A novel mucosal vaccine based on live lactococci expressing E7 antigen and IL-12 induces systemic and mucosal immune responses and protects mice against human papillomavirus type 16-induced tumors

被引:146
作者
Bermúdez-Humarán, LG
Cortes-Perez, NG
Lefèvre, F
Guimaraes, V
Rabot, S
Alcocer-Gonzalez, JM
Gratadoux, JJ
Rodriguez-Padilla, C
Tamez-Guerra, RS
Corthier, G
Gruss, A
Langella, P
机构
[1] INRA, Unite Ecol & Physiol Syst Digest, Jouy En Josas, France
[2] Unite Rech Laitieres & Genet Appl, Jouy En Josas, France
[3] Unite Virol & Immunol Mol, Jouy En Josas, France
[4] Univ Autonoma Nuevo Leon, Lab Immunol & Virol, Fac Ciencias Biol, Nuevo Leon, Mexico
关键词
D O I
10.4049/jimmunol.175.11.7297
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Current strategies to prevent or treat human papillomavirus type 16 (HPV-16) infection are promising, but remain costly. More economical but efficient vaccines are thus needed. In this study, we evaluated the protective effects of mucosally coadministered live Lactococcus lactis strains expressing cell wall-anchored E7 Ag and a secreted form of IL-12 to treat HPV-16-induced tumors in a murine model. When challenged with lethal levels of tumor cell line TC-1 expressing E7, immunized mice showed full prevention of TC-1-induced tumors, even after a second challenge, suggesting that this prophylactic immunization can provide long-lasting immunity. Therapeutic immunization with L. lactis recombinant strains, i.e., 7 days after TC-1 injection, induced regression of palpable tumors in treated mice. The antitumor effects of vaccination occurred through a CTL response, which is CD4(+) and CD8(+) dependent. Furthermore, immunized mice developed an E7-specitic mucosal immune response. These preclinical results suggest the feasibility of the low-cost mucosal vaccination and/or immunotherapy strategies against HPV-related cervical cancer in humans.
引用
收藏
页码:7297 / 7302
页数:6
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