2020
DOI: 10.1016/j.autrev.2020.102559
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SARS-CoV-2 infection complicated by inflammatory syndrome. Could high-dose human immunoglobulin for intravenous use (IVIG) be beneficial?

Abstract: SARS-CoV-2 infection complicated by inflammatory syndrome. Could high-dose human immunoglobulin for intravenous use (IVIG) be beneficial?

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Cited by 25 publications
(26 citation statements)
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“…Therefore, immunosuppressive therapy might be therapeutic options. Tocilizumab, a humanized monoclonal antibody against IL-6 receptor, and IVIG were reported to be options [4,5]. We used these drugs quickly when the patients exhibited ARDS.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, immunosuppressive therapy might be therapeutic options. Tocilizumab, a humanized monoclonal antibody against IL-6 receptor, and IVIG were reported to be options [4,5]. We used these drugs quickly when the patients exhibited ARDS.…”
Section: Discussionmentioning
confidence: 99%
“…The potential utility of therapy with human immunoglobulin for intravenous use (IVIG) has been recently reported by our group [55], based on the similar etiology and inflammatory pathogenesis of SARS-CoV-2 infection to diseases for which the use of IVIG has already been approved by the FDA or EMA (Table 1) [56][57][58][59][60][61][62][63], or for which IVIG are employed off-label (Table 2) [30,, including viral or bacterial septic shock [91] and the autoinflammatory syndrome with MAS [91][92][93]. To dam inflammation, IVIG should be given at a dosage not exceeding 0.4 g/kg/day for three to five consecutive days (maximum total dosage is 2 g/kg) and the patient should be well hydrated.…”
Section: Immunological Rationale For Targeting the Immune System To Fmentioning
confidence: 99%
“…In a very recent study, the administration of IVIG is recommended in COVID-19 patients, with or without MIS features, because it effects on the production of TNF-α and reduces the number of regulatory T cells, which control inflammation and T cell activation. All these therapeutic protocols could affect the cytokinemediated interstitial and alveolar wall edema in ARDS and consequently on the viral clearance [53].…”
Section: Potential Treatment Protocolsmentioning
confidence: 99%