Assay Development

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CFTR protein is shown at the apical surface of the cells (red signal).  Cytoplasm labelled with anti Cytokeratin antibody is  green and the nuclei are blue (DAPI).


In parallel with the development of gene therapy products there has been the development of clinical assays to gauge the effectiveness of gene therapy.

In many ways this type of research is as demanding as the development of the vectors themselves because without sufficiently powerful assays, it is impossible to determine the effectiveness of our technologies.

The types of assays we have developed can be broken down into a number of groups.

  • Clinical Biomarkers
  • Imaging Gene Transfer
  • Quantitative RT-PCR
  • Electrical Measurements of CFTR Function


Cinical Biomarkers

Clinical biomarkers are assays that can be performed to give a reliable measurement of the degree of disease severity in a disease.

In CF spirometry testing of lung function has been a classic biomarker for decades. However, for gene therapy clinical studies we wanted to be able to determine very subtle differences between patients that had received gene transfer vectors and those that had not. This required much more sensitive assays to be developed.

We have looked at a number of areas and you can find publications relating to these below. In particular we have been successful in developing lung clearance index assays (LCI) and believe this may be a more suitable approach to measuring changes in lung function in patients undergoing clinical trials.



Imaging Gene Transfer

One of the most meaningful ways of assessing the effectiveness of gene transfer efficiency is to use direct imaging technologies. For many preclinical studies we use fluorescent or luminescent reporter genes to be able to identify the cell types we have transfected in our models.

This allows us to answer one of the fundamental questions regarding gene transfer efficiency, "How many cells are we transfecting and how much do they express?"
Increasingly we are also using direct in-vivo imaging to make repeated measures of gene transfer in mice or in our ex-vivo models, thus reducing the number of animals and expense involved.

In many clinical trials, antibodies have been used to directly image CFTR protein expression. However, the range of antibodies available is limiting. Nevertheless our Antibody Working Group has developed a range of improved protocols to optimise such assays in our clinical trial and pre-clinical models.



Staining of clilia on an airway epithelium


Quantitative RT-PCR

Animation of a Taqman PCR reaction. Polymerisation from the primers forces the cleavage of the probe. The Reporter dye is freed from its quencher and fluoresces when excited by a laser.Imaging and biomarkers are very powerful tools to use to assess gene transfer. However, they are not truly quantitative and often fail to detect gene expression from inefficient gene transfer systems.

This can be particularly problematic for early stage projects where maximal sensitivity is desirable. Therefore the Consortium has a Taqman PCR core facility which is used to detect the presence of vector mRNA or DNA from most of our model systems and our ongoing clinical trial.

The sensitivity of Taqman is far greater than most other assays available and can be used to detect


Electrical Measurements of CFTR Function

CFTR forms an ion channel and passage of ions through this channel can be measured electrically.

In the clinical trial and in pre-clinical models we continue to make extensive use of such methods to assess the activity of the CFTR protein following gene transfer.



A pellet of E.coli containing a plasmid expressing a pink fluorescent protein.


Proposed 3D model of the CFTR protein.


Light microscope image of a human airway liquid interface cultures. Dark patches are mucous.


Large scale lentivirus production in suspension culture.


A CFTR Western blot, to confirm protein production in cell culture.


Human airway liquid interface cultures transduced with a lentivirus expressing Luciferase.


A frozen vial of GL67A (left) and a frozen vial of pGM169 plasmid DNA (right)


Purifying mRNA from tissue samples.