# An engineered oncolytic herpes virus expressing a full-length α-CD47 mAb for the treatment of GBM

> **NIH NIH U19** · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · 2021 · $173,914

## Abstract

PROJECT SUMMARY – PROJECT 1
The combination of oncolytic virotherapy (OV) and monoclonal antibody (mAb) immunotherapy has great
potential for the treatment of glioblastoma (GBM), the most common malignant brain tumor without a cure. An
OV carrying a mAb-coding gene can produce and release the mAb drug specifically at the tumor site as a safe,
effective, and innovative delivery system. Prior to our study, this approach has not been previously explored
using herpes simplex virus 1-based OV (oHSV). CD47 is a transmembrane protein widely expressed on cancer
cells including GBM. It acts as a “don’t eat me” signal by functioning as a ligand to signal regulatory protein-α
(SIRPα) expressed on macrophages, resulting in inhibition of phagocytosis. We have generated an oHSV that
expresses a full-length anti-CD47 mAb on an IgG1 scaffold (OV-αCD47-G1) that is capable of inducing antibody-
dependent cellular phagocytosis (ADCP) by macrophages and antibody-dependent cellular cytotoxicity (ADCC)
by natural killer cells to eradicate GBM cells in vitro and in vivo, in addition to blockade of the CD47-SIRPα “don’t
eat me” signaling pathway in macrophages. We have demonstrated that our novel OV-αCD47-G1 significantly
improves the survival of GBM-bearing mice in orthotopic, immunocompetent, and immunodeficient models. Our
central hypothesis is that OV-αCD47-G1 will be safe and effective at improving GBM treatment and its anti-
tumor activity in the brain will be reflected by markers in the peripheral blood. Importantly, we have optimized
and manufactured GMP-grade OV-αCD47-G1 to conduct the proposed studies and will initiate a phase I clinical
trial for adults with GBM. In this proposal, we will evaluate both the systemic and regional immune responses in
vivo following clinical-grade OV-αCD47-G1 administration and identify markers in the circulation that correlate
with anti-tumor activity in the brain in GBM animal models (Aim 1); we will perform Investigational New Drug
(IND)-enabling in vivo safety and efficacy studies using clinical-grade OV-αCD47-G1 (Aim 2); and we will
determine the safety of administering a single intracerebral infusion of OV-αCD47-G1 in adult patients with
recurrent GBM (Aim 3). To accomplish these objectives, we will utilize immunocompetent and
immunocompromised GBM mouse models for our correlative and preclinical studies evaluating OV-αCD47-G1
prior to the phase I clinical trial. Upon conclusion, we will understand how to optimize OV-αCD47-G1 therapy to
cure GBM. Further insight into this process, as will result from the implementation and completion of this
proposal, is impactful as it will ultimately lead to a reduction in mortality for adults suffering from GBM.

## Key facts

- **NIH application ID:** 10306304
- **Project number:** 1U19CA264512-01
- **Recipient organization:** BECKMAN RESEARCH INSTITUTE/CITY OF HOPE
- **Principal Investigator:** Jianhua Yu
- **Activity code:** U19 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2021
- **Award amount:** $173,914
- **Award type:** 1
- **Project period:** 2021-09-13 → 2026-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10306304

## Citation

> US National Institutes of Health, RePORTER application 10306304, An engineered oncolytic herpes virus expressing a full-length α-CD47 mAb for the treatment of GBM (1U19CA264512-01). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10306304. Licensed CC0.

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