Figure 5.
Figure 5. Effect of 2 subcutaneous injections (7 days apart) of 1 × 108 pfu of the Ad-sig-ecdhMUC1/ecdCD40L vector on the in vivo growth of the hMUC1-positive LL2/LL1hMUC1 cancer cell line in hMUC1.Tg mice. (A) Two subcutaneous injections (7 days apart) of 1 × 108 pfu Ad-sig-ecdhMUC1/ecdCD40L vector suppresses the growth of the human MUC1-positive LL2/LL1hMUC1 cancer cell line. The Ad-sig-ecdhMUC1/ecdCD40L vector or the Ad-sig-ecdhMUC-1 vector was injected twice at 7-day intervals or was not injected with any vector. One week after the second vector injection, the mice were injected with 5 × 105 LL2/LL1hMUC1 cancer cells, which were positive for hMUC1, and the growth of these cells was measured with calipers. (B) The Ad-sig-ecdhMUC1/ecdCD40L-induced suppression is specific for the hMUC1 antigen. hMUC1.Tg mice were injected twice subcutaneously (7 days apart) with 1 × 108 pfu Ad-sig-ecdhMUC1/ecdCD40L vector twice at 7-day intervals. One week after the second vector injection, the mice were injected with 5 × 105 LL2/LL1hMUC1 cells positive for the hMUC1 antigen or the same number of LL2/LL1 cells negative for the hMUC1 antigen. (C) Survival of LL2/LL1hMUC1 cell line-injected hMUC1.Tg mice that were twice (7 days apart) subcutaneously vaccinated or not vaccinated with 1 × 108 pfu Ad-sig-ecdhMUC1/ecdCD40L vector. Mice that received the injections outlined in panel A were monitored for survival after injection of the LL2/LL1hMUC1 cells. Continuous bold line indicates mice injected with the Ad-sig-ecdhMUC1/ecdCD40L vector. Broken bold line indicates mice not injected with a vector.

Effect of 2 subcutaneous injections (7 days apart) of 1 × 108 pfu of the Ad-sig-ecdhMUC1/ecdCD40L vector on the in vivo growth of the hMUC1-positive LL2/LL1hMUC1 cancer cell line in hMUC1.Tg mice. (A) Two subcutaneous injections (7 days apart) of 1 × 108 pfu Ad-sig-ecdhMUC1/ecdCD40L vector suppresses the growth of the human MUC1-positive LL2/LL1hMUC1 cancer cell line. The Ad-sig-ecdhMUC1/ecdCD40L vector or the Ad-sig-ecdhMUC-1 vector was injected twice at 7-day intervals or was not injected with any vector. One week after the second vector injection, the mice were injected with 5 × 105 LL2/LL1hMUC1 cancer cells, which were positive for hMUC1, and the growth of these cells was measured with calipers. (B) The Ad-sig-ecdhMUC1/ecdCD40L-induced suppression is specific for the hMUC1 antigen. hMUC1.Tg mice were injected twice subcutaneously (7 days apart) with 1 × 108 pfu Ad-sig-ecdhMUC1/ecdCD40L vector twice at 7-day intervals. One week after the second vector injection, the mice were injected with 5 × 105 LL2/LL1hMUC1 cells positive for the hMUC1 antigen or the same number of LL2/LL1 cells negative for the hMUC1 antigen. (C) Survival of LL2/LL1hMUC1 cell line-injected hMUC1.Tg mice that were twice (7 days apart) subcutaneously vaccinated or not vaccinated with 1 × 108 pfu Ad-sig-ecdhMUC1/ecdCD40L vector. Mice that received the injections outlined in panel A were monitored for survival after injection of the LL2/LL1hMUC1 cells. Continuous bold line indicates mice injected with the Ad-sig-ecdhMUC1/ecdCD40L vector. Broken bold line indicates mice not injected with a vector.

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