TY - JOUR
T1 - Enhancing immunomodulation on innate immunity by shape transition among RNA triangle, square and pentagon nanovehicles
AU - Khisamutdinov, Emil F.
AU - Li, Hui
AU - Jasinski, Daniel L.
AU - Chen, Jiao
AU - Fu, Jian
AU - Guo, Peixuan
N1 - Publisher Copyright:
© The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research.
PY - 2014/9/1
Y1 - 2014/9/1
N2 - Modulation of immune response is important in cancer immunotherapy, vaccine adjuvant development and inflammatory or immune disease therapy. Here we report the development of new immunomodulators via control of shape transition among RNA triangle, square and pentagon. Changing one RNA strand in polygons automatically induced the stretching of the interior angle from 60° to 90° or 108°, resulting in self-assembly of elegant RNA triangles, squares and pentagons. When immunological adjuvants were incorporated, their immunomodulation effect for cytokine TNF-α and IL-6 induction was greatly enhanced in vitro and in animals up to 100-fold, while RNA polygon controls induced unnoticeable effect. The RNA nanoparticles were delivered to macrophages specifically. The degree of immunostimulation greatly depended on the size, shape and number of the payload per nanoparticles. Stronger immune response was observed when the number of adjuvants per polygon was increased, demonstrating the advantage of shape transition from triangle to pentagon.
AB - Modulation of immune response is important in cancer immunotherapy, vaccine adjuvant development and inflammatory or immune disease therapy. Here we report the development of new immunomodulators via control of shape transition among RNA triangle, square and pentagon. Changing one RNA strand in polygons automatically induced the stretching of the interior angle from 60° to 90° or 108°, resulting in self-assembly of elegant RNA triangles, squares and pentagons. When immunological adjuvants were incorporated, their immunomodulation effect for cytokine TNF-α and IL-6 induction was greatly enhanced in vitro and in animals up to 100-fold, while RNA polygon controls induced unnoticeable effect. The RNA nanoparticles were delivered to macrophages specifically. The degree of immunostimulation greatly depended on the size, shape and number of the payload per nanoparticles. Stronger immune response was observed when the number of adjuvants per polygon was increased, demonstrating the advantage of shape transition from triangle to pentagon.
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U2 - 10.1093/nar/gku516
DO - 10.1093/nar/gku516
M3 - Article
C2 - 25092921
AN - SCOPUS:84941064568
SN - 0305-1048
VL - 42
SP - 9996
EP - 10004
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 15
ER -