Table 2.
Outcome and clinical measures among COVID-19 patients treated by IFN-β
| Author | IFN-β dose | Interferon type | Interferon administration | Resolved fever | Measured CBC | Hospitalization or discharge (intervention/control) | Mortality | Serious adverse effects | |
|---|---|---|---|---|---|---|---|---|---|
| WBC count | Lymphocyte count | ||||||||
| Rahmani et al. (2020) | 250 mcg subcutaneously every other day for two consecutive weeks | IFN β-1b | Subcutaneous | 54.5% vs. 63.6% | 5400 (4025–8250) vs. 5900 (4050–7650) | 924 (520–1400) vs. 869 (670-1000) | Discharge (78.79% vs 54.55%) | 6.06% vs. 18.18% | No |
| Dastan et al. (2020) | 44 μg subcutaneously every other day up to 10 days. (equivalent to 12 million international units) | IFN-β-1a | Subcutaneous | Resolved in all patients during first 7 days | Increased | Increased | Mean ±SD: 16.8 ± 3.4 days | 0% in 14 days | No |
| Monfared et al. (2020) | 44 micrograms/ml (12 million IU/ml) of interferon β-1a three times weekly for two consecutive weeks | IFN-β-1a | Subcutaneous | 8345±4632/7686±4033 | Not reported | 14.80 ± 8.45/12.25 ± 7.48 | 19%/43.6% in 28 days | Not different between the groups | |
| Payandemehr et al. (2020) | (44 μg every day until discharge or until 5 days of admission | IFN-β-1a | Subcutaneous | The most common symptom of the patients at onset of disease was fever. None of the patients had fever even in follow-up | 5.9×103 | 20.7% | 6.75 (±9.2) days | One of them died after 45 days of hospitalization | No adverse effects reported |
| Fan-Ngai Hung et al. (2020) | three doses of 8 million international units of interferon-beta-1b on alternate days | beta-1 | Subcutaneous | 81% vs 78% | 4.9 vs 5.4 × 109 per L | 1.0 vs 1.3 × 109 per L | 9.0 vs 14.5 days | 0.0% vs 0.0% | 0.0% vs 2% |