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April 19, 2026Cancer Research0 citations

Abstract LB021: Enhanced therapeutic efficacy of ApoA1-Anti CD99 antibody fusion protein for treatment of Ewing sarcoma

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HKHyungGyoo KangChildren's Hospital of Los AngelesBUBryon UptonJNJon Nagy

Key Points

  • The aim is to improve the targeting and efficacy of Ewing sarcoma treatments using a novel antibody fusion protein.
  • Developed a fusion protein by genetically linking apoA1 to human anti-CD99 antibodies.
  • Formulated irinotecan-loaded hybrid polymer-lipid nanoparticles (HPLNs) with the fusion protein for better targeting.
  • Evaluated antitumor efficacy in Ewing sarcoma xenograft models, comparing findings with traditional chemical conjugation methods.
  • Achieved a 5-fold higher affinity of nanoparticles to tumor cells with the ApoA1 fusion method.
  • NV105 demonstrated significantly greater tumor reduction compared to NV103 at much lower doses.
  • Complete tumor ablation was noted at doses as low as 5 mg/kg of NV105, outperforming conventional methods.

Abstract

Abstract Most conventional anticancer therapies suffer from poor target specificity, frequently resulting in significant off-target toxicity and limited therapeutic indices. To address these shortcomings, advanced drug delivery systems such as targetable hybrid polymer-lipid nanoparticles (tHPLNs) have been developed for improved tumor specificity. To date, tHPLNs have been formulated to enable covalent attachment of tumor-specific antibodies on their surfaces, with the aim of enhancing selective accumulation at tumor sites. However, current chemical conjugation strategies are often complex and rely on multi-step bioconjugation chemistry that can produce particles with misoriented or nonfunctional antibodies or antibody fragments, compromising targeting efficiency and reproducibility. By genetically fusing apolipoprotein A1 (ApoA1) to the Fc domain of human anti-CD99 antibodies, we generated a fusion protein that spontaneously associates with the HPLN surface, enabling effective antibody targeting of irinotecan-loaded nanoparticles (NV105) — all without modifying the core nanoparticle chemistry or performing additional antibody conjugation steps. Importantly, compared to chemical linkage methods, the ApoA1 attachment technology yields 5-fold higher affinity binding of our nanoparticles to tumor cells. In Ewing Sarcoma xenograft models, NV105 exhibited substantially greater antitumor efficacy than NV103, which was targeted via conventional chemical conjugation of human anti-CD99 antibodies. Much better tumor reduction has been observed at doses as low as 0. 5 mg/kg irinotecan, treated twice per week, which was superior to 1 mg/kg NV103 treated biweekly. Complete tumor ablation has been observed at doses as low as 5 mg/kg NV105, treated twice per week. In conclusion, HPLN/Ir formulated with anti-CD99 antibodies fused with ApoA1 demonstrated substantially greater efficacy against Ewing Sarcoma. We anticipate that this approach will enhance tumor cell binding and drug targeting broadly for other antibodies and nanoparticle formulations. Citation Format: HyungGyoo Kang, Bryon Upton, Jon Nagy, Timothy Triche. Enhanced therapeutic efficacy of ApoA1-Anti CD99 antibody fusion protein for treatment of Ewing sarcoma abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts) ; 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86 (8Suppl): Abstract nr LB021.

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Kang et al. (2026) studied this question.

synapsesocial.com/papers/69e472a8010ef96374d8eafchttps://doi.org/10.1158/1538-7445.am2026-lb021
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