Invention Title:

ARTIFICIAL ONCOLYTIC VIRUSES AND RELATED METHODS

Publication number:

US20240131095

Publication date:
Section:

Human necessities

Class:

A61K35/766

Inventors:

Applicant:

Drawings (4 of 19)

Smart overview of the Invention

Artificial viral compositions have been developed for the treatment of cancer and hyperproliferative disorders. These compositions aim to enhance the effectiveness of cancer therapies by utilizing engineered oncolytic viruses that selectively target and destroy cancer cells while minimizing damage to normal tissues.

Challenges in Current Cancer Treatments

Cancer treatment faces numerous challenges, particularly with solid tumors. Traditional therapies such as surgery, chemotherapy, and radiation are often applied at advanced stages and can have significant side effects. Solid tumors exhibit heterogeneity in antigen expression and can produce immune-suppressing agents, complicating treatment efforts. There is a critical need for more effective, precise therapies that improve patient outcomes.

Design of Artificial Oncolytic Viruses

The artificial oncolytic viruses are designed to selectively bind to cancer cells through engineered domains that target specific binding partners expressed at higher levels on these cells compared to normal cells. This selectivity allows for targeted therapy, potentially increasing the safety and efficacy of treatment. The viruses can be derived from naturally occurring strains but are modified to enhance their therapeutic properties.

Mechanism of Action

Upon administration, these viruses replicate within cancer cells, leading to cell death through mechanisms such as apoptosis or cytopathic effects. The cycle of infection and replication allows for localized amplification of the virus, continuing the therapeutic effect as long as target cells are present. This approach also includes additional modifications that may enhance tumor targeting or provide therapeutic benefits.

Methods for Production and Administration

The production of these oncolytic viruses involves designing specific viral DNA sequences, synthesizing them, and transfecting cells to generate the final viral product. Administration methods aim to effectively deliver these viruses to the target tissues while minimizing immune responses. The overall goal is to slow or reduce tumor growth in various cancers, making these engineered viruses a promising addition to cancer treatment strategies.