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All ABOut Blood Types - Immucor, Inc. Program... · All ABOut Blood Types –Objectives •Identify...
Transcript of All ABOut Blood Types - Immucor, Inc. Program... · All ABOut Blood Types –Objectives •Identify...
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All ABOut Blood TypesJanuary 23, 2019
LeeAnn Walker, MEd, MT(ASCP)SBB
Assistant Professor, CLS Department
University of Texas Medical Branch
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All ABOut Blood Types – Objectives
• Identify the genetic mechanism for inheritance of the ABH blood group antigens, including the Bombay phenotype.
• Differentiate the transferases and biochemical structures of the ABH antigens.
• Evaluate the characteristics of and relationship between antigens and antibodies in the ABO system.
• Identify lectin reagents that show ABO blood group specificity.
• Assess the effects of disease and age on production of ABO antigens and antibodies.
• Classify the A and B antigens into subgroups, including serologic characteristics, number of antigen sites and frequency in the population.
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ABO Blood Group History
• 1900-1901 – Discovery of A and B antigens and antibodies. • Serum of certain employees agglutinated red cells of other employees.
• Defined A, B and O blood groups.
• 1902 – Discovery of AB by Landsteiner’s students• Alfred von Decastello and Adriano Sturli
• 1930 – Landsteiner and colleagues received Nobel Prize in Medicine
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Karl Landsteiner 1868-1943
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Landsteiner’s Law
• Whenever an antigen is present on the red cells, the corresponding antibody is absent in the serum.
• The ABO system is the only system where the antibodies are predictably present.
• This is the foundation of all pre-transfusion testing.
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Genetics of ABO and H Systems
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What is a Blood Group System?
Defined by a series of allelic genes and their modifiers.
Produce chemically related but serologically distinct antigens.
Based on the presence of antigens and the genetic control of those antigens.
The antibody is usually the means by which the antigen is first recognized.
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Red Cell Antigens
• Chemical structures embedded in or protruding from the membrane of RBC or other cells.
• May also be found as soluble substances in body fluids.
• Genetics determines presence or absence of antigens (genotype).
• Gene products:• Specific protein or other substance that functions as an antigen.
• Enzyme (transferase) controls production of other protein, lipoprotein or carbohydrate substances.
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What do the ABO and H blood group genes do?
Genes code for specific transferases that add sugars onto a carbohydrate precursor structure.
H gene (FUT1) – Chromosome 19 Fucosyl transferase
Adds L-fucose to terminal sugar of precursor. Precursor is complex carbohydrate (glycoprotein or glycolipid)
Forms H substance – precursor for A and/or B antigen formation.
If H gene is not present, no A or B can be formed (Bombay).
ABO Genes – Chromosome 9 First known autosomal linkage in man –
ABO and Nail Patella syndrome
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ABO Genes7 exons – large genetic complex A and B genes code for transferases that add terminal sugar onto H
antigen structure.
A gene N-acetylgalactosamyl transferase
Adds N-acetylgalactosamine (GalNAC)
B gene D-Galactosyl transferase
Adds D-galactose (GAL)
AB blood group both A and B genes & transferases are present
O gene amorphic – codes for a non-functional transferase with no action
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ABO Inheritance• Genes are inherited according to Mendelian genetics and the
Hardy-Weinberg equilibrium for a 3-allele system.
• O gene is an amorph.• No gene expression.
• Phenotype O genotype OO
• A and B genes are codominant.• Phenotype A genotype AA or AO
• Phenotype B genotype BB or BO
• Phenotype AB genotype AB
• If one parent is A and the other is B:• May have children of any ABO type.
MOM →
DAD↓ A O
B AB BO
O AO OO
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Determining ABO Genotype
• Family Studies• Example: Mother Group O; Father Group A
• One child is group A and another is group O
• Therefore Father’s genotype would be AO
• Testing for presence of transferases
• Molecular studies• Testing for the presence of the gene
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ABH Biochemistry
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RBC Membrane Structure
• Soluble A, B and H antigens in secretions (if secretor gene is present) are carried on glycoprotein (Type 1 chains).
• A and B antigens are carried on glycolipids on RBC membranes, epithelial and endothelial cells (Type 2 chains).
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secretor
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GlcNAcGal
Gal Glc CER
GlcNAc
Gal
Gal GalNAc
Type 2 Structure
Type 1 Structure
β1-4
β1-4
β1-3
β1-4
β1-3
β1-3
Type 1 versus Type 2 Chains
Glycoproteins in plasma/secretions
Gal = Galactose,
GalNAc = N-acetyl-galactosamine,
Glc = glucose,
GlcNAc = N-acetyl-glucosamine,
Fuc = Fucose, CER = Ceramide
Glycolipids on RBCs
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A gene
A transferase
A Antigen
B gene
B transferase
B Antigen
CERGlcGal
Gal GlcNAC
Fuc
GalNAC
Type 2 Chains on RBCs
Gal
Fuc
Gal GlcNAC
Gal Glc CER
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ABO Antigen Development• Develop early in fetal life.
• In newborns, the number of A and B sites is fewer than in adults.
• Due to lack of H precursor on the cells.
• Primarily straight chain H precursor.
• 2-4 years of age – antigen strength = adults• Precursor chains become branched.
• Strength of RBC agglutinability varies among races. • B antigen strongest in Blacks.
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H Antigen• Expressed on all human red cells except Bombay type.
• Group O ONLY has H antigen.
• H antigen expression from MOST to LEAST:
O > A2 > B> A2B > A1 > A1B
• Bombay individual lacks H gene.
• Inherits 2 recessive genes: hh or Oh
• No fucosyl transferase produced, so no H antigen.
• If no H antigen, neither A nor B antigens can be formed.
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ABH on other cells, in secretions and other places
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• Cells:
• lymphocytes (not detected on granulocytes), platelets
• Other cells:
• endothelium of capillaries, veins, arteries, sinusoidal cells of spleen
• secretors only: glands, goblet cells, secreting surface epithelia
• secretors and non-secretors: gastric mucosa, pancreas, liver
• Secretions (if secretor gene is present):
• seminal fluid, tears, sweat, urine, digestive juices, bile, milk, pleural fluid, peritoneal fluid, pericardial fluid, amniotic fluid, hydroceles cyst, ovarian cyst
• Absent in connective tissues (cornea transplants) and central nervous system.
• Widely distributed in nature – Plants, Bacteria
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Antibodies of the ABO Blood Group• Primarily IgM.
• Some IgG, especially in Group O.• Group O has anti-A, Anti-B and anti-A,B.
• Anti-A and anti-B are not present at birth.• No serum testing on newborns!
• Produced in response to environmental contact with substances having similar carbohydrate structure to A and/or B antigens.
• By one year of age, antibodies will be present and can start as early as 3 months.
• Titers of anti-A and anti-B will reach adult levels by 5-10 yearsof age.
• Antibody titers often decline in later age.
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Anti-H• Produced by individuals lacking H antigen (Bombay
phenotype)
• Potent, IgM + IgG antibody, binds complement.
• May be hemolytic with wide thermal range (4C-37C).
• Reacts with all other normal Group O red cells.
• Can be produced as cold agglutinin.• Most often in group A1 or A1B individuals.
• These have the LEAST H antigen: O > A2 > B > A2B > A1 > A1B
• May be in combination with anti-I.
• IgM reactive at lower temps only.
• May cause problems with antibody screening and compatibility testing.
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Testing for A, B and H• Cell (forward) typing
• Anti-A and Anti-B reagents• Must meet FDA titer requirements
• Human source• Monoclonal
• Serum (reverse) typing• A1 and B reagent red cells
• Human source• Made of pools of donor red cells• Cells are confirmed as A1 and B
• Negative for D, C and E
• H typing• Anti-H lectin (Ulex europaeus)
• a flowering plant
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Forward (cells) Reverse (plasma)Blood
GroupAnti-A Anti-B A1 cells B cells
0 0 2-4+ 2-4+ O
3-4+ 0 0 2-4+ A
0 3-4+ 2-4+ 0 B
3-4+ 3-4+ 0 0 AB
Normal ABO Serology
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Lectins for AB and H typing• Extracts from plants, seeds or sometimes animal origin that
detect ABH antigens
• ABH Lectins• Anti-A - Dolichos biflorus (undiluted)
• Anti-A1 - Dolichos biflorus (diluted)
• Anti-B - Griffonia simplicifolia (aged)
• May also be found as GS II + GalNAc.
• Used to detect Acquired B antigen.
• Anti-A + B - Griffonia simplicifolia (fresh)
• has weak anti-A activity
• Anti-H - Ulex europeaus
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ABO Blood Groups
ABO Group
Prevalence (%) in US population
European Ethnicity
African Ethnicity
AsianEthnicity
O 45 49 40
A 40 27 28
B 11 20 27
AB 4 4 5
Bombay rare rare rare
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An Analogy…Building a House
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• You need the foundation to build the house.
This is the
precursor
substance.
An Analogy…Building a House
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• You frame and build the first floor…
H gene is present.
Now you have added
the fucose to make
the H antigen.
An Analogy…Building a House
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• Now you add the second floor…
If you have the A or B gene (or both), you add the
corresponding terminal sugars and now you have
A and/or B antigens.
An Analogy…Building a House
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• If you have 2 O genes, you only build a 1-story ranch… Fucose added but nothing else.
An Analogy…Building a House
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• If you have an A and/or B gene, you build a 2-story house… Either GalNAC or GAL added.
An Analogy…Building a House
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• If you LACK the H gene (Bombay), you only have the foundation!
An Analogy…Building a House
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Bombay Phenotype• Called Bombay phenotype because first identified in India (1952).
• Looks like Group O in routine forward and reverse testing.
• No H gene No H antigen No A or B antigens
• Makes potent anti-H and anti-A,B.
• Will only be detected in antibody screening or compatibility testing.
• Reactive at IS, 37C and AHG testing.
• Reactive with all group O cells tested.
• Negative with Anti-H lectin.
• Ulex europaeus
• Plasma is only compatible with other Bombay cells.
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Variations in A and B reactivity
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ABO and Disease Association No known function of ABO antigens has been proven.
No diseases are known to result from the lack of expression of ABO blood group antigens (ie. Bombay).
The susceptibility to a number of diseases has been linked with a person's ABO phenotype.
◦ Gastric cancer appears to be more common in group A individuals
◦ Gastric and duodenal ulcers occur more often in group O individuals
Group O individuals have about 25% less FVIII and vWF in their plasma.
Non-group O individuals have been shown to be at an increased risk of both arterial and venous disease.
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ABO and Disease Association
• Suppression of A antigen by disease (leukemia). • Myeloblastic leukemia – decreased H antigen.
• Polyagglutination• Acquired B
• Close serological relationship between E coli O86 and blood group A.
• Seen in patients with GI tract illnesses.
• Tn• May be associated with myelomonocytic leukemia.
• Seen in Group O and B with weak reaction with Anti-A or A1 lectin.
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Subgroups of A and B
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Subgroups of A• A1 and A2 most common and most important.
• Reactivity in cell typing same with reagent Anti-A.• Only detected when A2 person makes anti-A1.
• Anti-A1 may be detected in reverse type.
• Differentiate based on red cell reactivity with Anti-A1 reagent.• May be human source from A2 person.
• Or plant source: Lectin (Dolichos biflorus).
• May see slightly weaker reaction when combined with a B gene (A2B).
• A1 and A2 gene is same. • Codes for alpha-3-N-acetylgalactosaminyl transferase
• A1 and A2 transferases are the same, but different.• A2 transferase is less efficient in making A antigens.
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Action of A Gene
• Produces -3-N-acetylgalactosaminyl transferase
• N-acetyl galactosamine attaches to #4 carbon of terminal galactose
A Antigen
GalNAc
Gal = Galactose Fuc = Fucose
GlcNAc = N-acetylglucosamine
GalNAc = N-acetylgalactosamine
1-2
Gal
GlcNAc
1- 4 1- 3
Gal
Fuc
1- 4
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A1 versus A2- Quantitative differences
• A1 transferase converts almost all of the H precursor structure to A1 antigens
• A2 transferase converts about ¼ of the H precursor to A antigens.
• 4-6X more A antigen sites on A1 red cells.• >1,000,000 A antigen sites in A1.
• ~200,000 A antigen sites in A2.
• A1 agglutinated by diluted Dolichos biflorus lectin since so many antigen sites.
• A1 lectin will not react with weaker A subgroups since fewer antigen sites.
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A1 versus A2 – Qualitative differences
• A1 antigen structure is highly complex with many branches, forming many antigenic determinants.
• A2 antigen structure is simpler with less branching and fewer antigen sites.
• Group A infant appears to be A2 at birth with subsequent development of A1 phenotype.
• Likely due to conversion of branched H chains (H3 and H4) after birth.
• Precursors are same as for Ii antigens which go through a similar developmental process.
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H1
H2
H3
H4similar to H3 structure unknown
Aa
Ab
Ac
Ad
GLC GLCNAc GAL GALNAc FUC
H and A active oligosaccharides of glycolipids
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Why do Asub and AsubB individuals make anti-A1?
• Theory is that A2 individuals have mostly unbranched Aa and Ab
structures on their red cells.
• Anti-A1 is actually an anti-Acd (which is lacking on their cells).• Acd antigens can be found on all A1 cells.
• The AsubB individual has even less Acd on their cells since the A transferase competes with the B transferase.
• More likely to develop anti-A1.
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Building a House Analogy…
Precursor
H antigen
A and/or B antigen
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Building a House Analogy…
• The A1 gene…• Very efficient at producing the N-acetylgalactosamine transferase.
• Makes LOTS of A antigen!
• Causes branching of the sugar chains.• Very complex structures and even more A antigens present.
• What does your house look like?
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Really nice house!!
LOTS of A antigens!!
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What happens with the A2 gene?
• We have an A gene, but…• It’s not as efficient at producing the transferase to add the
terminal sugar.
• It doesn’t cause the branching of the sugar chains resulting in fewer antigen sites.
• So what does your house look like now?
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Much smaller, simpler house…
Much less A antigen…
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Weaker subgroups of A
• Other weaker A subgroups:• Rare
• Quantitative and qualitative differences.• GalNAc transferase less efficient.
• Decreased A antigen with increased H antigen.
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Subgroups of A
• ~20% of group A or AB are actually A2.• ~1-8% of group A2 will make anti-A1.
• ~20%-30% of group A2B will make anti-A1.
• Classification of weak subgroups of A:• Degree of reactivity with Anti-A and Anti-A1.
• Degree of reactivity with human anti-A,B.
• Degree of reactivity with anti-H lectin.
• Presence or absence of anti-A1 in the plasma.
• Presence of A and H substance in saliva of secretors.
• Adsorption/elution studies
• Family studies
• Molecular testing
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Subgroups of A
Reaction of cells with Anti-Reaction of plasma
with RBCs
RBC Pheno
A B A,B H A1 A1 A2 B
A1 4+ 0 4+ 0-1+ 4+ 0 0 4+
A2 4+ 0 4+ 2+ 0 0* 0 4+
A3 2+mf 0 2+mf 3+ 0 0* 0 4+
Am 0-1+ 0 0-1+ 4+ 0 0-2+ 0 4+
Ax 0-w+ 0 0-1+ 4+ 0 1-2+ 0 4+
Ael 0 0 0-w+ 4+ 0 1-3+ 0 4+
*Occurrence of anti-A1 is variable in these phenotypes.
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Characteristics of A Subgroups
• A3 typically shows mixed field reactions with Anti-A or Anti-A,B.
• Am will have A substance in saliva of secretors, while Ax, and Ael will not.
• Ael requires adsorption of anti-A onto cells with subsequent elution to prove antigen presence.
• The plasma of ANY person who is genetically A will have no reaction with A2 cells.
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Phenotype Frequencies (%)
Caucasian Black Asian Hispanic
A1 32 19 27 22
A2 8 8 Rare 6
B 11 20 27 13
O 45 49 40 55
A1B 3 3 5 4
A2B 1 1 Rare Rare
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Subgroups of B• Very rare!
• Serologically similar reactivity to weak subgroups of A.
• If Se gene present, B substance will be in secretions of:• B3
• Bm
• Rarely find weak anti-B in the serum of a B subgroup.
• Can occur in combination with A antigen.• ABsub
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Subgroups of B
Rxn of cells with Anti-Reaction of
plasma with RBCs
RBC Pheno
A B A,B H A1 B
B 0 4+ 4+ 0-1+ 4+ 0
B3 0 1+mf 2+mf 4+ 4+ 0
Bm 0 0-1+ 0-1+ 4+ 4+ 0
Bx 0 0-1+ 0-2+ 4+ 4+ 0-w+
Bel 0 0-w+ 0-w+ 4+ 4+ 0
B(A) w+-2+ 4+ 4+ 0 4+ 0
B3 may show mixed field reactions with Anti-B or Anti-A,B.
Bel requires adsorption of anti-B onto cells with subsequent elution
to prove antigen presence.
B(A) most often detected using Anti-A with MH04 clone.
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Summary• The ABH blood group antigens are inherited by Mendelian
genetics in a codominant manner.• O is an amorph.
• Gene products are transferases that add terminal sugars onto a precursor substance.
• H = L-Fucose
• A = N-Acetylgalactosamine
• B = D-Galactose
• If the antigen is absent, the antibody is predictable present.
• Anti-A1 lectin = Dolichos biflorus; Anti-H lectin = Ulexeuropeaus
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• Leukemias may suppress A antigens.
• Polyagglutination may result in weak A (Tn) or B antigens (Acquired B).
• There are quantitative and qualitative differences between A1 and other A subgroups.
• Weaker A subgroups are seen more often than B subgroups.
• Anti-A1 reacts with branched, complex A antigen structures, but not straight chains.
• A subgroups weaker than A2 and B subgroups are extremely rare.
Summary