GPA vasculitis wreaked havoc in my life, but I’m enduring

GPA vasculitis wreaked havoc in my life, but I’m enduring

Christine MacFadyen’s symptoms appeared 15 years ago, and she was diagnosed five years ago. (Photos courtesy of Christine MacFadyen) This is Christine MacFadyen’s story: I was a fun-loving, always smiling, energetic, adventurous woman. I was only 24 and had just graduated with my college degree in early childhood care…

Immune protein CX3CL1 may be biomarker of active MPA, GPA

High blood levels of the protein CX3CL1, a pro-inflammatory immune signal that appears to be associated with blood vessel inflammation, can accurately discriminate microscopic polyangiitis (MPA) and granulomatosis with polyangiitis (GPA) patients with active disease from those without, a study found. Importantly, high CX3CL1 levels were found to increase the…

Finding hope amid the life-changing challenges of vasculitis

Rob Nelson explores Peggy’s Cove in Nova Scotia, Canada, in fall 2021. (Photos courtesy of Rob Nelson) This is Rob Nelson’s story: Receiving a vasculitis diagnosis has a dramatic effect physically, emotionally, and socially on both those with the disease and their families. Like many conditions,…

ANCA antibodies against both PR3, MPO result in hybrid AAV features

People with ANCA-associated vasculitis (AAV) who are positive for antibodies against both myeloperoxidase (MPO) and proteinase 3 (PR3) show a combination of clinical characteristics from patients with each antibody type, according to a recent study in China. While double-positive patients are generally more similar to those with MPO-ANCAs, particularly…

My wife has EGPA; I have EGPA by proxy

This is Pam Squires’ story: Pam Squires says her life with her wife, Sarah Jones, who has eosinophilic granulomatosis with polyangiitis (EGPA), is like having EGPA by proxy. (Courtesy of Sarah Jones) My wife, Sarah, and I attended a support group a while back and one of the care…

Living with EGPA disease is one big game of whack-a-mole

Sarah Jones smiles for the camera. (Photos courtesy of Sarah Jones) This is Sarah Jones’ story: I thought on the day of my EGPA diagnosis — fully, eosinophilic granulomatosis with polyangiitis — that I was finally going to get on top of it and move on. Nothing could…

Argenx to stop clinical development of efgartigimod for AAV

Argenx has decided not to go ahead with its development plans for efgartigimod as a potential treatment for ANCA-associated vasculitis (AAV) after the therapy failed to show beneficial effects in late-stage clinical trials of two other autoimmune diseases. Efgartigimod is approved in the U.S. in two formulations for…