We’re sorry, something doesn't seem to be working properly.
Please try refreshing the page. If that doesn't work, please contact support so we can address the problem.
Anti-ribosomal P protein IgG autoantibodies in patients with systemic lupus erythematosus: diagnostic performance and clinical profile
BMC Medicinevolume 11, Article number: 98 (2013)
This study was devised to assess the performance of anti-ribosomal P (anti-Rib-P) antibodies in the diagnosis of systemic lupus erythematosus (SLE) and the association of these antibodies with the clinical features of SLE.
We used a fluorescence enzyme immunoassay to determine anti-Rib-P levels in an SLE group, a rheumatic disease control (RDC) group (rheumatoid arthritis (RA), ankylosing spondylitis, psoriatic arthritis and juvenile idiopathic arthritis), and a healthy control (HC) group. We also determined anti-Smith antigen (anti-Sm) and anti-double-stranded DNA (anti-dsDNA) antibody levels. Receiver operating characteristic (ROC) curves were constructed and the best cut-off points for positivity were determined. Using regression analysis, the relationship between clinical variables and autoantibody levels was analyzed.
In total, 127 patients with SLE, 256 controls with other rheumatic diseases, and 100 HCs were studied. Anti-Rib-P autoantibodies were positive in 18 (14.2%) of the patients with SLE (mean concentration of 30.6 ± 46.9 U/ml) and in 2 patients with RA (0.8% of the RDC group). In addition, 12 patients with SLE (9.4%) were positive for anti-Sm (31.1 ± 40.8 U/ml) and 63 (49.6%) were positive for anti-dsDNA autoantibodies (88.4 ± 88.5 U/ml). When we assessed the 18 patients with SLE who had tested positive for anti-Rib-P, we found that 4 of these were positive for anti-Rib-P only, whereas 12 were positive for anti-Rib-P plus anti-dsDNA, and 2 were positive for all three antibodies. There were no samples positive for anti-Rib-P plus anti-Sm. The specificity, sensitivity, positive likelihood ratio, and negative likelihood ratio of anti-Rib-P for SLE diagnosis were 99.4%, 14.2%, 23.7%, and 0.86%, respectively.
Caucasian ethnicity was associated with lower anti-Rib-P antibody levels. No relation was found between anti-Rib-P levels and neuropsychiatric or other clinical features.
Anti-Rib-P autoantibodies have high specificity for SLE, and measurement of these might improve the accuracy of SLE diagnosis. In this study, we found that Caucasian ethnicity was associated with lower anti-Rib-P antibody levels.
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by multi-organ involvement and by the production of autoantibodies directed against a variety of nuclear and cytoplasmic antigens [1, 2]. Autoantibodies can be detected in patients’ sera years before the diagnosis of SLE is made . Some antibodies are relevant to diagnosis, whereas others are associated with prognostic features or disease activity status [2, 4].
Antibodies against double-stranded DNA (anti-dsDNA) and Smith antigen (anti-Sm) are considered very specific for SLE diagnosis, and both are part of the immunologic classification criteria for this disease . Furthermore, high levels of anti-dsDNA are associated with higher disease activity in SLE .
One subset of SLE-specific autoantibodies is directed against ribosomal P (Rib-P) phosphoproteins . The Rib-P antigen consists of three protein components of the 60S ribosomal subunit designated P0 (38 kDa), P1 (19 kDa), and P2 (17 kDa). A pentameric complex of one copy of P0 and two copies each of P1 and P2 interacts with the 28S rRNA molecule to form a GTPase domain that is active during the elongation step of protein translation [7–12]. The major immunoreactive epitope of these ribosomal antigens has been localized to the 22 amino acid carboxy-terminal domain, which is present in all three proteins, and contains two phosphorylated serine residues proteins [2, 8–14].
Anti-Rib-P antibodies are directed against the three subunits [2, 9, 15], and are able to penetrate certain cells, binding to ribosomal proteins and blocking protein synthesis . Anti-Rib-P antibodies enhance the production of tumor necrosis factor (TNF) and interleukin (IL)-6 by activated monocytes and also upregulate the expression of TNF and IL-6 messenger RNA in activated monocytes, indicating that human peripheral blood monocytes express the ribosomal P epitope upon activation .
Ethnic background may influence the likelihood of anti-Rib-P antibodies occurring in patients with SLE, with the frequency ranging from 6% to 46% in different ethnic groups [2, 7, 11, 14–16]. In most ethnic groups, anti-Rib-P antibodies are present in 6 to 20% of patients, whereas 36% of Chinese patients with SLE were reported to be positive [7, 11, 12, 15].
Anti-Rib-P antibodies seem to be highly specific for SLE, and might also be a marker for SLE disease activity [12, 14, 15]. The presence of anti-Rib-P antibodies in patients with SLE has been reported to be associated with younger age at disease onset, multiple organ involvement, and an overall severe disease course , including presence of central nervous system involvement [2, 4, 7, 11, 12, 15], nephritis [2, 7, 12, 15], photosensitivity , malar rash , and hepatic involvement [2, 7, 12]. Moreover, it has become evident that anti-Rib-P antibodies are more prevalent in juvenile-onset than in adult onset SLE [11, 12]. Bonfa et al. first assessed the association of anti-Rib-P antibodies with psychiatric features in patients with psychosis secondary to SLE ; however, other studies have not confirmed this association [7, 8].
We hypothesized that anti-Rib-P autoantibodies might be useful for SLE diagnosis. To test this hypothesis, we used a new fluorescence enzyme immunoassay (FEIA) kit to quantify levels of anti-Rib-P in patients with SLE, controls with other rheumatic diseases (rheumatic disease control (RDC) group, which included rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), ankylosing spondylitis (AS), and psoriatic arthritis (PsA)), and healthy controls (HC group).
The study was conducted in accordance with the regulations governing clinical trials such as the Declaration of Helsinki, as amended in Seoul (2008), and was approved by the ethics committees of the Centro Hospitalar Lisboa Norte, Hospital de Santa Maria and the Hospital Garcia de Orta. All participants signed a written informed consent form before any protocol-specific procedure was carried out.
For this study, we used serum samples from Biobank (Instituto de Medicina Molecular, Lisboa, Portugal), collected between May 2007 and December 2009. Samples were selected from patients with the following diagnoses fulfilling the criteria of the relevant classifications: SLE (revised American College of Rheumatology (ACR) criteria, 1997), RA (revised American Rheumatism Association (ARA) criteria, 1987), JIA (International League of Associations for Rheumatology (ILAR) classification, second revision, 2001), AS (modified New York criteria, 1984) and PsA (modified European Spondyloarthropathy Study Group (ESSG) criteria, 2006). Samples from healthy volunteers were used as the HC group.
In total 127 patients with SLE, 256 RDCs (100 RA, 99 AS, 34 JIA, and 23 PsA), and 100 HCs were studied. Data on age, ethnicity, and gender were collected. For patients with SLE, the following data were obtained at the time of blood sample collection: age at disease diagnosis, disease duration, cumulative clinical features (in accordance with ACR classification criteria), presence of autoantibodies (anti-dsDNA, anti-Sm, anti-cardiolipin, anti-SSA, anti-SSB, and anti-ribonucleoprotein (anti-RNP) antibodies), current medication (including current dosage of corticosteroids and use of immunosuppressants, current disease activity (evaluated using the Systemic Lupus Erythematosus Disease Activity Index 2000 (SLEDAI2K) ), and cumulative organ damage (scored using the Systemic Lupus International Collaborating Clinics/ACR Damage Index (SLICC) ). Clinical features, particularly the occurrence of neuropsychiatric lupus syndromes in accordance with the ACR nomenclature , disease activity, and accumulated organ damage were assessed semi-annually thereafter.
Quantification of anti-Rib-P, anti-Sm and anti-dsDNA antibodies was carried out using FEIA kits (EliA™ Rib-P, EliA™ Sm, and EliA™ dsDNA; Phadia, Uppsala, Sweden; now part of Thermo Fisher Scientific) for in vitro diagnosis in accordance with the manufacturer’s instructions.
Results are reported as mean ± standard deviation for continuous variables or proportion for categorical variables. Anti-Rib-P, anti-Sm and anti-dsDNA concentrations are presented in U/ml.
Receiver operating characteristic (ROC) curves were performed for each test comparing the results from the patients with SLE with those of the HC or RDC groups. For both ROC curves for each antibody, a cut-off point was determined as the value of the parameter corresponding to the highest sensitivity without lowering the specificity. The area under the curve (AUC) was also determined.
Differences between the SLE and control groups were assessed using the t-test for continuous variables or χ2 or Fisher’s exact test for proportions.
The association between clinical variables and the various antibodies was investigated for patients with SLE using univariate followed by multivariate linear regression analyses. All variables relating to the studied outcome in the univariate analyses at P ≤ 0.20 were considered potential predictors, and were entered into the multivariate linear regression models along with neuropsychiatric features, because of their previously described association with these antibodies. The selection of covariates was stepwise by backward selection.
Statistical calculations were performed using SPSS statistical software (version 15.0; SPSS Inc., Chicago, IL, USA) and a two-tailed P-value of < 0.05 was considered significant.
The demographic characteristics of all studied subjects are presented in Table 1. Patients with SLE had a mean age at disease diagnosis of 34.2 ± 14.5 years, disease duration of 8.3 ± 6.5 years (range 0.5 to 34 years), mean SLEDAI2K of 3.3 ± 4.2, and SLICC damage score of 1.1 ± 2.1 at baseline evaluation. Of the 127 patients with SLE, 79 (62.2%) were receiving treatment with corticosteroids (mean daily dosage of prednisolone 12.4 mg), 90 (71%) with antimalarials, 50 (39%) with immunosuppressants, and 1 with a monoclonal antibody (rituximab).
ROC curves were constructed to obtain the most adequate cut-off values for the Portuguese population; these curves are of particular relevance for the new anti-Rib-P test kit. Curves were also constructed for the other tests for coherence analysis. The curves are presented in Figure 1 with the AUC and the corresponding P-values identified. For both the anti-Rib-P and anti-Sm tests, the cut-off values after analysis of the ROC curves were 4.45 U/ml and 3.4 U/ml, respectively. For anti-dsDNA, the cut-off value given by the manufacturer (15 U/ml) was used because it corresponds to the value obtained from the ROC curves. With these adjustment in cut-off values, we identified a higher number of patients with SLE who were positive for either anti-Rib-P or anti-Sm, without incurring more false-positive results in the control groups than we did with the manufacturer cut-off points (data not shown).
We found that the levels of anti-Rib-P autoantibodies were significantly higher in the SLE group (mean concentration of 4.9 ± 20.2 U/ml) than in the HC group (0.07 ± 0.21 U/ml; P = 0.016) or the RDC group (0.6 ± 1.8 U/ml; P = 0.017). In 18 samples of the SLE group (14.2%), anti-Rib-P was above the cut-off value of 4.45 U/ml for positivity (mean concentration of 30.6 ± 46.9 U/ml). Of note, in the RDC group, two patients with RA (0.8%) were positive for anti-Rib-P autoantibodies (18.9 ± 9.8 U/ml), whereas none of the HCs tested positive for this antibody.
The mean concentration of anti-Sm antibodies for the whole SLE group was 2.8 ± 13.8 U/ml, and 12 of these positive samples (9.4%) had a significantly higher mean concentration (31.1 ± 40.8 U/ml) than those of the HC group (0.02 ± 0.11 U/ml; P = 0.028) or the RDC group (0.1 ± 0.3 U/ml; P = 0.035). Positive results (above 3.4 U/ml) for anti-Sm autoantibodies were found only in the SLE group.
Patients with SLE also had a significantly greater mean concentration of anti-dsDNA antibodies (44.6 ± 73.8 U/ml) than found in the HC group (3.5 ± 8.1 U/ml; P < 0.001) or the RDC group (2.6 ± 4.2 U/ml; P < 0.001). Of the 127 patients with SLE, 63 (49.6%) were positive for anti-dsDNA (mean concentration 88.4 ± 88.5 U/ml.), compared with 6 samples (6.0%) in the HC group and 5 samples (2.0%) in the RDC group (1 RA, 1 JIA, and 3 AS samples).
These results are summarized in Table 2. The performance of the tests was evaluated, for sensitivity, specificity, positive likelihood ratio (LR+) and negative likelihood ratio (LR−), and found to be 14.2%, 99.4%, 23.7, and 0.86, respectively, for anti-rib-P; 9.4% 100%, ∞, and 0.90, respectively, for anti-Sm ; and 49.6%, 96.9%, 16, and 0.52 for anti-dsDNA.
Only 2 samples (1.6%) were positive for all three tested autoantibodies, whereas 12 (9.4%) were positive for both anti-Rib-P and anti-dsDNA, and 7 (5.5%) were positive for both anti-Sm and anti-dsDNA. Cross-positivity for anti-Rib-P and anti-Sm was not seen (Table 3).
The relationship between the clinical variables and the levels of anti-Rib-P, anti-Sm, and anti-dsDNA autoantibodies was further analyzed for the SLE group (Table 4).
Anti-Rib-P levels were related at (P ≤ 0.20) in univariate analysis with age (β = −0.125), Caucasian ethnicity (β = −0.190), erythrocyte sedimentation rate (ESR; β = 0.175), disease activity (SLEDAI2K; β = 0.154), malar rash (β = 0.142), renal disorder (β = 0.153), hematologic disorder (β = 0.130), and current corticosteroid dosage (β = 0.119). Hence, these variables were included in the multivariate analysis, which showed that Caucasian ethnicity (β = −0.190, P = 0.034) was the only factor independently associated with anti-Rib-P levels in patients with SLE (Table 4). Anti-Rib-P antibodies were not associated with previous neurologic disorder (seizure or psychosis) or with the occurrence of neuropsychiatric lupus features within the subsequent 3 years of follow-up.
The variables potentially associated with anti-Sm levels from the univariate analysis (at P ≤ 0.20) were Caucasian ethnicity (β = −0.060), ESR (β = 0.203), C-reactive protein (CRP) (β = 0.372), SLEDAI2K (β = 0.125), malar rash (β = −0.138), photosensitivity (β = 0.148), serositis (β = 0.277), renal disorder (β = 0.176), anti-RNP antibodies (β = 0.304), current corticosteroid dosage (β = 0.164), and use of immunosuppressants (β = 0.209). Higher CRP levels (β = 0.304, P = 0.003), serositis (β = 0.321; P = 0.002), and previous positivity for anti-RNP antibodies (β = 0.297; P = 0.003) were found to be independently associated with anti-Sm levels in patients with SLE (Table 4).
For anti-dsDNA levels, age (β = −0.237), age at disease onset (β = −0.169), disease duration (β = −0.176), ESR (β = 0.187), SLEDAI2K (β = 0.413), arthritis (β = −0.150), renal (β = 0.287), hematologic (β = 0.259), and immunologic disorders (β = 0.186), and current corticosteroid dosage (β = 0.130) came out as candidate predictors for higher anti-dsDNA levels (at P ≤ 0.20 in univariate analysis).In the multivariate analysis, SLEDAI2K (β = 0.338; P < 0.001), renal disorder (β = 0.252; P = 0.004), and shorter disease duration (β = −0.246; P = 0.005) were found to be independently associated with anti-dsDNA levels (Table 4).
Confirming earlier studies, the current work shows that anti-Rib-P protein autoantibodies are very specific for SLE diagnosis. The presence of antibodies against ribosomal P proteins was found to be very specific for patients with SLE compared with either HCs or with controls who had other rheumatic diseases. Moreover, the test had high levels of specificity and sensitivity. However, the choice of the most reliable test to determine these autoantibodies requires a comparative study between different tests and the study of a larger and multi-ethnic population.
In addition to determining the levels of anti-Rib-P autoantibodies, we used the same FEIA detection method to determine levels anti-Sm and anti-dsDNA autoantibodies in the same study groups. Both anti-Sm and anti-dsDNA antibodies have also been reported to be very specific for patients with SLE [21–23]; however, we found that anti-dsDNA antibodies were present at low levels in 6% of HCs and 2% of RDCs samples.
The commercial kit that we used for the determination of anti-Rib-P protein (EliA test) is an FEIA, designed as a sandwich immunoassay, containing a mixture of the three Rib-P antigens (P0, P1, and P2), which has been described previously as having high sensitivity and specificity [7, 11, 24]. We also used ROC curves to check the accuracy of this kit for the Portuguese population. ROC curves can be used to evaluate the diagnostic performance of a test, adjusting for a particular study population, and to determine the capability of a test to allow discrimination between the positive group and the control group [25, 26]. Based on the ROC curves, we adjusted the cut-off values for both anti-Rib-P and anti-Sm to 4.45 U/ml and 3.4 U/ml, respectively. These values corresponded to the lowest concentration that allowed the highest possible sensitivity without losing specificity, establishing a cut-off value for the SLE group in comparison with the HC and RDC groups. For anti-dsDNA determination, we used the manufacturer’s cut-off value (15 U/ml) in subsequent analyses, as this gave the best combination of sensitivity and specificity. The cut-off confirmation should be performed when using a new kit or when using an existing kit in a different population. The adjusted values might be either higher or lower than those established by the manufacturer, as confirmed by the work of Mahler and colleagues .
Our results showed increased levels of all the three autoantibodies in patients with SLE, and a higher percentage of positive samples for at least one of the autoantibodies in the SLE group. Although anti-dsDNA autoantibodies were present in more individuals in the SLE group than in the other two groups, the presence of anti-Rib-P or anti-Sm was more specific for SLE diagnosis.
We reviewed the medical records of the individuals in the HC and RDC groups who had a positive result for either anti-Rib-P or anti-dsDNA antibodies (none was positive for anti-Sm). Both of the anti-Rib-P-positive results were detected in patients with RA, one of these patients had presented with some lupus-like characteristics (skin rash, leucopenia, and aphthous ulcer) at some point in the disease course, and thus this case could be classified as an overlap RA/SLE. Interestingly, a similar case was previously reported, referring to a anti-Rib-P-positive patient with RA, who later developed renal disease, and their condition evolved into full-blown SLE . None of our HC or RDC group who were positive for anti-dsDNA autoantibodies had presented any lupus-like characteristics at any time.
When we used multivariate analysis on our SLE group, the only independent association with anti-Rib-P antibodies we identified was ethnicity: lower anti-Rib-P levels were present in individuals of Caucasian ethnicity. To our knowledge, no previous reports have established this association. However, given the small number of non-Caucasian patients in our group, these findings need to be replicated in larger SLE populations with different ethnic backgrounds.
Many previous studies have reported a relationship between the presence of anti-Rib-P antibodies and that of some clinical features, namely malar rash, renal involvement, and neuropsychiatric events, particularly psychosis [8, 11, 27, 28]. However, there are also reports that corroborate our findings of an absence of such an association between the presence of anti-Rib-P antibodies and clinical features or disease activity [7, 13, 16]. In addition, our analysis differed from previous reports because we also took into consideration anti-Rib-P levels.
We found that Rib-P positivity was not associated with previous neuropsychiatric features classifiable by the ACR criteria [29, 30], and the presence of these autoantibodies did not have a predictive value for the occurrence of neuropsychiatric symptoms in the subsequent 3 years. Thus, these autoantibodies seem to be very specific for SLE, but their value for diagnosis of neuropsychiatric lupus seems to be limited, possibly because both anti-Rib-P positivity and neuropsychiatric symptoms are relatively rare. However, given the high specificity, the inclusion of these autoantibodies as part of the SLE classification criteria might be useful. To confirm this, further studies encompassing a larger and multi-ethnic population are needed. Besides its possible use in established SLE, it will be important to assess the performance of such a test in patients with early-stage disease to confirm whether the inclusion of anti-Rib-P testing can improve diagnostic accuracy for SLE.
We performed a multivariate analysis for anti-Sm and anti-dsDNA levels, which revealed some associations of these antibodies with features of the disease. Serositis and CRP levels were positively associated with higher anti-Sm levels. High CRP levels are usually associated with an ongoing infection in patients with SLE, although they have been also associated with serositis, independently of the existence of an infection [31, 32]. This is in line with our results, as we found that CRP levels were increased in patients with serositis (P = 0.047). However, the association between serositis and anti-Sm antibodies contradicts the results of a previous report from Wang and co-workers .
The multivariate analysis also showed anti-RNP levels to be independently associated with anti-Sm levels. Both anti-Sm and anti-RNP antibodies recognize complexes that contain small nuclear RNA species, and the occurrence of anti-Sm antibodies along with anti-RNP antibodies has been reported previously .
Our observations regarding anti-dsDNA are in line with other classic findings depicting an association with renal involvement, as well as in relation to lower disease duration and higher disease activity .
We also evaluated cross-positivity for the three studied autoantibodies, and verified that 78% of the anti-Rib-P-positive patients were also positive for one or both of the other antibodies determined. Previous studies have also shown that the presence of anti-Rib-P antibodies is often associated with anti-dsDNA antibodies, but the simultaneous presence of anti-Rib-P and anti-Sm is not consensual between studies [2, 8, 11, 13]. However, we found that four patients (3.1%) in our SLE group (22% of the anti-Rib-P-positive patients) were positive for anti-Rib-P autoantibodies only. We reviewed the clinical records of these four patients, and found no particular clinical features in common.
The presence of anti-Rib-P antibodies in patients negative for anti-DNA and anti-Sm indicates that these autoantibodies might be useful for SLE diagnosis, as previously reported by Mahler and colleagues . Based on previous suggestions by other authors, and considering that disease classification criteria are constantly subject to confirmation and re-evaluation studies, as recently published by Petri and colleagues , we propose that further studies should be performed to evaluate the relevance of anti-Rib-P antibody testing for SLE diagnosis.
American College of Rheumatology
Area under the curve
Erythrocyte sedimentation rate
Fluorescence enzyme immunoassay
Juvenile idiopathic arthritis
Receiver operating characteristic
Systemic lupus erythematosus
SLE Disease Activity Index 2000
Systemic Lupus International Collaborating Clinics/ACR Damage Index
Tumor necrosis factor
Gualtierotti R, Biggioggero M, Penatti AE, Meroni PL: Updating on the pathogenesis of systemic lupus erythematosus. Autoimmun Rev. 2010, 10: 3-7. 10.1016/j.autrev.2010.09.007.
Heinlen LD, Ritterhouse LL, McClain MT, Keith MP, Neas BR, Harley JB, James JA: Ribosomal P autoantibodies are present before SLE onset and are directed against non-C-terminal peptides. J Mol Med. 2010, 88: 719-727. 10.1007/s00109-010-0618-1.
Arbuckle MR, McClain MT, Rubertone MV, Scofield RH, Dennis GJ, James JA, Harley JB: Development of autoantibodies before the clinical onset of systemic lupus erythematosus. N Engl J Med. 2003, 349: 1526-1533. 10.1056/NEJMoa021933.
Doria A, Zen M, Canova M, Bettio S, Bassi N, Nalotto L, Rampudda M, Ghirardello A, Iaccarino L: SLE diagnosis and treatment: when early is early. Autoimmun Rev. 2010, 10: 55-60. 10.1016/j.autrev.2010.08.014.
Hochberg MC: Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum. 1997, 40: 1725.
ter Borg EJ, Horst G, Hummel EJ, Limburg PC, Kallenberg CG: Measurement of increases in anti-double-stranded DNA antibody levels as a predictor of disease exacerbation in systemic lupus erythematosus. A long-term, prospective study. Arthritis Rheum. 1990, 33: 634-643. 10.1002/art.1780330505.
Gerli R, Caponi L, Tincani A, Scorza R, Sabbadini MG, Danieli MG, De Angelis V, Cesarotti M, Piccirilli M, Quartesan R, Moretti P, Cantoni C, Franceschini F, Cavazzana I, Origgi L, Vanoli M, Bozzolo E, Ferrario L, Padovani A, Gambini O, Vanzulli L, Croce D, Bombardieri S: Clinical and serological associations of ribosomal P autoantibodies in systemic lupus erythematosus: prospective evaluation in a large cohort of Italian patients. Rheumatology (Oxford). 2002, 41: 1357-1366. 10.1093/rheumatology/41.12.1357.
Olesinska M, Chwalinska-Sadowska H, Wiesik-Szewczyk E, Mielnik P, Zabek J: Clinical manifestation of systemic lupus erythematosus in patients with antiribosomal P protein antibodies. Pol Arch Med Wewn. 2010, 120: 76-81.
Agmon-Levin N, Gilburd B, Kivity S, Katz BS, Flitman-Katzevman I, Shoenfeld N, Paran D, Langevitz P, Shoenfeld Y: Anti-ribosomal-P antibodies in lupus patients and healthy controls: evaluation of three ELISA assays. Isr Med Assoc J. 2009, 11: 403-406.
Mahler M, Ngo JT, Schulte-Pelkum J, Luettich T, Fritzler MJ: Limited reliability of the indirect immunofluorescence technique for the detection of anti-Rib-P antibodies. Arthritis Res Ther. 2008, 10: R131-10.1186/ar2548.
Mahler M, Kessenbrock K, Szmyrka M, Takasaki Y, Garcia-De La Torre I, Shoenfeld Y, Hiepe F, Shun-le C, von Muhlen CA, Locht H, Hopfl P, Wiik A, Reeves W, Fritzler MJ: International multicenter evaluation of autoantibodies to ribosomal P proteins. Clin Vaccine Immunol. 2006, 13: 77-83. 10.1128/CVI.13.1.77-83.2006.
Mahler M, Kessenbrock K, Raats J, Fritzler MJ: Technical and clinical evaluation of anti-ribosomal P protein immunoassays. J Clin Lab Anal. 2004, 18: 215-223. 10.1002/jcla.20026.
Ghirardello A, Doria A, Zampieri S, Gerli R, Rapizzi E, Gambari PF: Anti-ribosomal P protein antibodies detected by immunoblotting in patients with connective tissue diseases: their specificity for SLE and association with IgG anticardiolipin antibodies. Ann Rheum Dis. 2000, 59: 975-981. 10.1136/ard.59.12.975.
Haddouk S, Marzouk S, Jallouli M, Fourati H, Frigui M, Hmida YB, Koubaa F, Sellami W, Baklouti S, Hachicha J, Bahloul Z, Masmoudi H: Clinical and diagnostic value of ribosomal P autoantibodies in systemic lupus erythematosus. Rheumatology (Oxford). 2009, 48: 953-957. 10.1093/rheumatology/kep142.
Toubi E, Shoenfeld Y: Clinical and biological aspects of anti-P-ribosomal protein autoantibodies. Autoimmun Rev. 2007, 6: 119-125. 10.1016/j.autrev.2006.07.004.
Chandran V, Upadhyaya SK, Haroon N, Aggarwal A, Misra R: Lack of clinical association with antibodies to ribosomal P proteins in Indian patients with systemic lupus erythematosus. J Rheumatol. 2006, 33: 1987-1989.
Bonfa E, Golombek SJ, Kaufman LD, Skelly S, Weissbach H, Brot N, Elkon KB: Association between lupus psychosis and anti-ribosomal P protein antibodies. N Engl J Med. 1987, 317: 265-271. 10.1056/NEJM198707303170503.
Gladman DD, Ibanez D, Urowitz MB: Systemic lupus erythematosus disease activity index 2000. J Rheumatol. 2002, 29: 288-291.
Gladman D, Ginzler E, Goldsmith C, Fortin P, Liang M, Urowitz M, Bacon P, Bombardieri S, Hanly J, Hay E, Isenberg D, Jones J, Kalunian K, Maddison P, Nived O, Petri M, Richter M, Sanchez-Guerrero J, Snaith M, Sturfelt G, Symmons D, Zoma A: The development and initial validation of the Systemic Lupus International Collaborating Clinics/American College of Rheumatology damage index for systemic lupus erythematosus. Arthritis Rheum. 1996, 39: 363-369. 10.1002/art.1780390303.
Ainiala H, Hietaharju A, Loukkola J, Peltola J, Korpela M, Metsanoja R, Auvinen A: Validity of the new American College of Rheumatology criteria for neuropsychiatric lupus syndromes: a population-based evaluation. Arthritis Rheum. 2001, 45: 419-423. 10.1002/1529-0131(200110)45:5<419::AID-ART360>3.0.CO;2-X.
Al-Jabri AA, Al-Gahdani AK, Al-Shuaili I: High frequency of Smith autoantibodies in Omani patients with systemic lupus erythematosus. Rheumatol Int. 2009, 30: 51-56. 10.1007/s00296-009-0909-4.
Zandman-Goddard G, Gilburd B, Shovman O, Blank M, Berdichevski S, Langevitz P, Shoenfeld Y: The homogeneous multiplexed system—a new method for autoantibody profile in systemic lupus erythematosus. Clin Dev Immunol. 2005, 12: 107-111. 10.1080/17402520500116723.
Alba P, Bento L, Cuadrado MJ, Karim Y, Tungekar MF, Abbs I, Khamashta MA, D'Cruz D, Hughes GR: Anti-dsDNA, anti-Sm antibodies, and the lupus anticoagulant: significant factors associated with lupus nephritis. Ann Rheum Dis. 2003, 62: 556-560. 10.1136/ard.62.6.556.
Lin JL, Dubljevic V, Fritzler MJ, Toh BH: Major immunoreactive domains of human ribosomal P proteins lie N-terminal to a homologous C-22 sequence: application to a novel ELISA for systemic lupus erythematosus. Clin Exp Immunol. 2005, 141: 155-164. 10.1111/j.1365-2249.2005.02816.x.
Metz CE: Basic principles of ROC analysis. Semin Nucl Med. 1978, 8: 283-298. 10.1016/S0001-2998(78)80014-2.
Zweig MH, Campbell G: Receiver-operating characteristic (ROC) plots: a fundamental evaluation tool in clinical medicine. Clin Chem. 1993, 39: 561-577.
Hanly JG, Urowitz MB, Su L, Bae SC, Gordon C, Clarke A, Bernatsky S, Vasudevan A, Isenberg D, Rahman A, Wallace DJ, Fortin PR, Gladman D, Romero-Dirz J, Sanchez-Guerrero J, Dooley MA, Bruce I, Steinsson K, Khamashta M, Manzi S, Ramsey-Goldman R, Sturfelt G, Nived O, van Vollenhoven R, Ramos-Casals M, Aranow C, Mackay M, Kalunian K, Alarcon GS, Fessler BJ: Autoantibodies as biomarkers for the prediction of neuropsychiatric events in systemic lupus erythematosus. Ann Rheum Dis. 2011, 70: 1726-1732. 10.1136/ard.2010.148502.
Briani C, Lucchetta M, Ghirardello A, Toffanin E, Zampieri S, Ruggero S, Scarlato M, Quattrini A, Bassi N, Ermani M, Battistin L, Doria A: Neurolupus is associated with anti-ribosomal P protein antibodies: an inception cohort study. J Autoimmun. 2009, 32: 79-84. 10.1016/j.jaut.2008.12.002.
The American College of Rheumatology nomenclature and case definitions for neuropsychiatric lupus syndromes. Arthritis Rheum. 1999, 42: 599-608.
Nived O, Sturfelt G, Liang MH, De Pablo P: The ACR nomenclature for CNS lupus revisited. Lupus. 2003, 12: 872-876. 10.1191/0961203303lu495oa.
Roy S, Tan KT: Pyrexia and normal C-reactive protein (CRP) in patients with systemic lupus erythematosus: always consider the possibility of infection in febrile patients with systemic lupus erythematosus regardless of CRP levels. Rheumatology (Oxford). 2001, 40: 349-350. 10.1093/rheumatology/40.3.349.
de Carvalho JF, Hanaoka B, Szyper-Kravitz M, Shoenfeld Y: C-reactive protein and its implications in systemic lupus erythematosus. Acta Reumatol Port. 2007, 32: 317-322.
Wang CL, Ooi L, Wang F: Prevalence and clinical significance of antibodies to ribonucleoproteins in systemic lupus erythematosus in Malaysia. Br J Rheumatol. 1996, 35: 129-132. 10.1093/rheumatology/35.2.129.
Combe B, Rucheton M, Graafland H, Lussiez V, Brunel C, Sany J: Clinical significance of anti-RNP and anti-Sm autoantibodies as determined by immunoblotting and immunoprecipitation in sera from patients with connective tissue diseases. Clin Exp Immunol. 1989, 75: 18-24.
Kiss E, Lakos G, Szegedi G, Poor G, Szodoray P: Anti-nuscleosome antibody, a reliable indicator for lupus nephritis. Autoimmunity. 2009, 42: 393-398. 10.1080/08916930903002446.
Petri M, Orbai AM, Alarcon GS, Gordon C, Merrill JT, Fortin PR, Bruce IN, Isenberg D, Wallace DJ, Nived O, Sturfelt G, Ramsey-Goldman R, Bae SC, Hanly JG, Sanchez-Guerrero J, Clarke A, Aranow C, Manzi S, Urowitz M, Gladman D, Kalunian K, Costner M, Werth VP, Zoma A, Bernatsky S, Ruiz-Irastorza G, Khamashta MA, Jacobsen S, Buyon JP, Maddison P: Derivation and validation of the Systemic Lupus International Collaborating Clinics classification criteria for systemic lupus erythematosus. Arthritis Rheum. 2012, 64: 2677-2686. 10.1002/art.34473.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1741-7015/11/98/prepub
We thank Dr. Teresa Araújo and Dr. Luísa Dupont (both Phadia (now Thermo Fisher Scientific) collaborators) for their technical advice, and Drs Elsa Vieira-Sousa, Filipa Mourão and Ana Maria Rodrigues for helping with data acquisition.
Laboratory expenses were supported by Phadia (now Thermo Fisher Scientific).
DCF was involved in the study design and performed the laboratory work, data analysis, and manuscript writing, MJS, HC, and JEF were involved in the study design; data acquisition, interpretation, and analysis; and critical revision of the article. All authors read and approved the final manuscript.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.