Centauri has developed an immunotherapeutics platform that can direct a potent natural immunity to target disease, via multifunctional molecules called Alphamers™. The Alphamer molecules are versatile structures consisting of three separate parts.
- A targeting domain which allows the Alphamer to bind specifically to the target of interest. We have exemplified antibodies, antibody fragments, peptides, oligonucleotides and chemicals within our IP estate
- An effector domain which comprises a variable number of natural carbohydrate structures which are recognised by pre-existing antibodies in humans. These antibodies are present at high titre in all humans, they are polyclonal consisting of a number immunoglobin subclasses and are able to trigger a potent immune response engaging both innate and adaptive immune mechanism concurrently
- The third part of the molecule is a proprietary Linker molecule, which covalently links effector and targeting domains. Linkers are stable, non-cleavable, and can be used in a modular fashion to link a targeting domain (the cell-binding component) to our effector molecules and engage the potent natural immune system mechanism. Linkers are critical to Alphamer properties and optimisation of functionality.
It is possible to select structurally diverse domains, for example a small molecule, peptide, aptamer, antibody or antibody fragment and use a linker to connect the targeting moiety to our effector domain.
Centauri’s approach is novel; unique in the anti-infective space and difficult to replicate by other ‘bi-specific’ modalities in oncology applications. Alphamer differentiation stems predominantly from four important features:
- The effector domain in an Alphamer is a natural sugar which is inherently non-toxic (an immunological hapten)
- Alphamers can be systemically delivered and repeatedly dosed
- Activation of the immune system only occurs on the target of interest driven by the targeting domain
- Alphamers, as a single agent, can engage multiple important immune mechanisms concurrently, including target cell killing and neo-antigen presentation, leading to a durable memory cell response (via complement activation, antibody dependant cellular toxicity, target cell phagocytosis)