part 2 terry kotrla, ms, mt(ascp)bb unit 3 immunology and complement
TRANSCRIPT
Part 2Terry Kotrla, MS, MT(ASCP)BB
Unit 3 Immunology and Complement
Overview of Immunity
ImmunoglobulinsHumans produce specific proteins or
immunoglobulins which can be differentiated on the basis of:SizeBiologic functionBiochemical propertiesSerological activity
Basic Structure of ImmunoglobulinsAn antibody digested by papain yields three fragments
Two Fab which consist of antigen binding site, can sensitize.One Fc, whic is the region that determines biological properties
of the Ig.
Basic Structure of ImmunoglobulinsAn antibody digested by pepsin yields two fragments:
One Fab2 which consist of 2 antigen binding sites joined together, able to agglutinate.
One Fc,the region that determines biological properties of the Ig.
Immunoglobulin Classes
IgM Class
IgM Largest of all the antibody molecules, consists of five of the
basic units (pentamer) mu heavy chains joined together by a structure known as J-chain.
Accounts for about 5-10% of the immunoglobulin pool. Restricted almost entirely to the intravascular space due to
its large size. Fixes complement, much more efficient than IgG in the
activation of complement and agglutination. First antibody to be produced and is of greatest
importance in the first few days of a primary immune response to an infecting organism.
Does not cross the placenta. Many blood group antibodies that are capable of
agglutinating antigen positive RBCs suspended in saline in tests performed at 22 C are IgM causing visible agglutination, ie, ABO antibodies.
IgM antibodies are potent agglutinators that activate complement very efficiently.
IgG Most abundant of the immunoglobulins in the plasma One basic structural unit, i.e. Y-shaped molecule having 2 light chains and 2
Gamma heavy chains. Produced in response to a wide variety of antigens, including bacteria,
viruses and RBC and WBC allo-antigens. Coats organisms to enhance phagocytosis by neutrophils and macrophages. Through its ability to cross the placenta, maternal IgG provides the
major line of defense against infection for the first few weeks of a baby's life.
It is the predominant antibody produced in the secondary response. The serologic behavior and characteristics of IgG antibodies make them one
of the most clinically significant in blood banking. Most blood group antigens capable of eliciting an immune response
result in the production of IgG antibodies. These antibodies are detected by serologic test procedures based on their behavior
characteristics, such as reactivity at 37 C, complement activation, indirect agglutination and hemolysis.
Much of routine blood banking involves serologic test procedures designed to detect and identify IgG antibodies.
Four subclasses which differ in their heavy chain composition and in some of their characteristics such as biologic activities. IgG1, IgG2, IgG3 and IgG4.
IgA Found in saliva, tears, colostrum breast milk and in nasal, bronchial
and intestinal secretions. IgA present in large quantities in colostrum and breast milk, is transferred
across the gut mucosa in the neonate and plays an important role in protecting the neonate from infection.
Produced in high concentrations by lymphoid tissues lining the gastrointestinal, respiratory and genitourinary tracts.
Plays an important role in protection against respiratory, urinary tract and bowel infections and preventing absorption of potential antigens in the food we eat.
Represents 10 to 15% of the total circulatory immunoglobulin pool. In plasma IgA may exist as a single basic structural unit or as two or three
basic units joined together. The IgA present in secretions exists as two basic units (a dimer) attached to
another molecule know as secretory component. 1) This substance is produced by the cells lining the mucous membranes. 2) It is thought to protect the IgA in secretions from destruction by digestive
enzymes. IgA does not cross the placenta and does not bind complement. For blood banking, an IgA deficient individual may produce anti-IgA which can
cause severe, life-threatening anaphylactic reactions during transfusion. Once identified these individuals must be transfused with blood and components which lack IgA.
IgA StructureThe dimeric IgA molecule.
1 H-chain, 2 L-chain, 3 J-chain, 4 secretory component
IgE
Trace plasma protein (only about 0.004%) in the plasma of non-parasitized individuals.
Major importance mediating some types of allergic reactions and is generally responsible for an individual's immunity to invading parasites.
Fc region binds strongly to a receptor on mast cells and basophils and, when antigen is bound it causes the basophil (or mast cell) to release histamines and heparin from these cells, resulting in allergic symptoms.
Clinical effects of IgE mediated reactions include increased vascular permeability, skin rashes, respiratory tract constriction (wheezing), and increased secretions from epithelium (watery eyes, runny nose).
Not much else is known about its biologic role. IgE does not fix complement and does not cross the
placenta. No blood group antibodies have been reported to belong to
this class.
IgE
IgDAccounts for less than 1% of the total
immunoglobulin pool.This is primarily a cell membrane
immunoglobulin found on the surface of B lymphocytes.
IgD does not fix complement and does not cross the placenta.
Little is known about the function of this class of antibody.
No blood group antibodies have been reported to belong to this class.
Clinical Significance of Blood Group AntibodiesA blood group antibody is considered
clinically significant if it has been associated with the following: Has caused hemolytic transfusion
reactions (destruction of transfused red cells) or
Implicated in Hemolytic disease of the fetus and newborn (HDFN) (destruction of fetal cells)
Blood Group AntigensAt least 30 blood groups with over 600
antigens.Individuals may produce antibodies to
blood group antigens they do not possess when exposed to blood through transfusion or pregnancy.
Second exposure may result in immune hemolysis of red blood cells.
Transfusion ReactionTerm used to describe an unfavorable
response by a recipient to the infusion of blood or blood products and include the following:In-vivo hemolysis (either immediate or delayed)Decreased survival of transfused cellsAnaphylaxisGraft-versus-host diseasePost-transfusion purpuraAlloimmunizationSepsis due to bacterial contaminated
components,Disease transmission.
Will be discussed in detail later
SeverityDepends on a number of factors, including the
characteristics of the antibody class involved.Antibodies to the ABO system antigens are predominantly
IgM, cause complement activation and intravascular hemolysis.
Other RBC antigens induce formation of IgG class antibodies which may cause accelerated RBC destruction extravascularly.
Symptoms of response to incompatible ABO transfusion may include fever, low back pain, nausea and vomiting, circulatory shock, anemia, jaundice, and kidney failure which may ultimately result in death.
Primary immune response may be asymptomatic due to slow destruction of RBCs.
Secondary response symptomatic due to memory B cells and rapid antibody production.
Antibody Mediated HemolysisHemolysis can be intravascular or extravascular. INTRAVASCULAR: Antibodies destroy the red cells IN THE
CIRCULATION. Due to of IgM and activation of complement with destruction of RBCs, VERY BAD, will see RED serum/plasma.
EXTRAVASCULAR: hemolysis is due to RBCs being coated with IgG and destroyed OUTSIDE the circulation in the RES system. If it occurs slowly may not be detectable.
Transfusion ReactionsScreening donor blood for disease markers
significantly decreased transfusion transmitted diseases.
Reactions to donor WBCs and platelets relatively common but usually not severe.
ABO reactions severe and PREVENTABLE by following protocols.
“Other” blood group antibodies may or may not be detectable.
It is YOUR duty to provide serologically compatible blood and blood components for transfusion.
ComplementSpend quality time on your notes from
Serology.
ComplementIntegral part of the immune system.Three pathways
ClassicalAlternative or properdinLectin
Three primary functions:Lysis of antibody coated cells, such as bacteria and
RBCs.Mediation of opsonization, preparation of foreign
cells for phagocytosis.Generation of peptide fragments that regulate
features of the inflammatory and immune response.
Importance in Blood BankingTwo major areas:
Some antigen-antibody complexes cause sufficient quantities of complement to be bound to RBCs to complete activation cycle, causing hemolysis.
Antigen-antibody complexes initiate complement binding in such a way that allows demonstration of the existence of such complexes by the use of serologic techniques.
Fresh serum necessary to detect complement mediated in-vitro reactions.
The Classic PathwayEleven components involved, numbered C1
to C9.Complement cascade requires presence of
cations, both calcium and magnesium.Activation of the classic pathway almost
always initiated by immunoglobulin.Requires only 1 molecule of IgM (has 5 Fc).Requires 2 molecules of IgG (has 1 Fc).
Two IgG, One IgM
The Classic PathwayRecognition Phase - Recognition unit:
C1q,C1r,C1s.Activation Phase -Activation Unit:
C4b,C2b,C3b,C5bAttack Phase – Attack Unit:
C5b,C6,C7,C8 and C9 Classic pathway:
C1,C4,C2,C3,C5,C6,C7,C8,C9Must go to completion for hemolysis
to occur. The next two slides are to assist you in your studies.
Classical Pathway
Alternative (Properdin) Pathway
Proteins in the alternative pathway perform activities similar to those in the classic pathway but are usually non-antibody triggered.
Any one of a variety of substances can initiate complement activation including:bacterial polysaccharides and lipopolysaccharides,endotoxins,cobra venom,trypsin like enzymes,aggregates of IgA and IgG4 that do not activate C1.
C1, C4 and C2 do not participate. Alternative pathway: C3,C5,C6,C7,C8,C9
Alternative Pathway
Lectin Pathway Activation begins when mannan-binding protein (MBP) binds to the
mannose groups of microbial carbohydrates. Two more lectin pathway proteins called MASP1 and MASP2
(equivalent to C1r and C1s of the classical pathway) now bind to the MBP.
This forms an enzyme similar to C1 of the classical complement pathway that is able to cleave C4 and C2 to form C4bC2a, the C3 convertase capable of enzymatically splitting hundreds of molecules of C3 into C3a and C3b.
The beneficial results are the same as in the classical complement pathway above: trigger inflammation (C5a>C3a>c4a); chemotactically attract phagocytes to the infection site (C5a); promote the attachment of antigens to phagocytes via enhanced
attachment or opsonization (C3b>C4b); serves as a second signal for the activation of naive B-lymphocytes
(C3d); cause lysis of gram-negative bacteria and human cells displaying foreign
epitopes (MAC); and remove harmful immune complexes from the body (C3b>C4b).
Lectin Pathway - FYI Overview of the lectin complement pathway. In humans, MBL
and ficolin that are lectins form complexes with MASPs (MASP-1,MASP-2 and MASP-3) and sMAP. Note that MBL consists of several sizes of oligomers and that the composition of MASPs and sMAP of each MBL oligomer has not been fully elucidated. Once the complexes bind to carbohydrates on the surfaces of microbes, activated MASPs cleave C4, C2 and C3.
Activation of Pathways
Order of Activation of 3 Pathways
Regulation of Complement
Activation of complement cascade results in complex series of molecular event with potent biologic consequences.
Modulating mechanisms are necessary to regulate complement activation and control production of biologically active split products.
First mechanism is spontaneous decay of activated components.
Second mechanism involves specific control proteins that modulate the activity of certain complement components at critical activation steps.C1 inhibitor blocks activities of C1r and C1s.Other factors inhibit activation of other complement
components. A number of proteins act to control the membrane attack
unit. Bottom line, gotta turn it off!
Referenceshttp://en.wikipedia.org/wiki/Antibody Complement: http://
www.medicine.uiowa.edu/martinlab/complement.html