| Literature DB >> 27037842 |
Aws Abdul-Wahid1,2, Marzena Cydzik2, Aaron Prodeus1,2, Mays Alwash2,3, Mile Stanojcic4, Megan Thompson2, Eric H-B Huang2, John E Shively5, Scott D Gray-Owen6, Jean Gariépy1,2,3.
Abstract
The engraftment of circulating cancer cells at distal sites represents a key step in the metastatic cascade, yet remains an unexplored target for therapeutic intervention. In this study, we establish that a vaccination strategy yielding an antigen-specific TH 9 response induces long term host surveillance and prevents the engraftment of circulating cancer cells. Specifically, we show that vaccination with a recombinant CEA IgV-like N domain, formulated with the TLR3 ligand poly I:C, elicits a CEA-specific TH 9 response, wherein IL-9 secreting TH cells act in concert with CEA N domain-specific antibodies as well as activated mast cells in preventing tumor cell engraftment. The development of this immune response was dependent on TLR3, since interference with the TLR3-dsRNA complex formation led to a reduction in vaccine-imparted protection and a shift in the resulting immune response toward a TH 2 response. These findings point to the existence of an alternate tumor targeting immune mechanism that can be exploited for the purpose of developing vaccine therapies targeting tumor dissemination and engraftment.Entities:
Keywords: TH9 immunity; cancer vaccine; metastatic dissemination; toll-like receptor 3; tumor cell engraftment
Mesh:
Substances:
Year: 2016 PMID: 27037842 DOI: 10.1002/ijc.30121
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396