Researchers found that ‘rational vaccinology’
increases potency by changing the structural location of antigens and
adjuvants.
Scientists globally are
investigating vaccines for cancer, some with ambitious goals. One such group of
scientists at from the International Institute for Nanotechnology (IIN) at
Northwestern University, US.
The
team recently discovered a new way to significantly increase the potency of
almost any vaccine. The scientists used chemistry and nanotechnology to change the structural location of
adjuvants and antigens on and within a nanoscale vaccine, greatly increasing
vaccine performance. The antigen targets the immune system, and the adjuvant is
a stimulator that increases the effectiveness of the antigen.
The
study was recently published in Nature Biomedical
Engineering.
“The work shows that vaccine structure and not just
the components is a critical factor in determining vaccine efficacy,” said lead
investigator Chad Mirkin, director of the IIN. “Where and how we position the
antigens and adjuvant within a single architecture markedly changes how the
immune system recognises and processes it.
This new heightened
emphasis on structure has the potential to improve the effectiveness of
conventional cancer vaccines, which historically have not worked well, Mirkin
said.
Mirkin’s team has studied the effect of vaccine
structure in the context of seven different types of cancer to date, including triple-negative breast cancer,
papillomavirus-induced cervical cancer, melanoma, colon cancer and prostate
cancer to determine the most effective architecture to treat each
disease.
With most conventional
vaccines, the antigen and the adjuvant are blended and injected into a patient.
There is no control over the vaccine structure, and, consequently, limited
control over the trafficking and processing of the vaccine components. Thus, there
is no control over how well the vaccine works.
“A challenge with
conventional vaccines is that out of that blended mish mosh, an immune cell
might pick up 50 antigens and one adjuvant or one antigen and 50 adjuvants,”
said study author Assistant Professor Michelle Teplensky. “But there must be an
optimum ratio of each that would maximise the vaccine’s effectiveness.”
Enter SNAs (spherical
nucleic acids), which are the structural platform — invented and developed by
Mirkin — used in this new class of modular vaccines. SNAs allow scientists to
pinpoint exactly how many antigens and adjuvants are being delivered to cells.
SNAs also enable scientists to tailor how these vaccine components are
presented, and the rate at which they are processed. Such structural
considerations, which greatly impact vaccine effectiveness, are largely ignored
in conventional approaches.
This approach to
systematically control antigen and adjuvant locations within modular vaccine
architectures was created by Mirkin, who coined the term rational vaccinology
to describe it. It is based on the concept that the structural presentation of
vaccine components is as important as the components themselves in driving
efficacy.
“Vaccines developed
through rational vaccinology deliver the precise dose of antigen and adjuvant
to every immune cell, so they are all equally primed to attack cancer cells,”
said Mirkin.
The team developed a
cancer vaccine that doubled the number of cancer antigen-specific T cells and
increased the activation of these cells by 30 percent by reconfiguring the
architecture of the vaccine to contain multiple targets to help the immune system
find tumour cells.
The team investigated
differences in how well two antigens were recognised by the immune system
depending on their placement — on the core or perimeter — of the SNA structure.
For an SNA with optimum placement, they could increase the immune response and
how quickly the nanovaccine triggered cytokine (an immune cell protein)
production to boost T cells attacking the cancer cells. The scientists also
studied how the different placements affected the immune system’s ability to
remember the invader, and whether the memory was long-term.
“Where and how we
position the antigens and adjuvant within a single architecture markedly
changes how the immune system recognises and processes it,” Mirkin said.