2014
DOI: 10.1097/md.0000000000000086
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Intravenous Immunoglobulin in the Therapeutic Armamentarium of Systemic Lupus Erythematosus

Abstract: Prepared from the plasma of thousands of blood donors, therapeutic intravenous immunoglobulin (IVIg) mostly consists of human polyspecific immunoglobulin G (IgG). The use of IVIg in systemic lupus erythematosus (SLE) is still considered experimental without any clear indications.The purpose of this systematic review is, therefore, to evaluate the available evidence to determine the therapeutic role of IVIg in SLE.A comprehensive, computerised search was performed in the MEDLINE (Pubmed), Scopus, EMBASE, and Co… Show more

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Cited by 53 publications
(31 citation statements)
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“…The combination of RTX and belimumab has recently been used in refractory disease. 85 Highdose intravenous immunoglobulin (2 g/kg) could be considered when there are contraindications to increasing glucocorticoids or immunosuppressive drugs, such as infection, 86 while plasma exchange is rarely indicated.…”
Section: Non-responding/refractory Diseasementioning
confidence: 99%
“…The combination of RTX and belimumab has recently been used in refractory disease. 85 Highdose intravenous immunoglobulin (2 g/kg) could be considered when there are contraindications to increasing glucocorticoids or immunosuppressive drugs, such as infection, 86 while plasma exchange is rarely indicated.…”
Section: Non-responding/refractory Diseasementioning
confidence: 99%
“…Despite being used since the 1980s, IVIG therapy is still considered to be experimental without any clear indications. A systematic review of observational studies highlighted the association of IVIG administration with significant improvement in disease activity scores and complement levels [53].…”
Section: Adjuvant Treatmentsmentioning
confidence: 99%
“…However, it holds great significance in identifying reliable, practical, and economical biomarkers to assist in diagnosing SLE and quantifying the disease activity of SLE patients. The immune system of SLE patients is abnormally activated by autoantigens, which results in immune complex deposition and complement system activation, followed by chronic inflammation (1,2,6,7,9). Furthermore, chronic inflammation stimulated by environmental and genetic factors is a common characteristic of autoimmune diseases including SLE (10,11).…”
Section: ' Introductionmentioning
confidence: 99%