Literature DB >> 16034547

The effect of a novel immunosuppressant, FTY720, in mice without secondary lymphoid organs.

Kiminobu Sugito1, Tsugumichi Koshinaga, Mikiya Inoue, Taro Ikeda, Noritsugu Hagiwara, Masahiro Fukuzawa.   

Abstract

PURPOSE: FTY720 is a novel immunosuppressive agent that is thought to reduce the number of peripheral blood lymphocytes (PBL) by directing them toward secondary lymphoid organs such as the lymph nodes and Peyer's patches. We studied the effects of FTY720 on aly/aly mice that do not have either lymph nodes or Peyer's patches, as well as on splenectomized aly/aly mice.
METHODS: FTY720 was orally administered by gavage (1 mg/kg) to aly/aly mice as well as to aly/+ mice with and without a splenectomy on 14 consecutive days. The number of lymphocytes was then counted using True Cell beads and flow cytometry. The number of B220-, CD3-, and CD4-positive cells was also determined. In addition, skin grafts from C3H donor mice were performed on these mice.
RESULTS: FTY720 was effective in significantly reducing the total lymphocyte count as well as the B220-, CD3-, and CD4-positive subtypes in the peripheral blood of aly/+ mice as well as in aly/aly mice with and without a splenectomy. While we did observe allograft skin graft rejection in both the aly/+ mice as well as the aly/aly mice recipients and splenectomized aly/aly mice, the graft survival was prolonged in all groups. The skin allografts treated by FTY720 thus demonstrated fewer lymphocytic cells and less infiltration of CD4-positive cells.
CONCLUSIONS: The administration of FTY720 to mice without lymph nodes, Peyer's patches, or spleens still results in peripheral lymphopenia. In all groups, FTY720 was found to prevent the infiltration of CD4-positive cells in skin allografts while also prolonging skin allograft survival. The fate of these lymphocytes, however, is unclear.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16034547     DOI: 10.1007/s00595-005-3011-x

Source DB:  PubMed          Journal:  Surg Today        ISSN: 0941-1291            Impact factor:   2.549


  12 in total

1.  FTY720: a novel transplantation drug that modulates lymphocyte traffic rather than activation.

Authors:  V Brinkmann; D Pinschewer; K Chiba; L Feng
Journal:  Trends Pharmacol Sci       Date:  2000-02       Impact factor: 14.819

2.  Alteration of lymphocyte trafficking by sphingosine-1-phosphate receptor agonists.

Authors:  Suzanne Mandala; Richard Hajdu; James Bergstrom; Elizabeth Quackenbush; Jenny Xie; James Milligan; Rosemary Thornton; Gan-Ju Shei; Deborah Card; CarolAnn Keohane; Mark Rosenbach; Jeffrey Hale; Christopher L Lynch; Kathleen Rupprecht; William Parsons; Hugh Rosen
Journal:  Science       Date:  2002-03-28       Impact factor: 47.728

3.  FTY720 immunosuppression impairs effector T cell peripheral homing without affecting induction, expansion, and memory.

Authors:  D D Pinschewer; A F Ochsenbein; B Odermatt; V Brinkmann; H Hengartner; R M Zinkernagel
Journal:  J Immunol       Date:  2000-06-01       Impact factor: 5.422

4.  Synthesis and biological evaluation of 2,2-disubstituted 2-aminoethanols: analogues of FTY720.

Authors:  M Kiuchi; K Adachi; T Kohara; K Teshima; Y Masubuchi; T Mishina; T Fujita
Journal:  Bioorg Med Chem Lett       Date:  1998-01-06       Impact factor: 2.823

5.  A new immunosuppressant, FTY720, induces bcl-2-associated apoptotic cell death in human lymphocytes.

Authors:  S Suzuki; X K Li; S Enosawa; T Shinomiya
Journal:  Immunology       Date:  1996-12       Impact factor: 7.397

6.  FTY720, a novel immunosuppressant, induces sequestration of circulating mature lymphocytes by acceleration of lymphocyte homing in rats. I. FTY720 selectively decreases the number of circulating mature lymphocytes by acceleration of lymphocyte homing.

Authors:  K Chiba; Y Yanagawa; Y Masubuchi; H Kataoka; T Kawaguchi; M Ohtsuki; Y Hoshino
Journal:  J Immunol       Date:  1998-05-15       Impact factor: 5.422

7.  Heterogeneity of CD4+ T cells involved in anti-allo-class I H-2 immune responses. Functional discrimination between the major proliferating cells and helper cells assisting cytotoxic T cell responses.

Authors:  S Kitagawa; S Sato; T Azuma; J Shimizu; T Hamaoka; H Fujiwara
Journal:  J Immunol       Date:  1991-04-15       Impact factor: 5.422

8.  CD4+ but not CD8+ cells are essential for allorejection.

Authors:  N R Krieger; D P Yin; C G Fathman
Journal:  J Exp Med       Date:  1996-11-01       Impact factor: 14.307

9.  CD4-positive helper T lymphocytes mediate mouse cardiac allograft rejection independent of donor alloantigen specific cytotoxic T lymphocytes.

Authors:  D K Bishop; S Chan; W Li; R D Ensley; S Xu; E J Eichwald
Journal:  Transplantation       Date:  1993-10       Impact factor: 4.939

10.  A novel immunosuppressant, FTY720, with a unique mechanism of action, induces long-term graft acceptance in rat and dog allotransplantation.

Authors:  S Suzuki; S Enosawa; T Kakefuda; T Shinomiya; M Amari; S Naoe; Y Hoshino; K Chiba
Journal:  Transplantation       Date:  1996-01-27       Impact factor: 4.939

View more
  1 in total

1.  CXCR4 antagonist AMD3100 redistributes leukocytes from primary immune organs to secondary immune organs, lung, and blood in mice.

Authors:  Qian Liu; Zhanzhuo Li; Ji-Liang Gao; Wuzhou Wan; Sundar Ganesan; David H McDermott; Philip M Murphy
Journal:  Eur J Immunol       Date:  2015-04-24       Impact factor: 5.532

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.