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Updated: Aug 23, 2026

Legionella pneumophila Outer Membrane Vesicles: Isolation and Analysis of Their Pro-inflammatory Potential on Macrophages
Published on: February 22, 2017
A case of legionellosis during treatment with a TNFalpha antagonist
Marielle J Wondergem1, Alexandre E Voskuyl, Michiel A van Agtmael
1Department of Internal Medicine, VU University Medical Centre, Amsterdam, The Netherlands.
Abstract:
We report a patient with Legionella pneumophila pneumonia after infliximab therapy for rheumatoid arthritis. Arguments are discussed for an emerging incidence of infections with intracellular microorganisms, granulomatous and non-granulomatous, in patients having received anti-TNFalpha therapy. These discussions consist of clinical and epidemiological data, experimental data in animals, theoretical evidence, and we provide a possible pathogenetic mechanism.
Insights
Infliximab therapy for rheumatoid arthritis may increase the risk of Legionella pneumonia. This suggests a potential rise in intracellular infections following anti-TNFalpha treatment.
Area of Science:
- Immunology
- Infectious Diseases
- Rheumatology
Background:
- Anti-tumor necrosis factor alpha (anti-TNFα) therapies, like infliximab, are used for rheumatoid arthritis.
- These therapies modulate the immune system, potentially increasing susceptibility to infections.
Observation:
- A patient developed Legionella pneumophila pneumonia after receiving infliximab for rheumatoid arthritis.
- This case highlights a potential link between anti-TNFα therapy and specific intracellular infections.
Findings:
- The study discusses an emerging incidence of intracellular microorganism infections (granulomatous and non-granulomatous) in patients treated with anti-TNFα therapy.
- Evidence includes clinical, epidemiological, and experimental data, alongside a proposed pathogenetic mechanism.
Implications:
- Physicians should consider the risk of intracellular infections, including Legionella, in patients on anti-TNFα therapy.
- Further research is warranted to understand and manage infection risks associated with immunomodulatory treatments for autoimmune diseases.
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