|
MIT
Works Toward Safer Gene Therapy
Friday, September 7, 2007
Biodegradable polymers
replace viruses to deliver genes
Structure of a piece of a
biodegradable polymer used for gene delivery.
Image Credit:
Jordan Green / MIT
|
In work that could lead to
safe and effective techniques for gene therapy, MIT researchers
have found a way to fine-tune the ability of biodegradable
polymers to deliver genes.
Gene therapy, which involves
inserting new genes into patients' cells to fight diseases like
cancer, holds great promise but has yet to realize its full
potential, in part because of safety concerns over using viruses
to carry the genes.
The new MIT work, published
this week in Advanced Materials, focuses on creating gene
carriers from synthetic, non-viral materials. The team is led by
Daniel Anderson, research associate in MIT's Center for Cancer
Research.
"What we wanted to do is
start with something that's very safe--a biocompatible,
degradable polymer--and try to make it more effective, instead of
starting with a virus and trying to make it safer," said
Jordan Green, a graduate student in biological engineering and
co-first author of the paper.
Gregory Zugates, a former
graduate student in chemical engineering now at WMR Biomedical,
Inc., is also a co-first author of the paper.
Gene therapy has been a field
of intense research for nearly 20 years. More than 1,000
gene-therapy clinical trials have been conducted, but to date
there are no FDA-approved gene therapies. Most trials use viruses
as carriers, or vectors, to deliver genes.
However, there are risks
associated with using viruses. As a result, many researchers have
been working on developing non-viral methods to deliver
therapeutic genes.
The MIT scientists focused on three
poly(beta-amino esters), or chains of alternating amine and
diacrylate groups, which had shown potential as gene carriers.
They hoped to make the polymers even more efficient by modifying
the very ends of the chains.
When mixed together, these
polymers can spontaneously assemble with DNA to form
nanoparticles. The polymer-DNA nanoparticle can act in some ways
like an artificial virus and deliver functional DNA when injected
into or near the targeted tissue.
A comparison of different
methods of gene delivery, showing delivery of DNA encoding
green fluorescent protein (from jellyfish) to human
umbilical vein endothelial cells. Image (A) shows delivery
by polyethylenimine, a leading non-biodegradable
commercially available polymer. Image (B) shows
poly(beta-amino esters) developed at MIT and (C) shows
adenovirus. High levels of DNA delivery are observed with
the MIT polymers one day after the addition of the
nanoparticles.
Image Credit:
Jordan Green / MIT
|
The researchers developed
methods to rapidly optimize and test new polymers for their
ability to form DNA nanoparticles and deliver DNA. They then
chemically modified the very ends of the degradable polymer
chains, using a library of different small molecules.
"Just by changing a couple
of atoms at the end of a long polymer, one can dramatically
change its performance," said Anderson. "These minor
alterations in polymer composition significantly increase the
polymers' ability to deliver DNA, and these new materials are now
the best non-viral DNA delivery systems we've tested."
The polymers have already been
shown to be safe in mice, and the researchers hope to ultimately
run clinical trials with their modified polymers, said Anderson.
Non-viral vectors could prove
not only safer than viruses but also more effective in some
cases. The polymers can carry a larger DNA payload than viruses,
and they may avoid the immune system, which could allow multiple
therapeutic applications if needed, said Green.
One promising line of research
involves ovarian cancer, where the MIT researchers, in
conjunction with Janet Sawicki at the Lankenau Institute for
Medical Research, have demonstrated that these polymer-DNA
nanoparticles can deliver DNA at high levels to ovarian tumors
without harming healthy tissue.
Other MIT authors on the paper
are Nathan Tedford, a former graduate student in biological
engineering now at Epitome Biosystems; Linda Griffith, professor
of biological engineering; Douglas Lauffenberger, head of
biological engineering, and Institute Professor Robert Langer.
Sawicki and Yu-Hung Huang of the Lankenau Institute are also
co-authors.
The research was funded by the
National Institutes of Health, the Department of Defense and the
National Science Foundation.
The MIT Center for Cancer
Research (CCR) was founded in 1974 and is one of eight National
Cancer Institute-designated basic research centers. Its mission
is to apply the tools of basic science and technology to
determine how cancer is caused, progresses and responds to
treatment.
Source:
MIT / Anne Trafton

|