TY - JOUR
T1 - Suppressive effect on Theiler's murine encephalomyelitis virus-induced demyelinating disease by the administration of anti-IL-12 antibody
AU - Inoue, Atsushi
AU - Koh, Chang Sung
AU - Yamazaki, Masashi
AU - Yahikozawa, Hiroyuki
AU - Ichikawa, Motoki
AU - Yagita, Hideo
AU - Kim, Byung S.
PY - 1998/11/15
Y1 - 1998/11/15
N2 - We examined the role of IL-12, a cytokine critical to the evolution of cellular responses, in the development of Theiler's murine encephalomyelitis virus-induced demyelinating disease (TMEV-IDD). Treatment with mAbs to IL- 12, especially during the effector phase, resulted in significant suppression of the development of this disease both clinically and histologically. In mice treated with these mAbs, the production of inflammatory and Th1-derived cytokines such as TNF-α and lieN-γ, in the spleen cells was decreased, and that of Th2-derived cytokines such as IL-4 and IL-10 was increased. The delayed type hypersensitivity and T cell proliferative response specific for TMEV were decreased by this treatment. These data suggest that IL-12 is critically involved in the pathogenesis of TMEV-IDD and that Abs to IL-12 could be a novel therapeutic approach in the clinical treatment of demyelinating diseases such as human multiple sclerosis.
AB - We examined the role of IL-12, a cytokine critical to the evolution of cellular responses, in the development of Theiler's murine encephalomyelitis virus-induced demyelinating disease (TMEV-IDD). Treatment with mAbs to IL- 12, especially during the effector phase, resulted in significant suppression of the development of this disease both clinically and histologically. In mice treated with these mAbs, the production of inflammatory and Th1-derived cytokines such as TNF-α and lieN-γ, in the spleen cells was decreased, and that of Th2-derived cytokines such as IL-4 and IL-10 was increased. The delayed type hypersensitivity and T cell proliferative response specific for TMEV were decreased by this treatment. These data suggest that IL-12 is critically involved in the pathogenesis of TMEV-IDD and that Abs to IL-12 could be a novel therapeutic approach in the clinical treatment of demyelinating diseases such as human multiple sclerosis.
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U2 - 10.4049/jimmunol.161.10.5586
DO - 10.4049/jimmunol.161.10.5586
M3 - Article
C2 - 9820536
AN - SCOPUS:0032533853
SN - 0022-1767
VL - 161
SP - 5586
EP - 5593
JO - Journal of Immunology
JF - Journal of Immunology
IS - 10
ER -