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Table 1 Effect of number of immunizations, antigen dose, and adjuvant dose on HBsAg-specific response a

From: Intranasal Immunization of Mice with CpG DNA Induces Strong Systemic and Mucosal Responses That Are Influenced by Other Mucosal Adjuvants and Antigen Distribution

 

Adjuvant

Number of Responders (of 5 immunized mice)

N° Doses

HBsAg

CT

CpG

Post-prime

Post-boost 1

Post-boost 2

Post-challenge

1

1

  

0

N/Db

N/D

0

1

1

1

 

0

N/D

N/D

3

1

1

 

1

0

N/D

N/D

1

1

1

1

1

0

N/D

N/D

4

3

1

  

0

0

0

0

3

1

1

 

0

0

0

5

3

1

 

1

0

0

1

3

3

1

1

1

0

0

2

5

3

1

10

 

1

2

4

N/D

3

1

 

10

0

3

5

N/D

3

1

 

50

0

1

3

N/D

3

1

1

10

1

4

5

N/D

3

10

1

 

5

5

5

N/D

3

10

10

 

3

4

5

N/D

3

10

 

1

3

5

5

N/D

3

10

 

10

2

5

5

N/D

3

10

 

50

2

5

5

N/D

3

10

1

1

5

5

5

N/D

3

10

1

10

5

5

5

N/D

  1. aBALB/c mice were immunized by intranasal (IN) inhalation of 1 or 10 µg of purified hepatitis B surface antigen (HBsAg) alone (none) or with 1, 10 or 50 µg cholera toxin (CT) and/or CpG-containing oligodeoxynucleotides (CpG) in a total volume of 20 µl. Some mice were boosted in an identical manner at 4 and 8 weeks. Other mice that failed to develop anti-HBs, such as those immunized with 1 µg HBsAg alone or with low dose adjuvant (1 µg), were challenged by intramuscular (IM) injection of 1 µg HBsAg without adjuvant, to determine if immune response had been primed. HBsAg-specific antibody titers were determined by ELISA in plasma taken 4 weeks after final immunization or 2 weeks after challenge. Titers were defined as the highest plasma dilution resulting in an absorbance value two times that of nonimmune plasma, with a cut-off value of 0.05. Values shown represent the number of responding mice (titers > 100).
  2. bN/D, not determined