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Table 23.1 Stem cell transplantation: potential 
donors. 
HLA-matching sibling 
Unrelated HLA-matching volunteer Allogeneic 
Umbilical cord blood 
Identical twin Syngeneic 
Self Autologous 
HLA, human leucocyte antigen. 
Table 23.2 Stem cell transplantation: 
indications. 
Allogeneic (or 
syngeneic) Autologous 
Acute lymphoblastic or 
myeloid leukaemia. 
Other malignant 
disorders of the 
marrow (e.g. chronic 
myeloid leukaemia, 
myelodysplasia, 
multiple myeloma, 
lymphoma, severe 
aplastic anaemia 
including Fanconi’s 
anaemia) 
Hodgkin lymphoma and 
non-Hodgkin 
lymphoma, multiple 
myeloma, AML, 
primary amyloidosis 
Inherited disorders: 
thalassaemia major, 
sickle cell anaemia, 
immune deficiencies, 
inborn errors of 
metabolism in the 
haemopoietic and 
mesenchymal system 
(e.g. osteopetrosis) 
Other acquired severe 
marrow diseases (e.g. 
paroxysmal nocturnal 
haemoglobinuria, red 
cell aplasia, 
myelofibrosis) 
AML, acute myeloid leukaemia.
Table 23.3 The human leucocyte antigens (HLA). 
Class I Class II 
Antigens HLA-A, -B, -C HLA-DR, -DP, -DQ 
Distribution All nucleated cells, platelets B lymphocytes 
Monocytes 
Macrophages 
Activated T cells 
Structure Large polypeptide chain (MHC coded) 
and a β2-microglobulin 
Two polypeptide chains (α and β) both 
MHC coded 
Interacts with CD8 lymphocytes CD4 lymphocytes 
MHC, major histocompatibility complex. 
Table 23.4 Complications of stem cell 
transplantation. 
Early (usually <100 
days) 
Late (usually >100 
days) 
Infections, especially 
bacterial, fungal, 
herpes simplex virus, 
CMV 
Infections, especially 
varicella-zoster, 
capsulate bacteria 
Haemorrhage Chronic pattern GVHD 
(arthritis, 
malabsorption, 
hepatitis, scleroderma, 
sicca syndrome, 
lichen planus, 
pulmonary disease, 
serous effusions) 
Acute pattern GVHD 
(skin, liver, gut) 
Chronic pulmonary 
disease 
Graft failure Autoimmune disorders 
Haemorrhagic cystitis Cataract 
Interstitial pneumonitis Infertility 
Others: veno-occlusive 
disease, 
cardiac failure 
Second malignancies 
CMV, cytomegalovirus; GVHD, graft-versus-host disease. 
Table 23.5 Acute pattern graft-versus-host disease: clinical staging (Seattle system). 
Stage Skin Liver (bilirubin, μmol/L) Gut (diarrhoea, L/day) 
I Rash <25% 20–35 0.5–1.0 
II Rash 25–50% 35–80 1.0–1.5 
III Erythroderma 80–150 1.5–2.5 
IV Bullae, desquamation >150 >2.5; severe pain, ileus

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Chapter23

  • 1. Table 23.1 Stem cell transplantation: potential donors. HLA-matching sibling Unrelated HLA-matching volunteer Allogeneic Umbilical cord blood Identical twin Syngeneic Self Autologous HLA, human leucocyte antigen. Table 23.2 Stem cell transplantation: indications. Allogeneic (or syngeneic) Autologous Acute lymphoblastic or myeloid leukaemia. Other malignant disorders of the marrow (e.g. chronic myeloid leukaemia, myelodysplasia, multiple myeloma, lymphoma, severe aplastic anaemia including Fanconi’s anaemia) Hodgkin lymphoma and non-Hodgkin lymphoma, multiple myeloma, AML, primary amyloidosis Inherited disorders: thalassaemia major, sickle cell anaemia, immune deficiencies, inborn errors of metabolism in the haemopoietic and mesenchymal system (e.g. osteopetrosis) Other acquired severe marrow diseases (e.g. paroxysmal nocturnal haemoglobinuria, red cell aplasia, myelofibrosis) AML, acute myeloid leukaemia.
  • 2. Table 23.3 The human leucocyte antigens (HLA). Class I Class II Antigens HLA-A, -B, -C HLA-DR, -DP, -DQ Distribution All nucleated cells, platelets B lymphocytes Monocytes Macrophages Activated T cells Structure Large polypeptide chain (MHC coded) and a β2-microglobulin Two polypeptide chains (α and β) both MHC coded Interacts with CD8 lymphocytes CD4 lymphocytes MHC, major histocompatibility complex. Table 23.4 Complications of stem cell transplantation. Early (usually <100 days) Late (usually >100 days) Infections, especially bacterial, fungal, herpes simplex virus, CMV Infections, especially varicella-zoster, capsulate bacteria Haemorrhage Chronic pattern GVHD (arthritis, malabsorption, hepatitis, scleroderma, sicca syndrome, lichen planus, pulmonary disease, serous effusions) Acute pattern GVHD (skin, liver, gut) Chronic pulmonary disease Graft failure Autoimmune disorders Haemorrhagic cystitis Cataract Interstitial pneumonitis Infertility Others: veno-occlusive disease, cardiac failure Second malignancies CMV, cytomegalovirus; GVHD, graft-versus-host disease. Table 23.5 Acute pattern graft-versus-host disease: clinical staging (Seattle system). Stage Skin Liver (bilirubin, μmol/L) Gut (diarrhoea, L/day) I Rash <25% 20–35 0.5–1.0 II Rash 25–50% 35–80 1.0–1.5 III Erythroderma 80–150 1.5–2.5 IV Bullae, desquamation >150 >2.5; severe pain, ileus