Bone Marrow Transplantation: Basic and Clinical Studies by Michael V. Wiles, Britt M. Johansson (auth.), Susumu Ikehara
By Michael V. Wiles, Britt M. Johansson (auth.), Susumu Ikehara M.D., Ph.D., Fumimaro Takaku M.D., Ph.D., Robert A. Good M.D., Ph.D., D.Sc., FACP (eds.)
In the decade, amazing advances were made in bone marrow transplantation (BMT), that's now turning into a robust device within the therapy of ailments corresponding to leukemia, aplastic anemia, and congenital immunodeficiency. In animal experiments, it's been came across that BMT can be utilized to regard not just systemic autoimmune ailments but in addition organ-specific autoimmune illnesses. In people, it has lately been proven that rheumatoid arthritis, ulcerative colitis, and Crohn's disorder may be effectively handled after BMT. This quantity comprises new info on tips to hinder graft rejection, how T telephone features could be thoroughly restored, and the way concomitant BMT can hinder the rejection of organ allografts with out using immunosuppressive brokers. BMT turns into an more and more important and robust therapy for numerous presently intractable ailments, and this ebook will give a contribution by means of delivering information of the most recent learn within the field.
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Extra resources for Bone Marrow Transplantation: Basic and Clinical Studies
These questions await further experiment and perhaps new reagents and approaches. ACKNOWLEDGEMENTS The authors acknowledge the many discussions and joint experiments performed with our friends and colleagues Ken Shortman and Wu Li. RS would like to thank the Japan Intractable Disease Foundation and Professor Susumu Ikehara for the opportunity to attend this conference. REFERENCES 1. Donskoy E, Goldschneider I. (1992) Thymocytopoiesis is maintained by blood-born precursors throughout postnatal life.
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The method of PCR-based cloning has been described previously . l Northern blot analysis of HTK expression in hematopoietic cell lines. Two micrograms ofpoly(A)+RNA was loaded per lane. SmaI-SmaI fragment of HTK cDNA (7 46 bps) was used as a probe. 39 HTK was isolated from UT-7 cells both with and without n-butyric acid treatment (which induces erythroid differentiation), but not with PMA treatment (megakaryocytic differentiation). Northern blot analysis showed the down-regulated expression of HTK mRNA during megakaryocytic differentiation induced by PMA (Fig.