Evidence map›Paper›PMID 38321023›Full record

Trial reportNature communications2024

A phase 1/2 clinical trial of invariant natural killer T cell therapy in moderate-severe acute respiratory distress syndrome.

Terese C Hammond, Marco A Purbhoo, Sapana Kadel, Jerome Ritz, Sarah Nikiforow, Heather Daley, Kit Shaw, Koen van Besien, Alexandra Gomez-Arteaga, Don Stevens and 20 more

Registry-linked trialAbstract readClinical Trial, Phase IIClinical Trial, Phase I
In one paragraph

Trial report in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04582201 (A Phase 1 Study of agenT-797 to Treat Moderate to Severe Acute Respiratory Syndrome in COVID-19 Patients), which is not on this map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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.

NCT04582201 phase1completednot on this map

A Phase 1 Study of agenT-797 to Treat Moderate to Severe Acute Respiratory Syndrome in COVID-19 Patients

TypeinterventionalSponsorMiNK TherapeuticsRan2020 to 2023Enrolled20ConditionsRespiratory Distress Syndrome, AdultArmsagenT-797
3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

  1. Article
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  12. From development to regeneration: the endothelial interface in lung injury and repair.American journal of physiology. Lung cellular and molecular physiology · 2025
    Review
  13. Article
  14. Review
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  20. Off-the-shelf allogeneic natural killer cells for the treatment of COVID-19.Molecular therapy. Methods & clinical development · 2024
    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

30 authors.

Terese C Hammond *Pulmonary Critical Care Sleep Medicine, Providence Saint John's Health Center, Santa Monica, CA, USA.
Marco A Purbhoo *MiNK Therapeutics, Lexington, MA, USA.
Sapana KadelMiNK Therapeutics, Lexington, MA, USA.
Jerome RitzDana Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0001-5526-4669
Sarah NikiforowDana Farber Cancer Institute, Boston, MA, USA.
Heather DaleyDana Farber Cancer Institute, Boston, MA, USA.
Kit ShawDana Farber Cancer Institute, Boston, MA, USA.
Koen van BesienUH Seidman Cancer Center, Cleveland, OH, USA.
Alexandra Gomez-ArteagaWeill Cornell Medicine, New York, NY, USA.
Don StevensNorton Cancer Center, Louisville, KY, USA.
Waldo OrtuzarAgenus, Lexington, MA, USA.
Xavier MicheletMiNK Therapeutics, Lexington, MA, USA.
Rachel SmithMiNK Therapeutics, Lexington, MA, USA.
Darrian MoskowitzMiNK Therapeutics, Lexington, MA, USA.
Reed MasakayanMiNK Therapeutics, Lexington, MA, USA.
Burcu YigitMiNK Therapeutics, Lexington, MA, USA.
Shannon BoiMiNK Therapeutics, Lexington, MA, USA.ORCID 0000-0001-9479-5665
Kah Teong SohAgenus, Lexington, MA, USA.ORCID 0000-0002-0146-0485
John ChamberlandMiNK Therapeutics, Lexington, MA, USA.
Xin SongAgenus, Lexington, MA, USA.
Yu QinMiNK Therapeutics, Lexington, MA, USA.
Ilya MishchenkoAgenus, Lexington, MA, USA.
Maurice KirbyAgenus, Lexington, MA, USA.
Valeriia NasonenkoAgenus, Lexington, MA, USA.
Alexa BuffaMiNK Therapeutics, Lexington, MA, USA.ORCID 0009-0007-4982-7788
Jennifer S BuellMiNK Therapeutics, Lexington, MA, USA.
Dhan ChandAgenus, Lexington, MA, USA.
Marc van DijkMiNK Therapeutics, Lexington, MA, USA.ORCID 0000-0002-0190-7814
Justin StebbingAnglia Ruskin University, Cambridge, UK. justin.stebbing@aru.ac.uk.ORCID 0000-0002-1117-6947
Mark A ExleyBrigham & Women's Hospital, Boston, USA.ORCID 0000-0002-5088-1032

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Invariant natural killer T (iNKT) cells, a unique T cell population, lend themselves for use as adoptive therapy due to diverse roles in orchestrating immune responses. Originally developed for use in cancer, agenT-797 is a donor-unrestricted allogeneic ex vivo expanded iNKT cell therapy. We conducted an open-label study in virally induced acute respiratory distress syndrome (ARDS) caused by the severe acute respiratory syndrome-2 virus (trial registration NCT04582201). Here we show that agenT-797 rescues exhausted T cells and rapidly activates both innate and adaptive immunity. In 21 ventilated patients including 5 individuals receiving veno-venous extracorporeal membrane oxygenation (VV-ECMO), there are no dose-limiting toxicities. We observe an anti-inflammatory systemic cytokine response and infused iNKT cells are persistent during follow-up, inducing only transient donor-specific antibodies. Clinical signals of associated survival and prevention of secondary infections are evident. Cellular therapy using off-the-shelf iNKT cells is safe, can be rapidly scaled and is associated with an anti-inflammatory response. The safety and therapeutic potential of iNKT cells across diseases including infections and cancer, warrants randomized-controlled trials.

Indexed as

Natural Killer T-CellsNeoplasmsRespiratory Distress SyndromeAnti-Inflammatory AgentsCytokinesHumansAnti-Inflammatory AgentsCytokines

Identifiers

PMID38321023
PMCPMC10847411

What OpenQuestion holds

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Registered trials

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.