2002
DOI: 10.1016/s1297-319x(02)00366-4
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Autoantibodies to ribosomal P proteins in systemic lupus erythematosus

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Cited by 10 publications
(7 citation statements)
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“…In addition, we studied their association with major clinical characteristics. As mentioned before, there existed relationship between major clinical manifestations and lupus-related autoantibodies in SLE patients [9][10][11][12], for example, anti-dsDNA and nephritis, anti-SM and skin damage, myositis and central nervous system disorder, AnuA and nephritis as well as neurologic disorder, etc., while rRNP was recognized to be correlated with neurologic disorder, liver involvement and LN. Our study demonstrates significant association of rRNP with photaesthesia and AHA with nephritis.…”
Section: Discussionmentioning
confidence: 86%
“…In addition, we studied their association with major clinical characteristics. As mentioned before, there existed relationship between major clinical manifestations and lupus-related autoantibodies in SLE patients [9][10][11][12], for example, anti-dsDNA and nephritis, anti-SM and skin damage, myositis and central nervous system disorder, AnuA and nephritis as well as neurologic disorder, etc., while rRNP was recognized to be correlated with neurologic disorder, liver involvement and LN. Our study demonstrates significant association of rRNP with photaesthesia and AHA with nephritis.…”
Section: Discussionmentioning
confidence: 86%
“…Twenty‐four additional publications (6, 8–13, 15–20, 22, 23, 25–29, 31–34) were retrieved from the database search, representing a total of 38 studies involving 3,713 lupus patients. Nevertheless, data for the comparison of NPSLE versus non‐NPSLE groups were available in only 18 of the 24 additional studies; data for other comparisons were available in even fewer reports (Table 3).…”
Section: Resultsmentioning
confidence: 99%
“…During the last 2 decades, several studies have explored the utility of antibodies to ribosomal P proteins (anti‐P) in detecting NPSLE (6, 8–35). These antibodies are directed toward 3 large‐subunit ribosomal phosphoproteins, called P0 (38 kd), P1 (19 kd), and P2 (17 kd), which share a common linear determinant in the carboxyl‐terminal 22–amino acid sequence (36).…”
mentioning
confidence: 99%
“…The HLA-DR3 phenotype has been detected in approximately 70% of patients with SCLE and psoriasiform lesions. 71 Anti-U1RNP antibodies are present in the serum of patients with MCTD and SLE. These antibodies are detected in 100% of patients with MCTD and in approximately 30% of patients with SLE, but may also occur in neonatal lupus and, very rarely, in systemic sclerosis.…”
Section: Discussionmentioning
confidence: 99%