2023
DOI: 10.1155/2023/1769290
|View full text |Cite
|
Sign up to set email alerts
|

New-Onset Crohn’s Disease following Initiation of Secukinumab: A Case Report and Review of the Role of IL-17 in the Pathogenesis of Crohn’s Disease

Abstract: Patients with autoimmune conditions show a high expression of proinflammatory cytokines including interleukin (IL)-17. While IL-17 inhibitors have demonstrated efficacy in managing autoimmune disorders, rare instances of de novo or exacerbated inflammatory bowel disease (IBD) have been reported. The factors that affect the onset and severity remain unclear. Here, we present a case of a 38-year-old female who developed manifestations of Crohn’s disease within 1 month of initiating secukinumab treatment for psor… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
2
0

Year Published

2023
2023
2023
2023

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 11 publications
0
2
0
Order By: Relevance
“…Within this context, other cytokines such as IL-1, IL-6, IL-23, and transforming growth factor-beta (TGF-β) contribute to the differentiation of a Th17 profile during the antigen presentation process among a subset of immature lymphocytes[ 27 ]. These cells are responsible for synthesizing IL-17, which stimulates the migration and activity of neutrophils, thereby promoting a more inflammatory environment, along with T regulatory (T-reg) cells[ 27 , 28 ]. Furthermore, the high levels of IL-17 present in the tissues affected by CD can act on the intestinal epithelium, triggering the release of chemokines that further enhance the chemotaxis of inflammatory agents[ 28 , 29 ].…”
Section: Pathophysiology and Crohn’s Disease Immunologymentioning
confidence: 99%
See 1 more Smart Citation
“…Within this context, other cytokines such as IL-1, IL-6, IL-23, and transforming growth factor-beta (TGF-β) contribute to the differentiation of a Th17 profile during the antigen presentation process among a subset of immature lymphocytes[ 27 ]. These cells are responsible for synthesizing IL-17, which stimulates the migration and activity of neutrophils, thereby promoting a more inflammatory environment, along with T regulatory (T-reg) cells[ 27 , 28 ]. Furthermore, the high levels of IL-17 present in the tissues affected by CD can act on the intestinal epithelium, triggering the release of chemokines that further enhance the chemotaxis of inflammatory agents[ 28 , 29 ].…”
Section: Pathophysiology and Crohn’s Disease Immunologymentioning
confidence: 99%
“…These cells are responsible for synthesizing IL-17, which stimulates the migration and activity of neutrophils, thereby promoting a more inflammatory environment, along with T regulatory (T-reg) cells[ 27 , 28 ]. Furthermore, the high levels of IL-17 present in the tissues affected by CD can act on the intestinal epithelium, triggering the release of chemokines that further enhance the chemotaxis of inflammatory agents[ 28 , 29 ]. Macrophages and antigen-presenting cells (APC) also contribute to the synthesis of IL-12, IL-6, TGF-β, and IL-23.…”
Section: Pathophysiology and Crohn’s Disease Immunologymentioning
confidence: 99%