Evidence map›Paper›PMID 36370065›Full record

ArticleRheumatology (Oxford, England)2023

Anti-rituximab antibodies demonstrate neutralizing capacity, associate with lower circulating drug levels and earlier relapse in lupus.

Chris Wincup, Nicky Dunn, Caroline Ruetsch-Chelli, Ali Manouchehrinia, Nastya Kharlamova, Meena Naja, Barbara Seitz-Polski, David A Isenberg, Anna Fogdell-Hahn, Coziana Ciurtin and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
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  5. CD22 as a Target for Hematological Malignancies and Autoimmune Diseases.International journal of molecular sciences · 2026
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Targeting CD20 for B-cell Depletion in Autoimmune Kidney Disease: Next Generation.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2025
    Review
  13. Article
  14. Review
  15. Article
  16. Article
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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

11 authors at 4 institutions in 3 countries.

Chris WincupCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.ORCID 0000-0002-8742-8311
Nicky DunnDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0001-9294-6124
Caroline Ruetsch-ChelliLaboratoire d'Immunologie, CHU de Nice, Université Côte d'Azur, Nice, France.
Ali ManouchehriniaDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0003-4857-5762
Nastya KharlamovaDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Meena NajaCentre for Adolescent Rheumatology Research, Division of Medicine, University College London, London, UK.
Barbara Seitz-PolskiLaboratoire d'Immunologie, CHU de Nice, Université Côte d'Azur, Nice, France.
David A IsenbergCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.ORCID 0000-0001-9514-2455
Anna Fogdell-HahnDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Coziana CiurtinCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.ORCID 0000-0002-8911-4113
Elizabeth C JuryCentre for Rheumatology Research, Division of Medicine, University College London, London, UK.ORCID 0000-0002-2389-3396
University College London · GBKarolinska University Hospital · SEInserm · FRUniversité Côte d'Azur · FR

Funding

Versus Arthritis 21992Versus Arthritis 22203Versus Arthritis 22908
6 · The paper itself

Abstract

objectivesHigh rates of anti-drug antibodies (ADA) to rituximab have been demonstrated in patients undergoing treatment for SLE. However, little is known with regard to their long-term dynamics, impact on drug kinetics and subsequent implications for treatment response. In this study, we aimed to evaluate ADA persistence over time, impact on circulating drug levels, assess clinical outcomes and whether they are capable of neutralizing rituximab.

methodsPatients with SLE undergoing treatment with rituximab were recruited to this study (n = 35). Serum samples were collected across a follow-up period of 36 months following treatment (n = 114). Clinical and laboratory data were collected pre-treatment and throughout follow-up. ADA were detected via electrochemiluminescent immunoassays. A complement dependent cytotoxicity assay was used to determine neutralizing capacity of ADA in a sub-cohort of positive samples (n = 38).

resultsADA persisted over the 36-month study period in 64.3% of patients undergoing treatment and titres peaked earlier and remained higher in those who had previously been treated with rituximab when compared with than those who were previously treatment naive. ADA-positive samples had a significantly lower median drug level until six months post rituximab infusion (P = 0.0018). Patients with persistent ADA positivity showed a significant early improvement in disease activity followed by increased rates of relapse. In vitro analysis confirmed the neutralizing capacity of ADA to rituximab.

conclusionsADA to rituximab were common and persisted over the 36-month period of this study. They associated with earlier drug elimination, an increased rate of relapse and demonstrated neutralizing capacity in vitro.

Indexed as

AntibodiesLupus Erythematosus, SystemicAntibodies, NeutralizingChronic DiseaseHumansRecurrenceRituximabAntibodiesAntibodies, NeutralizingRituximabautoantigens and autoantibodiesB cellsbiological therapyimmunological techniquesSLE

Identifiers

PMID36370065
PMCPMC10321108
OpenAlexW4308834405

What OpenQuestion holds

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Registered trials

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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.