Candidalysin: Anti-fungal target and immunotherapeutic candidate

The Problem


Candida albicans is an opportunistic fungal pathogen, which normally exists as a commensal of the oral cavity and gastrointestinal tracts and frequently causes superficial vaginitis infections. Moreover, common clinical procedures, such as gastrointestinal surgery, implantation of a central venous catheter or antibiotic treatment are major risk factors for life-threatening systemic candidiasis.  Systemic candidiasis is now the third most common cause of hospital-acquired bloodstream infections and is often fatal, having 30–50% mortality which equates to ~100,000 deaths/year. Damage of host cells and uncontrolled immune activation are the hallmarks of several diseases caused by C. albicans. In the USA, yearly healthcare costs for fungal infections are $3 billion, of which Candida infections account for $2 billion. EU healthcare costs are estimated to be similar. Therefore, Candida pathogens carry an immense health burden and represent a major socio-economic challenge for worldwide communities.


The Solution   


It is known that expression of the Candida gene ECE1 (extent of cell elongation 1) is upregulated during hypha formation and that the gene’s product, Ece1, can be proteolytically processed by Kex2 into eight peptide fragments. The inventors have now found that a single 31 amino acid proteolytic fragment of Ece1 (fragment 3; termed Candidalysin) acts both as a novel peptide pore-forming toxin and as an immunostimulant. No truncations have been found that produce cell lysis or inflammatory responses in epithelial cells, although the fragment’s carboxy-terminal K residue appears to be important for membrane interactions and damage induction, but not its immunostimulatory function. This opens a therapeutic window in which protective immunity may be generated without triggering damage.

To conclude, neutralisation of Candidalysin has the strong potential to prevent not only host damage during C. albicans infections but also deleterious inflammatory responses. Data obtained using multiple approaches supports Candidalysin representing a very promising new therapeutic target to treat C. albicans infections. Additionally, a modified fragment can form the basis of an antigen or adjuvant to provide mucosal protection against C. albicans and related infectious agents. Finally there are a range of diagnostic applications for the peptide and the specific binding partners for it.



Candidalysin represents a very promising new therapeutic target to treat C. albicans infections, overcoming growing resistance to existing anti-fungals. As a vaccine candidate peptide 3 can be delivered via a number of routes; oral or vaginal delivery would be favoured if  mucosal immunity was required and intravenous or intraperitoneal delivery might be preferred for systemic protection. Additionally, antibodies against Candidalysin might be used therapeutically to produce passive immunity. Application may be topical or, in the case or septicaemia, systemic.



We are seeking development partners wishing to take options / evaluation licences over the technology. Exclusivity in specified fields could be available for a suitable partner.

IP Status

Patents are pending in China, Europe and USA, taking priority from a GB filing (Priority date: 11 April 2013). The Joint Applicants are King’s College London, UK and Hans-Knöll Institut, Jena, DE. (In the US the patent has published as US 20160046699 A1; )  



Figure 1 is a graph showing the results of an experiment to determine which of the Ece1 peptides are haemolytic toxins.  Individual peptides were incubated with human erythrocytes for 1 hour and heamolysis assayed by measuring haemoglobin release (as measured by absorbance at 541nm, normalised to a 100% lysis control).





C. albicans


fungal infection




systemic infection


drug target


mucosal immunity



peptide fragment





Patent Information:
For Information, Contact:
Ian Durrant
IP & Licensing Manager
King's College London
Julian Naglik
Bernhard Hube
David Moyes
Sarah Höfs
Duncan Wilson
Shirley Tang
Jonathan Richardson