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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 :
Hammond TC
Purbhoo MA
Kadel S
Ritz J
Nikiforow S
Daley H
Shaw K
van Besien K
Gomez-Arteaga A
Stevens D
Ortuzar W
Michelet X
Smith R
Moskowitz D
Masakayan R
Yigit B
Boi S
Soh KT
Chamberland J
Song X
Qin Y
Mishchenko I
Kirby M
Nasonenko V
Buffa A
Buell JS
Chand D
van Dijk M
Stebbing J
Exley MA
Source :
Nature communications [Nat Commun] 2024 Feb 06; Vol. 15 (1), pp. 974. Date of Electronic Publication: 2024 Feb 06.
Publication Year :
2024

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.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
2041-1723
Volume :
15
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
38321023
Full Text :
https://doi.org/10.1038/s41467-024-44905-z