Detailed analysis for inducing specific CD8 T cells via a CpG-DNA adjuvant
- PMID: 19485751
- DOI: 10.1586/erv.09.36
Detailed analysis for inducing specific CD8 T cells via a CpG-DNA adjuvant
Abstract
An important question for vaccine development is how the adaptive immune system incorporates antigenic, costimulatory and inflammatory signals. Here, Cui et al. addressed the concept that antigenic and inflammatory signals were individually or cooperatively involved in effector CD8 T-cell expansion and differentiation by using a peptide-pulsed dendritic cell immunization system. The paper under evaluation introduced IL-12-enhanced effector CD8 T-cell expansion and differentiation to short-lived effector cells (SLECs). The authors also suggested that antigenic stimulation and inflammation needed to be coupled to induce SLEC formation, and that IL-12 produced by bystander cells played an important role in SLEC formation. IFN-gamma could be required for optimal IL-12 production. Their data also showed that CpG-B adjuvant increased SLEC formation, but did not increase the potential of CD8 T cells to differentiate into memory cells. Data in the paper should be considered in research into the development of new adjuvants.
Comment on
-
Effects of Signal 3 during CD8 T cell priming: Bystander production of IL-12 enhances effector T cell expansion but promotes terminal differentiation.Vaccine. 2009 Mar 26;27(15):2177-87. doi: 10.1016/j.vaccine.2009.01.088. Epub 2009 Feb 6. Vaccine. 2009. PMID: 19201385 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials