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. Author manuscript; available in PMC: 2016 Nov 1.
Published in final edited form as: Immunol Rev. 2015 Nov;268(1):296–310. doi: 10.1111/imr.12339

Table 1. FcγRIIa and FcγRIIIa alleles and their associations in HIV infection, vaccination and disease progression.

NE represents allele combinations that were not evaluated.

Observation HH HR RR VV VF FF Notes Ref.
Decline in proportion of subjects with CD4+ cells >=200/mm2 over time + RR faster decline (67)
Decline in proportion of subjects without AIDS over time + RR faster decline
Risk of P. jiroveci pneumonia as an AIDS-defining illness + HH higher risk, R lower risk
HIV viral RNA/ml setpoint at ~18 mo NE NE NE No association
Monocyte internalization of HIV immune complexes +++ ++ + NE NE NE HH highest internalization
Risk of Kaposi's sarcoma + VV higher risk
Risk of perinatal HIV-1 transmission based on infant allotype + (+) NE NE NE HH higher risk, RR lower risk (68)
Risk of perinatal HIV-1 transmission based on maternal allotype NE NE NE No association
Lower HIV replication post vaccination + + NE NE NE HH or H/R smaller increase (69)
Increased risk of infection + + V increased risk (70)
Risk of disease progression + + + VV and RR/FF increased risk
Rate of infection for placebo recipients (Vax004) No association (71)
Rate of infection for low risk vaccine recipients (Vax004) + VV increased rate
Risk of infection for vaccine trial participants (Step) No association (72)
Risk of infection (RV144) No association (73)