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Genocea Technology For many pathogens, protective immunity requires the generation of a cellular immune
response. One of the key components of a cellular immune response are T-lymphocytes (T-cells). T-cells can
be generally classified as CD8+ cytotoxic T-lymphocytes (CTL) and CD4+ Helper T-cells, that respectively,
recognize and eliminate pathogen-infected host cells or produce compounds (cytokines) that stimulate other
immune cells to help fight infection. To activate T-cell responses during a natural infection, invading pathogens
are initially engulfed by specialized antigen-presenting cells (APC). Pathogen-derived proteins (antigens) are
subsequently processed into smaller peptides and placed on the surface of the APC for recognition by CD8+
or CD4+ T-cells. Upon recognition of the presented antigenic peptide on the surface of the APC, T-cells are
then activated to help eliminate the infection. Activated T-cells also divide and become long-lived memory T-cells
that can rapidly respond to infection should the host contact the infectious agent again, thus providing
long-term protective T-cell memory. Genocea can rapidly identify the antigens that result in the in vivo stimulation of protective CD8+ and CD4+ T-cells, targets that can be immediately incorporated into existing antigen delivery systems to produce multivalent vaccine formulations that have the highest probability of generating protective cell-mediated immunity. Genocea's technology can essentially mimic the mammalian immune system in vitro and present it with every possible antigen from a disease-causing agent. Genocea can rapidly identify which antigens - out of the entire proteome of a disease target - will best stimulate the immune system in vivo, a task that was not only slow, but previously impossible. |
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