Professional Documents
Culture Documents
Transfusi Darah
Umi S Intansari
Fakultas Kedokteran UGM/
RSUP Dr. Sardjito
Beneficial and harmful immune responses
Immunological Complication of Blood Transfusion
Immune
Presentation response
Humoral Cellular
Immune
Antibodies
cells
Antigen
Components of the immune system
White blood cells
Lymphoid organ
Body tissues
effector sites for immune responses
Key molecules
Antigens: molecules that recognized by immune system
Receptors: Pattern, BCR, TCR
MHC/ HLA (Human Leucocyte Antgen)
Soluble mediator: ab, complement, cytokine, chemokine
Recognition
• Different pathogen/ antigen require different
response mechanism for detection, recognition
& destroying them
• Receptors:
Recognition
Antigen presenting cells (APCs)
Dendritic cells catch antigen in the periphery and present it in lymph nodes
Macrophages catch extracelular pathogen
B cells catch soluble antigens in the circulation and presents it in lymph nodes
Antigen Presentation
Phagocytes internalize
pathogens, degrade
them in endosomes
and present the
peptides on MHC II
Fc role
1. macrophage ingestion
Figure 9-31
1. Proliferation and
maturation: formation of
plasma cells
2. Secretion of antibodies
Repeated stimulation
with the same antigen
increases the antibody
concentration to that
antigen
Immunological memory
Ability of immune system to make second response to same ag more effective & efficiently
Application in Transfusion
Medicine
Agglutination
reaction
Blood type
Cross match
Immune-mediated Red Cell Destruction
Red cell alloimmunization
• The mechanism of red cell alloimmunization is not well
understood.
Allogeneic RBC
tranfused,degraded
Ab Blood
production circulation
Uptake by APCs,
B cells, presented
to T cell
Recognition of Alloantigens
Direct Presentation
Recognition of an intact MHC molecule displayed by donor APC in the
graft
Basically, self MHC molecule recognizes the structure of an intact
allogeneic MHC molecule
Involves both CD8+ and CD4+ T cells.
Indirect Presentation
• Hemolytic anemia
38
Hemolytic Transfusio Reaction
Acute
• Occur 24 hours of transfusion
• Intravascular:
• Most common: ABO incompatibility
• Involve Ab that strongly activate Comp
• Extravascular:
• RBC’s coated with recipient’s Ab/ Compl
• IgG-Fc/ Compl are recognized by MΦ receptors
Delayed
• 1 – 14 days after transfusion
• Ab are present in low amounts
Febrile non-hemolytic transfusion
reaction (FNHTR)
Anaphylaxis
TRALI
• Donor anti-leukocyte antibodies attack recipient’s
WBC
• WBC release inflammatory mediators increase
lung’s capillary permeability