Skip to main content
. Author manuscript; available in PMC: 2016 Sep 19.
Published in final edited form as: Curr Transplant Rep. 2014 Mar 13;1(2):78–85. doi: 10.1007/s40472-014-0012-y

Table 2.

Therapeutic options for acute AMR

Therapy Studies Mechanism of Action Effectiveness
Plasmapheresis Bonomini et al.
(1985)[37]
Kirubakaran et al.
(1981)[38]
Allen et al.
(1983)[39]
Blake et al.
(1999)[40]
Stegall et al.
2006[41]
Physical removal of
antibody
Temporarily effective at
reducing antibody level
depending on continued
antibody production.
Intravenous
Immunoglobulin
(IVIG)
Glotz et al.
(1993)[42]
Tyan et al.
(1994)[43]
Jordan et al.
(1998)[11]
Casadei et al.
(2001)[13]
Tyan et al.
1994 [43]
Stegall et al.
2006 [41]
Lafaucheur et al.
(2009)[44]
Multiple
immunomodulatory
actions
Variable efficacy
Splenectomy Locke et al.
2007 [17]
Tzvetanov et al.
2012[18]
Reduce B-cell and
Plasma Cell burden
Variable efficacy
Rituximab Kaposztas et al.
2009[45]
Lafaucheur et al.
2009 [44]
CD 20+ inhibitor
leading to reduction in
B-cells
Variable efficacy
Bortezomib Everly et al.
2008[26]
Walsh et al.
2010[27]
Wong et al.
2010[28]
Proteasome inhibitor
leads to plasma cell
apoptosis
Variable efficacy
Eculizumab Stegall et al.
2011[3]
Terminal complement
(C5) inhibitor
Very effective at inhibiting
acute AMR, but does not
prevent chronic AMR.
Expensive.