TY - JOUR
T1 - Allogeneic natural killer cell therapy
AU - Berrien-Elliott, Melissa M.
AU - Jacobs, Miriam T.
AU - Fehniger, Todd A.
N1 - Funding Information:
The authors apologize to investigators for not being able to cite them owing to space constraints. The authors thank Pamela Wong, David Russler-Germain, Jennifer Foltz, and other members of the Fehniger laboratory for critical review of the manuscript. All figures were created with BioRender.com. The research reported in this publication was supported by grants from the National Institutes of Health, National Cancer Institute P50CA171963 (T.A.F. and M.M.B.-E.), R01CA205239 (T.A.F.), P30CA91842 (T.A.F.), K12CA167540 (M.T.J.). Additional support was provided by the Siteman Cancer Center (T.A.F.), the ASCO Young Investigator Award via Conquer Cancer Foundation (M.T.J.), the Paula C. and Rodger O. Riney Blood Cancer Initiative (T.A.F.), and the Lymphoma Research Foundation (T.A.F.). Contribution: M.M.B.-E. M.T.J. and T.A.F. wrote the manuscript.
Funding Information:
The research reported in this publication was supported by grants from the National Institutes of Health, National Cancer Institute P50CA171963 (T.A.F. and M.M.B.-E.), R01CA205239 (T.A.F.), P30CA91842 (T.A.F.), K12CA167540 (M.T.J.). Additional support was provided by the Siteman Cancer Center (T.A.F.), the ASCO Young Investigator Award via Conquer Cancer Foundation (M.T.J.), the Paula C. and Rodger O. Riney Blood Cancer Initiative (T.A.F.), and the Lymphoma Research Foundation (T.A.F.).
Publisher Copyright:
© 2023 The American Society of Hematology
PY - 2023/2/23
Y1 - 2023/2/23
N2 - Interest in adoptive cell therapy for treating cancer is exploding owing to early clinical successes of autologous chimeric antigen receptor (CAR) T lymphocyte therapy. However, limitations using T cells and autologous cell products are apparent as they (1) take weeks to generate, (2) utilize a 1:1 donor-to-patient model, (3) are expensive, and (4) are prone to heterogeneity and manufacturing failures. CAR T cells are also associated with significant toxicities, including cytokine release syndrome, immune effector cell–associated neurotoxicity syndrome, and prolonged cytopenias. To overcome these issues, natural killer (NK) cells are being explored as an alternative cell source for allogeneic cell therapies. NK cells have an inherent ability to recognize cancers, mediate immune functions of killing and communication, and do not induce graft-versus-host disease, cytokine release syndrome, or immune effector cell–associated neurotoxicity syndrome. NK cells can be obtained from blood or cord blood or be derived from hematopoietic stem and progenitor cells or induced pluripotent stem cells, and can be expanded and cryopreserved for off-the-shelf availability. The first wave of point-of-care NK cell therapies led to the current allogeneic NK cell products being investigated in clinical trials with promising preliminary results. Basic advances in NK cell biology and cellular engineering have led to new translational strategies to block inhibition, enhance and broaden target cell recognition, optimize functional persistence, and provide stealth from patients’ immunity. This review details NK cell biology, as well as NK cell product manufacturing, engineering, and combination therapies explored in the clinic leading to the next generation of potent, off-the-shelf cellular therapies for blood cancers.
AB - Interest in adoptive cell therapy for treating cancer is exploding owing to early clinical successes of autologous chimeric antigen receptor (CAR) T lymphocyte therapy. However, limitations using T cells and autologous cell products are apparent as they (1) take weeks to generate, (2) utilize a 1:1 donor-to-patient model, (3) are expensive, and (4) are prone to heterogeneity and manufacturing failures. CAR T cells are also associated with significant toxicities, including cytokine release syndrome, immune effector cell–associated neurotoxicity syndrome, and prolonged cytopenias. To overcome these issues, natural killer (NK) cells are being explored as an alternative cell source for allogeneic cell therapies. NK cells have an inherent ability to recognize cancers, mediate immune functions of killing and communication, and do not induce graft-versus-host disease, cytokine release syndrome, or immune effector cell–associated neurotoxicity syndrome. NK cells can be obtained from blood or cord blood or be derived from hematopoietic stem and progenitor cells or induced pluripotent stem cells, and can be expanded and cryopreserved for off-the-shelf availability. The first wave of point-of-care NK cell therapies led to the current allogeneic NK cell products being investigated in clinical trials with promising preliminary results. Basic advances in NK cell biology and cellular engineering have led to new translational strategies to block inhibition, enhance and broaden target cell recognition, optimize functional persistence, and provide stealth from patients’ immunity. This review details NK cell biology, as well as NK cell product manufacturing, engineering, and combination therapies explored in the clinic leading to the next generation of potent, off-the-shelf cellular therapies for blood cancers.
UR - http://www.scopus.com/inward/record.url?scp=85147870057&partnerID=8YFLogxK
U2 - 10.1182/blood.2022016200
DO - 10.1182/blood.2022016200
M3 - Review article
C2 - 36416736
AN - SCOPUS:85147870057
SN - 0006-4971
VL - 141
SP - 856
EP - 868
JO - Blood
JF - Blood
IS - 8
ER -