Intravenous immunoglobulins (IVIG) in severe/critical COVID-19 adult patients

Biomed Pharmacother. 2023 Jul:163:114851. doi: 10.1016/j.biopha.2023.114851. Epub 2023 May 5.

Abstract

The coronavirus disease 2019 (COVID-19) pandemic has become a huge obstacle to the health system due to the high rate of contagion. It is postulated that intravenous immunoglobulins (IVIG) can lower the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-related inflammation and prevent the development of acute respiratory distress syndrome (ARDS). The main advantages of IVIG treatment might be targeting cytokine storm in severe and critical COVID-19 by influences on complement, innate immune cells, effector T-cells, and Tregs. Randomized clinical trials (RCTs) and non-RCTs evaluating the safety and efficacy of IVIG in patients with severe/critical COVID-19 were performed. It seems that early administration of high-dose IVIG (in the acceleration phase of the disease) in severe or especially critical COVID-19 may be an effective therapeutic option, but there are no strong data to use it routinely. The results regarding mortality reduction are inconclusive. Additionally, IVIG treatment carries a risk of complications that should be considered when initiating treatment. However, given the COVID-19 mortality rate and limited therapeutic options, the use of IVIG is worth considering. This review summarizes the development and highlights recent advances in treatment with IVIG of severe/critically ill COVID-19 patients.

Keywords: COVID-19; IVIG; Intravenous immunoglobulin; SARS-CoV-2.

Publication types

  • Review

MeSH terms

  • Administration, Intravenous
  • Adult
  • COVID-19*
  • Humans
  • Immunoglobulins, Intravenous / adverse effects
  • Inflammation / drug therapy
  • SARS-CoV-2

Substances

  • Immunoglobulins, Intravenous