“…Furthermore, because of marked differences in disease severity between different sickle genotypes, COVID-19 outcomes may vary between sickle cell patients. Interestingly, various studies observed that genotypes associated with milder SCD (i.e., HbSC, HbSE, HbSβ + ) had no different or worse outcomes than genotypes associated with more severe SCD (i.e., HbSS, HbSβ 0 ) [ 27 , 30 , 32 , 43 , 58 ]. We speculate that sickle cell anemia-specific therapies or pathophysiology, such as activation of the interferon-α signaling pathway as discussed earlier in this work, may provide a protective effect against COVID-19, but the reasons for this observation are unknown and require further investigation.…”