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Influence of human leucocyte antigen disparity and graft lymphocytes on allogeneic engraftment and survival after umbilical cord blood transplant in adults
Author(s) -
Van Heeckeren Willem J.,
Fanning Laura R.,
Meyerson Howard J.,
Fu Pingfu,
Lazarus Hillard M.,
Cooper Brenda W.,
Tse William W.,
KindwallKeller Tamila L.,
Jaroscak Jennifer,
Finney Marcie R.,
Fox Robert M.,
Solchaga Luis,
Forster Margaret,
Creger Richard J.,
Laughlin Mary J.
Publication year - 2007
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 - 10.1111/j.1365-2141.2007.06824.x
Subject(s) - medicine , cd34 , progenitor cell , immunology , umbilical cord , cord blood , transplantation , cd38 , haematopoiesis , stem cell , andrology , gastroenterology , biology , genetics
Summary The dose of graft‐nucleated cells and CD34 + haematopoietic progenitor cells are predictors of allogeneic engraftment and survival in umbilical cord blood (UCB) recipients. In this single institution prospective phase II trial, flow cytometric analyses of CD34 + progenitor and lymphocyte populations in unmodified single unit human leucocyte antigen (HLA)‐disparate UCB grafts infused into 31 consecutive adults (median age 41 years, range 20–64) receiving myeloablative conditioning were compared with clinical outcomes. Median infused UCB graft‐nucleated cells and CD34 + dose was 2·2 × 10 7 /kg and 1·2 × 10 5 /kg respectively. Day to absolute neutrophil count ≥0·5 × 10 9 /l with full donor chimerism averaged 27 d (range 12–41). Univariate analyses demonstrated that UCB graft‐infused cell doses of CD34 + ( P = 0·015), CD3 + ( P = 0·024) and CD34 + HLADR + CD38 + progenitors ( P = 0·043) correlated with neutrophil engraftment. This same analysis did not demonstrate a correlation between CD34 + ( P = 0·11), CD3 + ( P = 0·28) or CD34 + HLADR + CD38 + ( P = 0·108) cell dose and event‐free survival (EFS). High‐resolution matching for HLA‐class II (DRB1) resulted in improved EFS ( P = 0·02) and decreased risk for acute graft‐versus‐host disease (GVHD) ( P = 0·004). Early mortality (prior to post‐transplant day +28) occurred in three patients, while 26 patients achieved myeloid engraftment. These results suggest that UCB graft matching at DRB1 is an important risk factor for acute GVHD and survival, while higher UCB graft cell doses of CD34 + , committed CD34 + progenitors and CD3 + T cells favourably influence UCB allogeneic engraftment.