Fate Therapeutics, Inc.

The Scripps Research Institute

Juno Therapeutics Gmbh

Ian Hardy

Betsy Rezner

Eigen Peralta

Jonathan Rosen

Bahram Valamehr

Ryan Bjordahl

Leonard G Presta

Peter G Schultz

Travis Young

Daniel D Shoemaker

David Robbins

Chanhyuk Kim

Lucas James Thompson

Eric Hampton

Eduardo Laborda

David T Rodgers

Christian Maine

Compounds that either produced a higher proportion or greater absolute number of phenotypically identified nave, stem cell memory, central memory T cells, adaptive NK cells, and type I NKT cells are identified. Compositions and methods for modulating immune cells including T, NK, and NKT cells for adoptive cell therapies with improved efficacy are provided.

Compositions and methods for immune cell modulation in adoptive immunotherapies

Compounds that either produce a higher proportion or greater absolute number of phenotypically identified naive, stem cell memory, central memory T cells, adaptive NK cells, and type I NKT cells are identified. Compositions and methods for modulating immune cells including T, NK, and NKT cells for adoptive cell therapies, such as those providing improvements in one or more therapeutic outcomes, are provided.

Compounds that either produced a higher proportion or greater absolute number of phenotypically identified naive, stem cell memory, central memory T cells, adaptive NK cells, and type I NKT cells are identified. Compositions and methods for modulating immune cells including T, NK, and NKT cells for adoptive cell therapies with improved efficacy are provided.

Disclosed herein are chimeric antigen receptor effector cells (CAR-ECs) and CAR-EC switches. The switchable CAR-ECs are generally T cells. The one or more chimeric antigen receptors may recognize a peptidic antigen on the CAR-EC switch. The CAR-ECs and switches may be used for the treatment of a condition in a subject in need thereof.

Optimized PNE-based chimeric receptor T cell switches and uses thereof

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San Diego, CA, United States of America

Ian Hardy