Clinically translatable cytokine delivery platform for eradication of intraperitoneal tumors

Author:

Nash Amanda M.1ORCID,Jarvis Maria I.1ORCID,Aghlara-Fotovat Samira1ORCID,Mukherjee Sudip1ORCID,Hernandez Andrea1ORCID,Hecht Andrew D.1ORCID,Rios Peter D.2ORCID,Ghani Sofia2,Joshi Ira2,Isa Douglas2,Cui Yufei1,Nouraein Shirin1,Lee Jared Z.3ORCID,Xu Chunyu4,Zhang David Y.1ORCID,Sheth Rahul A.5ORCID,Peng Weiyi4ORCID,Oberholzer Jose26,Igoshin Oleg A.1ORCID,Jazaeri Amir A.7ORCID,Veiseh Omid1ORCID

Affiliation:

1. Department of Bioengineering, Rice University, Houston, TX, USA.

2. CellTrans Inc., Chicago, IL, USA.

3. Department of Chemistry, Rice University, Houston, TX, USA.

4. Department of Biology and Biochemistry, The University of Houston, Houston, TX, USA.

5. Department of Interventional Radiology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

6. Department of Surgery, University of Virginia, Charlottesville, VA, USA.

7. Department of Gynecologic Oncology and Reproductive Medicine, Division of Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

Abstract

Proinflammatory cytokines have been approved by the Food and Drug Administration for the treatment of metastatic melanoma and renal carcinoma. However, effective cytokine therapy requires high-dose infusions that can result in antidrug antibodies and/or systemic side effects that limit long-term benefits. To overcome these limitations, we developed a clinically translatable cytokine delivery platform composed of polymer-encapsulated human ARPE-19 (RPE) cells that produce natural cytokines. Tumor-adjacent administration of these capsules demonstrated predictable dose modulation with spatial and temporal control and enabled peritoneal cancer immunotherapy without systemic toxicities. Interleukin-2 (IL2)–producing cytokine factory treatment eradicated peritoneal tumors in ovarian and colorectal mouse models. Furthermore, computational pharmacokinetic modeling predicts clinical translatability to humans. Notably, this platform elicited T cell responses in NHPs, consistent with reported biomarkers of treatment efficacy without toxicity. Combined, our findings demonstrate the safety and efficacy of IL2 cytokine factories in preclinical animal models and provide rationale for future clinical testing in humans.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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