By Th. Büchner (auth.), W. Hinterberger, A. J. Barrett, K. Lechner, E. Deutsch (eds.)
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Additional resources for 11th Annual meeting of the EBMT: European Cooperative Group for Bone Marrow Transplantation
Residual cells were evaluated in comparison to complement treated marrow cells and seeded without cellularity adjustement. In vitro treatment of large volumes of marrowwas done along the same general procedure, except that whole marrow was processed on Haemonetics V50 and that marrow was cryopreserved in plasma and DMSO prior final clinical use. In vitro haematopo"ietic evaluation was done by GM-CFC assays in soft Agar with HPCM 15%. Lang term marrow culture was done using the technic of s. Gartner et al (3).
HematoL 12 (SuppL 15): 74. 3. , et aL (1982)- ldentical twin marrow Iransplantalion in multiple myeloma. Acta Haemat. 68: 215. 2 x I 0 8 marrow cells/Kg. Engraftment was prompt and on day 20 white cell and platelet counts exceeded 3 x 10 9 /1 and 50 x 10 9 /1, respectively. Bone marrow aspiration, performed on Day 18, revealed normal myelopoiesis and less than 5°/o polyclonal plasma cells. , et aL (1984)- Cyclosporin A (CyA) prophylaxis of graft versus host disease (GVHD) in allogencic 4. , Henderson ES.
These results are in agreement with the recent reports of A. Keating and Al. ( 7). , FERRONE S. et al Expression of Ia like and HLA A-B antigens on human pluripotential haematopo"ietic progenitor cells. S. , PIERES M. et al Distinct HLA-DR epitopes and distinct families of HLA DR molecules defined by 15 either anti DR or allo anti Ia K cross reacting with human cells. Eur. J. , V. der VAARTDUINKERKEN N. et al Polymorphie and monomorphic HLA-DR determinants on human hematopoietic progenitor cells.