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. Author manuscript; available in PMC: 2021 Jan 8.
Published in final edited form as: Sci Transl Med. 2020 Jan 8;12(525):eaav5701. doi: 10.1126/scitranslmed.aav5701

Fig. 3. PR8 hemagglutinin mRNA-LNP vaccine elicits protective antibody responses in the presence of matAbs.

Fig. 3.

(A) Mice (21 days old) were vaccinated intramuscularly with 1 μg of nucleoside-modified PR8 hemagglutinin (HA) mRNA-LNP vaccine, and influenza virus–specific serum antibody responses were measured by ELISA. *P < 0.05 after comparison of serum titers from mice vaccinated with PR8 HA mRNA-LNP vaccine versus PBS in the presence (blue *) or absence (orange *) of influenza virus–specific matAbs; one-way ANOVA with Tukey’s post hoc test at each time point. (B) Mice in (A) were challenged at 189 days after vaccination with 300 TCID50 of PR8 influenza virus intranasally, and weight loss was measured over 14 days. Data are shown as percentage of baseline weight (current weight divided by prechallenge weight). *P < 0.05 after comparison of percentage of baseline weight on each day for mice vaccinated as infants with PR8 HA mRNA-LNP vaccine versus PBS in the presence (blue *) or absence (orange *) of influenza virus–specific matAbs; one-way ANOVA with Tukey’s post hoc test at each day. (A and B) n = 3 (+matAbs) or n = 4 (−matAbs) mice per group. (C) Serum was collected at 100+ days after vaccination with 1 μg of PR8 HA mRNA-LNP vaccine or PBS in the presence or absence of influenza virus–specific matAbs and was pooled. Pooled serum (500 μl) was intraperitoneally transferred to 6- to 8-week-old naïve mice, and 4 to 5 hours later, mice were intranasally challenged with 300 TCID50 of PR8 influenza virus. Weight loss was measured over 14 days. n = 4 mice per group. *P < 0.05 after comparison of percentage of baseline weight on each day for mice that received sera from mice vaccinated with PR8 HA mRNA-LNP vaccine or PBS as infants in the presence of influenza virus–specific matAbs; one-way ANOVA with Tukey’s post hoc test at each day. (D) Sera from mice vaccinated with 1 μg of PR8 HA mRNA-LNP vaccine in the presence or absence of influenza virus–specific matAbs and from naïve mice were collected 189 days post-vaccination. Sera were analyzed for influenza virus–specific IgG1 (left) or IgG2a (right). n = 8 (blue), n = 9 (orange), or n = 4 (black) mice per group. Serum titers of mice vaccinated with PR8 HA mRNA-LNP vaccine in the presence or absence of influenza virus–specific matAbs were compared using an unpaired two-tailed t test. In (D), each point represents one mouse. Data are shown as means ± SD. Panels (A) to (D) show data from one experiment that is representative of two independent biological replicates.