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Novel innate immune variants causing autoinflammatory disease

Description 
We manage the Australian Autoinflammatory Disease Registry (AADRY.org), and collaborate widely to identify genetic variants that may be the cause of chronic inflammatory disease for patients from all over Australia. We now have several candidate variants of interest that we need to test to see if they are pathogenic, which could represent a novel mechanism, or in some cases the first time the disease has been identified. Given that Autoinflammatory diseases primarily feature inflammation from innate immune cells, we frequently examine the effect of the genetic variant using CRISPR in relevant cell lines (eg. monocytes) using readouts such as cytokine production (eg. ELISA or QPCR). More specific tests may need to be applied depending on the gene of interest. All results are confirmed using primary samples from patients (eg PBMC) where possible. At the conclusion of this project it should be possible to confirm the pathogenicity of a particular variant for a patient or family with Autoinflammatory disease, and add to the list of genes that are known to cause these conditions.
Essential criteria: 
Minimum entry requirements can be found here: https://www.monash.edu/admissions/entry-requirements/minimum
Keywords 
Inflammation, immune sensor, inflammasome, interferon, cytokine
School 
School of Clinical Sciences at Monash Health / Hudson Institute of Medical Research
Available options 
PhD/Doctorate
Time commitment 
Full-time
Top-up scholarship funding available 
No
Physical location 
Monash Health Translation Precinct (Monash Medical Centre)

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