Evidence map›Paper›PMID 39840060›Full record

ArticleFrontiers in immunology2024

Active withdrawal of corticosteroids using tocilizumab and its association with autoantibody profiles in relapsed Takayasu arteritis: a multicentre, single-arm, prospective study (the Ab-TAK study).

Tsuyoshi Shirai, Tomonori Ishii, Soshi Okazaki, Yuko Shirota, Yusho Ishii, Hiroko Sato, Hiroshi Fujii

Abstract readMulticenter Study
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Tsuyoshi ShiraiDepartment of Clinical Rheumatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Tomonori IshiiDepartment of Clinical Rheumatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Soshi OkazakiDepartment of Clinical Rheumatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Yuko ShirotaDepartment of Hematology and Rheumatology, Tohoku Medical and Pharmaceutical University, Sendai, Japan.
Yusho IshiiDepartment of Clinical Rheumatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Hiroko SatoDepartment of Clinical Rheumatology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Hiroshi FujiiDepartment of Clinical Rheumatology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: The feasibility of corticosteroid withdrawal (CW) for Takayasu arteritis (TAK) remains uncertain. Two autoantibodies (Abs) are identified against endothelial protein C receptor (EPCR) and scavenger receptor class B type 1 (SR-BI) in TAK, determining its three subgroups. This study aimed to evaluate CW using tocilizumab (TCZ) and its association with the Ab profile. Methods: This prospective study, lasted for 24 weeks, included patients with relapsed but stable TAK. Scheduled tapering of prednisolone (PSL) was performed with subcutaneous TCZ (CW at week 20). The primary endpoint was the difference in type A remission, defined by CW and the absence of inflammatory signs, according to the Ab profile at week 24. Results: Twenty patients were included and 18 patients with a mean PSL dose of 4.9 ± 2.8 mg/day were analysed. Anti-EPCR Ab-positive (E+), anti-SR-BI Ab-positive (S+), and double-negative (DN) groups included four (22.2%), eight (44.4%), and six (33.3%) patients, respectively. At week 24, the mean PSL dose was 2.0 ± 2.7 mg/day. Type A remission was observed in eight patients (44.4%), with significant differences based on the Ab profile: E+ (three patients, 75%), S+ (five patients, 62.5%), and DN (zero patients, 0%) (P=0.018). Besides, age, disease duration, PSL dose, type V arterial lesion, arterial dilation, and C-reactive protein >0.01 mg/dL were identified as risks for CW failure. Conclusion: CW using TCZ was achieved in 44.4% of patients with TAK relapse and was significantly higher in E+ and S+ patients. CW can be a feasible target, and the precise selection of patients is critical.

Indexed as

Adrenal Cortex HormonesAntibodies, Monoclonal, HumanizedAutoantibodiesPrednisoloneTakayasu ArteritisAdultFemaleHumansMaleMiddle AgedProspective StudiesRecurrenceTreatment OutcomeYoung AdultAdrenal Cortex HormonesAntibodies, Monoclonal, HumanizedAutoantibodiesPrednisolonetocilizumabautoantibodycorticosteroidTakayasu arteritistocilizumabwithdrawal

Identifiers

PMID39840060
PMCPMC11747699

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