Skip Navigation

Yerkes Researcher Finds Virus-Mimicking Nanoparticles Can Stimulate Long Lasting Immunity

February 23, 2011

Media Contacts

Holly Korschun, 404-727-3990, hkorsch@emory.edu; Emily Rios, 404-727-7732, erios@emory.edu; Lisa Newbern, 404-727-7709, lisa.newbern@emory.edu

Vaccine scientists say their “Holy Grail” is to stimulate immunity that lasts for a lifetime. Live viral vaccines such as the smallpox or yellow fever vaccines provide immune protection that lasts several decades, but despite their success, scientists have remained in the dark as to how they induce such long lasting immunity.

Scientists at the Emory Vaccine Center have designed tiny nanoparticles that resemble viruses in size and immunological composition and that induce lifelong immunity in mice. They designed the particles to mimic the immune-stimulating effects of one of the most successful vaccines ever developed – the yellow fever vaccine. The particles, made of biodegradable polymers, have components that activate two different parts of the innate immune system and can be used interchangeably with material from many different bacteria or viruses.

The results are described in this week’s issue of Nature.

“These results address a long-standing puzzle in vaccinology: how do successful vaccines induce long lasting immunity?” says senior author Bali Pulendran, PhD, Charles Howard Candler professor of pathology and laboratory medicine at Emory University School of Medicine and a researcher at Yerkes National Primate Research Center.

“These particles could provide an instant way to stretch scarce supplies when access to viral material is limited, such as pandemic flu or during an emerging infection. In addition, there are many diseases, such as HIV, malaria, tuberculosis and dengue, that still lack effective vaccines, where we anticipate that this type of immunity enhancer could play a role.”

One injection of the live viral yellow fever vaccine, developed in the 1930s by Nobel Prize winner Max Theiler, can protect against disease-causing forms of the virus for decades. Pulendran and his colleagues have been investigating how humans respond to the yellow fever vaccine, in the hopes of imitating it.

Several years ago, they established that the yellow fever vaccine stimulated multiple Toll-like receptors (TLRs) in the innate immune system. TLRs are present in insects as well as mammals, birds and fish. They are molecules expressed by cells that can sense bits of viruses, bacteria and parasites and can activate the immune system. Pulendran’s group demonstrated that the immune system sensed the yellow fever vaccine via multiple TLRs, and that this was required for the immunity induced by the vaccine.

“TLRs are like the sixth sense in our bodies, because they have an exquisite capacity to sense viruses and bacteria, and convey this information to stimulate the immune response,” Pulendran says.  “We found that to get the best immune response, you need to hit more than one kind of Toll-like receptor. Our aim was to create a synthetic particle that accomplishes this task.”

Emory postdoctoral fellow Sudhir Pai Kasturi, PhD, created tiny particles studded with molecules that turn on Toll-like receptors. He worked with colleague Niren Murthy, PhD, associate professor in the Wallace H. Coulter Department of Biomedical Engineering at Georgia Tech and Emory University.

“We are very excited about building on this platform to design improved vaccines for existing and emerging infectious diseases” says Kasturi, the primary author, working in Pulendran’s lab at the Emory Vaccine Center. One of the particles’ components is MPL (monophosphoryl lipid A), a component of bacterial cell walls, and the other is imiquimod, a chemical that mimics the effects of viral RNA.  The particles are made of PLGA—poly(lactic acid)-co-(glycolic acid)—a synthetic polymer used for biodegradable grafts and sutures.

All three components are FDA-approved for human use individually. For several decades, the only FDA-approved vaccine additive was alum, until a cervical cancer vaccine containing MPL was approved in 2009. Because of immune system differences between mice and monkeys, the scientists replaced imiquimod with the related chemical resiquimod for monkey experiments.

In mice, the particles can stimulate production of antibodies to proteins from flu virus or anthrax bacteria several orders of magnitude more effectively than alum, the authors found. In addition, the immune cells persist in lymph nodes for at least 18 months, almost the lifetime of a mouse. In experiments with monkeys, nanoparticles with viral protein could induce robust responses greater than five times the response induced by a dose of the same viral protein given by itself, without the nanoparticles.

The research was supported by the National Institutes of Health and the Bill and Melinda Gates Foundation.

For eight decades, the Yerkes National Primate Research Center, Emory University, has been dedicated to conducting essential basic science and translational research to advance scientific understanding and to improve the health and well-being of humans and nonhuman primates.

Today, the center, as one of only eight National Institutes of Health–funded national primate research centers, provides leadership, training and resources to foster scientific creativity, collaboration and discoveries. Yerkes-based research is grounded in scientific integrity, expert knowledge, respect for colleagues, an open exchange of ideas and compassionate quality animal care.

Within the fields of microbiology and immunology, neurologic diseases, neuropharmacology, behavioral, cognitive and developmental neuroscience, and psychiatric disorders, Yerkes research programs are seeking ways to: treat drug addiction; interpret brain activity through imaging; increase understanding of progressive illnesses such as Alzheimer's and Parkinson's diseases; unlock the secrets of memory; determine how the interaction between genetics and society shape who we are; develop vaccines for infectious and noninfectious diseases; and advance knowledge about the evolutionary links between biology and behavior.

Established in 1996, researchers at the Emory Vaccine Center (EVC), a division of the Emory School of Medicine housed at the Yerkes Research Center, study and develop vaccines for HIV/AIDS, cancers, hepatitis C, malaria, influenza and other global infectious disease threats. Rafi Ahmed, PhD, leads the division. The EVC provides an interdisciplinary focus for research in immunology and vaccines and fosters communication and collaboration among researchers to better understand the complexities of infectious diseases, cancer biology and vaccine development.


The Robert W. Woodruff Health Sciences Center of Emory University is an academic health science and service center focused on missions of teaching, research, health care and public service. Its components include the Emory University School of Medicine, Nell Hodgson Woodruff School of Nursing, and Rollins School of Public Health; Yerkes National Primate Research Center; Winship Cancer Institute of Emory University; and Emory Healthcare, the largest, most comprehensive health system in Georgia. Emory Healthcare includes: The Emory Clinic, Emory-Children's Center, Emory University Hospital, Emory University Hospital Midtown, Wesley Woods Center, and Emory University Orthopaedics & Spine Hospital. The Woodruff Health Sciences Center has a $2.5 billion budget, 17,600 employees, 2,500 full-time and 1,500 affiliated faculty, 4,700 students and trainees, and a $5.7 billion economic impact on metro Atlanta.

Learn more about Emory’s health sciences: http://emoryhealthblog.com -
@emoryhealthsci (Twitter) - http://emoryhealthsciences.org

###