blood bankAntibodies are passed on/the body acquired antibodies through a naturally occurring process.
· Blood typing
· Cross-matching
· Antibody screening
Pre-Transfusion Testing
1492
1st time a blood transfusion was recorded in history – Pope Innocent VII
William Harvey
In 1492, who identified that that blood flowed through the blood vessels in one direction.
F
3 young men
· In 1492, blood was taken from 5 young men and given to the stricken Pope Innocent VII in the hope of curing him. It is the first time a blood transfusion was recorded. (t/f)
1818
1st successful man to man blood transfusion was performed by British obstetrician James Blundell. He successfully transfused human blood to a px who had hemorrhage during childbirth
James Blundell
In 1818, 1st successful man to man blood transfusion was performed by British obstetrician - . He successfully transfused human blood to a px who had hemorrhage during childbirth
1869
Braxton Hicks recommended the use of sodium phosphate as an anticoagulant.
Braxton Hicks
In 1869, who recommended the use of sodium phosphate as an anticoagulant.
1901
Karl Landsteiner discovered the ABO blood groups.
Karl Landsteiner
In 1901, who discovered the ABO blood groups.
1901
Edward E. Lindeman introduced vein to vein transfusion of blood using multiple syringes & a special cannula for puncturing the vein through the skin. (time-consuming, complicated procedure that requires many skilled assistants)
Edward E. Lindeman
In 1901, who introduced vein to vein transfusion of blood using multiple syringes & a special cannula for puncturing the vein through the skin. (time-consuming, complicated procedure that requires many skilled assistants)
1901
Unger designed his syringe-valve apparatus that transfusions from donor to patient by unassisted physician became practical.
Unger
In 1901, who designed his syringe-valve apparatus that transfusions from donor to patient by unassisted physician became practical.
1914
Hustin reported the use of sodium citrate as an anticoagulant solution for transfusions.
Hustin
In 1914, who reported the use of sodium citrate as an anticoagulant solution for transfusions.
1915
Lewisohn determined the minimum amount of citrate needed for anticoagulation & demonstrated its nontoxicity in small amounts.
Lewisohn
In 1915, who determined the minimum amount of citrate needed for anticoagulation & demonstrated its nontoxicity in small amounts.
Anticoagulant
preservation of blood
1916
· Glucose was evaluated
1916
Rous & Turner introduced a citrate-dextrose solution for the preservation of blood.
Rous & Turner
In 1916, who introduced a citrate-dextrose solution for the preservation of blood.
1943
Loutit & Mollison introduced the formula for the preservative acid-citrate dextrose solution (ACD)
Loutit & Mollison
in 1943, who introduced the formula for the preservative acid-citrate dextrose solution (ACD)
1957
· Gibson introduced an improved preservative solution called citrate-phosphate-dextrose (CPD)
Gibson
In 1957, who introduced an improved preservative solution called citrate-phosphate-dextrose (CPD)
35 days expiration
CPDA-1 expiration
Immunohematology
Study of blood-related antigens and antibodies as applied to blood banking and transfusion services.
Immunohematology
Involves the study of immune response to the transfusion of cellular elements.
• Packed RBCs
• Platelets
• Plasma
Whole Blood Units
Immunology
- Study of components & processes of the immune system.
Immunology
- The study of a host’s reactions when foreign substances are introduced into the body.
concentrated with liquid
Cryoprecipitate
Cryosupernate
sa ibabaw
Innate / Natural Immunity
a non-specefic defense
Innate / Natural Immunity
involves anatomic & inflammatory responses
Adaptive / Acquired Immunity
response is specific for the stimulating antigen
Adaptive / Acquired Immunity
involves cell-mediated & humoral responses
Adaptive / Acquired Immunity
Acquired by contact with a specific foreign substance
Adaptive / Acquired Immunity
Initial contact with foreign substance triggers synthesis of specialized antibody proteins resulting in reactivity to that particular foreign substance
Adaptive / Acquired Immunity
Response improves with each successive encounter with the same pathogen
Adaptive / Acquired Immunity
- Is the most specific & allows the IS to have memory of pathogens it has encountered previously.
Active Natural Immunity
The body produced antibodies because of natural exposure to antigens.
Active Natural Immunity
Identify if active or passive Natural Immunity
· Natural infection
Active Natural Immunity
Identify if active or passive Natural Immunity
· Exposure to antigens in the environment.
Passive Natural Immunity
Identify if active or passive Natural Immunity
• IgG transfer from the mother to fetus through the placenta.
Passive Natural Immunity
Identify if active or passive Natural Immunity
• Colostrum rich in IgA (what babies get from breastfeeding)
Passive Natural Immunity
Antibodies are passed on/the body acquired antibodies through a naturally occurring process.
Active Artificial Immunity
The body produced antibodies due to artificial administration/injection of antigens.
Active Artificial Immunity
Identify if active or passive Artificial Immunity
• Live organism – small pox
Active Artificial Immunity
Identify if active or passive Artificial Immunity
• Attenuated / Weakened Organism - BCG
Active Artificial Immunity
Identify if active or passive Artificial Immunity
• Dead organism - cholera & typhoid fever
Active Artificial Immunity
Identify if active or passive Artificial Immunity
• Toxoid – toxin treated with chemicals
Active Artificial Immunity
Identify if active or passive Artificial Immunity
• Modified virus – polio virus
Passive Artificial Immunity
Identify if active or passive Artificial Immunity
· Anti-rabies
Passive Artificial Immunity
Identify if active or passive Artificial Immunity
· Heap B Immunoglobulin (HBIg)
Passive Artificial Immunity
Identify if active or passive Artificial Immunity
Rhogam – given to mothers with Rh-, & babies with Rh +
Passive Artificial Immunity
Antibodies are administered/injected to the body
o Acute inflammation
o Phagocytosis
o Activation of complement system
examples of natural / innate immunity
o Humoral response
o Cell mediated
example of Adaptive / Acquired Immunity
Phagocytosis
- Engulfment/destruction of foreign substance in the bodies which is done by the lymphocyte, macrophages etc.
Dendritic cells
Macrophages
Monocytes
Neutrophils
Cells most involved in Phagocytosis
· I – initiation
· C – chemotaxis (sensing the chemicals, chemotactic)
· E – engulfment
· D – digestion
Process of Phagocytosis
Neutrophil
- Is the #1 cell to attack, due to it small size which can easily roam around.
Phagosome
- Is characterized by the presence of vacuole in the cytoplasm.
Lysosome
- Are granulated (acid hydrolase) then they are released/emptied.
Cytokines
Protein molecules secreted by immune cells that act as chemical messengers in the immune response.
Cytokines
- Function as chemical messengers in your immune system. Your immune system is a network with several parts that work together to protect your body from threats, like germs that can make you sick.
Interleukin 1 (IL-1)
- Activated T helper cells
Interleukin 1 (IL-1)
Promotes inflammatory response & fever
Interferon Alpha
Inhibits viral replication / duplication
Tumor Necrosis Factor (TNF)
Kills tumor cells
Interleukin 6 & Colony Stimulating Factors (CSF)
Promote hematopoiesis
Antigens
- Are molecules that have the capability of reacting with a complementary antibody.
Antigens
Antibody generator because they have the capability of reacting with a complementary antibody.
F
NOT ALL ANTIGENS are IMMUNOGENS
T/F
ALL ANTIGENS are IMMUNOGENS
Immunogens
Antigens that can elicit an antibody-mediated immune response.
Hapten
A small molecule that can elicit an immune response only when attached to a larger carrier molecule.
Hapten
- A small molecule which can bind with the antibody binding site, but is not immunogenic unless attached to a larger molecular backbone. (5000 Dalton = Half of 10k Dalton) cannot elicit a response because the Dalton is not enough (should be >10k Dalton)
Hapten
- Nonimmunogenic materials that create new antigenic determinants when combined with a carrier.
Hapten
- Can react with the antibody, even without being complexed to a carrier molecule.
Hapten
- When bound to carriers, contribute to the development interconnected lattice that serves as the basis for precipitation and agglutination reactions.
Lattice Formation
· antigen & antibody complex. In order to see agglutination & precipitation we need a carrier. The most carrier are latex particle, charcoal & RBC. Hapten alone cannot form a -
latex particle, charcoal & RBC
· Lattice Formation – antigen & antibody complex. In order to see agglutination & precipitation we need a carrier. The most carrier are - . Hapten alone cannot form a lattice.
Epitope
where the antigen attach
Foreignness
Route, Dosage & Timing
Adjuvants
Size
Chemical Composition & Complexity
Factors Affecting Immunogenicity
Autoantigen
Foreignness
• - – body
Alloantigen
Foreignness
• - – foreign, acquired
Heteroantigen
Foreignness
• - – same species
Heterophile antigen
Foreignness
• – different species
F
The smaller the dose the less likely is the response
Route, Dosage & Timing (t/f)
- The larger the dose the less likely is the response
• Intravenous
• Intramuscular
• Intraperitoneal
• Intradermal
• Subcutaneous
• Inhalation – is the fastest route
Route, Dosage & Timing (t/f)
- Routes:
adjuvants
Is the ingredient used in some vaccines that helps create a stronger immune response in people receiving the vaccine. In other words, - help vaccines work better. (by protecting the antigens)
10k Daltons
Size needed for Immunogenicity
Anti-D
is the most immunogenic antigen.
D
most antigenic substance
0.70 - D Antigen
there will be severe transfusion reaction
Antibody / Immunoglobulin (Ig)
- Formerly Gamma globulins
Antibody / Immunoglobulin (Ig)
- Glycoproteins that recognize a particular epitope on an antigen & facilitate clearance of the antigen.
Antibody / Immunoglobulin (Ig)
- Production stimulated by antigens