Table 4.
Category | Glucocorticoids | Immunoglobulin | Anakinra | Tocilizumab |
---|---|---|---|---|
Population | All patients without contraindications | As corticosteroid‐sparing therapy or in combination as first‐line therapy | Patients with moderate to severe disease resistant to glucocorticoids | Patients with moderate to severe disease resistant to glucocorticoids |
Medication and dose use |
|
2 g/kg in 1 or 4 divided infusions within the first ten days from the disease onset alone or in combination with glucocorticoids | 100 mg daily by subcutaneous injection. Consider higher (often intravenous) doses, up to 10 mg/kg daily in cases of severe hyperinflammation |
8 mg/kg intravenously (to a maximum of 800 mg). If clinical improvement does not occur within 24 h after, up to 3 additional doses may be administered |
Mechanism of action | Glucocorticoids produce anti‐inflammatory and immunosuppressive effects through inhibition of proinflammatory cytokines and chemokines and inhibition of T and B cells | Immunoglobulin accelerates the clearance of circulating immunocomplexes, promotes the inhibition of complement deposition, and promotes the enhancement of regulatory T cells | Anakinra is a recombinant human IL‐1 receptor antagonist that promotes the downregulation of the downstream cascade events secondary to IL‐1 release | Tocilizumab inhibits the IL‐6 receptor and prevents the downstream activation of the IL‐6 pathway, the differentiation of CD4+ T cells, and the inhibition of T‐regulatory cells |
Adverse effects | Hyperglycemia and iatrogenic diabetes, psychiatric disturbances, immunosuppression, hypertension, peptic ulcer, osteoporosis, weight gain, adrenal suppression | Fever, dermatological adverse effects, arrhythmia, neutropenia, prothrombotic effects | Increased risk of serious infection, hepatitis, injection‐site reactions | Increased risk of serious infection, gastrointestinal perforations, neutropenia, and thrombocytopenia, increased level of hepatic indexes |
Contraindications | Systemic fungal infection, diabetes with poor glycemic control, known hypersensitivity, osteoporosis, glaucoma, joint infections | Active infective disease, known hypersensitivity, IgA‐deficient patients | Active infective disease, known hypersensitivity | Active infective disease, known hypersensitivity |
CS indicates cardiogenic shock; IgA, immunoglobulin A; IL‐1, interleukin 1; IL‐6, interleukin 6; and MIS‐A, multisystemic inflammatory syndrome in adults.