Connective
Tissue Disorders
Anti-Ribosome
P antibodies
Systemic
lupus erythematosus (SLE) is a multifaceted
autoimmune disease characterised by
the presence of a variety of circulating
autoantibodies.
Central
nervous system (CNS) manifestations
occur in a significant number of SLE
patients and elicit behavioural abnormalities
resembling schizophrenia. However, there
is no single test, that can detect CNS
manifestations of lupus with consistent
sensitivity and specificity.
There
is an association between cerebral lupus
and cytotoxic antibodies in the cerebrospinal
fluid against a neuroblastoma cell line.
In patients with psychotic SLE, a group
of autoantibodies is targeted against
the ribosomal phosphoproteins, called
P0 (38kD), P1 (19kD) and P2 (17kD).
Preceding the onset of psychotic episodes
in patients, a selective elevation of
anti-ribosome P antibodies has been
observed.
Anti-Ribosome
P antibody
reactions are difficult to recognise
by IFA but can be detected by BlueDot.
The BlueDot
anti-Ribosome P assays offer the investigator
valuable additional parameters and insight
into CNS involvement in episodes of
collagen-vascular disorders.
D-tek
BlueDot - Immunodot
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