TY - JOUR
T1 - Gamma delta T cells in acute myeloid leukemia
T2 - Biology and emerging therapeutic strategies
AU - Rao, Adishwar
AU - Agrawal, Akriti
AU - Borthakur, Gautam
AU - Battula, Venkata Lokesh
AU - Maiti, Abhishek
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
PY - 2024/2/27
Y1 - 2024/2/27
N2 - 3δT cells play an important role in disease control in acute myeloid leukemia (AML) and have become an emerging area of therapeutic interest. These cells represent a minor population of T lymphocytes with intrinsic abilities to recognize antigens in a major histocompatibility complex-independent manner and functionally straddle the innate and adaptive immunity interface. AML shows high expression of phosphoantigens and UL-16 binding proteins that activate the Vδ 2 and Vδ 1 subtypes of 3δT cells, respectively, leading to 3δT cell-mediated cytotoxicity. Insights from murine models and clinical data in humans show improved overall survival, leukemia-free survival, reduced risk of relapse, enhanced graft-versus-leukemia effect, and decreased graft-versus-host disease in patients with AML who have higher reconstitution of 3δT cells following allogeneic hematopoietic stem cell transplantation. Clinical trials leveraging 3δT cell biology have used unmodified and modified allogeneic cells as well as bispecific engagers and monoclonal antibodies. In this review, we discuss 3δT cells' biology, roles in cancer and AML, and mechanisms of immune escape and antileukemia effect; we also discuss recent clinical advances related to 3δT cells in the field of AML therapeutics.
AB - 3δT cells play an important role in disease control in acute myeloid leukemia (AML) and have become an emerging area of therapeutic interest. These cells represent a minor population of T lymphocytes with intrinsic abilities to recognize antigens in a major histocompatibility complex-independent manner and functionally straddle the innate and adaptive immunity interface. AML shows high expression of phosphoantigens and UL-16 binding proteins that activate the Vδ 2 and Vδ 1 subtypes of 3δT cells, respectively, leading to 3δT cell-mediated cytotoxicity. Insights from murine models and clinical data in humans show improved overall survival, leukemia-free survival, reduced risk of relapse, enhanced graft-versus-leukemia effect, and decreased graft-versus-host disease in patients with AML who have higher reconstitution of 3δT cells following allogeneic hematopoietic stem cell transplantation. Clinical trials leveraging 3δT cell biology have used unmodified and modified allogeneic cells as well as bispecific engagers and monoclonal antibodies. In this review, we discuss 3δT cells' biology, roles in cancer and AML, and mechanisms of immune escape and antileukemia effect; we also discuss recent clinical advances related to 3δT cells in the field of AML therapeutics.
KW - Hematologic Neoplasms
KW - Immunity, Cellular
KW - Immunotherapy, Adoptive
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U2 - 10.1136/jitc-2023-007981
DO - 10.1136/jitc-2023-007981
M3 - Review article
C2 - 38417915
AN - SCOPUS:85186432245
SN - 2051-1426
VL - 12
JO - Journal for immunotherapy of cancer
JF - Journal for immunotherapy of cancer
IS - 2
ER -