Table 1.
Modifications of SP-D found to increase or broaden antiviral activity for IAV.
SP-D preparation | Modification | Effect on antiviral activity |
---|---|---|
Full length recombinant human SP-D | Isolation of high molecular weight multimers | Increased activity compared to trimers or dodecamers (57, 70) |
Full length chimeric protein | Rat SP-D and conglutinin (NCRD) chimera | Increased activity compared with rat SP-D (69) |
Full length chimeric protein | Human SP-D and mannose-binding lectin (NCRD) chimera | Increased activity compared with similarly multimerized human SP-D (68) |
NCRD trimer of human SP-D | D325A or D325S mutation | Slight increase in activity compared to wild-type NCRD (76) |
NCRD trimer of human SP-D | R343V mutation | Strong increased activity compared with wild-type NCRD (75) |
NCRD trimer of human SP-D | D325A(or S) combined with R343V mutation | Increased activity compared to R343V or D325A alone; significant activity vs pandemic H1N1 and H3N2 (77) |
IAV, influenza A virus; SP-D, surfactant protein D; NCRD, neck and carbohydrate recognition domain.