Fig. 2: RVFV-specific antibodies are largely dispensable for survival in the presence of pre-existing RVFV-specific T cells. | npj Vaccines

Fig. 2: RVFV-specific antibodies are largely dispensable for survival in the presence of pre-existing RVFV-specific T cells.

From: Immune correlates of protection following Rift Valley fever virus vaccination

Fig. 2

Mice (n = 10 per experimental group) were depleted of CD20+ lymphocytes or mock-depleted, then vaccinated with 2 × 105 TCID50 DelNSsRVFV. Half were euthanized for immune assessment, and the other half were challenged with 2 × 105 TCID50 of WT RVFV (A). Animals were monitored for survival (B). Endpoint titers of RVFV-specific antibodies by ELISA (C) or neutralizing antibody titers (D) were measured 22 days after vaccination/prior to WT challenge, and again at the end of the experiment. The dotted line is the LOD (100 for ELISA, 40 for FRNT80). Negative values were plotted at 50 and 20, respectively. The geometric mean titer is noted for each group. The number of RVFV-specific T cells in total splenocytes was determined by IFN-γ ELISPOT assay, expressed as the number of spots per 1 × 105 splenocytes (n = 3, in duplicate) (E). Mean and standard deviation are noted.

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