Book contents
- Frontmatter
- Contents
- List of contributors
- Preface
- Part I Pathophysiology of acquired aplastic anemia
- Part II Epidemiology and clinical features of acquired aplastic anemia
- Part III Treatment of acquired aplastic anemia
- 9 Supportive treatment of patients with severe aplastic anemia
- 10 Immunosuppressive treatment of aplastic anemia
- 11 Role of cytokines in the treatment of aplastic anemia
- 12 HLA-identical sibling bone marrow transplantation to treat severe aplastic anemia
- 13 Alternative donor bone marrow transplantation for severe acquired aplastic anemia
- 14 Treatment of children with acquired aplastic anemia
- 15 Long-term follow-up of patients with aplastic anemia: clonal malignant and nonmalignant complications
- 16 Guidelines for treating aplastic anemia
- Part IV Fanconi's anemia
- Index
11 - Role of cytokines in the treatment of aplastic anemia
from Part III - Treatment of acquired aplastic anemia
Published online by Cambridge University Press: 18 August 2009
- Frontmatter
- Contents
- List of contributors
- Preface
- Part I Pathophysiology of acquired aplastic anemia
- Part II Epidemiology and clinical features of acquired aplastic anemia
- Part III Treatment of acquired aplastic anemia
- 9 Supportive treatment of patients with severe aplastic anemia
- 10 Immunosuppressive treatment of aplastic anemia
- 11 Role of cytokines in the treatment of aplastic anemia
- 12 HLA-identical sibling bone marrow transplantation to treat severe aplastic anemia
- 13 Alternative donor bone marrow transplantation for severe acquired aplastic anemia
- 14 Treatment of children with acquired aplastic anemia
- 15 Long-term follow-up of patients with aplastic anemia: clonal malignant and nonmalignant complications
- 16 Guidelines for treating aplastic anemia
- Part IV Fanconi's anemia
- Index
Summary
The rationale and potential aims of growth factor treatment in aplastic anemia
The standard treatment of aplastic anemia is allogeneic stem-cell transplantation or immunosuppressive treatment. These approaches are discussed in more detail in Chapters 10, 12 and 13 of this volume. This chapter concentrates on the use of hemopoietic growth factors in aplastic anemia. Essentially there are four possible indications for the use of growth factors in aplastic anemia:
Growth factors could be used therapeutically with the aim of inducing remission of the disease.
Growth factors could be used as adjuvant treatment for patients receiving concomitant immunosuppressive treatment with the aim of improving the rate and quality of remissions after immunosuppression.
Growth factors could be used as supportive care in order to reduce the risk of infection and bleeding associated with cytopenia.
Growth factors could be used to collect peripheral blood stem cells for allogeneic (and possibly even autologous) stem-cell transplantation.
Hemopoietic growth factors have been used in all four settings. Growth factors exert several possible effects that provide the rationale for their use in the treatment of aplastic anemia:
1. a. Growth factors stimulate the proliferation and differentiation of the residual primitive hemopoietic progenitor cells in aplastic anemia (Bacigalupo et al., 1991, 1993a; Bagnara et al., 1992; Gibson et al., 1994; Scopes et al., 1995, 1996; Wodnar Filipowicz et al., 1992, 1997).
b. Apoptotic activity in aplastic anemia bone marrow progenitor cells is accelerated (Maciejewski et al., 1995a,b; Philpott et al., 1995). Growth factors can exert antiapoptotic activity (Adachi et al., 1993; Philpott et al., 1997) and may therefore suppress the increased apoptotic activity in the bone marrow of those with aplastic anemia.
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- Aplastic AnemiaPathophysiology and Treatment, pp. 197 - 229Publisher: Cambridge University PressPrint publication year: 1999