TY - JOUR
T1 - Synthetic polymer as an adjuvant in collagen-induced arthritis
AU - Shakya, Akhilesh K.umar
AU - Nandakumar, Kutty S.elva
N1 - Publisher Copyright:
Copyright © 2014 John Wiley & Sons, Inc.
PY - 2014/3
Y1 - 2014/3
N2 - Collagen-induced arthritis (CIA), the classical animal model for experimental arthritis, resembles human rheumatoid arthritis in several aspects. However, the most widely used method of inducing CIA utilizes Freund's adjuvants, which can skew the elicited immune responses and also pose toxicity problems. This unit describes a new method of inducing CIA using a well defined stimuli-responsive synthetic polymer, poly-N-isopropylacrylamide-based adjuvant, mixed with the joint cartilage protein collagen type II (CII). PNiPAAm as an adjuvant is biodegradable and biocompatible, and does not skew immune responses. Thus, it is helpful in the development of arthritis models for studying antigen and tissue -specific autoimmune responses in an unbiased manner. This model is valuable for analyzing disease pathways, positional identification of genes regulating arthritis, validation of existing therapies, and exploring new therapeutic targets. Furthermore, this newly developed PNiPAAm adjuvant allows investigation of disease induction using specific autoantigens in several autoimmune diseases independently of toll-like receptors, as well as optimization of vaccine delivery systems for infectious diseases.
AB - Collagen-induced arthritis (CIA), the classical animal model for experimental arthritis, resembles human rheumatoid arthritis in several aspects. However, the most widely used method of inducing CIA utilizes Freund's adjuvants, which can skew the elicited immune responses and also pose toxicity problems. This unit describes a new method of inducing CIA using a well defined stimuli-responsive synthetic polymer, poly-N-isopropylacrylamide-based adjuvant, mixed with the joint cartilage protein collagen type II (CII). PNiPAAm as an adjuvant is biodegradable and biocompatible, and does not skew immune responses. Thus, it is helpful in the development of arthritis models for studying antigen and tissue -specific autoimmune responses in an unbiased manner. This model is valuable for analyzing disease pathways, positional identification of genes regulating arthritis, validation of existing therapies, and exploring new therapeutic targets. Furthermore, this newly developed PNiPAAm adjuvant allows investigation of disease induction using specific autoantigens in several autoimmune diseases independently of toll-like receptors, as well as optimization of vaccine delivery systems for infectious diseases.
KW - adjuvant
KW - arthritis
KW - collagen II
KW - poly-N-isopropylacrylamide
KW - polymer
UR - http://www.scopus.com/inward/record.url?scp=84944673814&partnerID=8YFLogxK
U2 - 10.1002/9780470942390.mo130226
DO - 10.1002/9780470942390.mo130226
M3 - Article
C2 - 25715674
AN - SCOPUS:84944673814
SN - 2161-2617
VL - 4
SP - 11
EP - 24
JO - Current protocols in mouse biology
JF - Current protocols in mouse biology
IS - 1
ER -