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

Authors :
Terese C. Hammond
Marco A. Purbhoo
Sapana Kadel
Jerome Ritz
Sarah Nikiforow
Heather Daley
Kit Shaw
Koen van Besien
Alexandra Gomez-Arteaga
Don Stevens
Waldo Ortuzar
Xavier Michelet
Rachel Smith
Darrian Moskowitz
Reed Masakayan
Burcu Yigit
Shannon Boi
Kah Teong Soh
John Chamberland
Xin Song
Yu Qin
Ilya Mishchenko
Maurice Kirby
Valeriia Nasonenko
Alexa Buffa
Jennifer S. Buell
Dhan Chand
Marc van Dijk
Justin Stebbing
Mark A. Exley
Source :
Nature Communications, Vol 15, Iss 1, Pp 1-15 (2024)
Publication Year :
2024
Publisher :
Nature Portfolio, 2024.

Abstract

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.

Subjects

Subjects :
Science

Details

Language :
English
ISSN :
20411723
Volume :
15
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
edsdoj.15d9c3789204f0f9cbf46c7c032881d
Document Type :
article
Full Text :
https://doi.org/10.1038/s41467-024-44905-z