Anti-CCR9 Chimeric Antigen Receptor T Cells for T Cell Acute Lymphoblastic Leukemia

T cell acute lymphoblastic leukemia (T-ALL) is an aggressive malignancy of immature T lymphocytes, associated with higher rates of induction failure in comparison to B-ALL. The potent immunotherapeutic approaches applied in B-ALL, which have revolutionized the treatment paradigm, have proven more ch...

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Veröffentlicht in:Blood 2022-07, Vol.140 (1), p.25-37
Hauptverfasser: Maciocia, PM, Wawrzyniecka, PA, Maciocia, NC, Burley, A, Karpanasamy, T, Deveraux, S, Hoekx, M, O’Connor, D, Leon, T, Rapoz D’Silva, T, Pocock, R, Rahman, S, Gritti, G, Yánez, DC, Ross, S, Crompton, T, Williams, O, Lee, L, Pule, MA, Mansour, MR
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Sprache:eng
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Zusammenfassung:T cell acute lymphoblastic leukemia (T-ALL) is an aggressive malignancy of immature T lymphocytes, associated with higher rates of induction failure in comparison to B-ALL. The potent immunotherapeutic approaches applied in B-ALL, which have revolutionized the treatment paradigm, have proven more challenging in T-ALL, largely due to a lack of target antigens expressed on malignant but not healthy T cells. Unlike B cell depletion, T cell aplasia is highly toxic. Here, we demonstrate that the chemokine receptor CCR9 is expressed in >70% of cases of T-ALL, including >85% or relapsed/ refractory disease, and only on a small fraction (
ISSN:0006-4971
1528-0020
DOI:10.1182/blood.2021013648