2021
DOI: 10.1016/j.addr.2021.04.016
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Prevention of diabetes-associated fibrosis: Strategies in FcRn-targeted nanosystems for oral drug delivery

Abstract: Prevention of diabetes-associated fibrosis: Strategies in FcRn-targeted nanosystems for oral drug delivery, Advanced Drug Delivery Reviews (2021), doi:

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Cited by 14 publications
(6 citation statements)
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References 239 publications
(485 reference statements)
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“…Such a need is not limited to refractory patients but should concern all patients. Most recently, biologics targeting compounds of the immunological system, such as B cells (46-49), pro-inflammatory cytokines (50, 51), and their receptors (52, 53), complement system (54), and Fc neonatal receptor (55)(56)(57), are emerging as promising critical therapeutic tools to provide faster symptoms remission and better corticosteroid-sparing effects than conventional treatments. It is noteworthy that RTX can be tried in patients with MG who have failed to respond to glucocorticoid and conventional immunosuppressive drug therapy (Class IV evidence), especially in patients with MusK-MG (58).…”
Section: Discussionmentioning
confidence: 99%
“…Such a need is not limited to refractory patients but should concern all patients. Most recently, biologics targeting compounds of the immunological system, such as B cells (46-49), pro-inflammatory cytokines (50, 51), and their receptors (52, 53), complement system (54), and Fc neonatal receptor (55)(56)(57), are emerging as promising critical therapeutic tools to provide faster symptoms remission and better corticosteroid-sparing effects than conventional treatments. It is noteworthy that RTX can be tried in patients with MG who have failed to respond to glucocorticoid and conventional immunosuppressive drug therapy (Class IV evidence), especially in patients with MusK-MG (58).…”
Section: Discussionmentioning
confidence: 99%
“…In contrast, a reasonably evident transcytosis mediated by the neonatal Fc receptor (FcRn, which can bind to the Fc domain of immunoglobulin G (IgG) or albumin) has the potential to enhance the bioavailability of orally delivered drugs. [ 144 , 145 ] FcRn is expressed on the epithelium. As a result, nanomaterials containing the Fc component of IgG or albumin bind FcRn at the apical surface of epithelial cells.…”
Section: Nanomaterials For Diabetes Prevention and Therapymentioning
confidence: 99%
“…These bound ligands are subsequently transcytosed via endosomes and released outside cells at physiological pH. 18 Therefore, FcRn can form strong bonds in the acidic small intestine, where most drugs are absorbed. 19 Also, in mice with hFcRn transgenes, human serum albumin (HSA) migrates more efficiently than human immunoglobulin G (hIgG) through mucosal lung barriers in vivo.…”
Section: Introductionmentioning
confidence: 99%
“…Substances with Fc portions of IgG or albumin can beneficially engage FcRn at the apical surface of epithelial cells, preventing lysosomal degradation. These bound ligands are subsequently transcytosed via endosomes and released outside cells at physiological pH . Therefore, FcRn can form strong bonds in the acidic small intestine, where most drugs are absorbed .…”
Section: Introductionmentioning
confidence: 99%