Epithelial Cell Biomarkers Are Predictive of Response to Biologic Agents in Crohn’s Disease

Author:

Osterman Mark T1,VanDussen Kelli L2,Gordon Ilyssa O3,Davis Elisabeth M4,Li Katherine5,Simpson Kate6,Ciorba Matthew7,Glover Sarah C8,Abraham Bincy9,Guo Xueyan4,Yee Eric U10,Allard Felicia D10,Perrigoue Jacqueline G5,Claggett Brian11,Shen Bo12,Stappenbeck Thaddeus S613,Liu Julia J4ORCID

Affiliation:

1. Division of Gastroenterology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA

2. Divisions of Gastroenterology, Hepatology, and Nutrition and of Developmental Biology, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH, USA

3. Department of Pathology, Cleveland Clinic Foundation, Cleveland, OH, USA

4. Division of Gastroenterology and Hepatology, University of Arkansas for Medical Sciences, Little Rock, AR, USA

5. Janssen Research and Development, Spring House, PA, USA

6. Departments of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, USA

7. Division of Gastroenterology and Hepatology, Washington University School of Medicine, St. Louis, MO, USA

8. Division of Gastroenterology and Hepatology, University of Florida, Gainesville, FL, USA

9. Division of Gastroenterology and Hepatology, Houston Methodist Hospital, Houston, TX, USA

10. Department of Pathology, University of Arkansas for Medical Sciences, Little Rock, AR, USA

11. Department of Medicine, Brigham and Women’s Hospital, Boston, MA, USA

12. Department of Gastroenterology, Hepatology, and Nutrition, Cleveland Clinic Foundation, Cleveland, OH, USA

13. Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA

Abstract

Abstract Background Therapeutic efficacy of biologics has remained at about 50% for 2 decades. In Crohn’s disease (CD) patients, we examined the predictive value of an epithelial cell biomarker, ileal microvillar length (MVL), for clinical response to ustekinumab (UST) and vedolizumab (VDZ) and its relationship to another biomarker, intestinal epithelial cell (IEC) pyroptosis, with respect to response to VDZ. Method Ileal biopsies from the UNITI-2 randomized controlled trial were analyzed for MVL as a predictor of clinical response to UST. In a 5-center academic retrospective cohort of CD patients, ileal MVL was analyzed to determine its predictive value for response to VDZ. Correlation between ileal MVL and IEC pyroptosis was determined, and the discriminant ability of the combination of 2 biomarkers to VDZ was examined. Results Clinical response in UST was significantly higher than placebo (65% vs 39%; P = 0.03), with patients with normal MVL (>1.7 µm) having the greatest therapeutic effect: 85% vs 20% (P = 0.02). For VDZ, clinical response with MVL of 1.35 to 1.55 µm was 82% vs 44% (<1.35 µm) and 40% (>1.55 µm; P = 0.038). There was no correlation between ileal MVL and IEC pyroptosis. The combination criteria of ileal pyroptosis <14 positive cells/1000 IECs or MVL of 1.35 to 1.55 µm could identify 84% of responders and 67% of nonresponders (P = 0.001). Conclusion Ileal MVL was predictive of response to UST and VDZ in prospective and retrospective CD cohorts. It was independent of ileal IEC pyroptosis, and combination of the 2 biomarkers enhanced the discriminate ability of responders from nonresponders to VDZ.

Funder

Janssen Discovery LLC

Takeda Pharmaceutical Company

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,Immunology and Allergy

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