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ABSTRACT To circumvent aGVHD in the early phase after allogeneic stem cell transplantation but to provide GVL activity later on, we performed alloPBSCT with CD34+ selected grafts followed by
delayed add-back of CD3+ T cells. Ten consecutive patients having an HLA-identical sibling donor were enrolled on to this trial. Four patients were in first CR of high-risk ALL, another
four in first CR of AML, one was in second myeloid blast crisis of CML, and one was in PR of relapsed NHL. Conditioning consisted of 2 × 60 mg/kg CY plus 12 Gy TBI. G-CSF (Filgrastim)
mobilized peripheral cells were CD34+selected using the Isolex 300i system in nine patients and the CliniMacs system in one. Median CD34+ purity was 86%. A median of 2.8 × 106/kg CD34+ cells
were transplanted. The number of CD3+ cells in the allografts was 5.7 × 104/kg (median) after Isolex 300i, and 0.2 × 104/kg after CliniMacs. All patients received G-CSF (Filgrastim) and
engrafted rapidly. Standard-dose CsA was administered, and until day +60 no aGVHD occurred. At that time point, seven patients received 2 × 106/kg CD3+ cells while CsA had been tapered to
50% of the starting dose. One of these patients died after a second T cell boost given on day +90 without concomitant immunosuppression due to grade IV intestinal aGVHD. Three others
developed cutaneous cGVHD. Taken together, T cell depletion by CD34+ selection does not impair rapid engraftment in the HLA-identical sibling donor setting. Using standard-dose CsA the risk
for acute GVHD seems to be minimized. Add-back of 2 × 106/kg CD3+ cells on day +60 with CsA protection is feasible. However, whether this is the optimal time point and number of T cells
remain to be further elucidated. _Bone Marrow Transplantation_ (2000) 25, Suppl. 2, S2–S5. Access through your institution Buy or subscribe This is a preview of subscription content, access
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February 2021 AUTHOR INFORMATION AUTHORS AND AFFILIATIONS * Medizinische Klinik III, Universitätsklinik Benjamin Franklin, Freie Universität, Berlin, Germany W Knauf, T Fietz, H
Schrezenmeier & E Thiel Authors * W Knauf View author publications You can also search for this author inPubMed Google Scholar * T Fietz View author publications You can also search for
this author inPubMed Google Scholar * H Schrezenmeier View author publications You can also search for this author inPubMed Google Scholar * E Thiel View author publications You can also
search for this author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Knauf, W., Fietz, T., Schrezenmeier, H. _et al._ CD34
selected alloPBSCT and adoptive immunotherapy. _Bone Marrow Transplant_ 25 (Suppl 2), S2–S5 (2000). https://doi.org/10.1038/sj.bmt.1702342 Download citation * Published: 01 May 2000 * Issue
Date: 01 May 2000 * DOI: https://doi.org/10.1038/sj.bmt.1702342 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a
shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative KEYWORDS * CD34+ selection * delayed
add-back of T cells * aGVHD