Table 1.
SARS-CoV-2 | Other | |
---|---|---|
Canonical immune response | Both humoral and cellular immunity weeks after infection. Resolution usually within weeks with a small percentage experiencing severe or fatal outcomes. | HCV: Adaptive immunity months after infection. Cellular immunity with some contribution from neutralising antibodies. |
Exposure duration and dose | Prolonged exposure not essential. Duration of exposure required is unclear. | HCV: Ongoing or recent exposure important for response maintenance. Potential role for low doses of virus. Responses peak earlier than in seropositive infection. |
Durability | Unknown | HCV: Limited, with waning of responses observed within one year |
Target antigens | Early translated antigens More non-structural targets than seropositive individuals |
HCV: Early life cycle peptides |
Cytokine profile | IL-2, IFNγ in some cases but not always | HBV: IFNγ production EBOV: IFNγ production |
Potential source of response | Cross-reactivity with HCoVs | MERS: Potential cross-reactivity with HCoVs |