Chapter 10: Serology Concepts

10.1: Serological Reagents

Immunogens and Antigens

• Immunogen: A foreign substance that is capable of eliciting antibody formation when introduced into a host.
• Natural immunogens are usually macromolecules such as proteins and polysaccharides.
• Epitope: Also known as determinant site; the molecular structure of an immunogen, usually a small portion recognized by an antibody.
• Multivalent: Multiple epitope in an immunogen.
• Antigen: A foreign substance that is capable of reacting with an antibody.   * Hapten: An example of a substance that is antigenic but not immunogenic. They are chemical compounds that are too small to elicit antibody production when they are introduced to a host animal.

Antibodies

• Antibodies: Also known as immunoglobulins, are capable of binding specifically to antigens and are designated with an Ig prefix.
• Isotypes: The immunoglobulins that differ based on the molecular variations in the constant domains of the heavy and light chains.
• The five major classes of immunoglobulins are designated: IgG, IgA, IgM, IgD, and IgE.   * IgD, IgE, and IgG are usually monomers.   * IgM can be a membrane-bound monomer or a cross-linked pentamer.   * IgA can be a monomer, dimer, or trimer.
• Further exposure to the immunogen can elicit a secondary response, producing IgG, IgA, IgE, and IgD immunoglobulins.   * IgG is the most abundant immunoglobulin in serum.
• Immunoglobulins are composed of four polypeptide chains: two heavy (H) chains and two light (L) chains.   * The H chain can be divided into fragment antigen-binding (Fab) and fragment crystallizable (Fc) fragments.   * The L chain consists of a Fab fragment only.
• A typical antibody has two identical antigen-binding sites and is thus considered bivalent.
• At the amino acid sequence level, both H and L chains have variable and constant domains.
• The variable domains are located at the N-terminal ends of the immunoglobulins.
• Additionally, three small hypervariable regions are located within the variable domain of each chain.

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Polyclonal Antibodies

• To produce an antibody, an immunogen is usually introduced into a host animal.
• A multivalent immunogen is capable of eliciting a mixture of antibodies with diverse specificities for the immunogen.
• As a result, a polyclonal antibody is produced by different B lymphocyte clones in response to the different epitopes of the immunogen.
• Humoral Antibodies: Circulating immunoglobulins.
• The blood from an immune host is drawn and allowed to clot, resulting in the formation of a solid consisting largely of blood cells and a liquid portion known as serum containing antibodies.
• Polyclonal Antiserum: Preparation of humoral antibodies.

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Monoclonal Antibodies

• To produce a monoclonal antibody, spleen cells are harvested from a host animal, such as a mouse, inoculated with an immunogen.
• Next, the plasma cells of the spleen, which produce antibodies, are fused with myeloma cells.
• The fused cells, called hybridoma cells, are immortal in cell cultures.
• Pools of hybridoma cells are diluted into single clones and are allowed to proliferate. The clones are then screened for the specific antibody of interest.
• Monoclonal antibodies have been utilized in many serological assays. However, it react with only a single epitope of a multivalent antigen and, therefore, cannot form cross-linked networks in precipitation assays.

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Antiglobulins

• If a purified foreign immunoglobulin or a fragment of a foreign immunoglobulin is introduced into a host, the antibodies produced are known as antiglobulins.
• Antiglobulins that are specific to a particular isotype can be produced in laboratories.
• It is possible to produce nonspecific antiglobulins, which recognize an epitope that is common to all isotypes of an immunoglobulin class.
• They are important reagents in many serological tests.

10.2: Strength of Antigen-Antibody Binding

• The binding of an antigen to its specific antibody is mediated by the interaction between the epitope of an antigen and the binding site of its antibody.
• Noncovalent bonds can be formed during antigen–antibody binding.
• Affinity: The energy of the interaction of a single epitope on an antigen and a single binding site on a corresponding antibody.   * Cross-reaction: Antibodies bind with a lower strength to antigens that are structurally similar to the immunogen.
• Avidity: The overall strength of the binding of an antibody and an antigen.   * It reflects the combined synergistic strength of the binding of all the binding sites of antigens and antibodies rather than the sum of individual affinities.   * It also reflects the overall stability of an antigen–antibody complex that is essential for many serological assays.

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10.3: Antigen-Antibody Binding Reactions

Primary Reactions

• It is the binding of a single epitope of an antigen (Ag) and a single binding site of an antibody (Ab) to form an antigen–antibody complex.

Secondary Reactions

• Precipitation   * If a soluble antigen is mixed and incubated with its antibody, the antigen–antibody complexes can form cross-linked complexes at the optimal ratio of antigen-to-antibody concentration.   * Precipitins: Antibodies that produce such precipitation.   * If an increasing amount of soluble antigen is mixed with a constant amount of antibody, the amount of precipitate formed can be plotted.   * Precipitin Curve: Illustrates the results observed when antigens and antibodies are mixed in various concentration ratios. It has three zones:     * Prozone: Here the ratio of antigen–antibody concentration is low.     * The Zone of Equivalence: As the concentrations of antigen increase, the amount of precipitate increases until it reaches a maximum.     * Post zone: Here the ratio of antigen–antibody concentrations is high or in excess.

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• Agglutination   * If the antigens are located on the surfaces of cells or carriers antibodies can bind to the surface antigens and can form cross-links among cells or carriers, causing them to aggregate.   * If the antigen is located on an erythrocyte, the agglutination reaction is designated hemagglutination.   * Initial Binding: The first step of the reaction involves antigen–antibody binding at a single epitope on the cell surface.   * Lattice Formation: The second step involves the formation of a cross-linked network resulting in visible aggregates that constitute a lattice.   * Agglutinins: Antibodies that produce agglutination.   * Complete Antibody: Capable of carrying out both primary and secondary interactions that result in agglutination.   * Incomplete Antibody: An antibody that can carry out initial binding but fails to form agglutination.

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