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The future of cystic fibrosis can be different thanks to personalized medicine

40% of patients with CF don't respond to treatment because of rare mutations

04-Oct-2019

Key points from article :

Researchers are growing mini gut and lung “avatars” derived from cells of children with cystic fibrosis.

Patients’ stem cells are collected at 11 CF clinics across Australia.

Stem cells are grown into miniature versions of the gut and lung.

Mini-organs are then frozen and preserved in the ECF biobank for future testing.

ECF AVATAR platform uses patient-derived mini-organs to assess the best medication for each patient.

Research is done by the University of New South Wales.

Mentioned in this article:

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Adam Jaffe

Professor and Paediatric Respiratory and Sleep Medicine Physician

University of New South Wales (UNSW)

Public Research university.

Topics mentioned on this page:
Precision Medicine