Cure8

Why This Matters

Perianal fistulizing Crohn's disease is a frequent, hard-to-treat complication; molecular and multiomic advances could lead to biomarkers that help choose better-targeted therapies and improve surgical–medical decision making.

Who Should Pay Attention

Patients with perianal Crohn's disease, gastroenterologists, colorectal surgeons, and researchers in IBD biology and biomarker development.

Study Snapshot

Story typeResearch paper
Evidence typeResearch paper
Source depthJournal abstract

What To Know

This is a review article (abstract-level content available) that synthesizes recent single-cell, spatial, and multiomic studies of fistula tissue and rectal mucosa.

The authors discuss how immune, stromal, epithelial, and microbial features identified by these methods expand understanding of PFCD biology and may enable biomarker development to stratify patients for different therapies.

The review also critically examines current and emerging pharmacological approaches and highlights the need to integrate molecular biomarkers with anatomical phenotype, surgical context, and standardized, multidimensional outcome measures for fistula healing.

Because the available content is an abstract, the brief summarizes the review's scope rather than detailed findings or specific biomarker candidates.

Keep In Mind

This entry is an abstract-level review on PubMed summarizing recent single-cell, spatial, and multiomic studies; it synthesizes existing research rather than reporting new trial results. Full-text review is needed for specific biomarker candidates or therapy recommendations.

Source Details

Review the original publication for the complete reporting, methods, and context.

Read Original Source
Research paper Evidence type derived from source or registry metadata.
PublicationTrends in pharmacological sciences
AuthorsVirginia Solitano, Lorenzo Bertani, Clelia Di Salvo +2 more
InstitutionDivision of Gastroenterology and Gastrointestinal Endoscopy, IRCCS Ospedale San Raffaele, Milan, Italy; Università Vita-Salute San Raffaele, Milan, Italy; Department of Epidemiology and Biostatistics, Western University, London, Ontario, Canada.
Study typeJournal article, review
Indexed viaPubMed
Source typeResearch paper
PublishedOct 20, 2026, 12:00 AM
Content availableJournal abstract

Conflict statement: Declaration of interests V.S. declares consulting fees from Janssen and Celltrion; speaker’s fees from Pfizer, Takeda, Giuliani, and Tillotts; travel grant from Eli Lilly and AbbVie. L.B. has received lecture fees, consultancy fees, or advisory board honoraria from AbbVie, Aliveda, Bromatech, Celltrion, Eli Lilly, Ferring, Johnson & Johnson, Giuliani, Italfarmaco, Lionhealth, Malesci, Noos, Novo Nordisk, PharmExtracta, PharmaNutra, Pfizer, Schwabe Pharma, and Takeda. L.A. has received lecture fees, consultancy fees, or advisory board honoraria from Alfasigma, Celltrion, Eli Lilly, Johnson & Johnson, and UCB. The other authors declare no competing interests.

This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.

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