Implants mimic Infection to rally immune system against tumors
January 22, 2009
Subcutaneous antigen-laden disks successfully marshal T cells against deadly melanoma
Contact: Steve Bradt
617-496-8070
CAMBRIDGE, Mass. - Jan. 22, 2009 – Bioengineers at Harvard University
have shown that small plastic disks impregnated with tumor-specific
antigens and implanted under the skin can reprogram the mammalian
immune system to attack tumors.
The research –
which ridded 90 percent of mice of an aggressive form of melanoma that
would usually kill the rodents within 25 days – represents the most
effective demonstration to date of a cancer vaccine.
Harvard’s David J. Mooney and colleagues describe the research in the current issue of the journal Nature Materials.
“Our immune systems work by recognizing and attacking foreign invaders,
allowing most cancer cells – which originate inside the body – to
escape detection,” says Mooney, Gordon McKay Professor of
Bioengineering in Harvard’s School of Engineering and Applied Sciences.
“This technique, which redirects the immune system from inside the
body, appears to be easier and more effective than other approaches to
cancer vaccination.”
Most previous work on cancer vaccines has focused on removing immune
cells from the body and reprogramming them to attack malignant tissues.
The altered cells are then reinjected back into the body. While Mooney
says ample theoretical work suggests this approach should work, in
experiments more than 90 percent of the reinjected cells have died
before having any effect.
The implants developed by Mooney and colleagues are slender disks
measuring 8.5 millimeters across. Made of an FDA-approved biodegradable
polymer, they can be inserted subcutaneously, much like the implantable
contraceptives that can be placed in a woman’s arm.
The disks are 90 percent air, making them highly permeable to immune
cells. They release cytokines, powerful attractants of immune-system
messengers called dendritic cells.
These cells enter an implant’s pores, where they are exposed to
antigens specific to the type of tumor being targeted. The dendritic
cells then report to nearby lymph nodes, where they activate the immune
system’s T cells to hunt down and kill tumor cells throughout the body.
“Much as an immune response to a bacterium or virus generates long-term
resistance to that particular strain, we anticipate out materials will
generate permanent and body-wide resistance against cancerous cells,
providing durable protection against relapse,” says Mooney, a core
member of the recently established Wyss Institute for Biologically
Inspired Engineering at Harvard.
The implants could also be loaded with bacterial or viral antigens to
safeguard against an array of infectious diseases. They could even
redirect the immune system to combat autoimmune diseases such as type 1
diabetes, which occurs when immune cells attack insulin-producing
pancreatic cells.
“This study demonstrated a powerful new application for polymeric
biomaterials that may potentially be used to treat a variety of
diseases by programming or reprogramming host cells,” Mooney and his
co-authors write in Nature Materials.
“The system may be applicable to other situations in which it is
desirable to promote a destructive immune response (for example,
eradicate infectious diseases) or to promote tolerance (for example,
subvert autoimmune disease).”
Mooney’s co-authors are Omar A. Ali,
Nathaniel Huebsch, and Lan Cao of Harvard’s School of Engineering and
Applied Sciences and Glenn Dranoff of the Dana-Farber Cancer Institute,
Brigham and Women’s Hospital, and Harvard Medical School. The research
was funded by the National Institutes of Health and Harvard University.

