Evidence map›Paper›PMID 36795280›Full record

ReviewEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2023

The use of TNF-α antagonists in tuberculosis to control severe paradoxical reaction or immune reconstitution inflammatory syndrome: a case series and literature review.

Lucas Armange, Adèle Lacroix, Paul Petitgas, Cédric Arvieux, Caroline Piau-Couapel, Patrice Poubeau, Matthieu Revest, Pierre Tattevin

Open access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
8.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  7. Disseminated PrimaryCase reports in infectious diseases · 2026
    Article
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  20. Therapeutic advances in neuroinfectious diseases.Therapeutic advances in infectious disease
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Lucas ArmangeInfectious Diseases and Intensive Care Unit, Pontchaillou University Hospital, F-35033, Rennes, France.
Adèle LacroixInfectious Diseases, General Hospital, Avignon, France.
Paul PetitgasInfectious Diseases and Intensive Care Unit, Pontchaillou University Hospital, F-35033, Rennes, France.
Cédric ArvieuxInfectious Diseases and Intensive Care Unit, Pontchaillou University Hospital, F-35033, Rennes, France.
Caroline Piau-CouapelMicrobiology, Pontchaillou University Hospital, Rennes, France.
Patrice PoubeauInfectious Diseases, Saint-Pierre Hospital, Saint-Pierre, La Réunion, France.
Matthieu RevestInfectious Diseases and Intensive Care Unit, Pontchaillou University Hospital, F-35033, Rennes, France.
Pierre TattevinInfectious Diseases and Intensive Care Unit, Pontchaillou University Hospital, F-35033, Rennes, France. pierre.tattevin@chu-rennes.fr.ORCID http://orcid.org/0000-0003-3617-5411
Hôpital Pontchaillou · FRPeuplements végétaux et bioagresseurs en milieu tropical · REUniversité d'Avignon et des Pays de Vaucluse · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paradoxical reaction (PR) and immune reconstitution inflammatory syndrome (IRIS) are common complications of tuberculosis treatment. Corticosteroids are first-line treatment for severe PR or IRIS, particularly neurological. We report four cases of severe PR or IRIS during tuberculosis treatment who required TNF-α antagonists, and identified 20 additional cases through literature review. They were 14 women and 10 men, with a median age of 36 years (interquartile range, 28-52). Twelve were immunocompromised before tuberculosis: untreated HIV infection (n=6), or immunosuppressive treatment (TNF-α antagonists, n=5; tacrolimus, n=1). Tuberculosis was mostly neuromeningeal (n=15), pulmonary (n=10), lymph node (n=6), and miliary (n=6), multi-susceptible in 23 cases. PR or IRIS started after a median time of 6 weeks (IQR, 4-9) following anti-tuberculosis treatment start, and consisted primarily of tuberculomas (n=11), cerebral vasculitis (n=8), and lymphadenitis (n=6). First-line treatment of PR or IRIS was high-dose corticosteroids in 23 cases. TNF-α antagonists were used as salvage treatment in all cases, with infliximab (n=17), thalidomide (n=6), and adalimumab (n=3). All patients improved, but 6 had neurological sequelae, and 4 had TNF-α antagonist-related severe adverse events. TNF-α antagonists are safe and effective as salvage or corticosteroid-sparing therapeutic for severe PR or IRIS during tuberculosis treatment.

Indexed as

HIV InfectionsImmune Reconstitution Inflammatory SyndromeTuberculosisTumor Necrosis Factor InhibitorsAdrenal Cortex HormonesAdultFemaleHumansMaleMiddle AgedAdrenal Cortex HormonesTumor Necrosis Factor InhibitorsImmune reconstitution inflammatory syndromeInfliximabParadoxical reactionTNF-α antagonistsTuberculosis

Identifiers

PMID36795280
OpenAlexW4321003203

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.