Schwannoma Gene Therapy via Adeno-Associated Viral Vector Delivery of Apoptosis-Associated Speck-like Protein Containing CARD (ASC): Preclinical Efficacy and Safety

• Published in: International journal of molecular sciences Vol. 23; no. 2; p. 819
• Main Authors: Ahmed, Sherif G, Maguire, Casey A, Cao, Shiliang Alice, Brenner, Gary J
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 13-01-2022; MDPI
• Subjects: AAV; Animal models; Animals; Antibodies; Antitumor activity; Apoptosis; ASC; Bevacizumab; CARD Signaling Adaptor Proteins - genetics; Caspase; Clinical trials; Cranial nerves; Dependovirus - genetics; Disease Models, Animal; Drug therapy; Fluorescent Antibody Technique; Gene Expression; Gene therapy; Gene Transfer Techniques; Genetic Therapy - adverse effects; Genetic Therapy - methods; Genetic Vectors - administration & dosage; Genetic Vectors - genetics; Humans; Immunocompetence; Immunohistochemistry; Inflammasomes; Mice; Morbidity; Myelin P0 protein; Nervous system; Neurilemmoma - genetics; Neurilemmoma - therapy; Neurotoxicity; neutralizing antibodies; Pain; Peripheral nervous system; Proteins; Schwann cells; schwannoma; Transduction, Genetic; Transgenes; Translation; Treatment Outcome; Tumors; Xenograft Model Antitumor Assays; Xenografts; Xenotransplantation; ASC; gene therapy; neutralizing antibodies; schwannoma; AAV
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms23020819

Schwannomas are tumors derived from Schwann-lineage cells, cells that protect and support myelinated nerves in the peripheral nervous system. They are typically slow-growing, encapsulated and benign. These tumors develop along peripheral, spinal and cranial nerves causing pain, sensory-motor dysfunction and death. Primary treatment for schwannoma is operative resection which can be associated with significant morbidity. Pharmacotherapy is largely restricted to bevacizumab, which has minimal or no efficacy for many patients and can be associated with treatment-limiting adverse effects. Given the suffering and morbidity associated with schwannoma and the paucity of therapeutic options, there is an urgent need for safe and effective therapies for schwannomas. We previously demonstrated that adeno-associated virus serotype 1 (AAV1) vector mediated delivery of the inflammasome adaptor protein, apoptosis-associated speck-like protein containing a caspase recruitment domain (
) under the control of the P0 promoter, produced a prolonged reduction in tumor volume and tumor-associated pain in human xenograft and mouse syngeneic schwannoma models. Here, we present data essential for the translation of our AAV1-P0-ASC schwannoma gene therapy to clinical trials. We determine the minimum effective dose of AAV1-P0-hASC required to induce an anti-tumor effect in the xenograft human-schwannoma model. We also show that the presence of preexisting AAV1 immunity does not alter the antitumor efficacy of AAV-P0-mASC in a syngeneic mouse schwannoma model. Furthermore, the maximum deliverable intratumoral dose of AAV1-P0-ASC was not associated with neuronal toxicity in immunocompetent mice. Taken together, these safety and efficacy data support the translation of the AAV1-P0-ASC schwannoma gene therapy strategy to clinical trials.