Respiratory infections associated with anti-TNFα agents

E Blanchard1, M-E Truchetet2, I Machelart3

  • 1Service des maladies respiratoires, hôpital Haut-Lévêque, CHU de Bordeaux, 1, avenue Magellan, 33604 Pessac cedex, France.

Insights

Anti-tumor necrosis factor alpha (TNFα) therapies can increase the risk of severe respiratory infections, especially within six months of starting treatment. Proactive screening and preventive measures are crucial for immunocompromised patients.

Area of Science:

  • Immunology
  • Infectious Diseases
  • Rheumatology

Background:

  • Anti-tumor necrosis factor alpha (TNFα) agents are effective for inflammatory, rheumatologic, dermatologic, and gastrointestinal diseases.
  • Patients on anti-TNFα therapy are immunocompromised due to underlying conditions and other immunosuppressants, complicating infection risk assessment.
  • Severe respiratory infections, including bacterial and fungal, are significant complications.

Purpose of the Study:

  • To evaluate the risk of severe respiratory tract infections in patients treated with anti-TNFα agents.
  • To identify specific pathogens and risk factors associated with these infections.
  • To emphasize the need for preventive strategies.

Main Methods:

  • Review of reported cases and incidence rates of infections in patients receiving anti-TNFα therapy.
  • Analysis of pathogen types, including bacteria, Mycobacterium tuberculosis, Legionella, and fungi.
  • Assessment of risk factors such as treatment type (monoclonal antibodies vs. soluble receptor) and duration of therapy.

Main Results:

  • An increased risk of infection is observed, particularly within the first six months of anti-TNFα therapy.
  • Monoclonal anti-TNFα antibodies are associated with a higher risk than soluble TNFα receptor agents.
  • Common pathogens include pyogenic bacteria, Mycobacterium tuberculosis (reactivation), Legionella pneumophila, and opportunistic fungi like Histoplasma, Aspergillus, and Pneumocystis.

Conclusions:

  • Anti-TNFα therapy necessitates careful evaluation of individual infection risk based on comorbidities and concomitant treatments.
  • Systematic screening for tuberculosis and chemoprophylaxis are warranted before initiating anti-TNFα therapy.
  • Empirical antibiotic coverage for Legionella should be considered for pneumonia in this patient population.

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