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I. IMMUNOHEMATOLOGY
the study of immunologic reactions involving all components of blood deals with antigens, antibodies and antigen-antibody reactions
II. APPLICATIONS OF IMMUNOHEMATOLOGY
transfusion of blood and its components diagnosis, prevention and management of immunization associated with pregnancy laboratory resolution of parentage problems
III. DISEASE WHERE BLOOD TRANSFUSION IS NEEDED
massive blood loss secondary to severe trauma dengue (where you have active bleeding and thrombocytopenia) patient with severe anemia
IV. DEFINITION OF TERMS
Antigen – any substance that stimulates production of antibodies (ANTIbody GENerator) Antibody – proteins produced by the Reticuloendothelial system in response to antigen stimulation Agglutinogen – antigen on the surface of RBC responsible for agglutination Agglutinin – antibody that attacks RBC antigens, manifest its activity by clumping of the RBCs Hemolysin – antibody that attacks RBC antigens, manifest its activity by lysis of the RBCs Agglutination – clumping of RBCs as a result of antibodies binding to the antigenic sites of the
adjacent cells Natural Antibodies – antibodies that appear without antigenic stimulation, usually these are present
during childhood and decreases as we age Acquired/Immune Antibodies – antibodies that appear upon introduction of antigen by disease,
transfusion, pregnancy and substances chemically related to RBC antigen Complete Antibodies - bivalent antibodies, can agglutinate RBCs Incomplete Antibodies - univalent antibodies, coats RBCs but cannot directly agglutinate them. They
require a special enzyme for agglutination to occur Isoantibodies/Alloantibodies – antibodies produced against antigen from genetically different
individuals coming from the same specie. Auto antibodies - antibodies produced against ones own tissue or self antigens ( as seen in
autoimmune diseases) Warm Antibodies
o antibodies which react best in vitro at body temp of 37oC o usually IgGo require exposure to foreign antigen before they are produced hence they are also called
“acquired antibodies” o Most are clinically significant except the (ABO blood group which are IgM)
Subject: Clinical PathologyTopic: ImmunohematologyLecturer: Dr. Joan Pascual RodriguezDate of Lecture: I forgotTranscriptionist: iorEditor: Pages: 10.5
o Coats red cells at body temperature and lead to removal by macrophages (extravascular hemolysis)
o IgG are small and therefore these antibodies can cross the placenta Cold Antibodies
o Antibodies which react best in vitro at 4-10oC or < 25oCo Usually IgMo Exist in humans regardless of whether they have been pregnant or transfused hence they
are also called “natural antibodies”o Most are not clinically significant except for the ABO IgM antibodieso When significant IgM antibodies are very efficient in fixing complement and causes
(intravascular hemolysis) o IgM are pentamers composed of 5 subunits of globulin chains therefore they are big and
cannot cross the placenta
V. BLOOD GROUP SYSTEM
A. ABO blood Group
first blood group discovered most significant for transfusion practice ABO compatibility is essential before other pre transfusion test is performed ABO antigens are the only antigens for which reciprocal antibodies exist in serum of normal individuals BIOCHEMISTRY: all of the antigens in the ABO blood group have the same core backbone the
PARAGLOBOSIDE composed of (glucose, galactose and N-acetylgalactosamine)o H antigen
Precursor to the A and B Made by adding fucose to paragloboside Only after the H antigen is made can the A or B antigens can be added A and B antigens functionally mask the H antigen (the more A and B that is made the
less H is present) Type O cells have no A or B antigen so they express the greatest amount of H antigen
o A antigen Formed by the addition of N-acetylgalactosamine to the H antigen
o B antigen Formed by the addition of galactose to the H antigen
(For people who are visual this is the picture of what is written above)
BLOOD GROUPSo Group A
Express A antigen on RBC surface Genotypes AA or AO Have naturally occurring, clinically significant, predominantly IgM with a small
amount of IgG antibodies against type B (antibody B) Subgroups
A1 – (80%) most common form of A antigen A2 – (20%) significant because it contains anti A1 antibodies
o Group B Express B antigen on their surface Genotypes BB or BO Have naturally occurring, clinically significant, predominantly IgM with a small
amount of IgG antibodies against type A antigen (antibody A)
o Group O Have neither A nor B antigens on their RBC surface Genotype OO Universal donors have naturally occurring, clinically significant very high titer anti A, anti B and
anti AB antibodies – the reason why it can only receive blood donors from blood type O
maternal anti A and B antibodies are IgG and therefore can cross the placenta to cause hemolytic disease of the newborn
o Group AB Express A and B antigen on RBC surface Genotypes A1B or A2B – remember that A antigen has two subgroups Have no ABO antibodies – therefore it is the universal recipient because it can
accept blood from all types without the risk of coagulation
BLOOD GROUP RBC ANTIGEN SERUM ANTIBODYA A BB B A
AB AB NoneO O A, B and AB
*** remember that antibodies are found circulating in the blood serum and that antigens are located on RBC surfaces
ABO BLOOD GROUP TESTINGo Forward Typing/Forward Grouping
Also called cell typing Testing antigens on red cells Patients red cells plus commercial sera (anti A and anti B)
ABO BLOOD GROUPFORWARD TYPING
(uses patients RBCs)Anti A Reagent Anti B Reagent
AB + +A + -B - +O - -
***NOTE: (+) indicates presence of agglutination : Since you are using the red cells you are testing for the Antigens present : The reagents contain the antibodies against the particular antigen present in the RBC : Blood type is determined in the reagent that has agglutination
o Reverse Typing also called serum or back typing uses patients serum versus commercial A1 and B cells analyzes patients serum for the presence of Anti A and Anti B antibodies Patients serum plus commercial A and B cells
ABO BLOOD GROUPREVERSE TYPING
(uses patients serum)A1 Cells B Cells
AB - -A - +B + -O + +
***NOTE: since you are using the serum you are looking for the ANTIBODIES present : Example: AB. It is (-) for A and (-) for B, therefore there are no antibodies present in AB : Testing antibodies are not reliable until 6 months of age because newborn serum may contain maternal IgG anti A or anti B which can interfere with the result.
COMMON CAUSES OF ABO DISCREPANCIES When the results of the forward and back typing are not compatible, that is
ABO discrepancy1. Abnormal Antigens
Person has A2 blood group with anti A1 formation
FORWARD TYPING REVERSE TYPING
Anti A Anti B A1 Cells B cells+ - + +
Forward blood type: A ; Reverse blood type: O (+) for B because blood type A has antibodies for B (+) for A1 because there are some people who have A2 blood group
with anti A1. Since A1 cells were used, it will react to that causing agglutination
To differentiate A1 from A1 you need a special lectin.2. Acquire B phenotype
Seen in group A patients with exposure to gram negative bacteria by way of intestinal obstruction, gram negative sepsis or colon cancer
Bacteria removes the N-acetyl group in the A antigen, leaving only the galactosamine.
The resultant chains is very much similar to the B antigen, such that the patients express weak B antigens
FORWARD TYPING REVERSE TYPING
Anti A Anti B A1 Cells B cells+++ + - +
Forward typing: AB ; Reverse typing: A (+) for A in forward typing because the patient is blood type A (+) for B in forward typing because they express weak B antigen (+) for B in reverse typing because blood type A has antibodies for B
3. Weak or Missing Antibodies
Common in newborn, elderly, immunosupressed individuals and other conditions that yield hypo/aggamaglobulinemia (decreased or absence of antibodies)
FORWARD TYPING REVERSE TYPING
Anti A Anti B A1 Cells B cells+ - - -
Forward Typing: A or B depends on the antigen present in here we used type A ; Reverse typing: AB due to absence of antibodies
Failure to produce antibodies will lead to AB like blood type4. Non ABO antibodies
Ex. Polyagglutinins and multiple myeloma. When present it can cause agglutination of red cells
FORWARD TYPING REVERSE TYPING
Anti A Anti B A1 Cells B cells+ + + +
Forward Typing: A, B, AB or O. in here we just used AB. ; Reverse typing: O
Since they cause agglutination of red cells they will type as O on reverse typing (+ for anti A and + for Anti B)
5. Bombay (Oh) Phenotype Patient lack the H gene and therefore cannot make H antigen nor A or B
antigen on their red cells (because you need the H antigen as precursor) Forward typing: O (because they do not have A and B antigens) Cause discrepancies on reverse typing
o Serum agglutinates A1, B and O cells (A and B antigens mask the H antigen. O cells do not because they don’t have A and B antigens). The Bombay phenotype will react to the O cells because they do not have the H antigen, which the O cells have
o Confirmatory testing is done using an anti H reagent made from Ulex europaeus plant
o Red cells + anti H = NO AGGLUTINATION (there will be no agglutination because there’s no H antigen. Even if you have H antibodies there is no antigen to act on.
o Have very strong anti A, anti B and anti H and can only receive blood from a Bombay Donor.
** I got confused with the mechanism so I tried to scan wiki. It says that Bombay phenotype doesn’t have any antigen (A, B, AB and O) because there’s no precursor which is the (H antigen) this is also the antigen of blood type O. Bombay’s can donate blood to all blood types because phenotypically it is O ( does not have antibody A and antibody B) but cannot accept A, B, AB and O because these set of antigens are not present on the Bombay persons blood and therefore it is not recognized and it will cause an immune reaction. Get it?
Rh BLOOD GROUPSo Complex blood group with > 50 described antigens
1. Nomenclature Systema. Fisher Race (English) – used by the British
Has 5 major antigens (D, C, E, c and e) The one used in the laboratory
Chromosome Antigen antibodyClosely
linked genesD D Anti DC C Anti Ce e Anti e
b. Weiner (American) Has 5 major antigens (Rho, rh’, rh’’, hr’,hr’’)
Chromosome Antigen Blood Factors Antibody
From a single gene R1 Rh1 Rho Anti Rhorh’ anti rh’hr’’ anti hr’’
2. Rh Antigens lacks corresponding naturally occurring antibodies produce antibodies only after exposure when Rh antibodies are present they are the result of sensitization caused by
previous transfusion or pregnancy
Fisher Race WeinerD RhoC rh’E rh’’c hr’e hr’’
These are the counterparts for the American and British version
3. Rh Antibodies Formation of antibodies may be secondary to transfusion or pregnancy Anti –D (Rho), anti – C (rh’), anti – E (rh’’), anti – c (hr’), and anti – e (hr’’) have
all been known to cause hemolytic transfusion reaction and hemolytic disease of the newborn.
Warm reacting, exposure-requiring IgG antibodies that are clinically significant Infants < 4 months usually do not form new antibodies against any incompatible
red cell antigens. (immature pa ung immune system nila)
4. Rh Blood Group Testing Testing for D (Rho) antigen is the most common Rh test performed (because it is
the most immunogenic) Rh – positive also means D positive D antigens are potent immunogens. (That’s why of D – negative patients, 80%
will develop an anti D when transfused with a single unit of D positive blood).
5. Weak D Phenotype (D’’) Weakly expressed D antigens that require more sensitive testing to detect it All apparently D negative blood donors must have a weak D test to avoid false
classification
When you have determined that a patient has a weak D phenotype, you label them as D positive this is because they still have the antigen its just that the antigen is weak, but the patient can still develop antibodies against the D antigen
OTHER BLOOD GROUPS SYSTEM1. Kell (K, k, kx)2. Duffy (Fy)3. MNSs4. P5. Lewis (Le)6. Lutheran (Lu)
o All of these may cause transfusion reactions are hemolytic disease of the newborn.o May interfere with cross matchingo For medico legal parenthood problems
TRANSFUSION RELATED TESTINGo Used to identify clinically significant antigens on red cellso To identify plasma antibodies to red cellso To detect antibodies and complement bound to red cellso IgM and IgG antibodies comprise 80% of the circulating antibodies and are the most
significant antibodies for transfusions related testing (because they can cause intra and extravascular hemolysis)
o To detect antibodies particularly IgG or complement bound to RBC, anti human globulin reagent (Coomb’s Reagent ) can be added
o Agglutination (clumping) of RBC’s is the end result of testing – indicating a positive reaction
COMMON TEST USED IN IMMUNOHEMATOLOGYo Antiglobulin (Coomb’s) Test
Remains the most important single test in antibody detection Principle: Red Blood Cells sensitized by IgG or complement can be made to
agglutinate by adding antihuman globulin 2 Types:
1. Direct Coomb’s Test (DAT – direct antibody test) Detects RBC’s that have already been sensitized with IgG Detects in vivo antibody coating (sensitization) of red cells Sample: Patients Red Cells Useful in
Detection of hemolytic disease of the newborn ( using infants red cells) Investigation of transfusion reactions Detection of autoimmune hemolytic anemia (AIHA) Detection of red cells sensitization by certain drugs (penicillin,
cephalothin, alpha methyldopa)
Patient’s red cells + Coombs Reagent. If you have antibodies coating the red cells you expect to see agglutination
2. Indirect Coombs Test (IAT – indirect antibody test) Detects antibodies to RBC antigens present in the patients serum Detects in vitro red cell sensitization if red cells contain antigen corresponding
to serum antibody Sample: Patients Serum Useful in
Detection and identification of unexpected antibodies Compatibility testing (cross matching) Red cell antigen phenotyping Investigation of transfusion reactions Detecting Du antigen (weak D phenotype)
Procedure Step 1: patients serum (with unknown Ab) + RBC with unknown (Ag) Step 2: product of step 1 + Coombs Reagent
In step 1: if the serum contains antibodies against antigens on the red cells, the antibodies will adhere to the antigen on the red cell.
In step 2: when you add the Coomb’s Reagent, if there are antibodies attached to the antigens on the red cells, there will also be agglutinations
o RBC Typing1. Forward Typing2. Reverse Typing3. D antigen
o Cross Matching Absence of agglutination or hemolysis is essential to the safety of blood
transfusion You do cross matching to check if your sample are compatible Uses
To detect antibodies to the donor or recipient To detect ABO typing discrepancies
Types:1. Major Cross match
Test’s patient’s (recipients) serum + donor cells Detects antibodies in the patients serum that may destroy transfused
donor RBCs Functions to determine the ABO compatibility of the donor cells Concept is like the indirect Coomb’s test
2. Minor Cross match Uses recipients red cells + donor serum Detects antibodies in the donor serum which may react with antigen in
the recipient No longer requires as part of the cross match procedure Concept is like the directs Coomb’s test
3 phases when performing a cross match
1. Immediate Spin in saline at room temperature
Patient’s serum + RBC will be mixed and centrifuged
Examine for hemolysis (red supernatant) or agglutinationIf there is agglutination, then it is positive on immediate spin phase
2. Incubation at 37 o C with enhancement medium
Patients Serum + donor RBC + enhancing medium (ex. Low ionic strength solution – LISS, polyethylene glycol – PEG or albumin)
Incubate at 37oC and centrifuge
Examine for hemolysis (red supernatant) or agglutination
3. Antiglobulin Phase after washing incubated cells with salineo After 37oC reading, wash RBCs with salineo Add AHG (Coomb’s Reagent) mix then centrifugeo Examine for hemolysis or agglutination
*** NOTE: all 3 phases must be negative for hemolysis if there is no hemolysis in all 3 phases then you’re ready for transfusion
Effects of Temperature on Antibodies IgM antibodies are usually cold antibodies and are often detected in the
immediate spin phase of testing ( so if you have + immediate spin phase, the antibodies are most likely IgM or cold antibodies)
IgG antibodies usually react at 37oC and are referred as warm antibodies and are often detected in the antihuman globulin phase of testing ( so if you have a + result on that phase the antibodies are most likely IgG or Warm antibodies)
o Antibody Screening Used to demonstrate unexpected antibodies in the serum of the recipient that
may destroy donor RBCs that were thought to be compatible on the basis of the Rh and ABO typing
Has replaced minor cross matching** minsan kahit same blood type there is still reaction so don’t give blood.
o Pre Transfusion/ Compatibility Testing You are testing the blood unit from the donor, if it is compatible with the
recipients blood1. Review recipients blood bank history
a. Check for ABO discrepancies or crossmatching problems that have been demonstrated in previous transfusion
2. ABO and Rh typing of recipient and donora. Should be compatible
3. Antibody screening of recipient and donor serum4. Major crossmatching
HEMOLYTIC DISEASE OF THE NEWBORN
o Also referred to as erythroblastosis fetalis or fetal hydropso Occurs when the mother is alloimmunized to antigens found on the RBC of the fetuso End result: destruction of fetal RBCs by mothers IgG antibodies
A. HDN due to Rh incompatibilityo Set up: Rh (-)mother and Rh (+) babyo Once Rh (-) person is exposed to Rh (+) blood he will develop reaction after 2-4 weekso Mother develops antibody against the Rh (+) blood coming from the babyo First baby is not affected: HDN occurs during subsequent pregnancies (because Rh
antibodies are exposure requiring) o May be prevented by giving anti Rh to Rh (-) mothers in the ante natal (28weeks) and
immediate postnatal period (within 72 hours after delivery) to neutralize the Rh antigens transfused into the mother
o On first exposure the mother develops antibodies against the Rh + blood of the babyo On subsequent exposure since the mom already has the antibodies it will react to the
baby’s Rh + blood cells causing hemolysis. This will destroy the fetal RBCs
HEMOLYSIS
ANEMIA HEMOGLOBIN DEGRADATION
EXTRAMEDULLARY HYPOXIC INJURY TO LIVER INCREASE BILIRUBIN AND HEART
HEPATOSPLENOMEGALY HYDROPS JAUNDICE KERNICTERUS (Anasarca of baby) (Deposition in tissue) (Deposition in
Brain)
PHYSIOLOGY OF HDN
o If hemolysis is not prevented it will lead to anemia and hemoglobin degradationo There is extramedullary hematopoiesis, so there will be an increase in RBC production in
organs like the spleen and liver aside from the bone marrow, resulting to hepatosplenomegaly
o Due to hypoxic injury to the liver, there will be decreased albumin. Since albumin controls oncotic pressure it will result to hydrops or generalized edema
o There will also be increase in bilirubin , primarily conjugated, due to the breakdown of hemoglobin leading to the pathological condition of jaundice and kernicterus
o Since bilirubin can cross the blood brain barrier it can be deposited in the brain causing kernicterus
Factors affecting maternal response to Rh + fetal RBCs:o Concurrent ABO incompatibilityo Dose of immunizing antigeno Isotype of antibody (IgM vs IgG)
B: HDN DUE TO ABO INCOMPATIBILITYo Set up : type O mother + type A or B babyo ABO incompatibility occurs in 20-25% of pregnancieso Hemolytic disease occurs only in 10% o Treatment warranted in 1 out of 200 caseso Most anti A and anti B are IgM (do not cross the placenta so you don’t have massive
destruction of your fetal RBCso A and B antigens are poorly expressed in neonatal RBCs