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Resolution: standard / high Figure 3.
Regeneration after immunoablative therapy of ACPA-IgG autoantibodies with low avidity.
(a) Low avidity of antibodies against anti-cyclic citrullinated protein (ACPA)-IgG (solid
lines) before and after immunoablative therapy when autoimmunity is reactivated with
rising levels of ACPA-IgG (dotted lines) in the three 'ACPA responders'. Levels below
the detection limit were arbitrarily assigned a value of 4 arbitrary units (AU)/ml
to optimize the graphical representation. Thick lines represent mean values. (b) Avidity of ACPA-IgG (solid lines) before and after immunoablative therapy in the three
'ACPA nonresponders', in whom, despite relatively stable ACPA-IgG levels (dotted lines),
reactivation of autoimmunity was accompanied by the avidity maturation of ACPA-IgG
autoantibodies. Thick lines represent mean values. (c) Avidity of tetanus toxoid (TT)-IgG (solid lines) before and after immunoablative therapy
in four patients. Increasing levels of TT-IgG (dotted lines) after repeated TT immunizations
(see Materials and methods) were accompanied by stably high avidity of TT-IgG, indicative
of an intact humoral recall response despite immunoablative therapy. Thick lines represent
mean values. DMARD, disease-modifying antirheumatic drug; NaSCN, sodium thiocyanate.
Teng et al. Arthritis Research & Therapy 2007 9:R106 doi:10.1186/ar2309 |