Moderated by:- Presented by:-
Dr. Maitrayee Roy Suchit Kumar
(Asst. Prof. ) Msc(mlt) 1st year
Department of pathology (MMISR)
M.M. Deemed to be university
 Bone Marrow is the soft spongy tissue that fills the
cores of larger bones.
 It serves an active function in the body by producing
all three types of blood cells, as well as lymphocytes,
which support the immune system.
 There are two types of bone marrow :-
1.Red bone marrow-
That is responsible for producing RBC’s ,
WBC’s and platelets.
2. Yellow bone marrow-
It consisting mainly of fat cells (adipocyte).
The bone marrow is removed from the back of
both hip bones.
 Stem cell can be collected from the
peripheral blood , bone marrow ,
umbilical cord blood.
 The donor is given a general anesthetic and
500-1200 ml marrow is harvested from pelvis.
 Fetal blood is a rich source of stem cells which
may be collected from cord blood.
 Because of the relatively small numbers of stem
cells collected from a single cord , they are
most useful for children who do not have a
fully matching sibling or unrelated donor
 Less stringent HLA matching is needed.
 A bone marrow transplant is a procedure to replace
damaged or destroyed bone marrow with healthy bone
marrow stem cells. Bone marrow is the soft, fatty tissue
inside your bones.
 The bone marrow produces blood cells. Stem cells are
immature cells in the bone marrow that give rise to all
of your different blood cells.
 It involves eliminating a patient’s hemopoietic
and immune system by chemotherapy and
replacing it with stem cells either from another
individual or with a previously harvested
portion of the patient’s own stem cells.
 The term bone marrow transplantation(BMT) ,
in which stem cells are collected from bone
marrow.
 Therearetwo main types ofbone marrow transplantation :
 Autologous bone marrow transplant:
Stem cells are removed from your body before you
receive chemotherapy and stored in a freezer. After
chemotherapy is done, your stem cells are put back in
your body to add to your normal blood cells. This is called
a «rescue» transplant
 Allogeneic bone marrow transplant:
Stem cells are removed from another person, called a
donor. Most times, the donor must at least partly match
you genetically, a brother or sister is most likely to be a
good match.
 A bone marrow transplant is a medical
procedure performed to replace bone
marrow that has been damaged or destroyed
by disease, infection, or chemotherapy.
 This procedure involves transplanting blood
stem cells, which travel to the bone marrow
where they produce new blood cells and
promote growth of new marrow.
1. Allogenic
transplants about
73%, Leukemia
28% for CML,
24% for AML:
20% for ALL and
1% for other
malignancies or
premalignant
disorders.
2. Autologous BMT : is
used only for malignancies,
NHL 25%;
Breast cancer,24%;
Hodgkin's disease 17%;
AML,11%;
Multiple myeloma, 4%;
ALL, 3%;
Neuroblastome 3%;
other Cancers, 13%.
 1. Fully matched sibling: Matching is
performed by serological typing of class I and
Class II MHC, as well as, bidirectionally
negative mixed lymphocyte culture.
 2.Other family donors: Including parents or
other sibling non- identical in one A or one B
class I MHC locus. For such cases typing of
class II MHC has to be performed both
serologically and at the DNA level.
 Prior to transplant, dental, ENT and
gynecological examinations are done for all
patients to exclude septic foci. Liver and
kidney function tests, respiratory function
tests, ECG, Echocardiography, chest X-ray and
abdominal sonography are performed to
exclude any organ function impairment.
 Serological tests for toxoplasmosis and the
following viruses: HBV, CMV, HIV, HCV,
EBV, HSV, and HZV are also performed.
Patients with recent infections are excluded.
 The major histocompatibility complex (MHC) is
a set of cell surface proteins essential for
the acquired immune system to recognize
foreign molecules in vertebrates, which in turn
determines histocompatibility.
 The MHC determines compatibility of donors
for organ transplant.
 The MHC molecules are classified in to three
classes namely :-
1. MHC class I
2. MHC class II
3. MHC class III
 MHC class I :-
In this molecule are a group of major histocompactibility
antigen. They are present on the surface of all
nucleated cells except nervous tissue and platelets. It
present antigen(HLA-A,-B,-C) to CD8+ T cells.
 MHC class II:-Class II molecule are present on the
surface of antigen presenting(HLA-DR, HLA-DQ, HLA-
DP) to CD4+ T cells.
 MHC class III :-The molecules include complements like
C2 and C4 and Bf (factor B).
 The natural role of HLA molecules is in
directing T- lymphocyte responses and the
greater the HLA mismatch the more severe is
the immune response b/w transplanted cells.
HLA typing is critical in donor selection for
allogeneic SCT.
 HLA typing may be carried out by serological
or molecular techniques. Serological testing
involves the use of antibodies that are specific
for individual HLA alleles or small families
alleles.
 This is caused by donor derived immune cells ,
particularly T – lymphocytes, reacting against
recipient tissues.
 In this , Lymphocytes from the donor graft
attack the cells of the host.
 GVHD can usually be treated with steroids or
other immunosuppressive agents.
These are two types :-
1. Acute GVHD :- In this , usually occurring in the
first 100 days, the skin , gastrointestinal tract
or liver are affected.
The skin rash typically affects the face ,
palms, soles and ears but may in several
cases affect the whole body.
2. Chronic GVHD :-which usually occurs after 100
days and may evolve from GVHD infections.
Malabsorption and pulmonary abnormalities
are frequent.
 Aplastic anemia, which is a disorder in which the
marrow stops making new blood cells
 cancers that affect the marrow, such as leukemia,
lymphoma, and multiple myeloma
 Damaged bone marrow due to chemotherapy
 Congenital neutropenia, which is an inherited disorder
that causes recurring infections
 Sickle cell anemia, which is an inherited blood disorder
that causes misshapen red blood cells
 Thalassemia, which is an inherited blood disorder
where the body makes an abnormal form of
hemoglobin, an integral part of red blood cells
Bone marrow transplantation

Bone marrow transplantation

  • 1.
    Moderated by:- Presentedby:- Dr. Maitrayee Roy Suchit Kumar (Asst. Prof. ) Msc(mlt) 1st year Department of pathology (MMISR) M.M. Deemed to be university
  • 2.
     Bone Marrowis the soft spongy tissue that fills the cores of larger bones.  It serves an active function in the body by producing all three types of blood cells, as well as lymphocytes, which support the immune system.
  • 3.
     There aretwo types of bone marrow :- 1.Red bone marrow- That is responsible for producing RBC’s , WBC’s and platelets. 2. Yellow bone marrow- It consisting mainly of fat cells (adipocyte).
  • 4.
    The bone marrowis removed from the back of both hip bones.
  • 6.
     Stem cellcan be collected from the peripheral blood , bone marrow , umbilical cord blood.
  • 7.
     The donoris given a general anesthetic and 500-1200 ml marrow is harvested from pelvis.
  • 8.
     Fetal bloodis a rich source of stem cells which may be collected from cord blood.  Because of the relatively small numbers of stem cells collected from a single cord , they are most useful for children who do not have a fully matching sibling or unrelated donor  Less stringent HLA matching is needed.
  • 9.
     A bonemarrow transplant is a procedure to replace damaged or destroyed bone marrow with healthy bone marrow stem cells. Bone marrow is the soft, fatty tissue inside your bones.  The bone marrow produces blood cells. Stem cells are immature cells in the bone marrow that give rise to all of your different blood cells.
  • 10.
     It involveseliminating a patient’s hemopoietic and immune system by chemotherapy and replacing it with stem cells either from another individual or with a previously harvested portion of the patient’s own stem cells.  The term bone marrow transplantation(BMT) , in which stem cells are collected from bone marrow.
  • 11.
     Therearetwo maintypes ofbone marrow transplantation :  Autologous bone marrow transplant: Stem cells are removed from your body before you receive chemotherapy and stored in a freezer. After chemotherapy is done, your stem cells are put back in your body to add to your normal blood cells. This is called a «rescue» transplant  Allogeneic bone marrow transplant: Stem cells are removed from another person, called a donor. Most times, the donor must at least partly match you genetically, a brother or sister is most likely to be a good match.
  • 13.
     A bonemarrow transplant is a medical procedure performed to replace bone marrow that has been damaged or destroyed by disease, infection, or chemotherapy.  This procedure involves transplanting blood stem cells, which travel to the bone marrow where they produce new blood cells and promote growth of new marrow.
  • 14.
    1. Allogenic transplants about 73%,Leukemia 28% for CML, 24% for AML: 20% for ALL and 1% for other malignancies or premalignant disorders. 2. Autologous BMT : is used only for malignancies, NHL 25%; Breast cancer,24%; Hodgkin's disease 17%; AML,11%; Multiple myeloma, 4%; ALL, 3%; Neuroblastome 3%; other Cancers, 13%.
  • 15.
     1. Fullymatched sibling: Matching is performed by serological typing of class I and Class II MHC, as well as, bidirectionally negative mixed lymphocyte culture.  2.Other family donors: Including parents or other sibling non- identical in one A or one B class I MHC locus. For such cases typing of class II MHC has to be performed both serologically and at the DNA level.
  • 16.
     Prior totransplant, dental, ENT and gynecological examinations are done for all patients to exclude septic foci. Liver and kidney function tests, respiratory function tests, ECG, Echocardiography, chest X-ray and abdominal sonography are performed to exclude any organ function impairment.  Serological tests for toxoplasmosis and the following viruses: HBV, CMV, HIV, HCV, EBV, HSV, and HZV are also performed. Patients with recent infections are excluded.
  • 17.
     The majorhistocompatibility complex (MHC) is a set of cell surface proteins essential for the acquired immune system to recognize foreign molecules in vertebrates, which in turn determines histocompatibility.  The MHC determines compatibility of donors for organ transplant.
  • 18.
     The MHCmolecules are classified in to three classes namely :- 1. MHC class I 2. MHC class II 3. MHC class III
  • 19.
     MHC classI :- In this molecule are a group of major histocompactibility antigen. They are present on the surface of all nucleated cells except nervous tissue and platelets. It present antigen(HLA-A,-B,-C) to CD8+ T cells.  MHC class II:-Class II molecule are present on the surface of antigen presenting(HLA-DR, HLA-DQ, HLA- DP) to CD4+ T cells.  MHC class III :-The molecules include complements like C2 and C4 and Bf (factor B).
  • 20.
     The naturalrole of HLA molecules is in directing T- lymphocyte responses and the greater the HLA mismatch the more severe is the immune response b/w transplanted cells. HLA typing is critical in donor selection for allogeneic SCT.  HLA typing may be carried out by serological or molecular techniques. Serological testing involves the use of antibodies that are specific for individual HLA alleles or small families alleles.
  • 21.
     This iscaused by donor derived immune cells , particularly T – lymphocytes, reacting against recipient tissues.  In this , Lymphocytes from the donor graft attack the cells of the host.  GVHD can usually be treated with steroids or other immunosuppressive agents.
  • 22.
    These are twotypes :- 1. Acute GVHD :- In this , usually occurring in the first 100 days, the skin , gastrointestinal tract or liver are affected. The skin rash typically affects the face , palms, soles and ears but may in several cases affect the whole body. 2. Chronic GVHD :-which usually occurs after 100 days and may evolve from GVHD infections. Malabsorption and pulmonary abnormalities are frequent.
  • 23.
     Aplastic anemia,which is a disorder in which the marrow stops making new blood cells  cancers that affect the marrow, such as leukemia, lymphoma, and multiple myeloma  Damaged bone marrow due to chemotherapy  Congenital neutropenia, which is an inherited disorder that causes recurring infections  Sickle cell anemia, which is an inherited blood disorder that causes misshapen red blood cells  Thalassemia, which is an inherited blood disorder where the body makes an abnormal form of hemoglobin, an integral part of red blood cells