcerative colitis (UC) is characterized by an extensive infiltrate of neutrophils into the mucosa and hence, increased proteolytic activity. Human neutrophil elastase (HNE) is a serine protease that has been reported to be increased in UC patients’ intestinal mucosa. Based on our previous studies, we hypothesized that HNE might induce proteolytic degradation and loss of function of therapeutic monoclonal antibodies in IBD patients. Patients and Methods: Elastase expression and elastinolytic activity were determined in mucosal explants from ulcerative colitis patients (n=6) and cultured ex vivo in the presence or absence of recombinant elafin. Enzymatic digestions of therapeutic monoclonal antibodies were performed using recombinant HNE and elafin. The integrity of the therapeutic antibodies was evaluated by immunoblotting and protein G binding assay, whereas their TNFneutralizing activity was assessed with a reporter cell line. Results: We found that HNE and its elastinolytic activity were increased in the gut mucosa of UC patients. We also demonstrated that HNE cleaved biological drugs, impairing the TNF-α neutralizing capacity of anti-TNF monoclonal antibodies. This proteolytic degradation was inhibited by the addition of the specific inhibitor, elafin. Conclusion: Our results suggest that the high level of proteolytic degradation by mucosal neutrophil elastase, along with a potential imbalance with elafin, contributes to the loss of function of biologic agents, which are currently used in patients with IBD. These findings might explain the non-responsiveness of UC patients to therapeutic monoclonal antibodies and suggest the potential beneficial concomitant use of elafin in this treatment. en
dc.format.extent 233-243 es
dc.language en es
dc.subject elastinolytic activity es
dc.subject elafin es
dc.subject anti-TNF es
dc.subject inflammatory bowel disease es
dc.subject biological drugs es
dc.title Human Neutrophil Elastase Proteolytic Activity in Ulcerative Colitis Favors the Loss of Function of Therapeutic Monoclonal Antibodies en
dc.type Articulo es
sedici.identifier.uri http://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC7251227&blobtype=pdf es
sedici.identifier.uri https://www.dovepress.com/human-neutrophil-elastase-proteolytic-activity-in-ulcerative-colitis-f-peer-reviewed-article-JIR es
sedici.identifier.other pmid:32547155 es
sedici.identifier.other pmcid:PMC7251227 es
sedici.identifier.other http://dx.doi.org/10.2147/jir.s234710 es
sedici.identifier.issn 1178-7031 es
sedici.creator.person Curciarello, Renata es
sedici.creator.person Sobande, Toni es
sedici.creator.person Jones, Samantha es
sedici.creator.person Giuffrida, Paolo es
sedici.creator.person Di Sabatino, Antonio es
sedici.creator.person Docena, Guillermo Horacio es
sedici.creator.person MacDonald, Thomas T. es
sedici.creator.person Kok, Klaartje es
sedici.subject.materias Ciencias Exactas es
sedici.subject.materias Ciencias Médicas es
sedici.description.fulltext true es
mods.originInfo.place Facultad de Ciencias Exactas es
mods.originInfo.place Instituto de Estudios Inmunológicos y Fisiopatológicos es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc/3.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Journal of Inflammation Research es
sedici.relation.journalVolumeAndIssue vol. 13 es


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Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)