Participation of factor B in residual immune complex red cell binding activity observed in serum from a C2‐deficient systemic lupus erythematosus patient may delay …
KH Traustadóttir, BO Rafnar… - … : Official Journal of …, 1998 - Wiley Online Library
KH Traustadóttir, BO Rafnar, K Steinsson, H Valdimarsson, K Erlendsson
Arthritis & Rheumatism: Official Journal of the American College …, 1998•Wiley Online LibraryObjective To investigate whether participation of factor B (FB) in immune complex transport
might explain long periods of clinical remissions in a homozygous C2‐deficient patient with
systemic lupus erythematosus (SLE) treated regularly with plasma infusions. Methods
Immune complex red cell binding (ICRB) was assayed as enzyme activity, C3d by enzyme‐
linked immunosorbent assay, and FB by immunoelectrophoresis. Results C2‐deficient sera
showed low‐grade ICRB, which correlated with levels of FB. This activity could be blocked …
might explain long periods of clinical remissions in a homozygous C2‐deficient patient with
systemic lupus erythematosus (SLE) treated regularly with plasma infusions. Methods
Immune complex red cell binding (ICRB) was assayed as enzyme activity, C3d by enzyme‐
linked immunosorbent assay, and FB by immunoelectrophoresis. Results C2‐deficient sera
showed low‐grade ICRB, which correlated with levels of FB. This activity could be blocked …
Objective
To investigate whether participation of factor B (FB) in immune complex transport might explain long periods of clinical remissions in a homozygous C2‐deficient patient with systemic lupus erythematosus (SLE) treated regularly with plasma infusions.
Methods
Immune complex red cell binding (ICRB) was assayed as enzyme activity, C3d by enzyme‐linked immunosorbent assay, and FB by immunoelectrophoresis.
Results
C2‐deficient sera showed low‐grade ICRB, which correlated with levels of FB. This activity could be blocked with antibodies to C1q, C4, or FB, but not by antibodies to C2. C3d levels in the patient's plasma changed during infusion, followed by a gradient increase during remission. Comparison of ICRB, C3d, and FB suggested an inverse relationship between FB levels and clinical symptoms.
Conclusion
In C2 deficiency, FB may interact with C4 to provide a low‐grade ICRB. This activity could be clinically significant in patients with C2 deficiency and explain why they are less prone to SLE than patients with C1q or C4 deficiency.
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