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463 Targeting a novel myeloid checkpoint Siglec-15 in GBM generates an extremely durable response with Zika virus oncolytic therapy
  1. Ashwani Kesarwani1,
  2. Amanda De Andrade Costa1,
  3. Tong Hu1,
  4. Jeremy N Rich2,
  5. Albert Kim1,
  6. Pei-Yong Shi3,
  7. Michael S Diamond1 and
  8. Milan Chheda1
  1. 1Washington University in St. Louis, St. Louis, MO, USA
  2. 2University of Pittsburgh, Pittsburgh, PA, USA
  3. 3University of Texas, Texas, TX, USA
  • Journal for ImmunoTherapy of Cancer (JITC) preprint. The copyright holder for this preprint are the authors/funders, who have granted JITC permission to display the preprint. All rights reserved. No reuse allowed without permission.


Background Glioblastoma (GBM) is a highly aggressive and malignant brain tumor. Despite aggressive treatment, GBM has a poor prognosis, and it is difficult to eliminate using current treatment strategy. Moreover, recurrence is a major challenge.

Methods To develop glioma model, we performed intracranial injection of CT2A and SB28 mouse glioma cells. ZIKV injection was given intratumorally 7 days post tumor implantation. Four doses of anti-siglec-15 and anti-PD1 injection were given intraperitonially.

Results We are developing Zika virus as a therapy for GBM. previously we showed ZIKV significantly increases survival in multiple syngeneic glioma mouse models. Like other oncolytic therapies, it generates a potent, anti-tumor CD8+ T-cell response. Post-ZIKV, we observe a 32-fold increase in myeloid cells in the GBM microenvironment. Siglec-15 is a novel myeloid immune checkpoint in cancer, which suppresses T-cell activation; an antibody targeting Siglec-15 is currently in clinical trial for lung cancer. Using immunostaining, we report for the first time that Siglec-15 is expressed on myeloid cells in human GBM specimens. Using syngeneic murine models, we observed that anti-Siglec-15 alone does not improve survival. However, in combination with ZIKV, anti-Siglec-15 significantly improves survival in the CT2A, SB28, and GL261 glioma models. Elaborating CT2A model, the combination treatment increased long-term survivors (at least 90 days) to 60%, compared to 20% with ZIKV alone and 0% with no treatment. To further confirm the role of Siglec-15, we used Siglec-15 knockout (KO) mice and observed 70% long-term survivor rate in Siglec-15 KO mice treated with ZIKV, compared to 40% in wild-type mice (C57BL/6J) with ZIKV. ZIKV treatment in Siglec-15 KO mice led to activation of CD8 T-cells and increased expression of cytotoxic molecules granzyme B and perforin, indicating enhanced anti-tumor activity. Additionally, we detected high levels IFN-gamma and TNF-alpha, further supporting the anti-tumor response. We further improved efficacy by targeting T-cells checkpoint marker PD-1. This combination resulted in 90% long-term survivors in Siglec-15 KO mice following ZIKV treatment. Moreover, in a model for recurrence, upon contralateral rechallenge with CT2A in long-term survivors, we observed long-term memory T-cell responses, with increased numbers of CD8+ T-cells displaying effector and resident memory cell phenotypes, compared to age-matched controls. We obtained similar results with immune-resistant SB28 model.

Conclusions This work suggests that ZIKV oncolytic therapy combined with blocking myeloid checkpoint Siglec-15, using an agent already in humans, and blocking CD8+ T cell checkpoint with anti-PD1, is worthy of study in humans.

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See

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