Immunoglobulins in systemic sclerosis management. A large multicenter experience.


Journal

Autoimmunity reviews
ISSN: 1873-0183
Titre abrégé: Autoimmun Rev
Pays: Netherlands
ID NLM: 101128967

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 08 08 2023
accepted: 03 09 2023
medline: 3 11 2023
pubmed: 15 9 2023
entrez: 14 9 2023
Statut: ppublish

Résumé

To analyze the effectiveness and safety of intravenous immunoglobulin (IVIG) given in routine care to patients with systemic sclerosis (SSc). A retrospective multicenter observational study was conducted in SSc patients treated with IVIG. We collected data on epidemiological parameters and clinical outcomes. Firstly, we assessed changes in organ manifestations during IVIG treatment. Secondly, we analyzed the frequency of adverse effects. The following parameters were collected from baseline to the last follow-up: the patient's weight, modified Rodnan Skin Score (mRSS), modified manual muscle strength scale (MRC), laboratory test(creatine kinase(CK), hemoglobin and protein levels), The University of California Los Angeles Scleroderma Clinical Trials Consortium gastrointestinal tract 2.0 (UCLA GIT 2.0) questionnaire, pulmonary function tests, and echocardiography. Data were collected on 78 patients (82% females; 59% with diffuse SSc). Inflammatory idiopathic myopathy was the most frequent concomitant overlap disease (41%). The time since Raynaud's phenomenon and SSc onset were 8.8 ± 18 and 6.2 ± 6.7 years respectively. The most frequent IVIG indication was myositis (38/78), followed by gastrointestinal (27/78) and cutaneous (17/78) involvement. The median number of cycles given were 5. 54, 53 and 9 patients have been treated previously with glucocorticoids, synthetic disease-modifying antirheumatic drugs and biologic therapies respectively. After IVIG use we found significant improvements in muscular involvement (MRC ≥ 3/5 92% IVIG, p = 0.001 and CK levels from 1149 ± 2026 UI to 217 ± 224 UI, p = 0.02), mRSS (15 ± 12.4 to 13 ± 12.5, p = 0.015) and improvement in total score of UCLA GIT 2.0 (p = 0.05). None Anti-RNA polymerase III patients showed an adequate response in gastrointestinal involvement (0/7) in comparison with other antibodies (0 vs. 25, p = 0,039). Cardiorespiratory involvement remained stable. A total of 12 adverse events were reported with only one withdrawn due to serious adverse effect. this study suggest that IVIG may improve myositis, gastrointestinal and skin involvement in SSc patients treated in routine care and seems to have a good safety profile.

Identifiants

pubmed: 37708984
pii: S1568-9972(23)00175-1
doi: 10.1016/j.autrev.2023.103441
pii:
doi:

Substances chimiques

Immunoglobulins, Intravenous 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

103441

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

J Tandaipan (J)

Department of Rheumatology and Systemic Autoinmune Diseases, Hospital Universitari de la Santa Creu i Sant Pau, Barcelona, Spain.

A Guillén-Del-Castillo (A)

Unit of Systemic Autoimmune Diseases, Department of Internal Medicine, Hospital Universitari Vall d'Hebrón, Barcelona, Spain.

C P Simeón-Aznar (CP)

Unit of Systemic Autoimmune Diseases, Department of Internal Medicine, Hospital Universitari Vall d'Hebrón, Barcelona, Spain.

P E Carreira (PE)

Department of Rheumatology, Hospital Universitario 12 de Octubre, Madrid, Spain.

C De la Puente (C)

Department of Rheumatology, Hospital Universitario Ramon y Cajal, Madrid, Spain.

J Narváez (J)

Department of Rheumatology, Hospital Universitari de Bellvitge, Hospitalet de Llobregat, Spain.

J Lluch (J)

Department of Rheumatology, Hospital Universitari de Bellvitge, Hospitalet de Llobregat, Spain.

M Rubio-Rivas (M)

Department of Internal Medicine, Hospital Universitari de Bellvitge, Hospitalet de Llobregat, Spain.

J J Alegre-Sancho (JJ)

Department of Rheumatology, Hospital Universitario Doctor Peset, Valencia, Spain.

G Bonilla (G)

Department of Rheumatology, Hospital Universitario La Paz, Madrid, Spain.

C Moriano (C)

Department of Rheumatology, Complejo Asistencial Universitario de León, León, Spain.

I Casafont-Sole (I)

Department of Rheumatology, Hospital Germans Trias i Pujol, Badalona, Spain.

R García-Vicuña (R)

Department of Rheumatology, Hospital Universitario de La Princesa, Madrid, Spain.

V Ortiz-Santamaría (V)

Department of Rheumatology, Hospital General de Granollers, Granollers, Spain.

E Riera (E)

Department of Rheumatology, Hospital Universitari Mútua de Terrassa, Terrassa, Spain.

B Atienza-Mateo (B)

Department of Rheumatology, Hospital Universitario Marques de Valdecilla, Santander, Spain.

R Blanco (R)

Department of Rheumatology, Hospital Universitario Marques de Valdecilla, Santander, Spain.

C Galisteo (C)

Department of Rheumatology, Hospital Universitari Parc Taulí, Sabadell, Spain.

J J Gonzalez-Martin (JJ)

Department of Rheumatology, Hospital Universitario HM San Chinarro, Madrid, Spain.

J M Pego-Reigosa (JM)

Department of Rheumatology, Complejo Hospitalario Universitario de Vigo, IRIDIS (Investigation in Rheumatology and Immune-Mediated Diseases)-VIGO Group, Galicia Sur Health Research Institute (IISGS), Vigo, Spain.

A Pros (A)

Department of Rheumatology, Hospital del Mar, Barcelona, Spain.

S Heredia (S)

Department of Rheumatology, Hospital Sant Joan Despí Moisès Broggi, Sant Joan Despí, Spain.

I Castellví (I)

Department of Rheumatology and Systemic Autoinmune Diseases, Hospital Universitari de la Santa Creu i Sant Pau, Barcelona, Spain; Department of Medicine, Universitat Autonoma de Barcelona, Spain. Electronic address: icastellvi@santpau.cat.

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Classifications MeSH