HLA DQA1*05 and Risk of Antitumor Necrosis Factor Treatment Failure and Anti-Drug Antibody Development in Children With Crohn's Disease

In a randomized trial of children with CD initiating anti-TNF, 40% were HLA DQ-A1*05 positive, which was associated with a trend toward increased risk of both treatment failure and ADA. These risks were mitigated, but not eliminated, by adding oral methotrexate. HLA DQ-A1*05 is an important biomarker for prognosis and risk stratification.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2024-10-18
DOI
https://doi.org/10.14309/ajg.0000000000003135
Citations
5
Primary Topic
Inflammatory Bowel Disease
Type
article
Field-Weighted Citation Impact
2.75

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article

HLA DQA1*05 and Risk of Antitumor Necrosis Factor Treatment Failure and Anti-Drug Antibody Development in Children With Crohn's Disease

Rana Ammoury, Traci Jester, Jillian S. Sullivan, Michael D. Kappelman et al.
5 citations
The American Journal of Gastroenterology
Inflammatory Bowel Disease
2.75
article

HLA DQA1*05 and Risk of Antitumor Necrosis Factor Treatment Failure and Anti-Drug Antibody Development in Children With Crohn's Disease

Rana Ammoury, Traci Jester, Jillian S. Sullivan, Michael D. Kappelman, Ann M. Firestine, Charles M. Samson, Jennifer Strople, Zarela Molle‐Rios, Steven J. Steiner, Jonathan Moses, Kelly Sandberg, Dinesh S. Pashankar, Jess L. Kaplan, Prateek Wali, Ian Leibowitz, Kelly Olano, Ajay Gulati, Tiffany M. Linville, Peter A. Margolis, Shehzad A. Saeed, Phillip Minar, Athos Bousvaros, Dawn R. Ebach, Jill Dorsey, Joseph A. Galanko, Hans Herfarth, Brendan Boyle, Keith Benkov, Lisa Pitch, Kelly Chun, Jeremy Adler, José Cabrera
article en
5 citations

Abstract

In a randomized trial of children with CD initiating anti-TNF, 40% were HLA DQ-A1*05 positive, which was associated with a trend toward increased risk of both treatment failure and ADA. These risks were mitigated, but not eliminated, by adding oral methotrexate. HLA DQ-A1*05 is an important biomarker for prognosis and risk stratification.

The American Journal of GastroenterologyVol. 120(5)
University of Vermont (US), University of North Carolina at Chapel Hill (US), University of Iowa (US), Cincinnati Children's Hospital Medical Center (US), Boston Children's Hospital (US), Lurie Children's Hospital (US), Nationwide Children's Hospital (US), Children's National (US), Harvard University (US), George Washington University (US), Wright State University (US), SUNY Upstate Medical University (US), Medical College of Wisconsin (US), Washington University in St. Louis (US), University of Michigan (US), LabCorp (United States) (US), Riley Hospital for Children (US), Children's of Alabama (US), University of Alabama at Birmingham (US), Yale University (US), Massachusetts General Hospital (US), Nemours Children's Health System (US), Michigan Medicine (US), Dayton Children's Hospital (US), Levine Children's Hospital (US), Children's Hospital of The King's Daughters (US), Rainbow Babies & Children's Hospital (US), C. S. Mott Children's Hospital (US), Nemours Children's Clinic (US), Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US), University of Cincinnati (US), Icahn School of Medicine at Mount Sinai (US)
Patient-Centered Outcomes Research Institute, Leona M. and Harry B. Helmsley Charitable Trust
Good health and well-being
Openalex Percentile: Top 9%
Inflammatory Bowel Disease
2.75
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