Evidence map›Paper›PMID 40481519›Full record

SynthesisCritical care (London, England)2025

Tumour necrosis factor-alpha inhibitors decrease mortality in COVID-19: a systematic review and meta-analysis.

Ágoston Jánosi, Blanka Bódy, Rita Nagy, Klementina Ocskay, Tamás Kói, Katalin Müller, Ibolya Túri, Miklós Garami, Péter Hegyi, Andrea Párniczky

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Critical care (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

10 authors.

Ágoston JánosiCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Blanka BódyCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Rita NagyCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Klementina OcskayHeim Pál National Paediatric Institute, Budapest, Hungary.
Tamás KóiCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Katalin MüllerCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Ibolya TúriCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Miklós GaramiCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Péter HegyiCentre for Translational Medicine, Semmelweis University, Budapest, Hungary.
Andrea PárniczkyCentre for Translational Medicine, Semmelweis University, Budapest, Hungary. andrea.parniczky@gmail.com.

Funding

CF Trust Strategic Research Consortium Grant NU-000600National Research, Development and Innovation Fund (NRDI Fund) FK 138929
6 · The paper itself

Abstract

backgroundDespite widespread vaccination efforts, effective treatment strategies remain critical for severe SARS-CoV-2 infection. Tumour necrosis factor-alpha (TNF-α) plays a central role in the cytokine storm characteristic of severe COVID-19. This systematic review and meta-analysis evaluates the effectiveness, efficacy, and safety of TNF-α inhibitors in the management of COVID-19. PATIENTS AND

methodsA systematic review of PubMed, Embase, and CENTRAL was conducted, focusing on studies involving SARS-CoV-2-infected patients treated with TNF-α inhibitors compared with those receiving standard of care without prior TNF-α inhibitor use. Data from studies published up to August 12, 2024, were analysed. Outcomes assessed included mortality, invasive mechanical ventilation, and C-reactive protein (CRP) levels. Odds ratios (ORs) and mean differences (MD) were calculated with 95% confidence intervals (CI), and subgroup analyses were performed for randomised controlled trials (RCTs) and non-randomised studies.

resultsSeven studies involving 1393 patients with moderate-to-critical COVID-19 were included. TNF-α inhibitor treatment was associated with a reduced odds of mortality (OR 0.67, 95% CI [0.44-1.00], P = 0.052), which was statistically significant in the RCT subgroup across three studies (OR 0.75, 95% CI [0.58-0.97], P = 0.042, certainty of evidence: very low). The number needed to treat for mortality was calculated to be 16 (95% CI 9.0-inf.), which indicates that one additional death could be avoided for every 16 patients treated with TNF-α inhibitors compared to standard of care. No significant reduction in the need for invasive mechanical ventilation was observed (OR 0.95 [95% CI 0.46-1.94]; P = 0.822). Additionally, TNF-α inhibitors resulted in a significant reduction in CRP levels (MD - 21.9 mg/L [95% CI - 38.46 to - 5.34]; P = 0.024) within three to seven days post-treatment.

conclusionOur study indicates a potential role for TNF-α inhibition in the treatment of COVID-19 as their use was associated with reduced mortality, but further studies are needed to provide robust evidence.

Indexed as

COVID-19COVID-19 Drug TreatmentTumor Necrosis Factor-alphaHumansSARS-CoV-2Tumor Necrosis Factor-alpha

Identifiers

PMID40481519
PMCPMC12144840

What OpenQuestion holds

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Registered trials

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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.