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1.
Figure 5

Figure 5. TIRAP-deficient mice develop antibody responses after Salmonella infection. From: Expression of Toll/IL-1R Domain-Containing Adaptor Protein (TIRAP) is detrimental to primary clearance of Salmonella and is not required for the generation of protective immunity.

Serum was obtained from infected Wt or TIRAP-/- mice, 3 months after intravenous infection with 5×105 BRD509, and from naïve Wt mice. IgG2a responses to Salmonella were determined by ELISA. Data show mean Salmonella-specific IgG2a titers ± SD of 8-9 mice per group.

Stu Jerke, et al. Immunol Lett. ;116(1):64-71.
2.
Figure 1

Figure 1. TIRAP is detrimental to the clearance of Salmonella infection. From: Expression of Toll/IL-1R Domain-Containing Adaptor Protein (TIRAP) is detrimental to primary clearance of Salmonella and is not required for the generation of protective immunity.

C57BL/6 Wt and TIRAP-/- mice were infected intravenously with 5×105 attenuated Salmonella, BRD509. (A) Spleens from infected mice were recovered at regular intervals after infection and the number of bacteria determined by plating serial dilutions. Data show the number of bacteria per spleen and are representative of at least 3 mice per group. (B) Spleens from infected mice were recovered 35 and 49 days after infection and the number of bacteria determined by plating serial dilutions. Data show the number of bacteria per spleen and are representative of at least 3 mice per group.

Stu Jerke, et al. Immunol Lett. ;116(1):64-71.
3.
Figure 6

Figure 6. Development of protective immunity against virulent Salmonella in TIRAP-deficient mice. From: Expression of Toll/IL-1R Domain-Containing Adaptor Protein (TIRAP) is detrimental to primary clearance of Salmonella and is not required for the generation of protective immunity.

C57BL/6 Wt and TIRAP-/- mice were infected intravenously with 5×105 attenuated Salmonella, BRD509 and 50 days later naïve or vaccinated mice were challenged intravenously with 1×105 virulent Salmonella SL1344. Cages were monitored daily for death or moribund mice. Data show percentage survival of mice using combined data from 2 individual experiments and at least 10 mice per group.

Stu Jerke, et al. Immunol Lett. ;116(1):64-71.
4.
Figure 3

Figure 3. Normal expansion and development of Salmonella-specific memory cells in a TIRAP-deficient environment. From: Expression of Toll/IL-1R Domain-Containing Adaptor Protein (TIRAP) is detrimental to primary clearance of Salmonella and is not required for the generation of protective immunity.

Wt and TIRAP-/- mice were adoptively transferred with SM1 T cells and infected intravenously the following day with 5×105 attenuated Salmonella, BRD509 or immunized intravenously with 1×108 HKST. Spleens were harvested at various time points later and stained using antibodies specific for CD4 and CD90.1. FACS plots show the percentage of SM1 T cells in the spleen of uninfected (Transfer Only), HKST immunized (HKST), and infected (Salmonella) mice. Numbers are the percentage of SM1 cells among all live gated spleen cells. Data are representative of 3 mice per group and 2 individual experiments.

Stu Jerke, et al. Immunol Lett. ;116(1):64-71.
5.
Figure 2

Figure 2. Enhanced IFN-γ production and resolution of splenic infiltration in TIRAP-deficient mice. From: Expression of Toll/IL-1R Domain-Containing Adaptor Protein (TIRAP) is detrimental to primary clearance of Salmonella and is not required for the generation of protective immunity.

C57BL/6 Wt and TIRAP-/- mice were infected intravenously with 5×105 attenuated Salmonella, BRD509. (A) Spleens from infected mice were harvested 35 days later and cultured in vitro in medium alone (-Ag) or with added HKST (+Ag). Supernatants were harvested 72 hours later and IFN-γ production measured by ELISA. Data shows the mean OD ± SD for 3 mice per group. (B) Spleens from infected mice were recovered 35 days after infection and stained with antibodies specific for cell-specific surface markers. Data show FACS plots for individual mice and are representative of 3 mice per group. Numbers show the percentage of cells within each boxed gate.

Stu Jerke, et al. Immunol Lett. ;116(1):64-71.
6.
Figure 4

Figure 4. Normal activation and cell division of Salmonella-specific T cells in a TIRAP-deficient environment. From: Expression of Toll/IL-1R Domain-Containing Adaptor Protein (TIRAP) is detrimental to primary clearance of Salmonella and is not required for the generation of protective immunity.

Wt and TIRAP-/- mice were adoptively transferred with CFSE-dyed SM1 T cells and infected intravenously the following day with 5×105 attenuated Salmonella, BRD509 or immunized intravenously with 1×108 HKST. Spleens were harvested at various time points later and stained using antibodies specific for CD4 and CD90.1 to identify SM1 cells, and CD11a to identify activated T cells. FACS plots show CFSE-dye dilution and CD11a expression on gated SM1 T cells in the spleen of uninfected (Transfer Only), HKST immunized (HKST), and infected (Salmonella) mice. There were too few SM1 cells at day 18 in infected mice to gather sufficient data for analysis. Data are representative of 3 mice per group and 2 individual experiments.

Stu Jerke, et al. Immunol Lett. ;116(1):64-71.

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