TY - JOUR
T1 - Induced production of anti-etanercept antibody in collagen-induced arthritis
AU - Yi, Hyoju
AU - Kim, Juryun
AU - Jung, Hyerin
AU - Rim, Yeri Alice
AU - Kim, Youngkyun
AU - Jung, Seung Min
AU - Park, Sung Hwan
AU - Ju, Ji Hyeon
PY - 2014/6
Y1 - 2014/6
N2 - Etanercept is a widespread biological drug for the treatment of rheumatoid arthritis, which inhibits tumor necrosis factor-α (TNF-α). Recently, the presence of antibodies targeting TNF-α inhibitors such as infliximab and adalimumab, was reported. However, few reports have studied etanercept in a mouse model of arthritis. We investigated the induction of anti-etanercept antibody production, along with the antibody's potential interfering effects on the biological function of etanercept, in mice with collagen-induced arthritis (CIA). CIA mice received an intraperitoneal injection of etanercept (25, 100 or 400 μg per mouse). The degree of inflammation and cartilage erosion was evaluated, and the number of osteoclasts in the ankle joints was assessed by TRAP staining. The level of pro-inflammatory cytokines in the serum was measured. To analyze the anti-osteoporotic effect of etanercept, microfocal computed tomography analyses of femurs and tibias were performed. Etanercept treatment decreased both the incidence and severity of arthritis in a dose-dependent manner, except for the highest dose of 400 μg. The mice that were treated with 25 and 100 μg etanercept showed an improvement in inflammation, cartilage damage, and even bone loss. However, mice treated with 400 μg etanercept showed no significant improvement in any of the tested parameters. Using a customized enzyme-linked immunosorbent assay (ELISA), the presence of the anti-etanercept antibody was detected in the serum in this treatment-refractory group. The therapeutic effect of etanercept was reduced in the CIA mice that developed the anti-etanercept antibody. In conclusion, the production of an anti-etanercept antibody can be induced in CIA mice, and this antibody can considerably reduce the anti-arthritic and anti-osteoporotic effects of etanercept.
AB - Etanercept is a widespread biological drug for the treatment of rheumatoid arthritis, which inhibits tumor necrosis factor-α (TNF-α). Recently, the presence of antibodies targeting TNF-α inhibitors such as infliximab and adalimumab, was reported. However, few reports have studied etanercept in a mouse model of arthritis. We investigated the induction of anti-etanercept antibody production, along with the antibody's potential interfering effects on the biological function of etanercept, in mice with collagen-induced arthritis (CIA). CIA mice received an intraperitoneal injection of etanercept (25, 100 or 400 μg per mouse). The degree of inflammation and cartilage erosion was evaluated, and the number of osteoclasts in the ankle joints was assessed by TRAP staining. The level of pro-inflammatory cytokines in the serum was measured. To analyze the anti-osteoporotic effect of etanercept, microfocal computed tomography analyses of femurs and tibias were performed. Etanercept treatment decreased both the incidence and severity of arthritis in a dose-dependent manner, except for the highest dose of 400 μg. The mice that were treated with 25 and 100 μg etanercept showed an improvement in inflammation, cartilage damage, and even bone loss. However, mice treated with 400 μg etanercept showed no significant improvement in any of the tested parameters. Using a customized enzyme-linked immunosorbent assay (ELISA), the presence of the anti-etanercept antibody was detected in the serum in this treatment-refractory group. The therapeutic effect of etanercept was reduced in the CIA mice that developed the anti-etanercept antibody. In conclusion, the production of an anti-etanercept antibody can be induced in CIA mice, and this antibody can considerably reduce the anti-arthritic and anti-osteoporotic effects of etanercept.
KW - Anti-drug antibody
KW - Collagen-induced arthritis
KW - Etanercept
KW - Rheumatoid arthritis
KW - Tumor necrosis factor-α
UR - https://www.scopus.com/pages/publications/84899667413
U2 - 10.3892/mmr.2014.2127
DO - 10.3892/mmr.2014.2127
M3 - Article
C2 - 24718553
AN - SCOPUS:84899667413
SN - 1791-2997
VL - 9
SP - 2301
EP - 2308
JO - Molecular Medicine Reports
JF - Molecular Medicine Reports
IS - 6
ER -