Figure 8.
Figure 8. Abrogation of antibodies' production and antitumor activity by the depletion of immune cell subsets. (A) Abrogation of antitumor activity by the depletion of immune cell subsets. Depletion of CD4 T lymphocytes showed complete abrogation of the antitumor activity of the qVEGFR vaccine (n = 10). In contrast, treatment with anti-CD8, anti-NK, or isotype controls (IgG2a and IgG2b) had no effect. Results showed the tumor volume on day 26 after tumor cell injection (mean ± SEM). (B) Abrogation of antibody production by the depletion of immune cell subsets. Sera obtained from mice immunized with qVEGFR were tested against qVEGFR (□) or mVEGFR (▪) by ELISA on day 7 after the fourth immunization. Treatment with anti-CD4 can abrogate the elevation of antibodies against qVEGFR and mVEGFR. In contrast, treatment with anti-CD8, anti-NK, or isotype control had no effect.

Abrogation of antibodies' production and antitumor activity by the depletion of immune cell subsets. (A) Abrogation of antitumor activity by the depletion of immune cell subsets. Depletion of CD4 T lymphocytes showed complete abrogation of the antitumor activity of the qVEGFR vaccine (n = 10). In contrast, treatment with anti-CD8, anti-NK, or isotype controls (IgG2a and IgG2b) had no effect. Results showed the tumor volume on day 26 after tumor cell injection (mean ± SEM). (B) Abrogation of antibody production by the depletion of immune cell subsets. Sera obtained from mice immunized with qVEGFR were tested against qVEGFR (□) or mVEGFR (▪) by ELISA on day 7 after the fourth immunization. Treatment with anti-CD4 can abrogate the elevation of antibodies against qVEGFR and mVEGFR. In contrast, treatment with anti-CD8, anti-NK, or isotype control had no effect.

Close Modal

or Create an Account

Close Modal
Close Modal