Prime-Boost Immunization

YZ Yilong Zhu
SD Shouwen Du
YZ Yang Zhang
JL Jingwei Liu
YG Yan Guo
CL Cunxia Liu
JB Jieying Bai
MW Maopeng Wang
FZ Fei Zhao
TC Tingting Cao
WX Wang Xu
BB Bing Bai
KZ Kelong Zhang
YM Yizhen Ma
CL Chang Li
NJ Ningyi Jin
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Seventy-two (72) female BALB/c mice were divided into three experimental groups (n = 24). Animals in the rFPVSg–Se group were primed with 1 × 107 PFU of rFPVSg–Se in 100 μL of PBS by the intramuscular route at day 0 and were boosted with the same dosage at day 21. The second group received 1 × 106 PFU of FPV282E4 (FPV282E4) at days 0 and 21, and the third group received 100 μL of PBS on days 0 and 21. Serum sample were collected at days 1, 7, 14, 21, 28, 35, 42, and 49 post immunization to detect SIV and vector-specific antibodies by ELISA. The experimental design is shown in Fig. 3a.

Quantifying the serum antigen specific IgG titer in BALB/c mice following a prime-boost rFPVsg–se immunization. a Schematic of the experimental design. Female BALB/c mice were used (n = 24/group). The mice were divided into three groups and immunized with rFPVsg–se, FPV282E4, or PBS. b SIV gag-specific IgG titers, c SIV gp120-specific IgG titers, and d vector-specific antibody levels were measured in the serum by ELISA

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