Systemic lupus erythematosus (SLE), more simply known as lupus, is an autoimmune disease where the body makes antibodies against its own DNA. It may involve a variety of genes, follow a variety of genetic pathways, and damage a variety of cell types. In many cases, the consequence is impairment of kidney function, which is known as glomerulonephritis.
Such a ‘moving target’ is difficult to pinpoint, track and ultimately treat, as one treatment may work for one particular genetic group, but not another. The Leukocyte Signalling Laboratory headed by A/Prof Margaret Hibbs, has identified a cellular pathway whereby once production of one particular signalling molecule called p110d PI3K is slowed down, the disease processes also slowed down. See journal article.
Such a ‘moving target’ is difficult to pinpoint, track and ultimately treat, as one treatment may work for one particular genetic group, but not another. The Leukocyte Signalling Laboratory headed by A/Prof Margaret Hibbs, has identified a cellular pathway whereby once production of one particular signalling molecule called p110d PI3K is slowed down, the disease processes also slowed down. See journal article.
No comments:
Post a Comment
Thankyou for your comment. We moderate all messages and may take a little time to review your comment. Please email inquiries to ccs.comms@monash.edu.