Not exact matches
«Finding the optimal conditions to avoid interfering with immune
cells working to eradicate cancer while preventing
graft rejection and GVHD is the holy grail of bone marrow
transplant,» says Leo Luznik, M.D., associate professor of oncology at the Johns Hopkins Kimmel Cancer Center.
A decade ago, he replicated the entire human leukemia disease process by introducing oncogenes into normal human blood
cells,
transplanting them into xenografts (special immune - deficient mice that accept human
grafts) and watching leukemia develop — a motherlode discovery that has guided leukemia research ever since.
Historically, clinicians evaluating a patient for
transplant have sought to identify donor
cells that are perfectly matched to the patient's
cell type, which is considered to be the optimal approach to help ensure successful outcomes and to minimize risk of
graft - versus - host disease (GVHD), a serious and potentially life - threatening complication that occurs when the donated immune
cells attack the patient's
cells as foreign tissue.
On the flipside, targeting this growth factor or BCL - 2 could reduce NK
cell numbers and offer potential therapies for immune disorders such as some types of autoimmune diseases, sepsis or
graft versus host disease, a side effect of bone marrow
transplants.
«Preventing
graft - versus - host disease and relapse after
transplant requires a difficult balance of eliminating the bad, overactive effector T
cells, without suppressing the good, regulatory T
cells,» said Kean, who is also an associate professor of pediatrics at the University of Washington School of Medicine and a member of the Fred Hutchinson Cancer Research Center.
«Given the serious threat of
graft - versus - host disease, new approaches to make stem
cell transplants safer for patients remain a critical unmet need,» said Dr. Leslie Kean, the trial's principal investigator and associate director of the Ben Towne Center for Childhood Cancer Research at Seattle Children's.
«Immunotherapy drug nearly eliminates severe acute
graft - versus - host disease: Drug used to treat rheumatoid arthritis improves survival after hematopoietic stem
cell transplant.»
One of the biggest challenges for medical researchers studying the effectiveness of stem
cell therapies is that
transplants or
grafts of
cells are often rejected by the hosts.
A new test may reveal which patients will respond to treatment for
graft versus host disease (GVHD), an often life - threatening complication of stem
cell transplants (SCT) used to treat leukemia and other blood disorders, according to a study led by researchers at the Icahn School of Medicine at Mount Sinai and published online today in the journal Lancet Haematology and in print in the January issue.
Wartman has a chronic form of
graft - versus - host disease (GVHD), a debilitating consequence of blood stem
cell transplants.
Now, in a study recently published in the journal PLOS ONE, a team of scientists from VCU Massey Cancer Center have shown a genetic relationship between the reactivation of hCMV and the onset of
graft - versus - host disease (GVHD), a potentially deadly condition in which the immune system attacks healthy tissue following a bone marrow or stem
cell transplant.
To eliminate the problem for good, Faustman borrowed an idea from the
transplant specialists, who have found that liver or spleen
cells can «reeducate» a
graft recipient's immune system to treat the
graft as native tissue.
Given to the patient shortly before the
transplant, the infusion of antibodies theoretically reduces the host's residual T
cells, minimizing the risk of
graft rejection while eliminating T
cells from the donor to thwart GVHD.
The research team tested the hypothesis by
transplanting cells onto the surface of mouse bone
grafts and studying the
cell behavior both in vivo — inside the animal — and in vitro — outside the body.
In some cases, the
transplanted marrow launches an immune attack against the host's
cells, a potentially lethal condition called
graft - versus - host disease.
In patients with GVHD, newly
transplanted T
cells from the bone marrow
graft attack the
transplant recipient's body.
While both eye fields and EFTF - expressing pluripotent
cells generated epidermis, forebrain, and olfactory tissue when
grafted to the anterior neural plate,
transplanted eye fields also formed muscle and head mesenchyme (Figure 4 and unpublished data).
Potentially everyone can benefit from gene modified T
cells and there's no danger of
graft versus host disease because it's not a
transplant from another person.
Sorting stem
cells before
transplant helps lower the risk of
graft - vs.
The only documented long - term complete remissions reported in multiple myeloma patients have occurred with allogeneic bone marrow transplantation, where a donor's blood stem
cells (
graft) are
transplanted into the patient (host) with multiple myeloma.
For the other adult patients that might still benefit from a cord blood donor, either two cord blood units are combined for a single
transplant, or more recently, there are some exciting new
graft engineering technologies that are emerging to expand stem or progenitor
cells in the laboratory before infusion or modify the
cells in some way to make them more potent at the time of
transplant.
But for blood cancer patients who receive donor hematopoietic stem
cell transplants as part of their treatment,
graft - versus - host disease (GVHD) often hampers their recovery.
Sorting stem
cells before
transplant helps lower risk of
graft - vs.
Indeed, postmortems of some of the people who had previously received fetal
cell transplants found evidence of the disease in some of the
cells in the
graft as though the protein involved in Parkinson's had caused disease in the
transplant.
Procedures include purging of cancerous
cells and purifying donor stem
cells to minimize
graft - versus - host disease (a serious side effect related to the use of donor
cells for
transplant).
Transplanted organs, tissues and
cells are targets of the host immune response, that, in the absence of adequate immunesuppression, lead to
graft loss.
Chloroquine Prevention Of Murine MHC Disparate Acute
Graft - Versus - Host Disease Correlates With Inhibition Of Spleenic Response To CpG Oligodeoxynucleotides And Alterations In T
Cell Cytokine Production, Biol Blood Marrow
Transplant 8 (12): 648 - 55, 2002.
His research interest is
graft - versus - host disease (GVHD), an immune complication after a donor stem
cell transplant.
Interestingly, when we looked at the splenocytes in these mice and compared them to controls, we were not able to detect a significant difference in the numbers of Tregs, suggesting that in the
transplant model, Tregs may be within the
graft - infiltrating population where they could regulate infiltrating host T
cells.
If these results are confirmed and one or more of these FLT3 - targeted drugs become approved by the FDA, testing for the FLT3 biomarker may eliminate the need for thousands of patients to undergo stem
cell transplantation (each allogeneic
transplant costs hundreds of thousands of dollars and place recipients at grave risk of infection and other complications such as
Graft vs. Host disease).
His research interest is
graft - versus - host disease, an immune complication after a donor stem
cell transplant.