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CLLS 3311 Advanced Clinical Immunohematology. Antigen and Antibody Reactions. Demonstration of red cell antigen-antibody reactions is key to immunohematology. AABB Technical Manual.

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clls 3311 advanced clinical immunohematology

CLLS 3311Advanced Clinical Immunohematology

Antigen and Antibody

Reactions

slide2
Demonstration of red cell antigen-antibody reactions is key to immunohematology.

AABB Technical Manual

slide3
Red cell antigen-antibody reactions that we study and perform include Patient ABO grouping, Rh typing, Antibody screens and identifications, Crossmatching, etc.
  • An awareness of how antigens and antibodies react is necessary to accurately perform the required testing including: quality control, trouble shooting, maintenance, etc.
immune response
Immune Response
  • Definition: Physiological mechanism to fight disease or clear foreign substances.
  • Primary immune response: First exposure of a foreign agent. IgM is the predominant antibody produced that attaches to and fights the foreign agent. In our case a foreign red blood cell antigen.
  • Secondary immune response: Subsequent exposure of the same foreign agent. Rapid response in which IgG is the predominant antibody produced.
antigen antibody reactions
Antigen:

Antigenicity:

Epitopes:

Substance capable of eliciting an immune response when introduced into a immunocompetent individual to whom it is foreign.

Ability of an antigen to react with the products of an immune response

Antigenic determinants - structural site where the antibody combines with the antigen.

Antigen/Antibody Reactions
characteristics of antigens
Antigenicity of an Antigen is affected by its:

Foreign:

Size:

Most common forms of Blood Group Antigens:

Size, shape, rigidity, location, number of determinants (epitopes), dose, route of entry, and genetic factors.

Normally…don’t forget autoimmune processes

>10,000 daltons

Glycoproteins: HLA

Glycolipids: ABH, Le, Ii and P antigens (Ag)

Proteins: Rh, M, N antigens

Characteristics of Antigens
characteristics of immunoglobulins antibodies
Characteristics of Immunoglobulins (Antibodies)
  • RBC Immune Vs. Non-RBC Immune
    • RBC Immune Antibody: antibody that results from exposure to foreign red cell antigen either by transfusion or pregnancy (anti-D, etc.)
    • Non-RBC Immune Antibody: antibody that is present without any evidence of exposure to foreign red cell antigen (anti-A, anti-N, etc.)
  • Clinically Significant Antibody: An antibody that decreases the red cell survival. Able to destroy red blood cells in vivo. (anti-A,B, Anti-Jka, etc.)
characteristics of igg class antibodies
Structure

Phase of Reactivity

Placenta

Complement (C’) Activation

Clinical Significance

Monomer

Warm: reacts best at 37oC

Can cross the placental barrier

Poor to good C’ activators. Two IgG required to activate C’ to completion.

Usually clinically significant RBC immune Antibody

Characteristics of IgG Class Antibodies
characteristics of igm class antibodies
Structure

Phase of reactivity

Placenta

Complement Activation

Clinical Significance

Pentamer

Cold: reacts best at 4-10oC

Cannot cross the placental barrier

GOOD (most) complement activators - one IgM can activate C’ to completion

“Usually” NOT clinically significant, Non RBC immune.

Characteristics of IgM Class Antibodies
slide10
We just stated that IgM antibodies are usually NOT clinically significant. There is a notable exception to this statement! What is it?
  • ABO antibodies are VERY CLINICALLY SIGNIFICANT.Most transfusion fatalities are the result of an ABO incompatibility.
  • Yet anti-M, anti-N, etc. are usually NOT clinically significant IgM antibodies.
slide11

IgG Antibody(Monomer Structure)

IgM Antibody(Pentamer Structure)

Images provided by textbook: Figure 14.3, page 97, Kuby

Immunology, 4th Edition, W.H. Freeman and Company

slide12

Cold reacting

  • Good complement activator
  • Pentamer
  • ABO, Ii, Lewis, MN, & P

IgM Antibody’s

  • Warm Reacting
  • Poorcomplement activators
  • Monomer
  • Rh, Kell, Kidd, Duffy, and Ss

IgG Antibody’s

separation of red blood cells
Separation of Red Blood Cells
  • In vivo red blood cells are built in such a way as to keep their distance from each other. It is a good thing. Theories include:
  • Waters of Hydration: Water bound by RBC membrane glycoproteins helps maintain the distance between rbc’s. (Water envelope)
  • Electrostatic charges: Electron cloud surrounds RBC with a net negative charge called the zeta potential.
  • To observe Ag/Ab reactions in vitro these forces need to be overcome to enable Ab’s to attach to their corresponding Ag.
in vitro in the test tube indicators of ag ab rxn s
In vitro (in the test tube) indicators of Ag/Ab Rxn’s
  • Antibody coating RBC without Agglutination
    • Sensitization: Attachment of antibody to antigen that requires antihuman globulin to detect.
  • RBC Hemolysis
    • Immune mediated lysis of red blood cells.
  • Agglutination
    • Antibody mediated clumping of red blood cells that express corresponding antigens on their surface.
antibody coating rbc membrane without agglutination
Antibody Coating RBC Membrane without Agglutination
  • Attachment of antibody to corresponding antigen on RBC membrane,ONLY.
  • This reaction is NOT SEEN at the Immediate Spin (IS), Room Temperature (RT), or 37oC (LISS) phases.
  • This reaction requires the use of an Antihuman Globulin reagent in the Direct (DAT) or Indirect Antiglobulin Tests (IAT) to observe.
hemolysis
Hemolysis
  • When antibody (IgG or IgM) has activated Complement to completion.
  • The complement (C’) cascade is the mechanism that actually destroys the red blood cell.
  • Antibody (immunoglobulin) by itself cannot tear a hole in the RBC membrane. It is the C’ that does that.
  • Seen when supernatant is CLEAR and RED.
  • Not seen at the AHG phase! Why??
agglutination reactions
Agglutination Reactions

Two Stage Process:

Stage 1

  • Sensitization: attachment of Antibody to Antigen on the RBC membrane. TM

Stage 2

  • Lattice formation: formation of bridges between the sensitized red cells to form the lattice that constitutes agglutination. TM
slide18

This represents what occurs during stage one of agglutination: Sensitization

Stage 1

Antibody molecules attach to their corresponding Antigenic site (epitope) on the red blood cell membrane. There is no visible clumping.

slide19

This represents what occurs during stage 2 of agglutination: Lattice Formation

Stage 2

Antibody molecules crosslink RBCs forming a lattice that results in visible clumping or agglutination.

stage 1 of agglutination sensitization
Stage 1 of Agglutination: Sensitization
  • Attachment of antibody to antigen
  • Attachment between Antigen and Antibody is dependent on spatial complementarity (Lock and Key concept) and on weak non-specific intermolecular forces including:
    • Electrostatic forces, Hydrogen Bonds, Hydrophobic forces, and van der Waals forces. (Does NOT involve covalent bonding.)
weak non specific intermolecular forces
Weak Non-specific Intermolecular Forces

Electrostatic forces

  • Attraction of oppositely charged or ionized molecules
  • Force of attraction is inversely proportional to square of the distance between charges: closer you get the stronger the attachment of Ag to Ab.

Hydrogen bonds

  • Weak, reversible hydrogen bridges between hydrophilic groups which are stronger at lower temperatures.
weak non specific intermolecular forces22
Weak Non-specific Intermolecular Forces

Hydrophobic forces

  • Water hating groups (valine, leucine) come into close contact and exclude water between them, resulting in lower free energy system disrupting the water envelope.
  • Disruption of water envelope is the result of hydrophobic forces: requires close proximity
weak non specific intermolecular forces23
Weak Non-specific Intermolecular Forces

van der Waals bonds

  • Temporary disruption of electrons in one molecule effectively forms a dipole which causes the formation of a dipole in another molecule, the two dipoles then exhibit an attraction for each other: Requires close proximity.
law of mass action
LAW OF MASS ACTION
  • Due to weakness of these forces Ag/Ab complexes obey the Law of Mass Action which is:

Antigen and antibody complexing is REVERSIBLE.

  • Equilibrium is the point at which the number of bonds being formed equals the number of bonds being broken.
factors affecting stage 1 of agglutination
Factors AffectingStage 1 of Agglutination

Temperature

  • Cold (4-10oC): Exothermic reactions occur when H+ bonds are made with carbohydrates at LOW temperatures.
    • ABO, P1, Lewis antibodies bond better at low temperatures due to carbohydrate nature of antigens
  • Warm (37oC): Entropy driven reactions associated with hydrophobic bonding to proteins.
    • Rh antibodies bond better at 37oC due to protein nature of Rh antigens.
factors affecting stage 1 of agglutination26
Factors AffectingStage 1 of Agglutination

pH

  • Changes in pH can affect electrostatic bonds.
  • Optimal range is physiologic pH
  • Some Ab’s like lowered pH particularly anti-M

Incubation Time

  • The time needed to reach equilibrium
  • Saline systems: 30-60 minutes at 37oC
  • Enhancement media can reduce incubation time significantly: LISS is 10-15 minutes
factors affecting stage 1 of agglutination27
Factors AffectingStage 1 of Agglutination

Ionic Strength

  • In normal saline, Na+ and Cl- ions cluster around and partially neutralize opposite charges on Ag and Ab molecules, which hinders the association of Ab with Ag.
  • If you lower the ionic strength of the test system then you increase rate of Ag-Ab association.
  • Using LISS (low ionic strength solution) decreases incubation time.
stage 2 of agglutination lattice formation
Stage 2 of Agglutination:Lattice Formation
  • Lattice formation: formation of bridges between the sensitized red cells to form the lattice that results in agglutination (clumping) of red blood cells.
slide29

Concentration of Ag and Ab also affects agglutination reactions, both the first and second stages.

factors affecting stage 2 of agglutination
Factors AffectingStage 2 of Agglutination

Size of the Immunoglobulin

  • IgG: Monomer, takes two to activate C’, etc.
  • IgM: Pentamer, takes one to activate C’, etc.

Number of binding sites

  • IgG: Two binding sites (anti-D, anti-Jka, etc.)
  • IgM: Ten binding sites (anti-A,B, anti-I, etc.)
factors affecting stage 2 of agglutination31
Factors AffectingStage 2 of Agglutination

Location and Number of Antigenic Determinants

  • A, B, M and N antigens: 600,000 to >1,000,000 antigen sites per RBC
  • Kidd: approximately 10-20,000 Ag sites/RBC

Centrifugation

  • Brings Ab’s and Ag’s into close proximity
  • Undercentrifugation: may result in false negative
  • Overcentrifugation: may result in false positive
factors affecting stage 2 of agglutination32
Factors AffectingStage 2 of Agglutination

Zeta Potential

  • Net negative charge surrounding RBC
  • Now considered a minor player

Waters of Hydration

  • Acts as an insulating bubble around RBC
  • Water molecules tightly bound to hydrophilic macromolecules on the red cell surface.
reading and interpreting ag ab reactions
Reading and Interpreting Ag/Ab Reactions

Agglutination

  • Grade reaction strength: Neg to 4+
  • Harmening Color Plate 2.

Hemolysis

  • ALWAYS observe the supernatant of the test tube after centrifugation. If the supernatant is clear and red Hemolysis is indicated. THIS IS A POSITIVE REACTION! And indicates a Nasty antibody.
reading and interpreting ag ab reactions34
Reading and Interpreting Ag/Ab Reactions

Rouleaux

  • Increased proteins can cause RBCs to clump and stack - false positive

Mixed Field Agglutination

  • Presence of two cell populations: such as Group O cells in a Group A patient. Anti-A will only agglutinate A cells resulting in a mixture of clumping cells and free cells.
potentiators
Potentiators
  • We have not covered the topic of potentiators. This is found on pages 60-62 in Harmening and is Objective #10.
  • We also did not cover Solid Phase and Gel testing techniques. This is found on page 62-63 in Harmening and is Objective #6.