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Multivalent 4-1BB binding aptamers costimulate [CD8.sup.+] T cells and inhibit tumor growth in mice

Authors :
McNamara, James O., II
Kolonias, Despina
Pastor, Fernando
Mittler, Robert S.
Chen, Lieping
Giangrande, Paloma H.
Sullenger, Bruce
Gilboa, Eli
Source :
Journal of Clinical Investigation. Jan, 2008, Vol. 118 Issue 1, p376, 11 p.
Publication Year :
2008

Abstract

4-1BB is a major costimulatory receptor that promotes the survival and expansion of activated T cells. Administration of agonistic anti-4-1BB Abs has been previously shown to enhance tumor immunity in mice. Abs are cell-based products posing significant cost, manufacturing, and regulatory challenges. Aptamers are oligonucleotide-based ligands that exhibit specificity and avidity comparable to, or exceeding, that of Abs. To date, various aptamers have been shown to inhibit the function of their cognate target. Here, we have described the development of an aptamer that binds 4-1BB expressed on the surface of activated mouse T cells and shown that multivalent configurations of the aptamer costimulated T cell activation in vitro and mediated tumor rejection in mice. Because aptamers can be chemically synthesized, manufacturing and the regulatory approval process should be substantially simpler and less costly than for Abs. Agonistic aptamers could therefore represent a superior alternative to Abs for the therapeutic manipulation of the immune system.<br />Introduction In addition to antigen-dependent TCR signaling, multiple costimulatory pathways regulate the potency, duration, and type of the T cell response. Experimental manipulation of costimulatory pathways offers an attractive way [...]

Details

Language :
English
ISSN :
00219738
Volume :
118
Issue :
1
Database :
Gale General OneFile
Journal :
Journal of Clinical Investigation
Publication Type :
Academic Journal
Accession number :
edsgcl.173646735