Evidence map›Paper›PMID 42315241›Full record

ArticleLupus science & medicine2026

Belimumab as a possible treatment for SLE-associated pulmonary arterial hypertension: the experience from a single centre.

Qianwen Wu, Zhangdi Zhou, Huangshu Ye, Miaojia Zhang, Xiaoxuan Sun, Qiang Wang

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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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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

6 authors.

Qianwen Wu *Department of Rheumatology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.ORCID 0000-0003-4365-7216
Zhangdi Zhou *Department of Rheumatology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Huangshu Ye *Department of Rheumatology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.ORCID 0000-0001-6548-0242
Miaojia ZhangDepartment of Rheumatology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Xiaoxuan Sun *Department of Rheumatology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China.
Qiang Wang *Department of Rheumatology, The First Affiliated Hospital With Nanjing Medical University, Nanjing, China jerrytortoise@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore clinical outcomes associated with belimumab use in patients with SLE-associated pulmonary arterial hypertension (SLE-PAH).

methodsWe performed an ambispective cohort study of 10 patients with SLE-PAH treated with intravenous belimumab (10 mg/kg) from January 2022 to January 2025 and compared them with 30 matched SLE-PAH controls receiving conventional immunosuppression without biologics. Patients were followed for 12 months by the same medical team. Clinical, laboratory, echocardiographic parameters, SLE Disease Activity Index 2000 and PAH risk stratification were compared between groups.

resultsAll patients were matched according to baseline age, sex, WHO functional class (WHO-FC), PAH treatment strategy and background SLE therapy. All enrolled patients received either dual or triple combination targeted therapy for PAH. In the SLE-PAH group treated with belimumab, rapid and sustained improvements were observed in multiple parameters, including N-terminal pro-B-type natriuretic peptide, WHO-FC, 6-minute walking distance, soluble suppression of tumorigenicity 2 levels, the ratio of tricuspid annular plane systolic excursion to pulmonary artery systolic pressure (TAPSE/PASP) and right ventricular end-diastolic basal dimension (RVDd). Compared with the matched control group, belimumab-treated patients showed greater improvement in TAPSE/PASP and RVDd at the 12-month follow-up, with statistically significant differences between groups. Additionally, at the 12-month follow-up, all patients in the belimumab group were stratified into the low-risk category, whereas one patient remained in the intermediate-low risk and four patients were categorised as intermediate-high risk in the matched group.

conclusionBelimumab combined with standard PAH-targeted therapy was associated with improvements in right ventricular structure and function in patients with SLE-PAH compared with conventional immunosuppression. Further large-scale, prospective investigations are warranted to confirm these findings.

Indexed as

Antibodies, Monoclonal, HumanizedImmunosuppressive AgentsLupus Erythematosus, SystemicPulmonary Arterial HypertensionAdultEchocardiographyFemaleHumansMaleMiddle AgedTreatment OutcomeAntibodies, Monoclonal, HumanizedbelimumabImmunosuppressive AgentsInflammationPulmonary Arterial HypertensionSystemic Lupus Erythematosus

Identifiers

PMID42315241
PMCPMC13289359

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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.