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Phenotype O frequency
45%
Phenotype A1 frequency
32%
Phenotype A2 frequency
8%
Phenotype A1B frequency
3.2%
Phenotype A2B frequency
0.2%
Respective sugar and enzyme for A
N-acetylgalactoseamine sugar and N-acetylgalactoseamine-transferase
Respective sugar and enzyme for B
galactose sugar and galactosyl-transferase
Respective sugar and enzyme for H
Fructose sugar and furctosyl-transferase
What genes are not present at the H locus in the Oh phenotype
A,B and H
What are the two methods to determine the actual ABO genotype or Phenotype for Oh
Anti-H lectin and family studies
What is the ABH red cell antigen expression for the Oh phenotype
no expression
What is the expected serum alloantibody activity for the Oh phenotype
strongly reacting allo-anti H ad naturally occurring in addition to anti-A, anti-B, and anti-A,B
What is the phenotype is expressed in Oh
Bombay phenotype hh
What is the immunoglobulin class of naturally occurring antibodies
IgM
What is the origin of ABO antibodies
environmental(IgM), mistransfusions, pregnancy, vaccinations(IgG)
What is the development of ABO antibodies
detectable around 3-6 months old, higher titer around 5-10yrs old, and elderly has the lowest titer
what is the predominate immunoglobulin class for ABO antibodies
Anti-A and Anti-B (IgM)
What is the in vitro serologic reactivity of ABO antibodies
room temp, IS, saline reaction, can bind complement(causing hemolysis) through agglutination
What is the clinical significance of ABO antibodies
hemolyica transfusion reactions(small amount of ABO incompatible blood will cause acute HTR) and hemolytic disease of thefts/newborn
Forward grouping
front type, reagent antisera is a known antibody, used to determine the patient's red blood cells' unknown antigen
Reverse grouping
back type, patient serum is unknown antibody and is used to determine the reagent RBCs known antigen
Type specific
transfuse a group A with a group A, and O with O, etc..
Type compatible
Transfuse a group a group AB with group A or a group B with group O
Type incompatible
never transfuse a group O with anything except group O, never give group A to B or B to A
Anti-A1 lectin
dolichos biflorus
Anti-H lectin
Ulex europaeus
Bombay phenotype(Oh)
homozygous amorphic genotype
Immune antibody
An antibody that is produced only after deliberate exposure to a foreign antigen
Precursor substance
A basic or “parent” antigenic structure on red blood cells that can be modified by enzymes to form more specific antigens
Subgroup
A variant form of a blood group antigen, often with weaker expression or slightly altered serologic characteristics
universal donor
Type o negative
universal recipient
Type AB positive
Partial D mechanism of production
Incomplete D antigen- actually missing part of antigen and may type weaker than expected but still detected without IAT
Genetic D mechanism of production
Inheritance of D genes that code for weakened expression of D antigen usually due to Ro gene, more common is AA pop
Position Effect D mechanism of production
D antigen is weakened when C is “trans”to D(usually with the r’ gene)
Clinical significance of the Weak D phenotypes in donors and blood recipients.
Can cause Immune production of an Anti-D
Rh system predominant immunoglobulin class
IgG
Rh system stimulus for production
unexpected antibodies
Rh system ability to bind complement
does not bind C’
Rh system clinical significance
Cause HTR and HDFN
Rh system characteristic serologic reactivity
immunogenicity (D>c>E>C>e)
purpose of Rh control
severs as a negative control for D testing that detects interference from unexpected antibodies coating the cells
Rh control composition
high protein reagents
Rh contorl expected results
negative(valid results)
Blood group system
groups of antigens on the red cell membrane that share related serologic properties and genetic patterns of inheritance
chromsome
gene-carrying structure
allele
a specific location on a chromosome where a gene resides and may be occupied by one or several genes
gene
a segment of DNA that codes for a particular protein; it its the basic unit for inheritance of any trait
gene locus
specific physical location of a gene or DNA sequence on a chromosome
trait
characteristic of an organism that can be observed or measured, which is influenced by genes
antithetical partner
antigens/allelic partners
linked genes
when two genes, located closely on the same chromosome, do not assort independently, they are said to be “linked”
crossing over
occurs when genes not closely linked “cross over” and exchange genetic information. Genes that are closely linked aren’t affected
amorphic
a silent gene
X-linked
inheritance pattern that only resides on the X chromosome
dosage effect
number of copies of a gene (gene dosage) directly influences the expression or intensity of a trait
gene interaction
where the effect of one gene is altered by the presence of another gene, a gene gets modified or suppressed
anamnestic response
remembered response
sensitization stage
primary stage of Ag-Ab reactions
visualization stage
secondary stage of Ag-Ab reactions
affinity
strength of a single Ag-Ab bond
avidity
combination of affinities
specificity
ability of an antibody or test to recognize and bind only to its intended antigen
cross reaction
antibody reacts not only with its intended antigen but also with a structurally similar, unintended antigen
zone of equivalence
Ag and Ab are in optional concentration, insoluble lattice structure
prozone
excess of unbound Ab
post zone
excel of Ag binding sites
Peer review Examples
AABB- Association for the Advancement of Blood and Biotherapies, CAP- College of American Pathologists
State review example
Indiana State Department of health
federal review example
FDA
phenotype
the observation of detectable traits; the outward expression of genes
genotype
an individuals genetic makeup
public antigen
high-frequency genes
private antigen
low-frequency genes
dominant
trait is seen anytime the gene is present, regardless of the zygosity of the gene
recessive
is seen only when the gene is present in a homozygous state
codominant
equal expression of two inherited genes
cis position
genes on the same chromosome (CDe/cde)
trans position
genes on homologous chromosomes (Cde/cDe)
Individual acquires his blood group genes according to Mendel’s Laws of Inheritance
Each parent contributes half of the inheritance, and individual traits are inherited independently of each other
pattern of inheritance most blood group systems follow
Codominance
direct exclusion
offspring possesses a trait that neither the mom the alleged dad possesses
Indirect exclsion
offspring does not possess a gene that should have been inherited
type of cells responsible to produce antibodies
B-cells
Primary stage
initial binding of Ag and Ab
Secondary stage
observable stage(agglutination, precipitation, C’-fix)
Tertiary stage
In vivo biologic expression of Ag-Ag rection or the immune response
primary response
large dose, long latency period(10 days-months), IgM produced and then IgG
Secondary response
Smaller dose, shorter latency period(1-2days), IgG produced and very small IgM
Immunogenicity
is the ability of an antigen to stimulate an antibody response. Because of differences in immunoglobins not all blood group antigens are equally immunogenic in vivo
main components that make up the red cell membrane.
Proteins(52%), Lipids(40%), Carbohydrates(8%)
Explain how the zeta potential effects the Ag-Ab reaction
Net charge and distance between the Ag-Ab affect the zeta potential
Explain the purpose of using enhancement media in antiglobulin tests.
Allows Ag and Ab to come closer together and reduces incubation time
Albumin enhancement media
collieded/high protein made media tat reduced ionic cloud
LISS- Low Ionic Strength Solution
reduced ionic cloud to bring cells closer together
PEG – Poly Ethylene Glycol
removes H2O and increases antibody concentration
Enzymes – Ficin, Papain, Bromelin
Cleaves some of the membrane’s glycoproteins, destroying some antigens, while exposing others
EDTA tubes
Purple pink, plasma sample
chelates Ca+ ions which prevents activation of the classical complement pathway
no complement activity in sample
Clot Tube
red top, serum sample
Component present in ‘fresh’ sample and C’ remains active for 24-28 hrs and stored at 4 °C
can be used to detect complement-dependent antibodies
Antigen known testing sources
manufacturer screening, panels, and A & B cells