Evidence map›Paper›PMID 31783909›Full record

Observational studyArthritis research & therapy2019

Increased levels of anti-dsDNA antibodies in immune complexes before treatment with belimumab associate with clinical response in patients with systemic lupus erythematosus.

Azita Sohrabian, Ioannis Parodis, Nellie Carlströmer-Berthén, Martina Frodlund, Andreas Jönsen, Agneta Zickert, Christopher Sjöwall, Anders A Bengtsson, Iva Gunnarsson, Johan Rönnelid

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Arthritis research & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.1field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 26 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Azita SohrabianDepartment of Immunology, Genetics and Pathology, Uppsala University, Rudbeck Laboratory, SE-75185, Uppsala, Sweden.
Ioannis ParodisRheumatology Unit, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Nellie Carlströmer-BerthénDepartment of Immunology, Genetics and Pathology, Uppsala University, Rudbeck Laboratory, SE-75185, Uppsala, Sweden.
Martina FrodlundRheumatology/AIR, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Andreas JönsenSection of Rheumatology, Department of Clinical Sciences, Lund University, Lund, Sweden.
Agneta ZickertRheumatology Unit, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Christopher SjöwallRheumatology/AIR, Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Anders A BengtssonSection of Rheumatology, Department of Clinical Sciences, Lund University, Lund, Sweden.
Iva GunnarssonRheumatology Unit, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
Johan RönnelidDepartment of Immunology, Genetics and Pathology, Uppsala University, Rudbeck Laboratory, SE-75185, Uppsala, Sweden. johan.ronnelid@igp.uu.se.ORCID 0000-0003-1186-3226
Karolinska University Hospital · SEUppsala University · SELinköping University · SELund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionImmune complexes are of importance in systemic lupus erythematosus pathogenesis, and autoantibodies are believed to participate in immune complex formation. Quantification of autoantibody levels in circulating IC might be of prognostic value.

methodsA C1q-binding-eluting technique was applied to purify immune complexes from 55 belimumab-treated systemic lupus erythematosus patients during a 24-month follow-up. Autoantibodies in serum and in solubilized immune complexes were quantified using addressable laser bead immunoassay. We investigated whether levels of autoantibodies in immune complexes associate with disease activity and response to belimumab treatment.

resultsHigh baseline anti-double-stranded DNA and anti-histone levels in immune complexes associated with attainment of zero scores in clinical systemic lupus erythematosus disease activity index 2000 during the 24-month follow-up (p = 0.003 and p = 0.048, respectively). Low complement levels associated with high serum anti-double-stranded DNA and anti-ribosomal P levels (p = 0.003 and p = 0.008, respectively) and high anti-double-stranded DNA (p = 0.002) but not anti-ribosomal P levels in immune complexes. Anti-SSA/SSB serum levels were lower in patients attaining lupus low disease activity state at month 6; these associations were stronger for corresponding immune complex levels. Serum levels of most autoantibodies had declined at month 3, whereas autoantibody levels in immune complexes, except for anti-double-stranded DNA, showed a more gradual decline over 1-2 years. Serum anti-double-stranded DNA levels decreased in all patients irrespective of systemic lupus erythematosus disease activity index 2000=0 attainment, whereas immune complex levels decreased only in achievers.

conclusionImmune complex levels of autoantibodies against double-stranded DNA and the SSA/SSB complex show more specific associations with treatment outcome compared with serum levels in belimumab-treated systemic lupus erythematosus patients. Characterization of autoantibody content in circulating immune complexes could prove useful in treatment evaluation in systemic lupus erythematosus and other immune complex-associated diseases.

Indexed as

AdultAntibodies, AntinuclearAntibodies, Monoclonal, HumanizedAntigen-Antibody ComplexDNAFemaleHumansImmunosuppressive AgentsLupus Erythematosus, SystemicMaleMiddle AgedPrognosisProspective StudiesSeverity of Illness IndexTreatment OutcomeAntibodies, AntinuclearAntibodies, Monoclonal, HumanizedAntigen-Antibody ComplexbelimumabDNAImmunosuppressive AgentsAnti-double-stranded DNAAnti-nuclear autoantibodiesBelimumabImmune complexesSystemic lupus erythematosusTherapy response

Identifiers

PMID31783909
PMCPMC6884768
OpenAlexW2990071069

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.