Evidence map›Paper›PMID 40924858›Full record

ArticleThe Journal of infectious diseases2026

Monkeypox Virus Shedding Despite Tecovirimat Treatment in a Cohort in Toronto, Canada.

Jacklyn R Hurst, Mary Addo, Abby Li, Shreya S Khera, Reva Persaud, Cassandra Bertucci, Misha Hummel, Oscar Javier Pico Espinosa, Adrienne K Chan, Sharon Walmsley and 3 more

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Jacklyn R HurstBiological Sciences, Sunnybrook Research Institute, Sunnybrook Hospital, Toronto, Ontario, Canada.ORCID 0000-0002-2858-0700
Mary AddoDepartment of Immunology, University of Toronto, Toronto, Ontario, Canada.ORCID 0009-0003-9391-8426
Abby LiMAP Centre for Urban Health Solutions, St. Michael's Hospital, Toronto, Ontario, Canada.
Shreya S KheraMAP Centre for Urban Health Solutions, St. Michael's Hospital, Toronto, Ontario, Canada.
Reva PersaudMAP Centre for Urban Health Solutions, St. Michael's Hospital, Toronto, Ontario, Canada.
Cassandra BertucciMAP Centre for Urban Health Solutions, St. Michael's Hospital, Toronto, Ontario, Canada.
Misha HummelMAP Centre for Urban Health Solutions, St. Michael's Hospital, Toronto, Ontario, Canada.
Oscar Javier Pico EspinosaMAP Centre for Urban Health Solutions, St. Michael's Hospital, Toronto, Ontario, Canada.
Adrienne K ChanDivision of Infectious Diseases, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.ORCID 0000-0002-9187-9465
Sharon WalmsleyDalla Lana School of Public Health, Institute of Health Policy Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0002-3959-5692
Sharmistha MishraMAP Centre for Urban Health Solutions, St. Michael's Hospital, Toronto, Ontario, Canada.ORCID 0000-0001-8492-5470
Darrell H S TanMAP Centre for Urban Health Solutions, St. Michael's Hospital, Toronto, Ontario, Canada.ORCID 0000-0002-3069-2875
Robert KozakBiological Sciences, Sunnybrook Research Institute, Sunnybrook Hospital, Toronto, Ontario, Canada.

Funding

CIHR MRR-184812Mathematical Modeling and Program ScienceTier 2 Canada Research Chair
6 · The paper itself

Abstract

backgroundTecovirimat (TPOXX) is an antiviral authorized for the treatment of mpox infections in Canada, but recent clinical trials found it has no impact on symptom duration.

methodsWe conducted a prospective cohort study of individuals diagnosed with mpox in Toronto, Canada. Skin lesion swabs were collected weekly to quantify infectious monkeypox virus (MPXV) shedding through cell culture. The presence of antiviral resistance mutations was assessed by PCR and sequencing the F13L gene.

resultsAmong 17 participants, 9 received tecovirimat, with a median initiation time of 14 days post-symptom onset. Infectious MPXV was detected in 31% (17/55) of lesion swabs from tecovirimat-treated participants and 32% (20/62) from untreated individuals. Shedding kinetics were similar between groups, with persistent infectious virus detected in several participants beyond 2 weeks of symptoms. Despite more than 7 days after tecovirimat initiation, 4 treated participants still shed viable virus in at least 1 sampled lesion, including up to 15 days after tecovirimat initiation. No known resistance mutations were identified in viral sequences from a subset of lesion swabs from both treated and untreated individuals, suggesting that tecovirimat resistance mutations were not widely circulating in Toronto during the 2022 outbreak.

conclusionsOur findings suggest that tecovirimat does not significantly impact the duration of infectious MPXV shedding from skin lesions, aligning with recent randomized trial results. These findings highlight the need for alternative antiviral strategies and continued genomic surveillance to monitor resistance emergence.

Indexed as

Antiviral AgentsBenzamidesGuanidinesIsoindolesMonkeypox virusMpox, MonkeypoxVirus SheddingAdolescentAdultAgedCanadaCohort StudiesDrug Resistance, ViralFemaleHumansMaleAntiviral AgentsBenzamidesGuanidinesIsoindolesPhthalimidestecovirimatantiviralMonkeypox virusviral shedding

Identifiers

PMID40924858
PMCPMC12811868

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.