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Table titled: The five immunoglobulin (Ig) classes. IgG monomer is a Y shaped molecule; the heavy chain is gamma, it has 2 antigen binding sites and a molecular weight of 150,000 daltons. It makes up 80% of the total antibodies in the serum. It crosses the placenta and fixes compliments and the Fc binds to phagocytes. It’s functions are: Neutralization, agglutination, complement activation, opsonization, and antibody-dependent cell-mediated cytotoxicity. IgM pentamer is 5 Y’s bound at their bases; the heavy chain is mu, it has 10 antigen binding sites and a molecular weight of 900,000 daltons. It makes up 6% of the total antibodies in the serum. It does not cross the placenta but does fix compliments and the Fc does not bind to a particular cell type. It’s functions are: Neutralization, agglutination, and complement activation. The monomer form serves as the B cell receptor. IgA dimer is 2 Y’s bound at their bases; the heavy chain is alpha, it has 4 antigen binding sites and a molecular weight of 385,000 daltons. It makes up 13% of the total antibodies in the serum. It does not cross the placenta nor fix compliments and the Fc does not bind to a particular cell type. It’s functions are: Neutralization and trapping of pathogens in mucus. IgD monomer is 1 Y; the heavy chain is delta, it has 2 antigen binding sites and a molecular weight of 180,000 daltons. It makes up <1% of the total antibodies in the serum. It does not cross the placenta nor fix compliments and the Fc does not bind to a particular cell type. It’s functions are: B cell receptors. IgE monomer is 1 Y; the heavy chain is epsilon, it has 2 antigen binding sites and a molecular weight of 200,000 daltons. It makes up <1% of the total antibodies in the serum. It does not cross the placenta nor fix compliments. The Fc binds to mast cells and basophils. It’s functions are: Activation of basophils and mast cells against parasites and allergens.
  • What part of an antibody molecule determines its class?
  • What class of antibody is involved in protection against parasites?
  • Describe the difference in structure between IgM and IgG.

Antigen-antibody interactions

Different classes of antibody play important roles in the body’s defense against pathogens. These functions include neutralization of pathogens, opsonization for phagocytosis, agglutination, complement activation, and antibody-dependent cell-mediated cytotoxicity. For most of these functions, antibodies also provide an important link between adaptive specific immunity and innate nonspecific immunity.

Neutralization involves the binding of certain antibodies (IgG, IgM, or IgA) to epitopes on the surface of pathogens or toxins, preventing their attachment to cells. For example, Secretory IgA can bind to specific pathogens and block initial attachment to intestinal mucosal cells. Similarly, specific antibodies can bind to certain toxins, blocking them from attaching to target cells and thus neutralizing their toxic effects. Viruses can be neutralized and prevented from infecting a cell by the same mechanism ( [link] ).

As described in Chemical Defenses , opsonization is the coating of a pathogen with molecules, such as complement factors, C-reactive protein , and serum amyloid A , to assist in phagocyte binding to facilitate phagocytosis . IgG antibodies also serve as excellent opsonins, binding their Fab sites to specific epitopes on the surface of pathogens. Phagocytic cells such as macrophages , dendritic cells , and neutrophils have receptors on their surfaces that recognize and bind to the Fc portion of the IgG molecules; thus, IgG helps such phagocytes attach to and engulf the pathogens they have bound ( [link] ).

Agglutination or aggregation involves the cross-linking of pathogens by antibodies to create large aggregates ( [link] ). IgG has two Fab antigen-binding sites , which can bind to two separate pathogen cells, clumping them together. When multiple IgG antibodies are involved, large aggregates can develop; these aggregates are easier for the kidneys and spleen to filter from the blood and easier for phagocytes to ingest for destruction. The pentameric structure of IgM provides ten Fab binding sites per molecule, making it the most efficient antibody for agglutination.

A virus is drawn as a circle with knobs on it. Antigens bind to the knobs, thereby surrounding the virus. Next image shows antibody binding to diphtheria toxin. Next image shows antibody binding to a bacterial cell.
Neutralization involves the binding of specific antibodies to antigens found on bacteria, viruses, and toxins, preventing them from attaching to target cells.
A macrophage with projections that are engulfing a pathogen with antibodies attached to it.
Antibodies serve as opsonins and inhibit infection by tagging pathogens for destruction by macrophages, dendritic cells, and neutrophils. These phagocytic cells use Fc receptors to bind to IgG-opsonized pathogens and initiate the first step of attachment before phagocytosis.
Bacterial cells with various epitopes (shown as different shapes). IgM antibodies are bound to multiple bacteria; all attached to the same shaped epitope which matches their binding sites.
Antibodies, especially IgM antibodies, agglutinate bacteria by binding to epitopes on two or more bacteria simultaneously. When multiple pathogens and antibodies are present, aggregates form when the binding sites of antibodies bind with separate pathogens.

Another important function of antibodies is activation of the complement cascade . As discussed in the previous chapter, the complement system is an important component of the innate defenses, promoting the inflammatory response, recruiting phagocytes to site of infection, enhancing phagocytosis by opsonization, and killing gram-negative bacterial pathogens with the membrane attack complex (MAC) . Complement activation can occur through three different pathways (see [link] ), but the most efficient is the classical pathway , which requires the initial binding of IgG or IgM antibodies to the surface of a pathogen cell, allowing for recruitment and activation of the C1 complex .

Yet another important function of antibodies is antibody-dependent cell-mediated cytotoxicity (ADCC) , which enhances killing of pathogens that are too large to be phagocytosed. This process is best characterized for natural killer cells ( NK cells ), as shown in [link] , but it can also involve macrophages and eosinophils . ADCC occurs when the Fab region of an IgG antibody binds to a large pathogen; Fc receptors on effector cells (e.g., NK cells) then bind to the Fc region of the antibody, bringing them into close proximity with the target pathogen. The effector cell then secretes powerful cytotoxins (e.g., perforin and granzymes ) that kill the pathogen.

FC receptors on an NK cell bind to the Fc region of the IgG bound to the antigen on the surface of a pathogen. This causes the NK cell to release toxins that kill the pathogen.
In this example of ADCC, antibodies bind to a large pathogenic cell that is too big for phagocytosis and then bind to Fc receptors on the membrane of a natural killer cell. This interaction brings the NK cell into close proximity, where it can kill the pathogen through release of lethal extracellular cytotoxins.
  • Where is IgA normally found?
  • Which class of antibody crosses the placenta, providing protection to the fetus?
  • Compare the mechanisms of opsonization and antibody-dependent cell-mediated cytotoxicity.

Key concepts and summary

  • Adaptive immunity is an acquired defense against foreign pathogens that is characterized by specificity and memory. The first exposure to an antigen stimulates a primary response , and subsequent exposures stimulate a faster and strong secondary response.
  • Adaptive immunity is a dual system involving humoral immunity (antibodies produced by B cells) and cellular immunity (T cells directed against intracellular pathogens).
  • Antigens , also called immunogens , are molecules that activate adaptive immunity. A single antigen possesses smaller epitopes , each capable of inducing a specific adaptive immune response.
  • An antigen’s ability to stimulate an immune response depends on several factors, including its molecular class, molecular complexity, and size.
  • Antibodies ( immunoglobulins ) are Y-shaped glycoproteins with two Fab sites for binding antigens and an Fc portion involved in complement activation and opsonization.
  • The five classes of antibody are IgM , IgG , IgA , IgE , and IgD , each differing in size, arrangement, location within the body, and function. The five primary functions of antibodies are neutralization, opsonization, agglutination, complement activation, and antibody-dependent cell-mediated cytotoxicity (ADCC).

Matching

Match the antibody class with its description.

___IgA A. This class of antibody is the only one that can cross the placenta.
___IgD B. This class of antibody is the first to appear after activation of B cells.
___IgE C. This class of antibody is involved in the defense against parasitic infections and involved in allergic responses.
___IgG D. This class of antibody is found in very large amounts in mucus secretions.
___IgM E. This class of antibody is not secreted by B cells but is expressed on the surface of naïve B cells.

d, e, c, a, b

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Fill in the blank

There are two critically important aspects of adaptive immunity. The first is specificity, while the second is ________.

memory

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________ immunity involves the production of antibody molecules that bind to specific antigens.

Humoral

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The heavy chains of an antibody molecule contain ________ region segments, which help to determine its class or isotype.

constant

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The variable regions of the heavy and light chains form the ________ sites of an antibody.

antigen-binding

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Short answer

What is the difference between humoral and cellular adaptive immunity?

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What is the difference between an antigen and a hapten?

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Describe the mechanism of antibody-dependent cell-mediated cytotoxicity.

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Questions & Answers

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Suppose the inflation rate is 6%, does it mean that all the goods you purchase will cost 6% more than previous year? Provide with reasoning.
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Source:  OpenStax, Microbiology. OpenStax CNX. Nov 01, 2016 Download for free at http://cnx.org/content/col12087/1.4
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