So, what’s new?
Nanovaccines that work to mount an immune response against a tumor basically consist of two components: the part that delivers the vaccine to the correct site, the lymph nodes, where immune system activation happens; and the part that activates the immune cells to expand and specifically target the tumor.
First author Guizhi Zhu, Ph.D. a post-doctoral fellow in the NIBIB Laboratory of Molecular Imaging and Nanomedicine (LOMIN) explained the new, simplified approach. “We designed a vaccine that binds to a protein called albumin normally found in the body, that also regularly filters through the lymph nodes. Thus, the vaccine essentially hitches a ride with albumin to travel to the lymph nodes, eliminating the need to create a separate delivery vehicle. Given that large-scale manufacturing and long-term safety are the primary hurdles of current nanovaccine technology, our approach offers a detour to accelerate eventual use of nanomedicines in the clinic.” The work is described in the 2017 December issue of Nature Communications.
How is it formulated?
Several nanovaccines were engineered, each with a different antigen—the component that stimulates the immune cells to attack a specific tumor type. To each antigen, the engineers also added a small dye molecule called Evans blue (EB), that binds to the albumin in the body and has been used for nearly a century in the clinic to study albumin binding proteins. The vaccine-EB complex was named AlbiVax (albumin-binding vaccine) because it immediately binds to albumin. The nanovaccine also included a small segment of DNA bound to the EB; the DNA is a “danger signal” to the immune system and so helps make the immune response more robust.
Thus, the complete formulation consists of an antigen and a DNA segment, both bound to EB. Upon injection, both components bind to albumin, which is why the vaccine is considered to be self-assembling. The albumin carrying the antigen and the DNA then delivers both to the lymph nodes where the antigen activates immune cells that specifically target the tumor, and the DNA enhances that activation, optimizing the immune attack.
Anti-tumor effects of the AlbiVax nanovaccine
The vaccines were tested on several tumor types and in several ways. In one experiment, tumor-free mice were vaccinated against mouse thymus tumor cells. The mice were immunized 3 times, with 2-week intervals.
At day 70 a large dose of the tumor cells was injected into seven immunized mice as a challenge. Five of the seven mice survived for more than four months. The five surviving mice were injected again with another large dose of the tumor cells, and four of the five mice survived for more than six months. Blood tests showed that four months after the last immunization, the mice still had circulating immune cells that were specifically killing the thymus tumor cells.
An AlbiVax nanocomplex vaccine was also engineered against a human colon cancer cell line. The human colon cancer cells are injected into the mouse where they establish tumors in various organs. Most tumors lodge in the lung, so the system is a good model of aggressive colon cancer cells that have metastasized to the lung. The mice were given the vaccine six days after the lung tumors were established. In this experiment the mice were also treated with an antibody called anti-PD-1, to counter the effects of the protein PD-1 that appears on the surface of some tumors and acts to slow down the immune attack. In this case, the combination of the nanovaccine and anti-PD-1 resulted in the complete regression of lung tumors in six of the 10 mice for four months.
The team is particularly optimistic about the long-lasting immunity that they were able to induce with the AlbiVax system, as evidenced by continued robust anti-tumor activity for up to six months. This was the longest time point tested in these experiments and represents a significant part of the lifespan of a mouse, which is about two years.
Zhu concludes, “albumin is an interesting protein and it has been studied for over 40 years for drug delivery using different technologies. Compared with other albumin-binding technologies, our proprietary technology has been developed using clinically safe EB, making it very promising for eventual clinical translation. By simply synthesizing albumin-binding vaccines, our technology can be applied to virtually any molecular vaccine or molecular therapeutics.”
The Chief of the NIBIB Laboratory of Molecular Imaging and Nanomedicine is Xiaoyuan Chen, Ph.D., who is the senior author of the publication. Additional laboratories at NIBIB in Bethesda, MD that contributed to the work include the Advanced Imaging and Microscopy Resource, the Laboratory of Cellular Imaging and Macromolecular Biophysics, and the Section on High Resolution Optical Imaging. Additional NIH collaborators included the Laboratory of Molecular Immunology at the National Institute of Allergy and Infectious Diseases, the Cancer and Inflammation Program, National Cancer Institute, Frederick, MD, and the Advanced Imaging and Microscopy resource, NIH, Bethesda. Additional collaborating laboratories included the Molecular Imaging Center, Department of Radiology, Keck School of Medicine, University of Southern California, Los Angeles, the School of Engineering, China Pharmaceutical University, Nanjing, China, the State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, Center for Molecular Imaging and Translational Medicine, and the School of Public Health, Xiamen University, Xiamen, China.