Collaborations & Alliances

IsoPlexis, Nektar Therapeutics in Immunotherapy Alliance

Will employ IsoCode Chip's single-cell functional profiling in collaboration with Nektar to profile effects of NKTR-214

By: Kristin Brooks

Managing Editor, Contract Pharma

IsoPlexis Corp. has entered a collaboration with Nektar Therapeutics focused on further defining the functional impact of NKTR-214 in the clinic, at the single-cell level, with the goal of revealing both mechanism and potential immune correlates with outcome. 

Recent preclinical data captured by IsoPlexis’ IsoCode Chip showed evidence that Nektar’s cytokine agonist NKTR-214 can significantly boost the activation of critical T cell subsets, termed polyfunctional T cells, in combination with adoptive cell transfer (ACT) therapies. 

Through this collaboration, IsoPlexis will employ its IsoCode Chip’s single-cell functional profiling in collaboration with Nektar Therapeutics to profile the effects of NKTR-214 in both monotherapy and combination immunotherapy in a clinical setting. IsoPlexis’ platform has previously highlighted the potential of polyfunctional T cells, those cells secreting multiple cytokines, as a promising correlate to clinical patient outcome in a variety of immunotherapies.

“We are excited to collaborate with Nektar Therapeutics and further demonstrate the broad impact of NKTR-214 and its ability to induce critical T cell responses in cancer immunotherapy,” said IsoPlexis chief executive officer, Sean Mackay. “We recently released preclinical data highlighting the ability of NKTR-214 to activate key subsets of highly functional immune cells, and look forward to further profile the therapy’s immune-based mechanisms and correlates in the clinic.”

“We see potential in utilizing IsoPlexis’ single-cell system to help provide deeper resolution into the functional impacts of our therapeutics,” said Jon Zalevsky, chief scientific officer of Nektar Therapeutics. “This collaboration will enable us to apply the sensitivity of this solution to further our understanding of patient-specific responses to our immune therapies.”

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