Evidence map›Paper›PMID 37138867›Full record

ReviewFrontiers in immunology2023

Biological therapy in systemic lupus erythematosus, antiphospholipid syndrome, and Sjögren's syndrome: evidence- and practice-based guidance.

António Marinho, José Delgado Alves, Jorge Fortuna, Raquel Faria, Isabel Almeida, Glória Alves, João Araújo Correia, Ana Campar, Mariana Brandão, Jorge Crespo and 8 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 4 pooled it
10.9field-weighted citation impact, top 1% 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

28 citing papers in PubMed, 4 syntheses or guidelines pooled it, 44 citations in OpenAlex.

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  17. Alcohol Consumption and Autoimmune Diseases.International journal of molecular sciences · 2025
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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

18 authors at 8 institutions in 2 countries.

António MarinhoUnidade de Imunologia Clínica, Centro Hospitalar Universitário do Porto, Porto, Portugal.
José Delgado AlvesSystemic Autoimmune Diseases Unit, Hospital Prof. Doutor Fernando Fonseca, Amadora, Portugal.
Jorge FortunaServiço de Medicina Interna, Departamento de Medicina, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal.
Raquel FariaUnidade de Imunologia Clínica, Centro Hospitalar Universitário do Porto, Porto, Portugal.
Isabel AlmeidaUnidade de Imunologia Clínica, Centro Hospitalar Universitário do Porto, Porto, Portugal.
Glória AlvesServiço de Medicina Interna, Hospital da Senhora da Oliveira - Centro Hospitalar Alto Ave, Guimarães, Portugal.
João Araújo CorreiaUnidade de Imunologia Clínica, Centro Hospitalar Universitário do Porto, Porto, Portugal.
Ana CamparUnidade de Imunologia Clínica, Centro Hospitalar Universitário do Porto, Porto, Portugal.
Mariana BrandãoUnidade de Imunologia Clínica, Centro Hospitalar Universitário do Porto, Porto, Portugal.
Jorge CrespoServiço de Medicina Interna, Departamento de Medicina, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal.
Daniela MaradoServiço de Medicina Interna, Departamento de Medicina, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal.
João Matos-CostaServiço de Medicina Interna, Hospital Distrital de Santarém, Santarém, Portugal.
Susana OliveiraSystemic Autoimmune Diseases Unit, Hospital Prof. Doutor Fernando Fonseca, Amadora, Portugal.
Fernando SalvadorUnidade de Doenças Autoimunes, Serviço de Medicina Interna, Centro Hospitalar de Trás-os-Montes e Alto Douro, Vila Real, Portugal.
Lelita SantosServiço de Medicina Interna, Departamento de Medicina, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal.
Fátima SilvaServiço de Medicina Interna, Departamento de Medicina, Centro Hospitalar Universitário de Coimbra, Coimbra, Portugal.
Milene FernandesReal-World Evidence & Late Phase, CTI Clinical Trial & Consulting Services Unipessoal Lda, Lisboa, Portugal.
Carlos VasconcelosUnidade de Imunologia Clínica, Centro Hospitalar Universitário do Porto, Porto, Portugal.
Hospitais da Universidade de Coimbra · PTCentro Hospitalar do Porto · PTUniversidade do Porto · PTHospital Prof. Dr. Fernando Fonseca · PTCentro Hospitalar de Trás os Montes e Alto Douro · PTClinical Trial and Consulting · USHospital da Senhora da Oliveira Guimarães · PTInstituto Politécnico de Santarém · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic lupus erythematosus (SLE), antiphospholipid syndrome (APS), and Sjögren's syndrome (SS) are heterogeneous autoimmune diseases. Severe manifestations and refractory/intolerance to conventional immunosuppressants demand other options, namely biological drugs, and small molecules. We aimed to define evidence and practice-based guidance for the off-label use of biologics in SLE, APS, and SS. Recommendations were made by an independent expert panel, following a comprehensive literature review and two consensus rounds. The panel included 17 internal medicine experts with recognized practice in autoimmune disease management. The literature review was systematic from 2014 until 2019 and later updated by cross-reference checking and experts' input until 2021. Preliminary recommendations were drafted by working groups for each disease. A revision meeting with all experts anticipated the consensus meeting held in June 2021. All experts voted (agree, disagree, neither agree nor disagree) during two rounds, and recommendations with at least 75% agreement were approved. A total of 32 final recommendations (20 for SLE treatment, 5 for APS, and 7 for SS) were approved by the experts. These recommendations consider organ involvement, manifestations, severity, and response to previous treatments. In these three autoimmune diseases, most recommendations refer to rituximab, which aligns with the higher number of studies and clinical experience with this biological agent. Belimumab sequential treatment after rituximab may also be used in severe cases of SLE and SS. Second-line therapy with baricitinib, bortezomib, eculizumab, secukinumab, or tocilizumab can be considered in SLE-specific manifestations. These evidence and practice-based recommendations may support treatment decision and, ultimately, improve the outcome of patients living with SLE, APS, or SS.

Indexed as

Antiphospholipid SyndromeBiological ProductsLupus Erythematosus, SystemicSjogren's SyndromeBiological TherapyHumansRituximabBiological ProductsRituximabantiphospholipid syndromebiological therapiesrecommendationsSjögren’s syndromesmall moleculessystemic autoimmune diseasessystemic lupus erythematosus

Identifiers

PMID37138867
PMCPMC10150407
OpenAlexW4366180241

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.