Background:
In recent years,
nanoparticle
materials have found
wide applications in
drug transport and
release systems.
Chitosan is a good
carrier for
proteins, peptides,
and nucleic acids
because of its
favorable release
properties and
ability to increase
membrane
permeability.
Objective: To
investigate the
effect of chitosan
microparticles
loaded with the
major epitope
peptide of mite
group 2 allergen Der
f 2 from
Dermatophagoides
farinae (Der f
2-47-67) in
alleviating asthma
in mice.
Methods: Der
f 2-47-67 was
entrapped in
chitosan to obtain
Der f 2-47-67-loaded
chitosan
microparticles,
which were injected
intraperitoneally
into BALB/c mice
prior to an
intranasal challenge
with a Der f extract
allergen. Airway
hyperreactivity was
measured via
whole-body
plethysmography, and
bronchoalveolar
lavage (BAL) fl uid
was collected to
calculate total cell
and eosinophil
counts. Changes in
lung histology were
assessed after
hematoxylineosin
staining, and serum
levels of Der
f-specific
immunoglobulin (Ig)
G2a and IgE were
determined by
enzyme-linked
immunoabsorbent
assay.
Results: Mice
immunized with Der f
2-47-67-loaded
chitosan
microparticles
displayed decreased
airway
hyperreactivity,
reduced numbers of
eosinophils in BAL
fl uid, alleviated
lung inflammation
and mucus
production, a
reduced serum level
of Der f-specifi c
IgE and an increased
serum level of Der
f-specific IgG2a.
Conclusion:
Our data showed that
Der f 2-47-67-loaded
chitosan
microparticles
inhibited airway
allergic
inflammation.
Key words:
Chitosan.
Dermatophagoides
farinae.
Polypeptide.
Microparticles.
Allergic airway
inflammation.
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