Juno Therapeutics Gmbh

Clinton Weber

Christopher Glen Ramsborg

Mark J Gilbert

He Li

Brian Christin

Claire L Sutherland

Ryan P Larson

Tina Albertson

Pascal Beauchesne

Nathan K Yee

Rachel K Yost

Jacob Randolph Garcia

Mary Mallaney

Jeff D Smith

Mark L Bonyhadi

Valerie Odegard

Kathryn Lindsay Pollock

Tom Kowski

Ryan L Crisman

Kedar Himanshu Dave

Andrew W Walker

Nikolaus Sebastian Trede

Sarah Y Lee

John Matthew Wesner

Michael Gerard Covington

Richard James Getto, Jr

James Boyd Whitmore

Travis Beckett

Samuel Charles Blackman

Nathaniel Chartrand

Nathaniel Lambert

Mel Davis-pickett

The present disclosure provides methods for genetically engineering T cells, such as CD4+ T cells, for use in cell therapy. In some aspects, the provided methods include one or more steps for incubating the cells under stimulating conditions, introducing a recombinant polypeptide to the cells through transduction or transfection, and cultivating the cells under conditions that promote proliferation and/or expansion. In some aspects, the incubation and/or the cultivation is performed in the presence of recombinant IL-2. In some aspects, the provided methods are an efficient, reliable means to produce genetically engineered T cells with a high degree of success.

Process for generating therapeutic compositions of engineered cells

Provided herein are methods, compositions and articles of manufacture for use in connection with cell therapy involving the administration of one or more doses of a therapeutic T cell composition. The cells of the T cell composition express recombinant receptors such as chimeric receptors, e.g. chimeric antigen receptors (CARs) or other transgenic receptors such as T cell receptors (TCRs). Features of the provided embodiments, including the numbers of cells or units of cells administered and/or the potency of administered cells, provide various advantages, such as lower risk of toxicity in subjects administered the T cell compositions.

Determining toxicity risk in CAR T-cell therapy

Provided are adoptive cell therapy methods involving the administration of doses of cells for treating disease and conditions, including certain B cell malignancies. The cells generally express recombinant receptors such as chimeric antigen receptors (CARs). In some embodiments, the methods are for treating subjects with non-Hodgkin lymphoma (NHL). In some embodiments, the methods are for treating subjects with relapsed or refractory NHL. Also provided are articles of manufacture and prophylactic treatments in connection with adoptive therapy methods.

Articles of manufacture and methods for treatment using adoptive cell therapy

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Seattle, WA, United States of America

Clinton Weber