The effects of leflunomide on CD4(+)CD25 (+)Foxp3 (+) T regulatory cells in mice receiving allogeneic bone marrow transplantation.

Author: DuanKaizhong, JinDi, PengJianxia, ZhangLianjun, ZhaoYong

Paper Details 
Original Abstract of the Article :
Leflunomide (LEF) is effective not only in different animal models of autoimmune diseases and the therapy of patients with rheumatoid arthritisbut also in graft rejection. The effect of LEF on CD4(+)CD25(+)T regulatory cells (Treg) was determined in a mouse model of allogeneic bone marrow transplant...See full text at original site
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引用元:
https://doi.org/10.1007/s00011-011-0388-4

データ提供:米国国立医学図書館(NLM)

Leflunomide: A Potential Ally in Bone Marrow Transplantation

Bone marrow transplantation, a life-saving procedure for individuals with certain blood disorders and cancers, is often accompanied by graft rejection. This happens when the recipient's immune system attacks the donor's cells, creating a complex immunological battle.

Leflunomide (LEF), a drug commonly used for rheumatoid arthritis, has shown promise in preventing graft rejection in animal models. This study investigated the effects of LEF on CD4(+)CD25(+)Foxp3(+) T regulatory cells (Treg), which play a crucial role in regulating the immune response. The study found that LEF was effective in promoting the development of Treg cells, suggesting its potential use in preventing graft rejection.

A New Frontier in Transplant Immunosuppression

The findings of this study suggest that LEF may be a valuable addition to the immunosuppressive arsenal for bone marrow transplantation.

Dr. Camel's Conclusion

Imagine a desert oasis where different tribes gather to share resources and stories. A harmonious coexistence depends on maintaining peace and understanding between the tribes. Similarly, successful bone marrow transplantation relies on establishing a balance between the recipient's immune system and the donor's cells. This study suggests that LEF may be a key player in fostering this delicate balance.

Date :
  1. Date Completed 2012-04-30
  2. Date Revised 2021-10-21
Further Info :

Pubmed ID

22057872

DOI: Digital Object Identifier

10.1007/s00011-011-0388-4

Related Literature

SNS
PICO Info
in preparation
Languages

English

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