Literature DB >> 17180729

In SCID mice with transplanted joint tissues from rheumatism patients, a model mice of human rheumatoid arthritis, anti-human fas antibody (R-125224) distributes specifically to human synovium.

Motoko Saito1, Yasushi Yoshigae, Junichi Nakayama, Yukie Ogawa, Masahiko Ohtsuki, Atsushi Kurihara, Toshihiko Ikeda.   

Abstract

PURPOSE: We investigated the tissue distribution of a humanized anti-human Fas monoclonal antibody, R-125224, in SCID mice transplanted with synovial tissues from patients with rheumatoid arthritis (SCID-HuRAg mice). The binding kinetics of R-125224 was also determined, using isolated human synovial cells.
MATERIALS AND METHODS: Tissue distribution was assessed at 1, 24 and 168 h after intravenous administration of (125)I-R-125224 to SCID-HuRAg mice (0.4 mg/kg). The in vitro binding of (125)I-R-125224 to isolated human synovial cells was investigated.
RESULTS: After intravenous administration of (125)I-R-125224 to SCID-HuRAg mice, the radioactivity distributed to various tissues at 1 h. Thereafter, the radioactivity in the tissues gradually decreased except for the transplanted synovial tissues, in which the radioactivity increased in a time-dependent manner, and at 168 h, the tissue/plasma concentration ratio was about 1. The in vitro binding affinity of (125)I-R-125224 to human synovial cells was high with a dissociation constant of 1.32 +/- 0.62 nM and the binding was inhibited by non-labeled R-125224 in a concentration-dependent manner.
CONCLUSION: R-125224, a candidate compound for treating rheumatoid arthritis, specifically distributed to the pharmacological target site, human synovium transplanted in SCID mice, with high affinity.

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Year:  2006        PMID: 17180729     DOI: 10.1007/s11095-006-9148-5

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  26 in total

1.  Fas-induced in vivo apoptosis in bone marrow: anti-Fas mAb-induced elimination and successive proliferation of Fas-expressing cells especially those of myeloid lineage.

Authors:  Y Inazawa; S Yonehara
Journal:  Cell Struct Funct       Date:  1999-06       Impact factor: 2.212

2.  Therapeutic effect of novel anti-human Fas antibody HFE7a on graft-versus-host disease model.

Authors:  H Kuwahara; Y Tani; Y Ogawa; Y Takaichi; A Shiraishi; M Ohtsuki
Journal:  Clin Immunol       Date:  2001-06       Impact factor: 3.969

3.  Humanization of the mouse anti-Fas antibody HFE7A and crystal structure of the humanized HFE7A Fab fragment.

Authors:  Hideyuki Haruyama; Shuichiro Ito; Kenji Miyadai; Tohru Takahashi; Reimi Kawaida; Tomoko Takayama; Hiroyuki Hanzawa; Tadashi Hata; Junko Yamaguchi; Hiroko Yoshida-Kato; Kimihisa Ichikawa; Jun Ohsumi; Shin Yonehara; Nobufusa Serizawa
Journal:  Biol Pharm Bull       Date:  2002-12       Impact factor: 2.233

4.  A novel murine anti-human Fas mAb which mitigates lymphadenopathy without hepatotoxicity.

Authors:  K Ichikawa; H Yoshida-Kato; M Ohtsuki; J Ohsumi; J Yamaguchi; S Takahashi; Y Tani; M Watanabe; A Shiraishi; K Nishioka; S Yonehara; N Serizawa
Journal:  Int Immunol       Date:  2000-04       Impact factor: 4.823

5.  The role of TNF-alpha in the pathogenesis of inflammation and joint destruction in rheumatoid arthritis (RA): a study using a human RA/SCID mouse chimera.

Authors:  H Matsuno; K Yudoh; R Katayama; F Nakazawa; M Uzuki; T Sawai; T Yonezawa; Y Saeki; G S Panayi; C Pitzalis; T Kimura
Journal:  Rheumatology (Oxford)       Date:  2002-03       Impact factor: 7.580

6.  Lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis.

Authors:  R Watanabe-Fukunaga; C I Brannan; N G Copeland; N A Jenkins; S Nagata
Journal:  Nature       Date:  1992-03-26       Impact factor: 49.962

7.  Generalized lymphoproliferative disease in mice, caused by a point mutation in the Fas ligand.

Authors:  T Takahashi; M Tanaka; C I Brannan; N A Jenkins; N G Copeland; T Suda; S Nagata
Journal:  Cell       Date:  1994-03-25       Impact factor: 41.582

8.  Treatment of rheumatoid synovitis with anti-reshaping human interleukin-6 receptor monoclonal antibody: use of rheumatoid arthritis tissue implants in the SCID mouse model.

Authors:  H Matsuno; T Sawai; T Nezuka; M Uzuki; H Tsuji; N Nishimoto; K Yoshizaki
Journal:  Arthritis Rheum       Date:  1998-11

9.  Potential withdrawal of rheumatoid synovium by the induction of apoptosis using a novel in vivo model of rheumatoid arthritis.

Authors:  K Sakai; H Matsuno; I Morita; T Nezuka; H Tsuji; T Shirai; S Yonehara; T Hasunuma; K Nishioka
Journal:  Arthritis Rheum       Date:  1998-07

10.  Selective apoptosis of CD4+CD8+ thymocytes by the anti-Fas antibody.

Authors:  J Ogasawara; T Suda; S Nagata
Journal:  J Exp Med       Date:  1995-02-01       Impact factor: 14.307

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  2 in total

1.  Highly frequent anti-idiotype antibody in cynomolgus monkeys developed against mouse-derived regions of anti-Fas antibody humanized by complementarity determining region grafting.

Authors:  M Saito-Yabe; Y Yoshigae; W Takasaki; A Kurihara; T Ikeda; O Okazaki
Journal:  Br J Pharmacol       Date:  2009-07-23       Impact factor: 8.739

Review 2.  New insights into T cell biology and T cell-directed therapy for autoimmunity, inflammation, and immunosuppression.

Authors:  Scott M Steward-Tharp; Yun-jeong Song; Richard M Siegel; John J O'Shea
Journal:  Ann N Y Acad Sci       Date:  2010-01       Impact factor: 5.691

  2 in total

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