2. A. HOST VS. GRAFT RXN
B. GRAFTT VS. HOST RXN
C. TYPES OF GRAFT RXN
3. • WILL OCCUR WHEN VIABLE
RECIPIENT’S T-CELL PROLIFERATE,
ARE NOT RECOGNIZED BY THE
DONOR’S T-CELL AS FOREIGN, BUT
RECOGNIZE AND REJECT THE GRAFT
AS FOREIGN
4. DEFINITION
• CAN OCCUR WHEN VIABLE DONOR’S
T-CELL PROLIFERATE, ARE NOT
RECOGNIZED BY THE RECIPIENT’S
IMMUNE SYSTEM AS FOREIGN, BUT
RECOGNIZE AND REJECT THE HOST
AS FOREIGN.
– RESULTING TRANSFUSION-ASSTD
GRAFT-VS-HOST DISEASE
5. • COMMON CASES
– STEM CELL TRANSPLANT
– LUNG AND LIVER
I. ACUTE GVHD
– Occurs during the first 100 days post infusion
and targets the skin, GIT, & liver.
– In mismatched allogeneic stem cell
transplantation, the targets of GVHD are the
mismatched HLA proteins
– while in matched stem cell
transplantation, minor histocompatibility
antigens are targeted.
6. • The incidence and severity of GVHD is
related to the match status of the donor
and recipient as well as other factors.
• The infused T cells can mediate GVHD
in several ways:
1. massive release of cytokines due to largescale activation of the donor cells by MHC
mismatched proteins
2. by infiltration and destruction of tissue.
7.
8. Cases at risk of TA-GVHD
• Congenital cellular
immunodeficiency
• Hematopoietic progenitor cell
transplantation
• Hodgkin lymphoma
• Granulocytes transfusion
• Intrauterine transfusions
(IUT)
• Transfusion to neonates who
have received IUT
• Transfusions from biological
relatives
• Chemotherapy w/ purine
analogs
•
•
•
•
•
•
•
Cases does not inc. risk
TA-GVHD
HIV infection
Hemophilia
Small-volume transfusions
of term infants who did not
received IUT
Elderly Px
Typical dose
immunosuppressive
therapy
Pregnancy
RC membrane, metabolic
or Hb disorders
9. • Beyond 100 days post-transplant
• This condition resembles autoimmune
disease, with fibrosis affecting the skin, eyes,
mouth, and other mucosal surfaces.
10.
11. 1. Immunosuppressive therapy in the
early post-transplant period
2. removal of T lymphocytes from the
graft
– T-cell reduction is very effective in lowering
the incidence of GVHD, but it can also
reduce the graft-versus-leukemia (GVL)
effect of the infused cells and increase the
incidence of graft failure
12. 1. AUTOGRAFT
Is the transfer of tissue from one area of the body to
another of the same individual
2. SYNGENEIC GRAFT
Is the transfer of cells or tissues between identical
twins
3. ALLOGRAFT
Is the transfer of cells or tissue between two
individuals of the same specie
4. XENOGRAFT
Is the transfer of tissue between two individuals of a
different species
13. 1. Hyperacute rejection occurs within minutes to
hours after the vascular supply to the transplanted
organ is established.
– This type of rejection is mediated by preformed
antibody that reacts with donor vascular endothelium.
ABO, HLA,and certain endothelial antigens may elicit
hyperacute rejection. Binding of preformed antibodies
to the alloantigens activates the complement cascade
and clotting mechanisms and leads to thrombus
formation. The result is ischemia and necrosis of the
transplanted tissue.
14. • Days to weeks after transplant, individuals
may develop (2.)acute rejection. This is a
cellular-type rejection but may involve
antibody as well. Acute rejection is
characterized
by
parenchymal
and
vascular injury. Interstitial cellular infiltrates
contain a predominance of CD8-positive T
cells as well as CD4 T cells and
macrophages.
15. 3. Chronic rejection results from a process
of graft arteriosclerosis characterized by
progressive fibrosis and scarring with
narrowing of the vessel lumen due to
proliferation of smooth muscle cells.13
Several predisposing factors impact the
development of chronic rejection, including
prolonged cold ischemia, reperfusion, acute
rejection episodes, and toxicity from
immunosuppressive drugs.
Hinweis der Redaktion
T-cell of the donor’s bone marrow can mediate GVHD