Evidence map›Paper›PMID 42508961›Full record

ArticleLupus science & medicine2026

Targeting type I interferon in lupus autoimmune haemolytic anaemia: first report with anifrolumab.

Fulvia Ceccarelli, Rossella De Angelis, Francesca Bottazzi, Danila Madonna, Melania Alessia Coscia, Noemi Italiano, Emanuela Praino, Emanuela Sabatini, Leonardo Santo, Lorenzo Cavagna and 1 more

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Article in Lupus science & medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Fulvia CeccarelliUniversity of Rome La Sapienza, Rome, Italy fulviaceccarelli@gmail.com.ORCID 0000-0001-5026-8783
Rossella De AngelisPolytechnic University of Marche, Ancona, Italy.ORCID 0000-0001-5169-3511
Francesca BottazziUniversity of Pavia, Pavia, Italy.
Danila MadonnaPolytechnic University of Marche, Ancona, Italy.
Melania Alessia CosciaAzienda Ospedaliera di Caserta Sant'Anna e San Sebastiano, Caserta, Italy.
Noemi ItalianoAzienda Ospedaliera di Caserta Sant'Anna e San Sebastiano, Caserta, Italy.
Emanuela PrainoBarletta Hospital, Barletta, Italy.
Emanuela SabatiniOspedale Clinicizzato SS Annunziata, Chieti, Italy.
Leonardo SantoBarletta Hospital, Barletta, Italy.
Lorenzo CavagnaUniversity of Pavia, Pavia, Italy.
Fabrizio ContiUniversity of Rome La Sapienza, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAutoimmune haemolytic anaemia (AIHA) occurs in approximately 5-10% of patients with SLE and it is traditionally associated with higher disease activity, increased damage accrual and reduced survival. SLE management recommendations partially address disease-related haematological manifestations without specific indication for AIHA treatment. Indeed, therapeutic approaches are prevalently extrapolated from the haematology field. In the present report, we aimed at describing a case series of patients with SLE and AIHA successfully treated with anifrolumab (ANF).

methodsWe described patients with SLE treated by ANF with active AIHA at the drug initiation. Clinical and laboratory data were reported in a standardised electronic form, including laboratory evidence of haemolysis. Overall disease activity was assessed by using the SLE Disease Activity Index 2000 (SLEDAI-2k). We collected patients data at baseline (T0), after 1 month (T1) and every 3 months thereafter.

resultsWe included seven patients (6F/1M, median age 61 years (IQR 33), median disease duration 48 months (IQR 72)). All the patients had a positive direct Coombs test and laboratory evidence of active haemolysis at ANF starting. During treatment, we observed a progressive increase in haemoglobin (Hb) levels, with a statistically significant difference compared with baseline after 3 months of treatment (p=0.02). In parallel we registered the increase in RBC count, without the need to perform RBC transfusions after ANF starting. Overall disease activity significantly improved during the follow-up, with significant reduction of mean SLEDAI-2k values after 6 months of treatment (p=0.01).

conclusionIn the present case-series study, we provide the first report about the benefit of ANF in the treatment of SLE-related AIHA, a rare but potentially severe manifestation associated with increased morbidity and mortality. In our cohort, ANF treatment was associated with a rapid and sustained increase in Hb levels, evident already at 1 month and progressively improving up to 6 months.

Indexed as

Anemia, Hemolytic, AutoimmuneAntibodies, Monoclonal, HumanizedInterferon Type ILupus Erythematosus, SystemicAdultAgedCoombs TestFemaleHemoglobinsHumansMaleMiddle AgedTreatment OutcomeanifrolumabAntibodies, Monoclonal, HumanizedHemoglobinsInterferon Type IAutoimmunityHematologyInterferon Type ISystemic Lupus Erythematosus

Identifiers

PMID42508961
PMCPMC13409081

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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.