Anti-SIRPα antibody immunotherapy enhances neutrophil and macrophage antitumor activity.

Abstract:

:Cancer immunotherapy has emerged as a promising therapeutic intervention. However, complete and durable responses are only seen in a fraction of patients who have cancer. A key factor that limits therapeutic success is the infiltration of tumors by cells of the myeloid lineage. The inhibitory receptor signal regulatory protein-α (SIRPα) is a myeloid-specific immune checkpoint that engages the "don't eat me" signal CD47 expressed on tumors and normal tissues. We therefore developed the monoclonal antibody KWAR23, which binds human SIRPα with high affinity and disrupts its binding to CD47. Administered by itself, KWAR23 is inert, but given in combination with tumor-opsonizing monoclonal antibodies, KWAR23 greatly augments myeloid cell-dependent killing of a collection of hematopoietic and nonhematopoietic human tumor-derived cell lines. Following KWAR23 antibody treatment in a human SIRPA knockin mouse model, both neutrophils and macrophages infiltrate a human Burkitt's lymphoma xenograft and inhibit tumor growth, generating complete responses in the majority of treated animals. We further demonstrate that a bispecific anti-CD70/SIRPα antibody outperforms individually delivered antibodies in specific types of cancers. These studies demonstrate that SIRPα blockade induces potent antitumor activity by targeting multiple myeloid cell subsets that frequently infiltrate tumors. Thus, KWAR23 represents a promising candidate for combination therapy.

authors

Ring NG,Herndler-Brandstetter D,Weiskopf K,Shan L,Volkmer JP,George BM,Lietzenmayer M,McKenna KM,Naik TJ,McCarty A,Zheng Y,Ring AM,Flavell RA,Weissman IL

doi

10.1073/pnas.1710877114

subject

Has Abstract

pub_date

2017-12-05 00:00:00

pages

E10578-E10585

issue

49

eissn

0027-8424

issn

1091-6490

pii

1710877114

journal_volume

114

pub_type

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