Dos Santos Luara Isabela, Galvão-Filho Bruno, de Faria Paula Cristina, Junqueira Caroline, Dutra Miriam Santos, Teixeira Santuza Maria Ribeiro, Rodrigues Maurício Martins, Ritter Gerd, Bannard Oliver, Fearon Douglas Thomas, Antonelli Lis Ribeiro, Gazzinelli Ricardo Tostes
Centro de Pesquisas René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, Minas Gerais, 30190-002, Brazil.
Cancer Immunol Immunother. 2015 Mar;64(3):311-23. doi: 10.1007/s00262-014-1634-8. Epub 2014 Nov 18.
The development of cancer immunotherapy has long been a challenge. Here, we report that prophylactic vaccination with a highly attenuated Trypanosoma cruzi strain expressing NY-ESO-1 (CL-14-NY-ESO-1) induces both effector memory and effector CD8(+) T lymphocytes that efficiently prevent tumor development. However, the therapeutic effect of such a vaccine is limited. We also demonstrate that blockade of Cytotoxic T Lymphocyte Antigen 4 (CTLA-4) during vaccination enhances the frequency of NY-ESO-1-specific effector CD8(+) T cells producing IFN-γ and promotes lymphocyte migration to the tumor infiltrate. As a result, therapy with CL-14-NY-ESO-1 together with anti-CTLA-4 is highly effective in controlling the development of an established melanoma.
癌症免疫疗法的发展长期以来一直是一项挑战。在此,我们报告称,用表达NY-ESO-1的高度减毒克氏锥虫菌株(CL-14-NY-ESO-1)进行预防性疫苗接种可诱导效应记忆和效应CD8(+) T淋巴细胞,从而有效预防肿瘤发展。然而,这种疫苗的治疗效果有限。我们还证明,在疫苗接种期间阻断细胞毒性T淋巴细胞抗原4(CTLA-4)可提高产生IFN-γ的NY-ESO-1特异性效应CD8(+) T细胞的频率,并促进淋巴细胞向肿瘤浸润部位迁移。因此,CL-14-NY-ESO-1与抗CTLA-4联合治疗在控制已形成的黑色素瘤发展方面非常有效。