bc2006219_si_001.pdf (422.43 kB)
Download fileT Cell-Specific siRNA Delivery Using Antibody-Conjugated Chitosan Nanoparticles
journal contribution
posted on 2012-06-20, 00:00 authored by Jangwook Lee, Kyoung-Soo Yun, Chang
Seon Choi, Seung-Hwa Shin, Hong-Seok Ban, Taiyoun Rhim, Sang Kyung Lee, Kuen Yong LeeThe intracellular delivery of small interfering RNA (siRNA)
plays
a key role in RNA interference (RNAi) and provides an emerging technique
to treat various diseases, including infectious diseases. Chitosan
has frequently been used in gene delivery applications, including
siRNA delivery. However, studies regarding the modification of chitosan
with antibodies specifically targeting T cells are lacking. We hypothesized
that chitosan nanoparticles modified with T cell-specific antibodies
would be useful for delivering siRNA to T cells. CD7-specific single-chain
antibody (scFvCD7) was chemically conjugated to chitosan by carbodiimide
chemistry, and nanoparticles were prepared by a complex coacervation
method in the presence of siRNA. The mean diameter and zeta potential
of the scFvCD7-chitosan/siRNA nanoparticles were approximately 320
nm and +17 mV, respectively, and were not significantly influenced
by the coupling of antibody to chitosan. The cellular association
of antibody-conjugated nanoparticles to CD4+ T cell lines as well
as gene silencing efficiency in the cells was significantly improved
compared to nonmodified chitosan nanoparticles. This approach to introducing
T cell-specific antibody to chitosan nanoparticles may find useful
applications for the treatment of various infectious diseases.