Camel antibodies survive trek to tumor cells

"These viruses are already engineered to replicate only in tumors," says David T. Curiel. "These camelid antibodies would enable them to become even more tumor-specific and open the door for use in metastatic cancer." (Credit: Charles Roffey/Flickr)

Antibodies from camels and alpacas can bring anticancer viruses straight to tumor cells, while leaving other types of cells uninfected, report researchers.

The researchers used human cells grown in the lab for the study. They say it demonstrates the possibility of directly delivering genetically engineered viruses to specific cells. The goal is to infect only cancer cells and then trigger the virus to replicate until the cells burst, killing them and releasing more of the targeted viruses.

The scientists showed that unlike human antibodies or those of most other animals, the antibodies of camels and alpacas survive the harsh environment inside cells and retain the ability to seek out targets, potentially solving a longstanding problem in the field of gene therapy.

“For decades, investigators have been putting human or mouse antibodies on viruses, and they haven’t worked—the antibodies would lose their targeting ability,” says senior author David T. Curiel, professor of radiation oncology at Washington University School of Medicine in St. Louis.

“It was a technical problem. During replication, the virus is made in one part of the cell, and the antibody is made in another. To incorporate the two, the antibody is dragged through the internal fluid of the cell. This is a harsh environment for the antibodies, so they unfold and lose their targeting ability.”

Flip the switch

Antibodies are proteins of the immune system that travel through the bloodstream and recognize potential threats to the body, whether bacteria, viruses or abnormal cells. Most antibodies have a characteristic Y shape. The tips of the Y form a “lock” that binds to a specific “key” carried by foreign bodies that the immune system should destroy.

According to Curiel, recent work by other groups has identified an unusually small and stable class of antibodies made by camels, alpacas, and related species collectively classified as camelids. The “lock” of camelid antibodies consists of the stem of the Y only, so it can’t unfold in the harsh internal environment of the cell.

“We found that when we incorporated the camelid antibodies into the virus, they retained their binding specificity,” Curiel says. “This opens the door to targeting these antibodies to specific tumor markers.”

Currently available viral-based cancer therapeutics and those in human trials are not targeted directly to tumor cells. These therapeutic viruses can infect almost any cell type, but they are genetically engineered to replicate only inside tumor cells.

The viral DNA code is rewritten so that only tumor cells carry the molecular switch that activates the virus’s replication machinery. Once that switch is flipped, the virus replicates until the cell bursts, killing the cell and releasing more viruses that can potentially infect other cells.

‘Even more tumor-specific’

Limiting virus replication and cell death only to cancer cells is helpful in reducing side effects of the treatment. But the technology is still inefficient because so much of the injected virus never finds the tumor and is essentially wasted.


“We want this new level of targeting specificity because it would allow us to inject the virus into the bloodstream, where it would exclusively infect and replicate in tumor cells, even if they are disseminated throughout the body,” Curiel says.

“These viruses are already engineered to replicate only in tumors. These camelid antibodies would enable them to become even more tumor-specific and open the door for use in metastatic cancer.”

After demonstrating this proof of concept, the next step is to design viruses with camelid antibodies against a specific tumor and test it in an animal model of the disease, Curiel says.

The National Institutes of Health, the Stichting Jo Kolk Studiefonds, and the Dutch Cancer Society supported the work, which appears in Molecular Therapy—Oncolytics.

Source: Washington University in St. Louis