OP37 Direct intra-bone injection of unrelated cord blood cells overcomes the problem of delayed engraftment or failure to engraft and improves the feasibility of hematopoietic transplant in adult patients

2007 ◽  
Vol 31 ◽  
pp. S49-S50
Author(s):  
A.M. Raiola ◽  
M. Podestà ◽  
A. Ibatici ◽  
F. Gualandi ◽  
N. Sessarego ◽  
...  
Blood ◽  
2006 ◽  
Vol 108 (11) ◽  
pp. 3190-3190 ◽  
Author(s):  
Adalberto Ibatici ◽  
Anna Maria Raiola ◽  
Marina Podesta ◽  
Sarah Pozzi ◽  
Silvia Lucchetti ◽  
...  

Abstract The major limit of cord blood (CB) transplant in adult patients is represented by the delayed engraftment. Newer approaches have been suggested including double cord blood transplant and infusion of CD34+ selected cells from a relative to achieve a transient engraftment until CB cells generate mature blood cells. Our initial pre-clinical studies showed that intra-bone injection of hematopoietic cells in the mouse was associated with an engraftment about 10 times more efficient with respect to the usual intravenous injection. Moreover, we had already demonstrated that the defect of cord blood cells in term of delayed engraftment was not related to the lower number of hematopoietic cells infused since the capacity to reconstitute the host stem cell reservoir was higher than adult bone marrow. Therefore, we set-up a pilot study to evaluate whether this type of transplant could shorten the time of engraftment. Five patients [4 male (M) and 1 female (F)] have been enrolled in this study. Clinical characteristics at transplant were: three patients had acute myeloid leukaemia: 2 refractory-relapsing and one in 1st CR (age 37 M, 50 M, 60 M) and 2 acute lymphoblastic leukaemia: one in 1st CR and one in 2nd CR (age 42 F, 18 M). Cord Blood grafts were matched as follows: 3/6 in one patients, 4/6 in three patients, and 5/6 in one patient for HLA-A, B, DRB1 (serology for HLA class I and allelic for class II). Patients were prepared with standard conditioning including TBI. Anti-Thymocyte-Globulin 3.75mg/kg was given on day −3,−2. GVHD Prophylaxis was cyclosporine from day -7 (therapeutic range 200–400 ng /ml) plus mycophenolate-mofetil 15mg/kg b.i.d. from day +1 to +28. The number of cord blood cells infused was 2.4, 1.6, 2.4, 3.0, 2.7 x 10^7/kg b.w. Cells were infused under very short general anaesthesia (propofol) of 5–10 minutes in the posterior iliac crest with a standard bone marrow aspiration needle (gauge n. 14). Before infusion, CB cells were washed to eliminate DMSO. Sustained engraftment of PMN (more than 3 consecutive days > 500 PMN x10^9/l) was recorded at day: + 20, 25, 18, 20, 23. Platelets sustained engraftment (more than 3 consecutive days > 20.000 Platelets x10^9/l) was recorded at day: +32, 42, 25, 29, 31.Acute GVHD was absent in these five patients. This is a pilot study with very short follow-up (2 to 5 months). Thus, no conclusive answer can be drawn on the impact of this technique on the final outcome of these patients. However, the time to PMN and Platelets engraftment is much shorter with respect to the available data obtained with intra-venous (IV) injection of the same amount of cells. Seeding efficiency experiments have shown that less than 10% of the injected cells via IV actually seed in the active hematopoietic sites. Cord blood cells, injected directly into the bone marrow, may undergo a better homing without loss, proliferate and finally colonise the rest of the bone marrow; thus, improving considerably the seeding efficiency. Alternatively, CB cells may undergo faster maturation if injected intra-bone marrow and, at the same time, colonise more efficiently the rest of active hematopoietic sites. If confirmed in larger studies, this approach may render cord blood cells transplant suitable for a greater number of adult patients who so far were excluded from this therapeutic option. This work was supported by AIRC, CARIGE; Compagnia di San Paolo.


2007 ◽  
Vol 13 (11) ◽  
pp. 1397
Author(s):  
A. Ibatici ◽  
A.M. Raiola ◽  
F. Gualandi ◽  
N. Sessarego ◽  
A. Parodi ◽  
...  

2008 ◽  
Vol 9 (9) ◽  
pp. 831-839 ◽  
Author(s):  
Francesco Frassoni ◽  
Francesca Gualandi ◽  
Marina Podestà ◽  
Anna Maria Raiola ◽  
Adalberto Ibatici ◽  
...  

1998 ◽  
Vol 22 (2) ◽  
pp. 193-196 ◽  
Author(s):  
S Weinreb ◽  
JC Delgado ◽  
OP Clavijo ◽  
EJ Yunis ◽  
L Bayer-Zwirello ◽  
...  

Hematology ◽  
2004 ◽  
Vol 2004 (1) ◽  
pp. 354-371 ◽  
Author(s):  
Nelson J. Chao ◽  
Stephen G. Emerson ◽  
Kenneth I. Weinberg

Abstract Allogeneic stem cell transplantation is an accepted treatment modality for selected malignant and non-malignant diseases. However, the ability to identify suitably matched related or unrelated donors can be difficult in some patients. Alternative sources of stem cells such as cord blood provide a readily available graft for such patients. Data accumulated over the past several years have demonstrated that the use of cord blood is an accepted source of stem cells for pediatric patients. Since the cell numbers of hematopoietic progenitors in cord blood is limited and the collection can occur only in a single occasion, its use in adult patients can be more problematic. Here, new developments in the use of cord blood for adults and studies aimed at expansion of cord blood cells and immune reconstitution are described. In Section I, Dr. Nelson Chao describes the early data in cord blood transplantation in adult patients. The patient outcomes are reviewed and analyzed for various factors such as cell dose, HLA typing, and patient selection that could have contributed to the final outcome of these adult patients. Myeloablative as well as nonmyeloablative approaches are presented. Discussion of the various benefits and risks are presented. More recent data from multiple single institutions as well as larger registry data comparisons are also provided. Analyses of these studies suggest methods to improve on the outcome. These newer data should lead to a logical progression in the use of cord blood cells in adult patients. In Section II, Dr. Stephen Emerson describes the historical efforts associated with expansion of hematopoietic stem cells, specifically with cord blood cells. These efforts to expand cord blood cells continue with novel methods. Moreover, a better understanding of stem cell biology and signaling is critical if we are to be able to effectively expand these cells for clinical use. An alternative, more direct, approach to expanding stem cells could be achieved by specific genetic pathways known or believed to support primitive HSC proliferation such as Notch-1 receptor activation, Wnt/LEF-1 pathway induction, telomerase or the Homeobox (Hox) gene products. The clinical experience with the use of expanded cord blood cells is also discussed. In Section III, Dr. Kenneth Weinberg describes immune reconstitution or lack thereof following cord blood transplantation. One of the hallmarks of successful hematopoietic stem cell transplantation is the ability to fully reconstitute the immune system of the recipient. Thus, the relationship between stem cell source and the development of T lymphocyte functions required for protection of the recipient from infection will be described, and cord blood recipients will be compared with those receiving other sources of stem cells. T cell development is described in detail, tracking from prethymic to postthymic lymphocytes with specific attention to umbilical cord blood as the source of stem cells. Moreover, a discussion of the placenta as a special microenvironment for umbilical cord blood is presented. Strategies to overcome the immunological defects are presented to improve the outcome of these recipients.


Sign in / Sign up

Export Citation Format

Share Document