Today, clinicians can choose from a variety of extracorporeal immunomo
dulatory procedures such as plasma exchange, double filtration, immuno
adsorption, chemoadsorption, photopheresis, and cytoapheresis. The mec
hanisms underlying extracorporeal immunomodulation (ECIM) comprise rem
oval of pathogenic antibodies and circulating immune complexes as well
as reticuloendothelial system deblockage; modification of immune comp
lex structure and processing can be induced by changing the antigen/an
tibody ratio and by modulation of immune complex solubility via comple
ment activation. Finally, cellular components like lymphocyte subsets,
can be modified. Clinical examples of ECIM include lupus erythematosu
s, Goodpasture's syndrome, antineutrophil cytoplasmatic antibodies-med
iated systemic vasculitis, myasthenia gravis, and, hypothetically, sep
sis.