Jump to content

Photopheresis: Difference between revisions

From Wikipedia, the free encyclopedia
Content deleted Content added
ECP also used for experimental treatment of NSF
additional external link
Line 9: Line 9:
== External links ==
== External links ==
* [http://www.cancer.gov/Templates/db_alpha.aspx?CdrID=403135 Extracorporeal photopheresis] entry in the public domain NCI Dictionary of Cancer Terms
* [http://www.cancer.gov/Templates/db_alpha.aspx?CdrID=403135 Extracorporeal photopheresis] entry in the public domain NCI Dictionary of Cancer Terms
* [http://www.emedicine.com/derm/topic566.htm Extracorporeal photopheresis] definition at ''eMedicine.com''


[[Category:Medical treatments]]
[[Category:Medical treatments]]

Revision as of 15:55, 3 April 2008

This article is about the medical treatment of blood. For the optical phenomenon see: photophoresis.

In medicine, photopheresis or extracorporeal photopheresis is a form of apheresis in which blood is treated with photoactivable drugs which are then activated with ultraviolet light.

Photopheresis is currently standard FDA-approved therapy for cutaneous T-cell lymphoma. In this procedure, buffy coat (WBC + platelets) is separated from whole blood, chemically treated with 8-Methoxypsoralen (instilled into collection bag or given per os in advance), exposed to ultraviolet light, and returned to the patient. 8-Methoxypsoralen irreversibly binds covalently to both strands of the DNA of nucleated cells following photoactivation. The photochemically damaged T-cells returned to the patient appear to induce cytotoxic effects on T-cell formation. The mechanism of such “antitumor” action has not been elucidated. Minimal observed side effects for patients receiving photopheresis include hypotension and syncope resulting from volume shifts during leukapheresis phase of treatment. Photopheresis is also used as an experimental treatment in patients with cardiac, pulmonary and renal allograft rejection, graft-versus-host disease, autoimmune diseases, nephrogenic systemic fibrosis and ulcerative colitis.