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Targeting TLR7 to limit auto-immunity

Description 
Systemic lupus erythematosus (SLE) and related autoimmune diseases remain incurable, with therapies largely directed at suppressing downstream inflammation rather than targeting disease‑maintaining mechanisms. Our pioneering studies have recently identified TLR7 as a key modulator of SLE (Brown et al. 2022 Nature; Alharbi et al. 2026 Nature Immunology). In this project we are exploring how aberrant TLR7 function can be targeted by short RNA fragments to limit auto-immunity, beyond the case of SLE. The successful candidate will gain cutting edge practical knowledge in molecular, cellular and animal biology, working on a project with a strong translational angle.
Essential criteria: 
Minimum entry requirements can be found here: https://www.monash.edu/admissions/entry-requirements/minimum
Keywords 
immunology inflammation DNA Lupus
School 
School of Clinical Sciences at Monash Health / Hudson Institute of Medical Research » Molecular and Translational Sciences
Available options 
PhD/Doctorate
Masters by research
Honours
Time commitment 
Full-time
Top-up scholarship funding available 
No
Physical location 
Monash Health Translation Precinct (Monash Medical Centre)
Co-supervisors 
Dr 
Sunil Sapkota

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