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C. Gravekamp, B. Leal, A. Denny, R. Baher, S. Lampkin, F. Castro, S. H. Kim, D. Moore and R. Riddick, “In vivo Responses to Vaccination with Mage-b, GM-CSF and Thioglycollate in a Highly Metastatic Mouse Breast Tumor Model, 4T1,” Cancer Immunology Immunotherapy, Vol. 57, No. 7, 2008, pp. 1067-1077. doi:10.1007/s00262-007-0438-5

has been cited by the following article:

• TITLE: Construction and Evaluation of a Combined Cyclophosphamide/Nanoparticle Anticancer Vaccine

  AUTHORS: Kurt Andrew Yaeger, Robert Anthony Kurt

  KEYWORDS: Nanoparticle Vaccine, Breast Cancer, Metastasis, 4T1

  JOURNAL NAME: Journal of Cancer Therapy, Vol.2 No.3, August 18, 2011

  ABSTRACT: Tumor immunotherapy is a rapidly emerging form of cancer treatment. In the current study, a nanoparticle-based vaccine was constructed and the efficacy was assessed through analysis of immune cell populations, tumor growth rates, and metastasis. The vaccine was fabricated through encapsulation of plasmid DNA encoding the tumor-associated antigen Mage-b, and the TLR9 agonist CpG oligodeoxynucleotides by a biodegradable polymer, poly(L,D-lactic-coglycolic acid) (PLGA). The size and shape of the nanoparticles suggested that they were an appropriate size for uptake by professional antigen presenting cells; dendritic cells. Furthermore, effects of the immunopotentiating drug cyclo-phosphamide was included to decrease systemic populations of regulatory T cells (Treg); immune system sentinels that down-regulate immune responses. The vaccine was assessed using the 4T1 murine mammary carcinoma model which is a model for stage IV breast cancer. The combined cyclophosphamide/nanoparticle vaccine was shown to significantly reduce 4T1 tumor growth rates and lung metastasis in female BALB/c mice.