At 5, 20, or 40 weeks after inoculation with SIVmac239Δnef, groups of 6 macaques each were challenged by high-dose vaginal inoculation with SIVmac251UCD. Serum collected the day of challenge was evaluated for neutralization of SIVmac251UCD (A–C) and ADCC against SIVmac251UCD-infected cells (D–F). Symbols appear in color for immunized macaques that remained uninfected by SIVmac251UCD, and in black for the immunized animals that became infected. Target cells infected with SHIVSF162P3 served as a negative control for ADCC assays (gray). Dashed lines indicate 50% activity. The groups challenged on weeks 5, 20, and 40 were combined for statistical analysis (G–J). The SIVmac239Δnef-immunized macaques remaining uninfected by SIVmac251UCD had higher 50% ADCC titers than those that became infected (2-tailed Mann-Whitney U test, P = 0.0487) (G). A similar but non-significant trend was observed in AUC values for ADCC (2-tailed Mann-Whitney U test, P = 0.0761) (H). Non-significant trends were in the direction of lower peak SIVmac251UCD viral loads for animals with higher 50% ADCC titers (RS = −0.4615, P = 0.1124) (I) and higher AUC measurements of ADCC activity (RS = −0.4560, P = 0.1173) (J). Linear regression lines are shown. The macaque with the lowest ADCC titers among those remaining uninfected was the only animal possessing the protective combination of MHC class I alleles Mamu-A*01 and -B*17
[70].