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Technology

Gylden are developing an extensive range of T cell-priming vaccines and immunotherapy candidates for infectious diseases and other indications using core proprietary technologies designed to elicit broad and long-lasting cellular immune responses.

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 Gylden product candidates are comprised of the core technologies described below:

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  1. Immunoproteomics and Multi-Omic Technologies
    • An MHC Class I expression ‘ligandome library’ of pathogen-derived protein fragments (peptides) are experimentally-determined to be expressed on the surface of pathogen-infected cells and therefore represent the targets of the T cell response during an infection.
  1. Nanotechnology Particles: An ultrasmall carbohydrate-passivated nanocluster delivery system
    • Fully synthetic peptides are designed to be efficiently delivered to the skin-resident immune system to elicit a robust T cell immune response.
  1. Microneedle Array Patch [MAP] Technology
    • Advanced delivery and R&D assets were acquired via the purchase of Zosano Pharma in 2022. Preliminary studies were completed that combine Zosano MAP technology with our T cell-priming candidates, consolidating the platform’s potential and supporting the development of our many other T cell-priming candidates.
  1. In-house GMP Nanomedicine Manufacturing Capabilities
    • Issued by the UK’s MHRA, the Company received its MIA(IMP) license and cGMP accreditation in 2024.

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With Gylden’s product candidates, viral peptides are presented to T cells as in the natural immune response.

  • Gylden’s approach is designed to deliver fully synthetic viral peptides to antigen presenting cells (eg. dendritic cells ), activating naïve T cells with specificity to a virus that are then expanded to a memory phenotype.
  • Such virus-specific memory CD8+ T cells have the potential to migrate to tissue sites of potential pathogen exposure following a second vaccination.
  • A pre-existing population of virus-specific CD8+ T cells is thus created that, upon subsequent pathogen encounter, would be able to immediately kill infected cells before they can release virions, and the infection is rapidly terminated.

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An approach designed to mimic natural immunity

Our goal is to create a critical mass of ‘primed’ tissue-resident memory CD8+ T cells and shorter-lived CD8+ T effector cells with specificities to early pathogen peptides, equipped to provide broad and long-lasting cellular immunity upon subsequent infection. T cell adaptive vaccines evoke the course of cellular immunity that is prompted through natural infection but halt the infection locally — at the site of transmission — before progression to full-blown disease would take place.

Product candidates designed to prime the immune system to enable a rapid response to future infection

The adaptive immune response to an infection includes CD8+ T cells that recognize pathogen-derived peptides (below, from a viral infection) associated with MHC Class I molecules expressed on the surface of infected cells.
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