Enhancing the antitumor functions of invariant natural killer T cells using a soluble CD1d-CD19 fusion protein

Blood Adv. 2019 Mar 12;3(5):813-824. doi: 10.1182/bloodadvances.2018028886.

Abstract

Invariant natural killer T (iNKT) cells comprise a unique lineage of CD1d-restricted lipid-reactive T lymphocytes that potently kill tumor cells and exhibit robust immunostimulatory functions. Optimal tumor-directed iNKT cell responses often require expression of the antigen-presenting molecule CD1d on tumors; however, many tumor cells downregulate CD1d and thus evade iNKT cell recognition. We generated a soluble bispecific fusion protein designed to direct iNKT cells to the site of B-cell cancers in a tumor antigen-specific but CD1d-independent manner. This fusion protein is composed of a human CD1d molecule joined to a single chain antibody FV fragment specific for CD19, an antigen widely expressed on B-cell cancers. The CD1d-CD19 fusion protein binds specifically to CD19-expressing, but not CD19-negative cells. Once loaded with the iNKT cell lipid agonist α-galactosyl ceramide (αGC), the CD1d-CD19 fusion induces robust in vitro activation of and cytokine production by human iNKT cells. iNKT cells stimulated by the αGC-loaded CD1d-CD19 fusion also strongly transactivate T-, B-, and NK-cell responses and promote dendritic cell maturation. Importantly, the αGC-loaded fusion induces robust lysis of CD19+CD1d- Epstein-Barr virus immortalized human B-lymphoblastoid cell lines that are otherwise resistant to iNKT cell killing. Consistent with these findings; administration of the αGC-loaded fusion protein controlled the growth of CD19+CD1d- tumors in vivo, suggesting that it can "link" iNKT cells and CD19+CD1d- targets in a therapeutically beneficial manner. Taken together, these preclinical studies demonstrate that this B cell-directed fusion protein can be used to effectively induce iNKT cell antitumor responses in vitro and in vivo.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, CD19 / immunology*
  • Antigens, CD1d / genetics*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Heterografts
  • Humans
  • Lymphocyte Activation / drug effects
  • Mice
  • Natural Killer T-Cells / physiology*
  • Oncogene Proteins, Fusion / genetics
  • Oncogene Proteins, Fusion / pharmacology
  • Oncogene Proteins, Fusion / therapeutic use*
  • Protein Engineering / methods
  • Single-Chain Antibodies / genetics
  • Solubility
  • Tumor Burden / drug effects

Substances

  • Antigens, CD19
  • Antigens, CD1d
  • CD1D protein, human
  • Oncogene Proteins, Fusion
  • Single-Chain Antibodies