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Record W4407285818 · doi:10.1093/jcag/gwae059.165

A165 IL-6 ENHANCES THE ANTI-COLITIC THERAPEUTIC POTENTIAL OF HUMAN IL-4 POLARIZED MACROPHAGES

2025· article· en· W4407285818 on OpenAlex

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

affAt least one author lists a Canadian institution in the pinned OpenAlex snapshot.
aboutThe title or abstract carries a Canadian signal from the geographic lexicon.

Bibliographic record

VenueJournal of the Canadian Association of Gastroenterology · 2025
Typearticle
Languageen
FieldMedicine
TopicMicroscopic Colitis
Canadian institutionsUniversity of Calgary
Fundersnot available
KeywordsMedicineImmunology

Abstract

fetched live from OpenAlex

Abstract Background Inflammatory bowel disease (IBD) is a group of inflammatory disorders, including Crohn’s disease and ulcerative colitis, that affect the gastrointestinal tract and can significantly impact patients’ quality of life. Forty percent of individuals with IBD are unresponsive to current therapies and a cure remains elusive. Macrophages play key roles in inflammation and tissue repair, with IL-4 treated macrophages, M(IL4)s, exerting an anti-inflammatory effect. We showed that systemic administration of human M(IL4)s reduced disease severity in murine colitis. Interleukin-6 is considered a pro-inflammatory cytokine, the levels of which are increased in IBD gut tissue. Murine studies suggest IL-6 may reinforce an M(IL4) phenotype, raising the possibility, and perhaps challenging dogma, that IL-6 could promote the beneficial effects of M(IL4)s. Therefore, I hypothesize that local tissue signal IL-6 enhances the anti-inflammatory properties of human M(IL4)s. Aims 1. Determine the effect of IL-6 on the phenotype of human M(IL4)s. 2. Determine the effect of IL-6 on M(IL4) function, assessing (a) wound healing capacity and (b) cell death. 3. Compare the efficacy of M(IL4) and M(IL4+IL6) in the DNBS-rag1-/- mouse colitis. Methods M(IL4)s were differentiated from blood monocytes from male and female healthy volunteers and individuals with Crohn’s disease. M(IL4)s ± IL-6 (10 ng/mL; 24h) were assessed for (1) phenotype (mRNA expression) and (2) function. Function was evaluated through testing (a) conditioned medium from M(IL4+IL6)s in an in vitro Caco2 epithelial scratch-wound assay and (b) viability in response to hydrogen peroxide (H2O2) (oxidative stress) via LDH release. (3) M(IL4)s or M(IL4+IL6)s were delivered intraperitoneally (106 cells) and 48h later, rag1-/- mice received 5mg intra-rectal DNBS. Colitis was assessed 72h later. Non-treated M(0) and M(IL6) serve as controls. Results M(IL4)s and M(IL4+IL6)s show similar increased expression of CD206 and CCL18, and decreased CD14 mRNA (n=6-7). Conditioned media from both M(IL4)s and M(IL4+IL6)s promoted a similar degree of epithelial migration in the wound healing assay (n=5). Macrophages from patients had increased susceptibility to H2O2-induced death, which was reduced in the M(IL4+IL6) group (n=6 healthy donors; n=6 Crohn’s). M(IL4+IL6)s were more effective than M(IL4)s in protecting against murine colitis as determined by body weight, colon length and a macroscopic disease score (n=8 mice, 3 exps.). Conclusions IL-6 does not abrogate the M(IL4) phenotype or wound healing capacity and protects the cell from H2O2-induced cytotoxicity. Also, M(IL4+IL6)s have a superior anti-colitic effect when compared to M(IL4)s from the same donor. The data support macrophage transfer to treat colitis and indicate that an element of an inflamed environment can enhance the anti-colitic effect of human M(IL4)s. Funding Agencies CIHRCartier Family Student Research Award in Gastroenterology and Hepatology, Alberta Graduate Excellence Scholarship, Helmsley Grant

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.337
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.006
GPT teacher head0.257
Teacher spread0.251 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it