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001), gender (p?selleck compound CI: 388.0�C442.1?mIU/mL), respectively. The seroconversion and GMT were similar across groups who got different substrains of YFV: 67.0% seroconversion and GMT of 384.7?mIU/mL (95% CI: 359.9�C411.2?mIU/mL) 17-DMAG (Alvespimycin) HCl in children in the 17D-213 group; 65.2% seroconversion and GMT equal to 362.6?mIU/mL (95% CI: 340.0�C386.7?mIU/mL) in the 17-DD group (p?=?0.497). Reverse cumulative distribution curves for antibody titers after MMR, support the finding of similar immunogenicity across groups defined by YFV substrains, and groups in which YFV and MMR were given either simultaneously or 30 days apart (data not shown). For mumps, the curves were also consistent with the small difference in the GMT shown above. For each of the three components, the proportions of seroconversion, did not differ substantially in children who received MMR vaccine from different producers, whereas GMTs were slightly higher among those who received the MSD vaccine (data not shown). The proportion of seroconversion and magnitude of immune response (GMT and distribution of postvaccination antibody titers) were greater in the group vaccinated with an interval of 30 days compared to simultaneous vaccination (p??0.5, Table 2 and Fig. 2). The logistic model this website (data not shown) showed a strong association of seroconversion (OR?=?4.53, 95% CI: 3.12�C6.57) and post-vaccination seropositivity (OR?=?7.60, 95% CI: 5.06�C11.40) with the interval between administration of YFV and MMR, adjusted for the interval between blood collection and vaccination with MMR. In multivariate linear model (data not shown) log10 post-vaccination antibody titers against yellow fever were strongly correlated to the interval between YFV and MMR (p?