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Mouse in Science
MONOCLONAL ANTIBODIES
see also READINGS AND RESOURCES ON MABS
In 1975, Kohler and Milstein first fused lymphocytes to produce a cell line which was both immortal and a producer of specific antibodies. The two scientists were awarded the Nobel Prize for Medicine in 1984 for the development of this "hybridoma." The value of hybridomas to the field was not truly appreciated until about 1987, when MAbs were regularly produced in rodents for diagnostics.What are Monoclonal Antibodies?
Monoclonal antibodies (MAbs) are:
antibodies of exceptional purity and specificity
components of the immune system
able to recognize and bind to a specific antigen
Uses
Monoclonal antibodies are currently utilized in many diagnostic procedures, including:
measuring protein and drug levels in serum
typing tissue and blood
identifying infectious agents
identifying clusters of differentiation for the classification and follow-up therapy of leukemias and lymphomas
identifying tumor antigens and auto-antibodies
identifying the specific cells involved in the immune response
identifying and quantifying hormones
Technology: The first step in the production of MAbs is to immunize a mouse with an antigen. When the mouse begins to produce antibodies to the antigen, its spleen is removed. Antibody-producing cells from the spleen are then fused with a myeloma cell line, one which is not Ab-producing and has been maintained in culture. The new fused cell line, which does produce antibodies, is grown briefly in culture and then re-injected into another mouse's peritoneum. Finally, the ascites fluid which contains monoclonal antibodies is harvested from the mouse.
Factors Affecting MAb Production
The purity of the antigen, the mouse strain which is used, the age
and sex of the mouse, the tolerance of the individual mouse, and many other
factors may affect the outcome of Ab-producing procedures. Because so many
variables are present, one general way to maximize the animal's immune response
is to use adjuvants. Adjuvants hold the antigen at the site of
immunization and release it over a long period of time. Freund's Complete
Adjuvant, which is more widely used than any other adjuvant, includes killed
mycobacteria which serve to increase inflammation upon injection, and thereby
enhance the mouse's immune response. This inflammation often results in painful
lesions at the injection site.
ELISA
The Enzyme
Linked ImmunoSorbent Assay (ELISA) was first developed by Engvall and Perlman in
1971. ELISA makes it possible to create a simple color test to detect and
quantify the presence of an antigen, antibody, or hormone. This system is widely
used because it can process large numbers of samples in a short time and can
handle complex antigens, such as bacteria.
In this assay, the MAb is an antigen which has been anchored to a surface. This antibody then can be detected by a polyclonal antibody preparation which binds the monoclonal antibody. These polyclonal antibodies are linked to enzymes which generate a colored product in the presence of the MAb.
Commercial uses of the ELISA test are in high demand. Over-the-counter pregnancy tests make use of this principle by using MAbs directed to protein samples in urine. To monitor diabetes, glucose levels can be determined using a mediator molecule to interface biological and electronic components of a sensor which results in a current reading. Antibiotic residues in milk may be detected using an ELISA system which monitors the inhibition of a test organism's growth. ELISA is also used in food safety by indicating the presence of salmonella. This test is used to predict salmonella carrier status in cattle.
Human Monoclonal Antibodies
The production of MAbs has opened many doors in the area of
immunotherapy. Human antibodies, however, are much more useful in this capacity
than are those of mice, which may be rejected by the human immune system. Also,
in some cases, MAbs from mice may elicit different responses than those from
humans.
Human MAb production has proved to be quite complex. One current strategy involves transforming cells with Epstein-Barr virus and stabilizing them by extensive cloning. Another popular technique is the "humanization" of mouse MAbs. In this procedure, regions of the human myeloma protein are joined to the variable region of a mouse antibody. The production of true human antibodies is possible with the use of the Polymerase Chain Reaction, but limitations of this procedure are still in need of attention.
In Vitro Production.
The expansion of hybridomas in animals is becoming less acceptable
due to humane and economic concerns. Several European countries have
incorporated legislation limiting antibody production in mice. MAbs are
extensively produced in vitro in Switzerland and Germany. Although in
vivo production is relatively inexpensive, ascites fluid of mice may yield
commercially unsuitable antibody. Two popular alternatives are bulk tissue
culture in encapsulated or hollow fibre systems, and the expression of cloned
antibody genes in high producing eukaryotes. The latter is accomplished through
recombinant DNA technology.
Quality of Life for Mice: A Dilemma.
Freund's Complete Adjuvant (FCA) is the most effective
adjuvant for antibody production in mice, but it creates inflammatory lesions at
the inoculation site. The resulting discomfort to mice is a subject of
widespread concern. When FCA is used, specific guidelines commonly require using
smaller doses at each injection site and avoiding foot pad or intradermal
injections. Due to the pain FCA causes, large-scale FCA use has been banned in
the Netherlands and the United Kingdom. Alternative adjuvants are effective in
certain situations.
GLOSSARY
adjuvant a substance that increases the antigenic response and is used to increase production of antibody.
antibody (Abs) a protein secreted by B lymphocytes in response to an antigen.
antigen a substance that induces the formation of antibodies.
ascites the accumulation of serum in the peritoneal cavity of the abdomen.
Freund's Complete Adjuvant (FCA) the adjuvant that produces very high antibody levels by stimulating a hypersensitive, painful inflammation at the injection site.
hybridoma the cell produced by the fusion of an antibody-producing cell and a multiple myeloma cell; this cell can produce a continuous supply of antibody.
lymphocyte a particular type of white blood corpuscle; B lymphocytes arise in bone marrow; lymphocytes in the thymus develop into T-cells.
monoclonal arising from a single cell, as in antibodies specific for a particular antigen and derived from hybridoma cells.
myeloma a tumor of B lymphocyte cells arising in the bone marrow.
Lynette A. Hart, Professor, SVM:PHR
Amy Dassler, Undergraduate intern 1996
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