Video: Every Case Tells a Story| Webinar: ACR/CHEST ILD Guidelines in Practice

An official publication of the ACR and the ARP serving rheumatologists and rheumatology professionals

  • Conditions
    • Axial Spondyloarthritis
    • Gout and Crystalline Arthritis
    • Myositis
    • Osteoarthritis and Bone Disorders
    • Pain Syndromes
    • Pediatric Conditions
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Sjögren’s Disease
    • Systemic Lupus Erythematosus
    • Systemic Sclerosis
    • Vasculitis
    • Other Rheumatic Conditions
  • FocusRheum
    • ANCA-Associated Vasculitis
    • Axial Spondyloarthritis
    • Gout
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Systemic Lupus Erythematosus
  • Guidance
    • Clinical Criteria/Guidelines
    • Ethics
    • Legal Updates
    • Legislation & Advocacy
    • Meeting Reports
      • ACR Convergence
      • Other ACR meetings
      • EULAR/Other
    • Research Rheum
  • Drug Updates
    • Analgesics
    • Biologics/DMARDs
  • Practice Support
    • Billing/Coding
    • EMRs
    • Facility
    • Insurance
    • QA/QI
    • Technology
    • Workforce
  • Opinion
    • Patient Perspective
    • Profiles
    • Rheuminations
      • Video
    • Speak Out Rheum
  • Career
    • ACR ExamRheum
    • Awards
    • Career Development
  • ACR
    • ACR Home
    • ACR Convergence
    • ACR Guidelines
    • Journals
      • ACR Open Rheumatology
      • Arthritis & Rheumatology
      • Arthritis Care & Research
    • From the College
    • Events/CME
    • President’s Perspective
  • Search

Increased Risk of Serious Infections During Early Anti-TNF Treatment

Will Boggs, MD  |  June 16, 2015

NEW YORK (Reuters Health)—The risk of serious infections increases in the early months of anti-TNF treatment for inflammatory bowel disease, researchers from Denmark report.

“The pro-inflammatory cytokine TNF-alpha plays an important role in the immune system and therefore it is biologically plausible that TNF-alpha inhibitors may increase the risk of infections,” said Dr. Nynne Nyboe Andersen from Statens Serum Institute in Copenhagen.

ad goes here:advert-1
ADVERTISEMENT
SCROLL TO CONTINUE

“Our findings of an increased risk of infections in the early phase after treatment initiation and a subsequent decline in risk are in accordance with other studies based on people with rheumatoid arthritis,” she told Reuters Health by email.

For their study, online June 5 in BMJ, Dr. Andersen’s team used data from linked Danish registries on nearly 52,400 people with inflammatory bowel disease, among whom 4,300 were treated with TNF-alpha inhibitors.

ad goes here:advert-2
ADVERTISEMENT
SCROLL TO CONTINUE

The risk of serious infections in the first 90 days of treatment increased by 63%, from an incidence of 9 per 100 person-years among nonusers to an incidence of 14 per 100 person-years among anti-TNF-alpha users, the researchers found.

The increased risk was limited to women, whose risk increased 2.08-fold.

The risk of serious infection over the first 365 days, however, was not significantly different between TNF-alpha inhibitor users and nonusers.

In matched analyses, the use of TNF-alpha inhibitors was associated with an 81% higher risk of serious infections in the first 90 days of treatment and a 52% increased risk of serious infections in the first 365 days of treatment.

“It is important to stress that the benefit of TNF-alpha inhibitor treatment in people with inflammatory bowel disease is unquestionable,” Dr. Andersen concluded. “However, our findings call for a clinical awareness of potential infectious complications among people using these drugs, particularly early in the course of treatment.”

Dr. Andersen added, “We would like to point out that the study’s ability to conclude on specific infections and on different TNF-alpha inhibitors separately was limited because of power issues and should be assessed in future even larger-scale population-based studies.”

Dr. Julio Maria Fonseca Chebli from Inflammatory Bowel Disease Center, Federal University of Juiz de Fora in Brazil, said, “All physicians who use TNF-alpha inhibitors must have in their mind that a strict evaluation must be done about patient’s immunity in reference to those infections that are more frequent in such circumstances, including tuberculosis, influenza, hepatitis B and C, pneumonia, and others, if appropriate vaccines are not employed before beginning treatment.”

Page: 1 2 | Single Page
Share: 

Filed under:ConditionsDrug UpdatesOther Rheumatic Conditions Tagged with:anti-TNF agentInfectioninflammationinflammatory bowel disease

Related Articles

    TNF Blockade for SLE

    September 1, 2010

    Reckless approach versus missed opportunity?

    Treating IBD with Anti-TNF Tied to Higher Risk of Demyelinating Disease

    October 9, 2015

    NEW YORK (Reuters Health)—Treating inflammatory bowel disease (IBD) with tumor necrosis factor (TNF) inhibitors is associated with a doubling of the risk of central nervous system demyelinating disease, researchers from Denmark report. “Based on the current evidence anti-TNF should be used cautiously in patients with an own or family history of demyelinating disease,” Dr. Nynne…

    Are We Playing It Safe?

    October 1, 2010

    Tumor necrosis factor alpha inhibition and the risk of solid malignancies

    Skin Exam Advised Before Anti-TNF-Alpha Therapy

    January 16, 2018

    NEW YORK (Reuters Health)—Using tumor necrosis factor alpha (TNF-alpha) inhibitors for atypical dermatoses may unmask, or perhaps even worsen, cutaneous lymphoma, according to new research. “Our findings suggest that careful skin examination might be required in all patients prescribed anti-TNF-alpha agents, especially those with atypical presentations of benign skin conditions,” says Dr. Joan Guitart of…

  • About Us
  • Meet the Editors
  • Issue Archives
  • Contribute
  • Advertise
  • Contact Us
  • Copyright © 2025 by John Wiley & Sons, Inc. All rights reserved, including rights for text and data mining and training of artificial technologies or similar technologies. ISSN 1931-3268 (print). ISSN 1931-3209 (online).
  • DEI Statement
  • Privacy Policy
  • Terms of Use
  • Cookie Preferences