Evidence map›Paper›PMID 40822329›Full record

ArticleOpen forum infectious diseases2025

Standardized Infliximab Regimen to Treat Severe Central Nervous System Tuberculosis: A Case Series of 18 Patients.

Johan Benhard, Gentiane Monsel, Vincent Dubée, Patricia Pavese, Vero Rasoldier, Valérie Garrait, Marie Talleux, Fanny Vuotto, Romain Gueneau, Xavier Pouget-Abadie and 9 more

Abstract read
In one paragraph

Article in Open forum infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
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

19 authors.

Johan BenhardINSERM UMR 1136, AP-HP, Infectious and Tropical Diseases Department, Pitié-Salpêtrière Charles Foix University Hospitals, Sorbonne University, Paris, France.ORCID https://orcid.org/0009-0003-1393-9551
Gentiane MonselINSERM UMR 1136, AP-HP, Infectious and Tropical Diseases Department, Pitié-Salpêtrière Charles Foix University Hospitals, Sorbonne University, Paris, France.
Vincent DubéeINSERM, Immunology and New Concepts in ImmunoTherapy (INCIT), Infectious and Tropical Diseases Department, Angers University Hospital, Angers University, Nantes University, Angers, France.ORCID https://orcid.org/0000-0002-9982-4741
Patricia PaveseInfectious and Tropical Diseases Department, Grenoble University Hospital, Grenoble, France.
Vero RasoldierDepartment of Infectious Diseases, Rouen University Hospital, Rouen, France.
Valérie GarraitDepartment of Internal Medicine, Inter-municipal Hospital Centre, Créteil, France.
Marie TalleuxPaediatric Department, Amiens-Picardie University Hospital, Amiens, France.
Fanny VuottoInfectious and Tropical Diseases Department, Lille University Hospital, Lille, France.ORCID https://orcid.org/0000-0002-3908-7655
Romain GueneauAP-HP, Infectious and Tropical Diseases Department, Bicêtre Hospital, Paris-Saclay University, Le Kremlin-Bicêtre, France.
Xavier Pouget-AbadieDepartment of Internal Medicine and Infectious Diseases, La Rochelle Ré Aunis Hospital Group, La Rochelle, France.
Michael ThyAP-HP, Infectious and Tropical Diseases Department, Bichat-Claude Bernard Hospital, Paris, France.ORCID https://orcid.org/0000-0001-9366-505X
Christia PalaciosDepartment of Infectious Diseases, Tenon Hospital, Paris, France.
Marwa BachirDepartment of Infectious Diseases, Tenon Hospital, Paris, France.
Felix DjossouTropical and Infectious Diseases Department, Andrée Rosemon Hospital, Cayenne, French Guiana.
Simone TunesiInternal Medicine Unit, Jean Verdier Hospital, Bondy, HUPSSD, APHP, Sorbonne Paris Nord Universit, Bobigny, France.ORCID https://orcid.org/0000-0002-4943-4446
Mathilde Fréchet JachymSanatorium, Bligny Hospital, Briis-sous-Forges, France.ORCID https://orcid.org/0000-0003-3909-6380
Valérie PourcherINSERM UMR 1136, AP-HP, Infectious and Tropical Diseases Department, Pitié-Salpêtrière Charles Foix University Hospitals, Sorbonne University, Paris, France.ORCID https://orcid.org/0000-0002-3879-1480
Nicolas VezirisCentre for Immunology and Infectious Diseases (Cimi-Paris), UMR 1135, Department of Bacteriology, Saint-Antoine Hospital, AP-HP, Sorbonne University, National Reference Centre for Mycobacteria, Paris, France.
Anne BourgaritInternal Medicine Unit, Jean Verdier Hospital, Bondy, HUPSSD, APHP, Sorbonne Paris Nord Universit, Bobigny, France.ORCID https://orcid.org/0000-0002-4788-9105

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Morbidity associated with central nervous system tuberculosis (CNS TB) remains high due to persistent inflammation despite standard-of-care (SOC) treatment, including antituberculosis therapy and corticosteroids. Tumor necrosis factor alpha (TNF-α) is a key cytokine driving this inflammatory response, and a limited number of case reports suggest that TNF-α inhibitors may improve outcomes. We report the 1-year outcome of a cohort of consecutive patients treated with infliximab for severe CNS TB. Methods: Following the guidance provided by the French Tuberculosis Consilium, a standardized regimen of intravenous infliximab at 5 mg/kg per dose was used to treat CNS TB unresponsive to SOC. We retrospectively included consecutive patients who received at least 1 infliximab injection for CNS TB from 2017 to September 2021. Results: Eighteen patients with CNS TB, 94% with tuberculous meningitis, were included. Most had severe disease: 82% were classified as British Medical Research Council grade II or III, and 44% required intensive care unit admission. All demonstrated clinical and radiological worsening despite SOC; in 89% due to paradoxical reaction. At infliximab initiation, symptoms remained disabling, with a median modified Rankin scale (mRS) score of 3.5 (interquartile range, 3-4). One month after the first infusion, 38% showed improved mRS scores, increasing to 78% at 1 year. One-year survival was 94%; 1 death occurred 12 months after a single infliximab dose and was unrelated to TB treatment. Conclusions: Infliximab may represent a promising adjunctive treatment for CNS TB unresponsive to SOC, including paradoxical reaction. Prospective studies are needed to confirm these findings.

Indexed as

central nervous system tuberculosisinfliximabparadoxical reactionTNF-α inhibitortuberculous meningitis

Identifiers

PMID40822329
PMCPMC12351261

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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.