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SHIP-1 knockout (SHIP-1−/−) mice on BALB/c background were immunized with ovalbumin (OVA) plus aluminum hydroxide, a strong Th2-inducing immunization, and challenged with OVA.
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Mice of various genetic backgrounds were immunized with DEC-HER2 in combination with DC maturation stimuli (poly IC ± CD40 Ab).
For ovalbumin/alum immunization, BALB/cJ mice and PI3KγKD/KD mice of BALB/cJ background were immunized at tail base with 50 μg ovalbumin (Grade V, Sigma-Aldrich)/alum mixture.
To broaden antiviral immunity, the RM were immunized with multimeric HIV clade C (HIV-C) gp160 and HIV Tat.
Genetically altered immunoglobulin heavy chain deficient Jh (Balb/c background) and T cell deficient nude mice (Balb/c) were immunized with IsdB, or BSA using the same protocol as above.
Mice were immunized with HBsAg as described.
Female C57BL/6 mice were immunized with MOG35 55.
In present study, mice were immunized with SARS CoV S DNA vaccine.
Donor animals were immunized with AAV-SEAP at a dose of 4 × 1011 vg kg−1.
C3H/HeN mice were immunized with idiotypic immunoglobulin M (IgM) and its molecular subunits from the syngeneic 38C13 lymphoma.
Six control animals were immunized with the Qß platform alone.
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