Fig. 1 | Signal Transduction and Targeted Therapy

Fig. 1

From: Long-term stability and protection efficacy of the RBD-targeting COVID-19 mRNA vaccine in nonhuman primates

Fig. 1

Humoral and cellular immune responses in ARCoV-immunized cynomolgus macaques. Cynomolgus macaques were immunized i.m. with 50 μg (n = 3) or 200 μg (n = 4) of ARCoV or a Placebo (n = 3) and boosted with the same dose on day 14 after first vaccination. a Schematic diagram of vaccination, sampling, and viral challenge in cynomolgus macaques. b SARS-CoV-2 RBD-specific IgG antibody titers of the immunized animals were determined by ELISA. c, d The NT50 and PRNT50 titers of the immunized animals were detected using VSV-based pseudovirus and live SARS-CoV-2, respectively. The dashed lines indicate the detection limit of the assay. Data are shown as mean with floating bars (min to max). Symbols represent individual animals. Statistical significance was calculated using a Student’s t test (n.s. not significant; *p < 0.05, **p < 0.01, ****p < 0.0001). e, f Serum cross-neutralization assays against SARS-CoV-2 epidemic strains and variants of concern in animals immunized with 200 μg of ARCoV. PRNT50 were performed using animal sera collected on day 28 after the first vaccination. The data were analyzed by a Paired t-test. g, h ELISpot assays for IFN-γ and IL-4 in PBMCs of the ARCoV-immunized cynomolgus macaques. Data are shown as mean ± SEM. Significance was calculated using a Student’s t test (*p < 0.05, ****p < 0.0001)

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