Adoptive immunotherapy following allogeneic bone marrow transplantation
1Department of Haematology, Royal Postgraduate Medical School, London, United Kingdom. f.dazzi@rpms.ac.uk
Annual Review of Medicine
|March 24, 1998
Summary
Adoptive cell therapy, including virus-specific T cells and donor leukocyte infusions, offers new strategies to combat infections and leukemia relapse after bone marrow transplantation (BMT). These immunotherapies show promise in improving BMT outcomes.
Area of Science:
- Immunology
- Transplantation Medicine
- Cell Therapy
Background:
- Allogeneic bone marrow transplantation (BMT) faces challenges including post-transplant infections (Epstein-Barr virus, cytomegalovirus) and graft-versus-host disease (GVHD).
- GVHD, while a risk, is linked to a beneficial graft-versus-leukemia (GVL) effect, crucial for preventing leukemia relapse.
Purpose of the Study:
- To explore recent advances in immune recognition for overcoming BMT disadvantages.
- To highlight the role of adoptive T-cell transfer in managing post-BMT complications.
- To discuss the efficacy of donor leukocyte infusions (DLI) in GVL and leukemia remission.
Main Methods:
- Adoptive transfer of virus-specific cytotoxic T lymphocytes to restore immunity.
- Utilizing donor leukocyte infusions (DLI) to leverage the graft-versus-leukemia (GVL) effect.
- Investigating leukemia-specific antigens to refine immunotherapy.
Main Results:
- Virus-specific T-cell therapy can reconstitute immunity and treat viral diseases in BMT patients.
- Donor leukocyte infusions (DLI) demonstrate efficacy in inducing long-lasting remissions, particularly in chronic myeloid leukemia relapse post-BMT.
- GVHD is associated with a potent graft-versus-leukemia (GVL) response.
Conclusions:
- Allogeneic cell therapy, though currently basic, is a promising immunotherapy approach for BMT.
- Further research into leukemia-specific antigens will enhance cell therapy outcomes and applications.
- Adoptive immunotherapy strategies show potential to improve survival and reduce complications following allogeneic BMT.
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