AI Article Synopsis

  • - CD40L and GITRL are immune molecules from the tumor necrosis factor superfamily that can enhance vaccine effectiveness.
  • - Previous research showed that a specific DNA vaccine in mice using multimeric forms of CD40L (multiple trimers) activated stronger CD8(+) T-cell responses compared to single or natural forms.
  • - Similar multimeric versions were created for macaques, showing efficacy in stimulating B-cell and CD4(+) T-cell responses, offering promising tools for vaccine development against simian immunodeficiency virus.

Article Abstract

CD40 ligand (CD40L) and GITR ligand (glucocorticoid-induced tumor necrosis factor receptor-related protein ligand [GITRL]) are tumor necrosis factor superfamily molecules that can be used as vaccine adjuvants. In a previous human immunodeficiency virus (HIV) DNA vaccine study in mice, we found that plasmids expressing multimeric soluble forms of trimeric CD40L (i.e., many trimers) were stronger activators of CD8(+) T-cell responses than were single-trimer soluble forms or the natural membrane-bound molecule. This report describes similar multimeric soluble molecules that were constructed for studies in macaques. Both two-trimer and four-trimer forms of macaque CD40L were active in B-cell proliferation assays using macaque and human cells. With human cells, four-trimer macaque GITRL costimulated CD4(+) T-cell proliferation and abrogated the immunosuppressive effects of CD4(+) CD25(+) regulatory T cells on a mixed leukocyte reaction. These molecular adjuvants provide new tools for vaccine development in the simian immunodeficiency virus system and other macaque models.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1656546PMC
http://dx.doi.org/10.1128/CVI.00198-06DOI Listing

Publication Analysis

Top Keywords

multimeric soluble
12
cd40 ligand
8
gitr ligand
8
tumor necrosis
8
necrosis factor
8
immunodeficiency virus
8
soluble forms
8
human cells
8
macaque
5
ligand
5

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!