Sensitization and Agglutination

Slides:



Advertisements
Similar presentations
PREPARED BY: JOSEPHINE C. MILAN, RMT, MSMT WAGGAS AHMEDELAAS; M.Sc, MLT (Revised, Feb 2014)
Advertisements

When can you use an antibody to find another antibody?
Antiglobulin Test (Coomb’s Test)
Rh Grouping.
Module One Precipitation and Agglutination Methods
© 2004 Wadsworth – Thomson Learning Immunology Tutorial Introduction & Course outline By: Moh’d J. Al Khatatneh.
Immuoagglutination test Yasser M. alatawi Pharm.D College of Pharmacy Umm Al-Qura University.
ABO & Rh Discrepancies.
Sensitization and Agglutination
Introduction to Immunoassays
ABO & Rh Discrepancies.
Immunology vs. Serology Immunology –Study of immune system Serology –Detecting/measuring elements of humoral immune system (I.e., antibodies) –Help diagnose.
Detecting Antibodies The Antibody Screen CLS 422
Drmsaiem IMMUNOGLOBULINS DR. Mohammed Saiemaldahr FACULTY OF APPLIED MEDICAL SCIENCES KAAU.
Immunology  The interaction between antigen and antibody  ag - ab reaction  Antigen-antibody reaction is characterized by following salient features.
2. Basic Immunologic Procedures
Immunologic Methods Part One Definitions Part Two Antigen-Antibody Reactions CLS 420 Clinical Immunology and Molecular Diagnostics Kathy Trudell MLS SBB(ASCP)
Antigen-Antibody Reactions. Antigen-antibody interactions:  Are reversible specific non-covalent biochemical reactions: – Hydrogen bonds (A chemical.
Immunologic Methods Part One Antigen-Antibody Reactions CLS 420 Clinical Immunology & Molecular Diagnostics.
Serology and Immunology
When can you use an antibody to find another antibody?
Antiglobulin Test.
Proteins I BCH 302 [practical].
2. Basic Immunologic Procedures Part 5 Agglutination
CLLS 3311 Advanced Clinical Immunohematology Antigen and Antibody Reactions.
Faculty of Allied Medical Science Blood Banking (MLBB 201)
Terry Kotrla, MS, MT(ASCP)BB Unit 4 Principles of Serological Testing in Immunohematology.
Human Blood Typing Lab Objective: 1. Apply blood typing method to determine the blood type for a sample of synthetic human blood 2. Describe the appearance.
Antigen and Antigenicity Antigen and Antigenicity
Compatibility Testing practical NO 4 Dr: Dalia Kamal Eldien.
Immunology Review Part Two Antibodies and Antigens.
Compatibility Testing  Compatibility testing is performed to determine if a particular unit of blood can be transfused safely into a certain patient.
Practical Blood Bank Lab 3 Rh Grouping.
Enzymes. What are enzymes? Special proteins that coordinate the cell’s activities Important: 1)All enzymes are proteins 2)All proteins are NOT enzymes.
Enzymes All enzymes are proteins. Not all proteins are enzymes. Enzymes are catalysts. A catalyst is a substance which increases the rate of chemical reaction.
Reagents and Methods for Testing in the Blood Bank
Lab 3 Practical Blood Bank. Practical Aspects of Rh Grouping Rh grouping in routine use for donors and patients involves testing for Rh (D) antigen only.
The Antiglobulin Test ( Direct & Indirect )
Agglutination 1.
Practical Blood Bank Anti-Globulin Test Direct, Indirect Lab 5.
Practical Blood Bank Lab 5.
Practical Blood Bank Anti-Globulin Test Direct, Indirect Lab 5.
Blood Groups.
Blood Grouping Or Blood Types
The Antiglobulin Test (Direct & Indirect )
COOMB’S TECHNIQUES MLS 522.
Agglutination test It is one of important laboratory method to detect antigen antibody reaction. It provides flexible and useful method for semi quantitating.
Coombs test practical(3)
MLAB Hematology Keri Brophy-Martinez
Qualitative tests of protein
Methods for Ag-Ab detection
ANTIGEN-ANTIBODY REACTIONS
ANTIGEN-ANTIBODY REACTIONS
b. Explain how enzymes function as catalysts.
Detection and Identification of alloantibodies to Red Cell Antigens
Introduction to Lab Ex. 23: Hemagglutination
Blood group and cross matching
Blood Typing Lab.
Antigen-Antibody reactions
Cross-matching.
19-3 Blood Types Surface antigens
Sensitization and Agglutination
Practical Blood Bank Lab 1 ABO Grouping.
Practical Blood Bank Antibody Titration.
Practical Blood Bank Antibody Titration.
Lecture 14 Antibody-Antigen Reactions
Practical Blood Bank - Lab 2 - Rh Grouping Lab 2.
Enzymes.
Experimental Systems and Methods
Antibody/ Antigen Reactions.
Presentation transcript:

Sensitization and Agglutination

Antigen-Antibody reaction Red cell Ag-Ab reaction can detected by a number of techniques Most frequently used Hemolysis Occurs if the entire complement sequence is activated following Ag-Ab interaction Frequently stops at C3 – no lysis Agglutination Used as indicator of Ag-Ab reaction

Agglutination Reactions Two Stage Process: Stage 1 Sensitization: attachment of Antibody to Antigen on the RBC membrane. Stage 2 agglutination: formation of bridges between the sensitized red cells to form the lattice that constitutes agglutination.

Stage 1: Sensitization This represents what occurs during stage one of agglutination. Antibody molecules attach to their corresponding antigenic site (epitope) on the red blood cell membrane. There is no visible clumping. Red cells must be close enough for the Fab portion of Ab to bind and make bridges between cells

Stage 2: agglutination Antibody molecules crosslink RBCs forming a lattice that results in visible clumping or agglutination.

Sensitization by IgG does not result in agglutination IgG is too small to span the distance between two red cells IgM can easily cause agglutination For agglutination to occur, the repulsive forces keeping red cells apart must be overcome

The Zeta Potential The electric repulsion between cells This explains why cells do not agglutinate Red cells have negative charge due to sialic acid molecules When red cells are in solution containing free ions: Cations are attracted to the –vely charged red cells This forms a repelling cloud around the cell

The Zeta Potential can be varied by altering the charge on red cells This can affect both sensitization and agglutination Reducing the cloud density allow Abs to approach the cells, sensitize and then agglutinate them

Factors affecting the Zeta Potential Removal of sialic acids by enzymes Introduction of bipolar Albumin Albumin dissipates some of the +ve charges around cells, reducing zeta potential Albumin

Increase the ionic strength of the medium Increasing conc. of cations in medium cause Increase in the density of ions around the red cell which cause Size of cloud of cations is decreased Zeta potential decreases Red cell approach each other easily Agglutination is facilitated

Decreasing the ionic strength of medium by using low ionic strength saline (LISS) Decreasing conc. of cations in medium Leads to decrease in density of ions around red cells This increases sensitization But decreases agglutination

Factors affecting Red Cell Sensitization 1- Ratio of Ab to Ag Sensitization occurs easily when at higher conc. of Ab This can be done by increasing conc. of serum containing the Ab to conc. of cells

2- The pH of reaction mixture At a pH below the pI, Abs have +ve charges This makes it easier for the Ab to bind to the –vely charged red cells Optional pH for sensitization is 6.5 to 7.5 (Ab +vely charged) pH 8 pH 7

Factors affecting Red Cell Sensitization 3- Temperature Ab -Ag reactions are exothermic Therefore, Abs bind to a greater degree at lower temperature But at lower temperatures, rate of reaction is reduced To speed up reaction, tests are done at 37oC

Temperature can also affect Ag accessibility on red cells Some IgM Abs bind best at 4oC (cold Abs) Temperature can make conformational changes in the Ag More Ag sites are exposed as the temperature is lowered allowing increased binding of Ab Most naturally occurring cold Abs are of no clinical significance Compatibility testing is done at 37oC 37oC 4oC

4- Ionic strength of the medium When RBCs are suspended in LISS the cloud of ions around the cell is less dense than in isotonic saline Reduced conc. of cations surrounding RBCs allow +vely charged Abs easier to access Ag sites Rate of sensitization increases

Factors Influencing RBCs Agglutination Agglutination occurs when RBCs are close enough allowing the Ab to bridge adjacent cells 1- Ionic strength of Medium Rate of sensitization increases in LISS Agglutination impaired because of increase in zeta potential

2- Presence of Albumin in medium 3- Enzyme treatment of red cells Remove –vely charged sialic acid therefore reduce the zeta potential This make cells come closer & agglutinate But, certain Ags can be destroyed by enzymes (M, N, S, Fya, Fyb) 4- Temperature

5- Antigen Density The greater the number of Ags on red cell, the greater the sensitization Binding of +vely charged Abs to red cells lower the zeta potential And therefore enhances agglutination Increased Ag density also increases chance of bridging

6- Ag Clustering and Mobility Clustering facilitates agglutination by increasing likelihood of Ab binding at that site Cluster of some Ags like (Rh) can occur after enzyme treatment of cells Clustering of Ags

7- Antibody Characteristics Ability of Ab to agglutinate cells depend on the Ig class IgM has a wider span than IgG, and therefore more effective agglutination IgG can be chemically modified to increase its span 250-300 Ao 300 Ao 150 Ao IgM Ag IgG IgG

Summary Sens. Agg. Removal of RBCs sialic acid by enzymes Introduction of bipolar albumin ___ Increasing ionic strength of the medium decreasing ionic strength of the medium