Repeat doses of antibody to serum amyloid P component clear amyloid deposits in patients with systemic amyloidosis

Author:

Richards Duncan B.1ORCID,Cookson Louise M.1,Barton Sharon V.1,Liefaard Lia1,Lane Thirusha2,Hutt David F.2,Ritter James M.3ORCID,Fontana Marianna2,Moon James C.4ORCID,Gillmore Julian D.2,Wechalekar Ashutosh2,Hawkins Philip N.2,Pepys Mark B.25ORCID

Affiliation:

1. GlaxoSmithKline Research and Development, Stevenage, Herts SG1 2NY, UK.

2. National Health Service National Amyloidosis Centre, Centre for Amyloidosis and Acute Phase Proteins, University College London and Royal Free Hospital, London NW3 2PF, UK.

3. Quintiles Drug Research Unit, Guy’s Hospital, London SE1 1YR, UK.

4. University College London Institute of Cardiovascular Science and Barts Heart Centre, St Bartholomew’s Hospital, London EC1A 7BE, UK.

5. Wolfson Drug Discovery Unit, Centre for Amyloidosis and Acute Phase Proteins, University College London, London NW3 2PF, UK.

Abstract

Repeat cycles of miridesap, to deplete circulating serum amyloid P component (SAP), followed by the anti-SAP antibody, dezamizumab, cleared visceral amyloid deposits in patients with systemic amyloidosis.

Funder

GlaxoSmithKline

Publisher

American Association for the Advancement of Science (AAAS)

Subject

General Medicine

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