Novel CD19-targeted TriKE restores NK cell function and proliferative capacity in CLL.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
26 03 2019
Historique:
received: 04 12 2018
accepted: 10 02 2019
entrez: 21 3 2019
pubmed: 21 3 2019
medline: 28 3 2020
Statut: ppublish

Résumé

Chronic lymphocytic leukemia (CLL) is characterized by chronic clonal expansion of mature CD19-expressing B lymphocytes and global dysfunction of immune effectors, including natural killer (NK) cells. CLL remains incurable, and novel approaches to refractory CLL are needed. Our group has previously described trispecific killer engager (TriKE) molecules that redirect NK cell function against tumor cells. TriKE reagents simultaneously bind an activating receptor on NK cells, CD16, and a tumor antigen while also providing an NK cell expansion signal via an interleukin-15 moiety. Here we developed the novel CD19-targeting 161519 TriKE. We demonstrate that 161519 TriKE induced killing of a CD19-expressing Burkitt's lymphoma cell line and examined the impact on primary CLL targets using healthy donor and patient NK cells. 161519 TriKE induced potent healthy donor NK cell activation, proliferation, and directed killing. Furthermore, 161519 TriKE rescued the inflammatory function of NK cells obtained from CLL patient peripheral blood samples. Finally, we show that 161519 TriKE induced better directed killing of CLL in vitro when compared with rituximab. In conclusion, 161519 TriKE drives a potent activating and proliferative signal on NK cells, resulting in enhanced NK cell expansion and CLL target killing. Our findings indicate the potential immunotherapeutic value of 161519 TriKE in CLL.

Identifiants

pubmed: 30890546
pii: bloodadvances.2018029371
doi: 10.1182/bloodadvances.2018029371
pmc: PMC6436008
doi:

Substances chimiques

Antigens, CD19 0
Antineoplastic Agents, Immunological 0
FCGR3B protein, human 0
GPI-Linked Proteins 0
IL15 protein, human 0
Interleukin-15 0
Receptors, IgG 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

897-907

Subventions

Organisme : NCI NIH HHS
ID : P30 CA077598
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002494
Pays : United States
Organisme : NCI NIH HHS
ID : P01 CA065493
Pays : United States
Organisme : NCI NIH HHS
ID : R21 CA150085
Pays : United States
Organisme : NCATS NIH HHS
ID : KL2 TR002492
Pays : United States
Organisme : NCI NIH HHS
ID : P01 CA111412
Pays : United States

Informations de copyright

© 2019 by The American Society of Hematology.

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Auteurs

Martin Felices (M)

Division of Hematology, Oncology, and Transplantation, Department of Medicine, and.

Behiye Kodal (B)

Division of Hematology, Oncology, and Transplantation, Department of Medicine, and.

Peter Hinderlie (P)

Division of Hematology, Oncology, and Transplantation, Department of Medicine, and.

Michael F Kaminski (MF)

Division of Hematology, Oncology, and Transplantation, Department of Medicine, and.

Sarah Cooley (S)

Division of Hematology, Oncology, and Transplantation, Department of Medicine, and.

Daniel J Weisdorf (DJ)

Division of Hematology, Oncology, and Transplantation, Department of Medicine, and.

Daniel A Vallera (DA)

Department of Radiation Oncology, University of Minnesota, Minneapolis, MN.

Jeffrey S Miller (JS)

Division of Hematology, Oncology, and Transplantation, Department of Medicine, and.

Veronika Bachanova (V)

Division of Hematology, Oncology, and Transplantation, Department of Medicine, and.

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Classifications MeSH