The Osler I nstitute

P}Chaffin (2/12/2013) Blood Bank I page 1

Blood Bank I
D. Joe Chaffin, MD
Cedars-Sinai Medical Center, Los Angeles, CA

We finish this WHEN???
A. Blood Bank I
Blood Groups
B. Blood Bank II
Blood Donation and Autologous Blood
Pretransfusion Testing
Transfusion-transmitted Diseases
C. Blood Bank III
Component Therapy
D. Blood Bank IV
Transfusion Reactions
E. Blood Bank Practical
Management of specific clinical situations
Calculations, Antibody ID and no-pressure sample
questions



Blood Bank I
Blood Groups
I. Basic Antigen-Antibody Testing
A. Basic Red Cell-Antibody Interactions
1. Agglutination
a. Clumping of red cells due to antibody coating
b. Two stages:
1) Cell Coating (sensitization)
a) Affected by antibody specificity, zeta potential,
pH, temperature, antigen and antibody amounts
b) Low Ionic Strength Saline (LISS) decreases
repulsive charges between RBCs; tends to
enhance cold antibodies and autoantibodies
c) Polyethylene glycol (PEG) excludes H
2
O; tends
to enhance warm antibodies and autoantibodies.
2) Bridge Formation
a) Lattice structure formed by antibodies and RBCs
b) IgG isnt great at this; too small to bridge gap
c) IgM is better because of its pentameric structure.
2. Hemolysis
a. Direct lysis of RBCs due to antibody coating and
subsequent complement fixation
Pathology Review Course
page 2 Blood Bank I P}Chaffin (2/12/2013)
b. Uncommon, but equal to agglutination.
1) IgM antibodies do this better than IgG
B. Tube testing (Classic blood bank testing)
1. Immediate spin phase
a. Mix serum, 2-5% RBC suspension; spin 15-30 sec.
1) Most common: 2 drops serum, 1 drop RBCs.
b. Antibodies reacting here are us IgM and insignificant
if not ABO
2. 37 C phase
a. Add potentiator if desired, incubate at 37 C, spin.
b. Potentiators and incubation times:
1) 10-15 minutes for LISS
2) 15 minutes for PEG (do not READ PEG at 37C!)
3) 30-60 minutes for no potentiation (saline)
3. Indirect antiglobulin test (IAT) phase
a. Wash above to remove unbound globulins.
b. Immediately add antihuman globulin (AHG), spin.
c. Detects RBCs coated with IgG +/ complement
d. Antibodies reacting at IAT are more often significant
C. Modern alternatives to tube testing
1. Column agglutination technology (Gel testing)
a. Add RBCs/plasma to gel column top, incubate, spin.
b. Microtubes filled with gel particles and anti-IgG
1) Gel particles separate RBC clusters physically
(bigger agglutinates, less migration through gel).
2) Anti-IgG grabs onto IgG-coated RBCs and inhibits
their migration through gel immunologically
c. Results:
1) Negative: RBCs in button at bottom of microtube.
2) Positive: RBCs stopped in areas through the
microtube (more positive = higher position in tube)

Image courtesy of Ortho
d. Also done without anti-IgG in gel (ABO, other testing)
e. Can be automated (ProVue machine)
f. Similar sensitivity to PEG-enhanced tube testing
2. Solid-phase Red Cell Adherence (Solid phase)
a. Antibody binds to lysed or intact RBC antigens that
are bound by manufacturer to bottom of microwells
b. Add patient plasma, incubate, wash: If positive, IgG
binds to RBC antigens all over bottom of the well.
c. Wash, add indicator RBCs coated with anti-IgG,
centrifuge (RBCs bind diffusely to bottom of well)
The Osler I nstitute
P}Chaffin (2/12/2013) Blood Bank I page 3
d. Interpretation:
1) Negative: RBCs in a button at bottom of microwell,
(No bound IgG for indicator cells to attach to).
2) Positive: RBCs spread in diffuse carpet across
bottom of well (attached to bound IgG).

Image courtesy of Immucor
e. Can be automated (Echo, NEO)
f. Similar sensitivity to PEG tube testing and to gel
D. The Antiglobulin Test (Coombs Test)
1. Indirect: see above; demonstrates in-vitro RBC coating
with antibody and/or complement.
2. Direct: red cells from patient washed, then mixed with
antihuman globulin; demonstrates in-vivo RBC coating
with antibody and/or complement.

Image credit: Zarandona JM and Yazer MH. The role of the Coombs test in the evaluation
of hemolysis in adults. Canadian Medical Association Journal 2006;174:305-307
3. IAT variations
a. Unknown antibody check: Use RBCs with a known
antigen profile to search for RBC antibodies
b. Unknown RBC antigen check: Use serum with known
antibody specificity to search for RBC antigens
c. Can be used to check for an unknown antigen OR
unknown antibody, as in the crossmatch procedure
d. Can be done in tubes, gel, solid-phase, microwells
4. Specificity possibilities for the antiglobulin
a. Anti-IgG, C3d (polyspecific); most commonly used
1) Detect red cells coated with either of the above
2) May also detect other immunoglobulins (anti-IgG
detects shared kappa/lambda light chains)
b. Anti-IgG and anti-IgG (heavy chain-specific)
1) Anti-IgG used for PEG, gel, and solid phase tests
Pathology Review Course
page 4 Blood Bank I P}Chaffin (2/12/2013)
c. Anti-C3b, C3d
1) Detects either of the above complement components
2) Useful in IgM-related hemolysis, cold agglutinin dz
5. IgG-sensitized RBCs (Coombs control, check cells)
a. Use after negative DAT or IAT tube test (not gel or
solid-phase) to ensure functioning AHG reagent
b. Add IgG-coated cells to AHG-cell mixture
c. Negative = bad AHG or no AHG added
E. Dosage
1. Some antibodies react more strongly with RBC antigens
that have double-dose (homozygous) gene expression.
2. Most common in Kidd, Duffy, Rh and MNS systems
3. For example, imagine a hypothetical anti-Z
a. Patient 1 genotype: ZZ (more Z because of 2 genes)
b. Patient 2 genotype: ZY (less Z; only 1 gene)
c. Anti-Z shows dosage by stronger rxn with ZZ RBCs
RBC Genotype Reaction with anti-Z
ZZ 3+
ZY 1+
F. Enzymes
1. Proteolytic enzymes (e.g., ficin, papain) cleave RBC
surface glycoproteins
a. This may destroy certain RBC antigens
b. Can also strengthen reactions by allowing antibodies
to bind better to previously shielded antigens
2. Useful in antibody identification to confirm or refute a
particular antigen as target of an antibody (see table)
3. The Enzyme Classification
Enhanced Decreased Unaffected
ABO-related
ABO, H Systems
Lewis System
I System
P System
Rh System
Kidd System
MNS System
Duffy System
Lutheran System
Kell System
Diego System
Colton System
G. Neutralization
1. Certain substances, when mixed with a red cell antibody,
inhibit the activity of that antibody against test red cells.
Neutralization of Antibodies
ABO Saliva (secretor)
Lewis Saliva (secretor for Le
b
)
P1
Hydatid cyst fluid
Pigeon egg whites
Sd
a
Human urine
Chido, Rodgers Serum
The Osler I nstitute
P}Chaffin (2/12/2013) Blood Bank I page 5
H. Lectins
1. Seed/plant extracts react with certain RBC antigens
2. Especially useful in polyagglutination studies (T, Tn, etc)
Lectin Specificity
Dolichos biflorus A
1

Ulex europaeus H
Vicia graminea N
Arachis hypogea T
Glycine max T, Tn
Salvia Tn
II. Blood Groups
A. General characteristics
1. Definition
a. Blood group antigen: Protein, glycoprotein, or
glycolipid on RBCs, detected by an alloantibody
b. Blood group system: Group of blood group antigens
that are genetically linked (30 total systems per ISBT)
2. Significance
a. Significant = antibody causes HTRs or HDFN
b. Most significant antibodies are IgG and warm
reactive; meaning they react best at IAT (+/ 37 C).
c. Most insignificant antibodies are IgM and cold
reactive; meaning they react best below 37 C.
1) Also typically naturally occurring (no transfusion
or pregnancy required for their formation).
d. ABO is the exception; see asterisks in table below
WARM-REACTIVE COLD-REACTIVE
IgG IgM
Require exposure Naturally occurring
Cause HDN No HDN*
Cause HTRs No HTRs*
Significant Insignificant*
B. ABO and H Systems
1. Basic biochemistry (see figure on page 6)
a. Type 1 and 2 chains
1) Type 1: Glycoproteins and glycolipids in secretions
and plasma carrying free-floating antigens
2) Type 2: Glycolipids and glycoproteins carrying
bound antigens on RBCs.
b. Se (secretor) gene (FUT2; fucosyltransferase)
1) Required to make A or B antigens in secretions
2) FUT enzyme adds fucose to type 1 chains at
terminal galactose; product is type 1 H antigen
3) 80% gene frequency
c. H gene (FUT1)
1) Closely linked to Se on chrom 19
Pathology Review Course
page 6 Blood Bank I P}Chaffin (2/12/2013)
2) FUT enzyme adds fucose to type 2 chains at
terminal galactose; product is type 2 H antigen.
3) Virtually 100% gene frequency (Bombay = hh).
d. H antigen required before A and/or B can be made on
RBCs (type 2 H) or in secretions (type 1 H).
1) Single sugar added to a type 1 or 2 H antigen chain
makes A or B antigens and eliminates H antigen.
a) Group A sugar: N-acetylgalactosamine
b) Group B sugar: Galactose
2) As more A or B is made, less H remains.
a) H amount: O > A
2
> B > A
2
B > A
1
> A
1
B
2. ABO antigens
a. Genotype determined by three alleles on long arm of
chromosome 9: A, B and O
b. A and B genes make transferase enzymes, not directly
for an antigen (O makes nonfunctional enzyme)
c. ABO antigens begin to appear on fetal RBCs at 6
weeks gestation; reach adult levels by age 4.
1) Also platelets, endothelium, kidney, heart, lung,
bowel, pancreas tissue
3. ABO antibodies
a. Antibodies clinically significant, naturally occurring
b. Appear age 4 months; adult levels age 10, may fade
with advanced age
f. Three antibodies: anti-A, anti-B and anti-A,B;
1) Group A and B: Anti-A or B predominantly IgM,
but each reacts strongly at body temperatures.
2) Group O: Anti-A and B are predominantly IgG,
and react best at body temperatures
3) Group O: Anti-A,B is IgG reacting against A and/or
B cells (cant separate into individual specificities).
4. ABO blood groups
a. Group O (Genotype OO)
1) The most common blood group across racial lines
2) Antigen: H (Ulex europaeus lectin positive)
3) Antibodies: Anti-A, anti-B, anti-A,B (see above)
a) Because of IgG component to all antibodies,
mild HDFN common in O moms
The Osler I nstitute
P}Chaffin (2/12/2013) Blood Bank I page 7
b) Why not severe? Weak fetal ABH expression,
soluble ABH antigens (neutralize antibodies)
b. Group A (Genotypes AA or AO)
1) Antigens: A, H
2) Antibody: anti-B (primarily IgM).
3) A subgroups
a) A
1
(80%) and A
2
(~20%) most important
b) Monoclonal anti-A agglutinates both types well
c) A
1
red cells carry about 5x more A on RBC
surfaces than A
2
cells
d) Qualitative differences also exist in the structure
of the antigenic chains (type 3 and 4 for A
1
).
e) 1-8% of A
2
and 25% of A
2
B form anti-A
1
.
Usually clinically insignificant IgM
Common cause of ABO discrepancies.
If reactive at 37C, avoid A
1
RBC transfusion.
f) Dolichos biflorus lectin: A
1
RBCs +, A
2
RBCs .
c. Group B (Genotypes BB or BO)
1) Antigens: B, H
2) Antibodies: Anti-A (primarily IgM).
3) B subgroups: Usually unimportant and less frequent
d. Group AB (Genotype AB)
1) Least frequent ABO blood type (about 4%)
2) Antigens: A and B (very little H)
a) Can be further subdivided into A
1
B or A
2
B
depending on the status of the A antigen
3) Antibodies: No ABO antibodies
5. ABO testing
Cell Serum
ABO
Group
Anti-A Anti-B A
1
cells B cells
4+ 0 0 4+ A
0 4+ 4+ 0 B
4+ 4+ 0 0 AB
0 0 4+ 4+ O
a. Red cell grouping (forward grouping)
1) Patient red cells agglutinated by anti-A, anti-B.
b. Serum grouping (reverse grouping, back typing)
1) Patient serum (or plasma) against A
1
and B RBCs.
c. Note the opposite reactions!
1) If forward reactions are not opposite of reverse, an
ABO discrepancy is present.
Type Whites Blacks Asians Native Americans
O 45% 49% 40% 79%
A 40% 27% 28% 16%
B 11% 20% 27% 4%
AB 4% 4% 5% <1%
Pathology Review Course
page 8 Blood Bank I P}Chaffin (2/12/2013)
d. Red cell and serum grouping required unless:
1) Testing babies < 4 months of age
2) Reconfirming ABO testing done on donor blood
6. ABO discrepancies
a. Disagreement between the interpretations of red cell
and serum grouping (e.g., forward = A, reverse = O)
b. Antigen problems
1) Missing antigens
a) A or B subgroups
b) Transfusion or transplantation
c) Leukemia or other malignancies
2) Unexpected antigens
a) Transfusion/transplantation out-of-group
b) Acquired B phenotype (more below)
c) Recent marrow/stem cell transplant.
d) Polyagglutination
c. Antibody problems
1) Missing antibodies
a) Immunodeficiency
b) Neonates, elderly, or immunocompromised
c) Transplantation or transfusion
d) ABO subgroups
2) Unexpected antibodies
a) Cold antibodies (auto- or allo-)
b) Anti-A
1
c) Rouleaux/plasma expanders (false positive)
d) Transfusion or transplantation
e) Reagent-related antibodies
d. Technical errors
1) Sample/reagent prep, mix-ups, interpretation errors
7. Weird stuff about ABO
a. Acquired B phenotype
1) A
1
RBC contact with enteric gram negatives: Colon
cancer, intestinal obstruction, gram-negative sepsis
2) AB forward (with weak anti-B reactions), A reverse
3) Bacterial enzymes deacetylate group A GalNAc;
remaining galactosamine looks like B and reacts
with forms of monoclonal anti-B (ES-4 clone).
4) Use monoclonal anti-B that does NOT recognize
acquired B, acidify serum (no reaction with anti-B)
Cell Typing Serum Typing
Anti-
A
Anti-
B
Interp
A
1

cells
B
cells
Interp
4+ 1-2+ AB 0 4+ A
b. B(A) phenotype
1) Opposite of acquired B (group B patients with weak
A activity); this condition is inherited, not acquired
The Osler I nstitute
P}Chaffin (2/12/2013) Blood Bank I page 9
2) Cross-reaction with a specific monoclonal anti-A;
test using different anti-A shows the patient as B.
c. Bombay (O
h
) phenotype
1) Total lack of H, A and B antigens due to lack of H
and Se genes (genotype: hh, sese)
2) Naturally occurring strong anti-H, anti-A, anti-B
3) Testing: O forward, O reverse, but antibody screen
wildly positive and all units incompatible
4) Require H-negative blood (Bombay donors)
d. Para-Bombay phenotype
1) Like Bombays, are hh, but unlike Bombays, have at
least one Se gene
2) Phenotypes: A
h
, B
h
, AB
h

3) RBCs may be Bombay-like, but may also show free
or RBC A or B antigens (unless group O).
4) Allo-anti-H present in serum.
5) Require H-negative blood (Bombay donors)
8. Consequences of ABO incompatibility
a. Severe acute hemolytic transfusion reactions
1) Among most common blood bank fatalities
2) Clerical errors
b. Most frequent HDFN; usually mild, however
C. Lewis System
1. Biochemistry (see figure below)
a. Type 1 chains only
b. One gene: Le (FUT3)
1) Second gene, le, is nonfunctional
c. FUT3 enzyme adds fucose to subterminal GlcNAc
(left side of figure).
1) This makes Le
a
(Lewis A) antigen.
2) Le
a
antigens cannot be modified to make Le
b
.
d. In secretors (right side of figure), Se enzyme adds
fucose, then Le enzyme adds fucose: Result = Le
b

1) In secretors, Le
b
formation occurs preferentially.
2) As a result, the vast majority of the chains of those
who carry Le and Se are Le
b
rather than Le
a
.
3) In non-secretors, Le
a
is only possible Lewis antigen.

Pathology Review Course
page 10 Blood Bank I P}Chaffin (2/12/2013)
e. Unlike ABO, antigens are not tightly bound
(remember, they are made from type 1 chains); rather,
they adsorb onto the surface of RBCs.
1) Le
b
does this better than Le
a
; another reason that
most adults with both Le and Se will be Le(a-b+).
2) Le(a-b+) people still have Le
a
, just in much smaller
quantities that may not show up on RBCs.
f. Same chain can carry Le and ABO antigens (unlike the
relationship between ABO antigens and H antigen).
2. Lewis phenotypes, antigens, and antibodies
a. Phenotypes: Le(a-b+), Le(a+b-), Le(a-b-)
b. 22% of blacks are Le(a-b-), vs. only 6% of whites.
c. Antibodies are naturally occurring, cold-reacting IgM.
1) Primarily in Le(a-b-)
2) Neutralize with saliva from secretors.
3) Antibodies commonly show ABH specificity (e.g.,
anti-Le
bH
reacts best with Le
b
+, O or A
2
RBCs)
3. Consequences of incompatibility
a. Antibodies are generally insignificant
b. Rare HTRs (more commonly seen with anti-Le
a
)
c. Minimal to no HDFN (antibody doesnt cross placenta
and Le antigens are not present on fetal RBCs).
4. Weird stuff about Lewis
a. Lewis antigens decrease during pregnancy.
1) Pregnant patients may appear Le(a-b-) and have
transient, insignificant Lewis antibodies.
2) Increased plasma volume dilutes the antigens and
increased plasma lipoproteins strip the antigens
b. Le(a-b+) people dont make anti-Le
a
.
1) Still have Le
a
, just not on their RBCs (see above)
c. Childrens Lewis type may vary, as antigen chains are
converted [more Le
a
than Le
b
initially, with a transient
period of Le(a+b+)]; by age 2, most are Le(a-b+)
d. Infection associations:
1) H. pylori attaches to gastric mucosa via Le
b
antigen.
2) Norwalk virus also attaches via Le
b

3) Le(a-b-) are at risk for Candida and E. coli infection
D. I System
1. Antigens built on type 2 chains.
2. Expression is age-dependent.
a. Simple chains found on neonates make i antigen.
b. Branched chains in adults make I antigen (I expression
generally parallels ABO antigen expression)
c. Big I in big people, little i in little people
d. Occasional adults lack I; they are known as i
adult
;
more common in Asians
3. Antibodies (usually autoantibodies)
a. Cold reacting IgM, with auto-anti-I seen commonly
b. Naturally occurring, common, usually insignificant
The Osler I nstitute
P}Chaffin (2/12/2013) Blood Bank I page 11
c. Like Lewis, antibodies commonly have H specificity
as well (e.g., anti-IH reacts better against O and A
2
)
4. Classic associations
a. Auto-anti-I
1) Cold agglutinin disease
2) Mycoplasma pneumoniaeinfection
b. Auto-anti-i
1) Associated with infectious mononucleosis
2) Less often a problem than auto-anti-I
c. i
adult
phenotype
1) Cataracts
2) HEMPAS
E. P System (the cool one)
1. Also built on ABO-related chains
2. Antigens
a. P1 is the only antigen in the P system
1) P, P
k
not officially in P system, but along with P1,
define the overall P phenotype
2) Most common P phenotype: P
1
(P+P1+P
k
).
b. Rare lack of all three leads to anti-PP1P
k
(anti-Tj
a
)
1) Acute HTR; HDFN leading to spontaneous abortion
c. P antigen is parvovirus B19 receptor.
d. P
k
antigen is receptor for various bacteria and toxins
3. Antibodies (anti-P1)
a. Cold reacting, naturally occurring, insignificant IgM;
rare anti-P1 reactive at AHG is potentially significant
b. Titers elevated in those with hydatid cyst disease
(Echinococcus) and bird handlers
1) Bird feces contains P1-like substance.
c. Neutralized by hydatid cyst fluid, pigeon egg whites
4. Auto-anti-P (paroxysmal cold hemoglobinuria)
a. Biphasic IgG autoantibody with unique features
1) Binds in cold temps, hemolyzes when warmed
2) Donath-Landsteiner biphasic hemolysin
b. Historically in syphilis, now after viral infx in children
F. Rh System
1. Second most important blood group (after ABO)
2. Old (incorrect) Rh antigen terminology systems
a. Fisher-Race (DCE or CDE)
1) Five major antigens: D, C, E, c, e
a) Rh positive really means D positive.
b) Absence of D designated d (no d antigen)
c) C/c and E/e are antithetical (e.g., cant have both
C and c or E and e from same chromosome)
2) Eight potential combinations based on presence of
genes for above antigens (ie, DCe, dce, etc.)
b. Wiener (Rh-Hr)
1) Different, archaic names for the five main antigens
Pathology Review Course
page 12 Blood Bank I P}Chaffin (2/12/2013)
2) Believed that main Rh genes (for presence or
absence of D, for C or c and for E or e) inherited as
one genetically linked group, or haplotype.
3) Shorthand names to the haplotypes; nomenclature is
still in use and is essential to know (though theory
of how these are inherited has been disproven).
Wieners Haplotypes
(with DCE Equivalents)

R
1
: DCe r : dCe
R
2
: DcE r: dcE
R
0
: Dce r : dce
R
z
: DCE r
y
: dCE
a) Rules for converting Wieners modified
haplotypes into Fisher-Race terminology:
R = D, r = d
1 or prime = C
2 or double prime = E
0 or blank = ce
Any sub- or superscript letter = CE
4) Only four of the above combinations occur with
significant frequency: R
1
, R
2
, R
0
and r. (~97% of
blacks and whites use only these four).
R
0
most common in blacks, least common in
whites.
r is always second in frequency.
R
1
always comes before R
2
.
The Big Four
Whites: R
1
> r > R
2
> R
0

Blacks: R
0
> r > R
1
> R
2

5) Asians us. D+; order is R
1
> R
2
> r = R
0
.
c. Current understanding of Rh genetics/structure
1) Two genes, RHD and RHCE (chromosome 1) code
for two main Rh proteins (RHD and RHCE)
2) D type determined by presence/absence of RHD
3) One protein (RHCE) carries both C/c and E/e
antigens; combination determined by which alleles
of RHCE are present (CE, Ce, cE, or ce)
3. Rh antibodies
a. Exposure-requiring, warm-reacting IgG
b. D induces the most antibodies, then c and E
1) Traditional: 80% of D negatives make anti-D when
exposed to one unit of D pos RBCs
2) Recent data: 22% in hospital patients
c HTRs with extravascular hemolysis
d Severe and prototypical HDFN with anti-D, severe
HDFN with anti-c, mild HDFN with anti-C, -E, -e
The Osler I nstitute
P}Chaffin (2/12/2013) Blood Bank I page 13
4. Weird stuff about Rh
a. D-negative phenotype
1) Unusual because caused by mutations and deletions
rather than by synthetic actions of a gene product
2) Caucasians: D-negatives have deletion of RHD gene
3) African-Americans: Point mutations in RHD gene
(pseudogene)
4) Asians: Usually have inactive RHD gene
b. D Variants
1) Weak D (formerly D
u
)
a) A quantitative defect in D antigen (less D than
normal); generally the D antigen is normally
formed (see partial D discussion later)
b) Usual D testing: Monoclonal IgM with
polyclonal IgG read only at immediate spin
Almost all D+ test as D+ this way
Weak D requires IAT to detect D presence

c) Possible reasons for weak D
Mutated form of RHD (most common by far)
Point mutation causing altered amino acids
in membrane or inner part of RHD
Type 1 common in Caucasians
RHCe on opposite chromosome to RHD (C
in trans) inhibits D expression
d) Testing requirements
Weak D test for all D-negative blood donors
The idea is that weak D RBCs could
potentially induce anti-D in a D recipient
Not required for D-negative blood recipients
Previously a concern, for fear of wasting D-
neg units on weak D patients
Testing above makes this very unlikely
In fact, calling a partial weak D (see below)
recipient D is exactly what is desired
Only non-donors who definitely need weak
D testing are D babies born to D moms.
e) Weak D moms do not need RhIG prophylaxis
2) Partial D (formerly D Category, D mosaic)
a) Usually considered a qualitative D antigen
defect (abnormal forms, missing parts of the
antigen) not quantitative (like weak D)
Not quite that simple; some partial D are also
quantitatively defective (partial weak D)
Pathology Review Course
page 14 Blood Bank I P}Chaffin (2/12/2013)
b) Cause: RHD gene mutations leading to alteration
of exterior part of RHD antigen
c) Antibodies form against absent parts of RHD;
this antibody appears to be anti-D at first glance
d) Classic: Anti-D in a D-positive person
e) Most common: DVI (say D six) in whites,
DIIIa (D three A) in African-Americans
Monoclonal anti-D usually types DVI as D-
negative on immediate spin (weak D is +
though)
f) Why partial D vs. weak D matters:
Partial D moms need HDFN prophylaxis
(RHIG), while weak Ds commonly do not
(disagreement on this, though)
Partial D recipients may make anti-D when
receiving D+ RBCs, weak D recipients
generally do not
Partial D OR weak D donor RBCs may
induce anti-D in a D-negative recipient
g) Partial D vs. weak D distinction may be
impossible without molecular testing; if in doubt
for prenatal testing, consider patient D-negative
3) DEL (D-E-L, formerly D
el
)
a) Appear D-neg but have tiny amounts of D seen
after elution of reagent anti-D from RBCs
b) Primarily seen in Asian populations (up to 1/3 of
D-negative Asians)
c. These antibodies go together
1) Anti-E formation commonly accompanied by anti-c
(not necessarily vice-versa)
2) Think Big 4; R
2
R
2
gives both E and c exposure
d. Compound Rh antigens
1) G = Antigen present when either C or D is present
Anti-G reacts against (D+C-), (D-C+), or
(D+C+) RBCs (rarely against D-C-G+)
Common presentation: D-negative person forms
anti-D + anti-C despite no exposure to D
Important because if D-neg mom has anti-G, she
DOES still need RhIG to prevent anti-D
Can cause HTRs (give D-C- blood)
See bbguy.blogspot.com/2011/08/g-whiz.html
2) f = Present when RHce is inherited (r and R
0
).
Anti-f is often seen with anti-e or anti-c
Can cause mild HDFN and HTR
G. Kidd System
1. Kidd antigens
a. Jk
a
, Jk
b
, Jk3 (very high frequency)
b. Jk
a
slightly more common than Jk
b
in African
Americans but similar in whites and Asians
The Osler I nstitute
P}Chaffin (2/12/2013) Blood Bank I page 15
c. Antigens reside on a urea transport protein
1) Jk(a-b-) are resistant to hemolysis in 2M urea (no
urea transport, so no resultant osmotic lysis)
2. Kidd antibodies
a. Exposure requiring, warm-reacting IgG (often with
IgM component as well)
1) Can fix complement (with IgM component)
2) Severe acute HTRs possible
b. Marked dosage effect
1) Antibodies may not react at all against cells with
genetic single dose (heterozygous) Kidd antigens
c. Variable antibody expression
1) Antibody often disappears with time/storage.
3. Weird stuff about Kidd
a. Delayed HTRs (most famous association)
1) Anamnestic response
2) Intravascular and often severe
b. Mild HDFN at worst
1) Child can only be one antigen different from mom;
remember dosage discussion above.
H. MNS System
1. Basic biochemistry
a. Glycophorin A (GPA) carries M or N antigens
b. Glycophorin B (GPB) carries S or s, and U antigens
c. GPA/GPB both receptors for P. falciparum
2. MNS antigens
a. M frequency roughly equals N (each ~75%)
b. s (~90%) is more frequent than S (~50%W, ~30%B)
c. If S-s- (as seen in 2% of African-Americans), may also
be U-negative (U is extremely high frequency).
d. Vicea graminea lectin reacts against N antigens
e. Mur: Hybrid antigen seen in nearly 10% of Chinese
1) Significant antibodies; common in Asians
3. MNS antibodies
a. Anti-M and N are mostly opposite of anti-S, -s and -U
Anti-M & anti-N Anti-S, -s and -U
Naturally occurring Require exposure
Cold IgM Warm IgG
Dosage Minimal dosage
Insignificant Significant
b. Anti-M and anti-N can usually be ignored unless
reactive at 37C; not so with anti-S and anti-s
1) Though anti-M is usually insignificant, it has been
rarely associated with severe HDFN.
c. Effect varies by enzyme, but enzymes generally
decrease all MNS antigens except U
Pathology Review Course
page 16 Blood Bank I P}Chaffin (2/12/2013)
4. Weird stuff about MNS
a. N-like antigen (N)
1) GPB always has terminal 5 amino acid sequence
that matches the N version of GPA; known as N.
a) Not really true N antigen, but its close enough
to prevent most M+N- from making anti-N.
2) Seen in all except those who lack glycophorin B.
a) <1% of blacks lack S, s, and U; rare in whites
b) Anti-N nearly exclusive to African-Americans
b. Auto-anti-N induced by hemodialysis
1) Formaldehyde sterilization of machine
2) Modification of N leads to rare autoantibody
I. Duffy System
1. Duffy antigens and genes
a. Fy
a
from Fy
a
gene; high frequency in Asians
b. Fy
b
from Fy
b
gene; high frequency in caucasians
c. Fy (a-b-) is most common Fy phenotype in African-
Americans (68%; even higher in Africa).
1) Due to inheritance of two copies of Fy gene, which
gives no functioning Duffy glycoprotein
2) Fy is an Fy
b
gene variant, and gives Fy
b
antigen in
non-RBC tissues
2. Duffy antibodies
a. Anti-Fy
a
more common and significant than anti-Fy
b

b. Exposure requiring, warm-reactive IgG
c. Marked dosage and variable expression like Kidd Abs
3. Consequences of incompatibility
a. Severe HTRs, usually delayed and extravascular
b. Often mild, occasionally severe HDFN
4. Weird stuff about Duffy
a. Fy(a-b-) and malarial resistance
1) Fy(a-b-) humans are resistant to Plasmodium vivax
and P. knowlesi infection.
J. Kell System
1. Extremely important group clinically and serologically
2. Kell antigens
a. Low frequency: K, also known as KEL1 (9%
whites, 2% blacks), Js
a
, Kp
a

b. High frequency: k or KEL2 (99.8%), Js
b
, Kp
b

c. Kx antigen: Bound to Kell glycoprotein on the red cell
membrane; required for proper Kell antigen expression
1) Actually a separate blood group (Kx system)
2) When Kell antigens decrease, Kx increases (as in
K
0
,

aka Kell null)
3) When Kx decreases (as in McLeod syndrome, see
later), Kell antigens decrease, too.
d. Kell system antigens destroyed by thiol reagents (2-
ME, DTT, ZZAP) but not by enzymes alone.

The Osler I nstitute
P}Chaffin (2/12/2013) Blood Bank I page 17
3. Kell antibodies
a. Anti-K
1) Most common non-ABO antibody after anti-D
2) Exposure-requiring, warm reacting IgG1
3) More common from transfusion than pregnancy
b. Anti-k
1) Very uncommon due to high antigen frequency
2) Antibody is just like anti-K
4. Consequences of incompatibility
a. Severe HTRs
1) May be acute or delayed; usually extravascular.
b. Severe HDFN
1) Less common than ABO or RHD HDFN
2) Damages EARLY RBC precursors, so tends to be
suppressive rather than hemolytic
a) Lower bilirubin and reticulocytopenia than with
anti-D HDFN
b) Significant at lower titers (1:8 = critical)
5. Weird stuff about Kell
a. Kell null phenotype (K
0
)
1) All Kell antigens decreased, Kx increased
2) Significant anti-Ku (universal) with exposure
b. McLeod phenotype
1) Kx absent, all Kell antigens markedly decreased
2) No anti-Ku, but can form anti-Kx and anti-Km
(Kell McLeod); only McLeod RBCs compatible
3) Phenotype is part of McLeod syndrome
a) Hemolytic anemia with acanthocytes
b) Myopathy, ataxia, peripheral neuropathy,
cognitive impairment, cardiomyopathy
c) Association with X-linked chronic
granulomatous disease
NADPH oxidase deficit
Organisms phagocytized but not killed
Catalase-positive organisms (Staph)
K. Diego System
1. Over 20 antigen system built on band 3
a. Important RBC membrane structure
b. Carries HCO
3
-
anions out of RBCs (for CO
2
removal),
and anchors membrane to cytoskeleton
2. Diego antigens
a. Di
a
and Di
b
antithetical pair
1) Di
a
very low frequency except in some South
Americans and Asians
2) Di
b
very high frequency in all populations
b. Wr
a
and Wr
b
antithetical pair
1) Wr = Wright
2) Wr
a
very low frequency, Wr
b
very high frequency

Pathology Review Course
page 18 Blood Bank I P}Chaffin (2/12/2013)
3. Diego antibodies
a. Di antibodies are IgG, while Wr antibodies may have
IgM component
b. Both anti-Di
a
and Di
b
can cause HDFN that may be
severe but generally not HTRs
c. Anti-Di
b
can show marked dosage effect
d. Anti-Wr
a
is common, naturally occurring, and may
cause both HTRs and severe HDFN (IgG + IgM)
e. Anti-Wr
b
, on the other hand, is rarely seen as an
alloantibody but may be an autoantibody in
autoimmune hemolytic anemia (AIHA)
L. Colton System
1. Antigens (Co
a
and Co
b
) located on water transport
membrane protein (aquaporin 1)
2. Co
a
very high frequency (near 100%), Co
b
about 10%
3. Both antibodies may cause significant HDFN
M. A few other systems and antigens (in brief)
1. Dombrock System
a. Do
a
/Do
b
antigens; Do
b
more frequent
1) Either antibody may cause HTRs but generally
dont cause HDFN
2) Warm-reactive IgG
b. High frequency antigens Jo
a
, Gy
a
, Hy
1) Mild HTRs or HDFN possible, but antibodies are
very rare
2) Near 100% incidence for all of these
3) Jo
a
- and Hy negative exclusively in blacks
4) Gy
a
negative in Japanese and eastern Europeans
2. Lutheran (Lu) System
a. Lu
a
(low frequency; 5-8%) and Lu
b
(very high
frequency; 99.8%) antigens
b. Antibodies uncommon, may be naturally occurring
(anti-Lu
a
), and not usually significant
c. Most enzymes decrease Lu antigen activity.
3. Xg System
a. Gene carried on X chromosome (X-linked)
1) Seen in 66% of males and 90% of females
b. Antibody insignificant
4. Yt System
a. Formerly Cartwright
b. Yt
a
(very high frequency; 99.8%), Yt
b
(8%)
c. Antibodies are IgG but not usually significant
(occasional anti-Yt
a
can cause HTRs, however)
5. Vel Antigen
a. Extremely high frequency antigen (>99% in all
populations)
b. Antibody is mix of IgG and IgM
1) May cause severe HTRs and HDFN
The Osler I nstitute
P}Chaffin (2/12/2013) Blood Bank I page 19
2) May interfere with ABO typing due to reaction at
room temperatures
3) May be allo- or autoantibody
6. Landsteiner-Wiener (LW) System
a. LW
a
antigen is more abundant on D-positive RBCs
b. LW antigens were originally thought to be Rh antigens
c. Antibodies are not generally significant
7. Sd
a
(Sid) antigen
a. High frequency (96%)
b. Refractile, small immune complexes with naturally
occurring IgM
c. Lectin of Dolichos biflorus agglutinates Sd
a
positive
RBCs (like A
1
)
d. Neutralize with guinea pig or human Sd
a
+ urine!
8. Antibodies with high titer, low avidity (HTLA) features
(HTLA-like antibodies)
a. High frequency antigens that are generally clinically
benign (no HTRs or HDN)
b. Chido, Rodgers most frequent
1) Complement components (C4)
c. Multiple others known
1) Knops (Kn
a
), McCoy (McC
a
), JMH
d. Must be careful, because some antibodies with similar
features may be significant (anti-Vel, anti-Yt
a
)