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Transplantation of HLA‐mismatched CD34 + selected cells in patients with advanced malignancies: severe immunodeficiency and related complications
Author(s) -
Bacigalupo A.,
Mordini N.,
Pitto A.,
Piaggio G.,
Podestà M.,
Benvenuto F.,
Van Lint M. T.,
Valbonesi M.,
Lercari G.,
Carlier P.,
Lamparelli T.,
Gualandi F.,
Occhini D.,
Bregante S.,
Figari O.,
Soracco M.,
Vassallo F.,
De Stefano G.
Publication year - 1997
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1046/j.1365-2141.1997.2773094.x
Subject(s) - medicine , thiotepa , gastroenterology , total body irradiation , transplantation , immunology , cd34 , cyclophosphamide , stem cell , chemotherapy , biology , genetics
This trial was designed to test the use of CD34 + selected haemopoietic stem cells (HSC) in HLA‐mismatched donor–recipient pairs, following intensive conditioning with thiotepa, antilymphocyte globulin (ALG), cyclophosphamide and single‐dose total‐body irradiation (sTBI). 10 patients aged 16–50 with advanced malignancies and a two‐ or three‐antigen mismatched family donor entered this study. Donor marrow and G‐CSF primed peripheral blood cells were processed separately on CD34 columns (Ceprate). The median number of infused CD34 + cells were 5.66 × 10 6 /kg, with 0.55 × 10 6 /kg CD3 + cells. Nine patients received cyclosporin for graft‐versus‐host disease (GvHD) prophylaxis. Median neutrophil counts on day 21 were 2 × 10 9 /l with a median platelet count of 60 × 10 9 /l, but CD4 counts remained extremely depressed throughout the study. Acute GvHD was scored as grade 0–I in two patients, as grade II in seven, and grade III in one. Eight patients died at a median interval of 72 d from HSCT (range 20–144) due to cytomegalovirus (CMV) associated interstitial pneumonitis (IP) ( n = 5), renal failure ( n = 1), GvHD ( n = 1) and Aspergillus meningitis ( n = 1). Two patients are alive 365–495 d post transplant, one in remission and one in relapse. This study suggests that large numbers of positively selected mismatched HSC can rapidly engraft after intensive conditioning regimen: however, profound post‐transplant immunodeficiency leads to a high risk of lethal infectious complications.