Printer Friendly

Enzyme immunoassay (EIA)/enzyme-linked immunosorbent assay (ELISA).

Enzyme immunoassay (EIA) and enzyme-linked immunosorbent assay (ELISA) have become household names for medical laboratories, manufacturers of in vitro diagnostic products, regulatory bodies, and external quality assessment and proficiency-testing organizations. This brief historical note spotlights the development of enzyme labels in immunoassay from the invention of this method in the 1960s through its development and early use during the 1970s and 1980s.

The first published EIA and ELISA systems differed in assay design, but both techniques are based on the principle of immunoassay with an enzyme rather than radio-activity as the reporter label. Two scientific research groups independently and simultaneously developed this idea and executed the necessary experiments to demonstrate its feasibility. The ELISA technique was conceptualized and developed by Peter Perlmann, principal investigator, and Eva Engvall at Stockholm University, Sweden, and the EIA technique by Anton Schuurs, principal investigator, and Bauke van Weemen at the Research Laboratories of NV Organon, Oss, The Netherlands.

RIA was first described in 1960 for measurement of endogenous plasma insulin by Solomon Berson and Rosalyn Yalow of the Veterans Administration Hospital in New York (1). Yalow would later be awarded the 1977 Nobel Prize for Medicine for "the development of the RIA for peptide hormones' (2), but because of his untimely death in 1972, Berson could not share the award. Also in 1960, Dr. Roger Ekins of Middlesex Hospital in London published his findings on "saturation analysis" used to estimate thyroxine in human plasma (3).

The immunoassay technique with a radioactive label immediately caught the imagination of many researchers and clinicians, and in the ensuing decade RIAs for new analytes were published at a rapid pace and variants of the method were rapidly developed. In 1968, Miles and Hales published their first results of an "immuno-radio-metric" technique with radioactive labeled antibodies rather than labeled antigen for measuring insulin in human plasma (4).

In many laboratories around the world, special facilities were built in which investigators could safely work with the amounts of radioactivity required for the labeling of antigens or antibodies, but concern persisted with regard to the safety of laboratory personnel, the radioactive waste problem, the requirements of building special laboratory facilities, and the procurement of expensive counting equipment. It should be recalled that in the original studies (1, 3, 4) iodine-131 ((3 and y radiation) was used for the labeling because no alternatives were available at that time. The potential health problems related to the use of radioactive materials were greatly diminished when manufacturers such as Amersham and NEN began marketing iodine-125 (weak y radiation) preparations of sufficiently high specific activity and purity.

At meetings, such as the ERIAC (European RadiolmmunoAssay Club) in Basel in the early 1970s, the idea of using enzyme labels was met with skepticism and incredulity. How could so bulky and large a molecule as an enzyme be attached to an antigen or antibody without sterically hindering the immunochemical reaction between antigen and antibody? This objection on principle was nullified by carefully planned and executed experiments to demonstrate the feasibility of enzyme assays. Initial results were encouraging, and later the resounding success of the enzyme-(linked) immunoassay technique proved all skeptics wrong.

How did Perlmann and Schuurs each invent a method that others found inconceivable? These two principal investigators, when personally contacted by this author, could not report an anecdote about a particular or spectacular moment of insight. Instead, the classic pattern of research was followed, building on results published by colleagues in other fields, notably Stratis Avrameas of Villejuif, France (5, 6), G.B. Pierce of Los Angeles, California (7), and L. Wide of Uppsala, Sweden (8).

Between 1966 and 1969, the group in Villejuif reported their successful results of coupling antigens or antibodies with enzymes such as alkaline phosphatase (EC, glucose oxidase (EC, and others (5, 6). Avrameas and colleagues (5, 6) described the optimal coupling of these molecules by means of glutaraldehyde. Their purpose was to use the enzyme-labeled antigens and antibodies to detect antibodies or antigens by immunofluorescence, and they applied their tools to histopathology. In Los Angeles, Pierce and colleagues (7) had successfully developed the same line of research, also for histochemical purposes. The Uppsala group had developed a so-called (radio) immunosorbent technique in which antibodies were insolubilized by coupling them to cellulose or Sephadex beads.

Engvall and Perlmann published their first paper on ELISA in 1971 (9) and demonstrated quantitative measurement of IgG in rabbit serum with alkaline phosphatase as the reporter label. In the same year, van Weemen and Schuurs (10) published their innovative work on EIA and reported that it was possible to quantify human chorionic gonadotropin concentrations in urine. They used the enzyme horseradish peroxidase (EC 1.11.17), coupled by means of glutaraldehyde, as the reporter label. The Schuurs group secured patents on their findings [US patent application 762120, filed September 24, 1968 (11); Dutch patent applications 7016396, filed November 10, 1970, and 7018838, filed December 28, 1970 (12)].

Perlmanri s further research included cytotoxicity of human lymphocytes (13) and immunogen selection and epitope mapping for malaria vaccine development (14). Engvall's group applied the ELISA measurement tool to parasitology [e.g., malaria (15) and trichinosis (16)], microbiology (17), and oncology (18-20). Engvall then focused her scientific interests on the biochemistry of tissues, e.g., fibronectin, laminin, integrins, and muscular dystrophies. Engvall's laboratory is currently investigating the use of differentiation factors for muscle regeneration and myogenic cells from nonmuscle tissues for muscle cell replacement (21).

During the late 1960s and early 1970s, many RIA test systems were essentially "home-brew" methods developed by individual researchers who could not keep pace (particularly financially) with the possibilities and facilities of commercial manufacturers such as Boehringer-Mannheim (Germany), Abbott (United States), and Organon Teknika (The Netherlands), to name only a few. Commercialization of EIA/ELISA test kits had started. Solid-phase techniques (8, 22) were used in the development of microtiter plates (96 wells) in which either an antigen or an antibody is noncovalently bound to a solid-phase support. Technical advances led to automated pipetting devices (Micromedics; Hamilton), multichannel pipettes (Lab Systems), and microtiter plate readers and washers (Fig. 1), and in the 1980s fully automated test instruments were manufactured by Boehringer-Mannheim and Abbott, among others. Such automated systems have come to stay in medical laboratories.

The spectacular invention EIA/ELISA generated a whole series of test formats, from the immunoenzymo-metric [already mentioned in Ref. (4)] to the many variants of "sandwich" test procedures. For a comprehensive review of the possibilities the reader is referred to Ref. (23). The Dutch group at Organon/Organon Teknika successfully developed EIA systems in the field of reproductive endocrinology, including assays for human chorionic gonadotropin (10, 24), total estrogens, and human placental lactogen (25) in plasma. However, the new tests did not become commercially successful until the late 1970s and early 1980s, when they matched the exquisite sensitivity of existing RIA systems for the same analytes.

In the early 1970s, blood-bank screening for virologic diseases such as hepatitis B antigen was done either by (semi)automated RIA or nonradioactive but rather cumbersome hemagglutination tests. In 1976, Organon Teknika developed and marketed a highly successful EIA system for the hepatitis B surface antigen (HbsAg) (26), featuring a 96-well microtiter plate format. This test became the first commercially available EIA (Fig. 2). Other microbiological and virologic diagnostic tests soon followed, e.g., for hepatitis B "e" (HBe) antigens (27), rubella antibodies, toxoplasma antibodies, and in the 1980s, an EIA system for detection of human immunodeficiency virus antibodies.



The impact of diagnostic immunoassays, be they RIA, EIA, or ELISA, on patients, clinicians, and the healthcare system in general is virtually unsurpassed. To substantiate this subjective statement, this author searched PubMed with the search terms "enzyme-immunoassay", "enzyme-linked immunoassay", and "RIA", in clusters of 5 years from 1960 to 2005. The estimates of the number of articles quoting these keywords are given in Fig. 3. The sheer numbers are astounding! The peak of RIA quotations seems to have occurred between 1980 and 1990. The number of citations decreased from 1990 to 2000, but is still quite substantial. The number of articles with EIA or ELISA as a keyword increased rapidly in the 1980s and plateaued at an amazing ~40 000 quotations per 5 years in the 1990s. A decrease in this trend is not yet in sight.



In conclusion, the number of analytical and clinical investigations relying on these measurement procedures worldwide is exceedingly large. Thus, one can imagine that the numbers of measurements and determinations using immunoassay for routine patient care are astronomical. The clinical impact of EIA/ELISA as nonradioactive variants of immunoassays is indeed overwhelming. Perlmann, Schuurs, Engvall, and van Weemen were honored for their inventions when they received the German scientific award of the "Biochemische Analytik" in 1976 (Fig. 4), 5 years after they had published their first papers. Given the impact that their inventions have had on clinical diagnosis and healthcare in general, as well as on the development of a well-established in vitro diagnostic industry, these inventors deserve to be honored again.

During submission of this historical note for manuscript review, the sad news arrived that Dr. Perlmann had died on April 19, 2005, in Stockholm. He had received the submitted draft of this paper, however, in March 2005.

Received March 23, 2005; accepted August 5, 2005.

Previously published online at DOI: 10.1373/clinchem.2005.051532


(1.) Yalow RS, Berson SA. Immunoassay of endogenous plasma insulin in man. Clin Invest 1960;39:1157-75.

(2.) Nobel Prize home page. (accessed June 2005).

(3.) Ekins RP. The estimation of thyroxine in human plasma by an electrophoretic technique. Clin Chim Acta 1960;5:453-9.

(4.) Miles LEM, Hales CN. Labelled antibodies and immunological assay systems. Nature 1968;219:186-9.

(5.) Avrameas S, Uriel J. Methode de marquage d'antigenes et d'anticorps aver des enzymes et son application en immunodiffusion. C R Acad Sci Hebd Seances Acad Sci D 1966;262:2543-5.

(6.) Avrameas S. Coupling of enzymes to proteins with glutaraldehyde. Immunochemistry 1969;6:43-52.

(7.) Nakane PK, Pierce GB. Enzyme-labeled antibodies for the light and electron microscopic localization of tissue antigens. J Cell Biol 1967;33:307-18.

(8.) Wide L, Porath J. Radioimmunoassay of proteins with the use of Sephadex-coupled antibodies. Biochem Biophys Acta 1966;30: 257-60.

(9.) Engvall E, Perlmann P. Enzyme-linked immunosorbent assay (ELISA). Quantitative assay of immunoglobulin G. Immunochemistry 1971;8:871-4.

(10.) van Weemen BK, Schuurs AHWM. Immunoassay using antigen-enzyme conjugates. FEBS Letts 1971;15:232-6.

(11.) US Patent 762120. United States Patent and Trademark Office home page. (accessed June 2005).

(12.) Patents 7016396 and 7018838. Deutsches Patent- and Markenamt. (accessed June 2005).

(13.) Pape GR, Troye M, Axelsson B, Perlmann P. Simultaneous occurrence of immunoglobulin-dependent and immunoglobulin-independent mechanisms in natural cytotoxicity of human lymphocytes. J Immunol 1979;122:2251-60.

(14.) Perlmann P, Berzins K, Perlmann H, Troye-Blomberg M, Wahlgren M, Wahlin B. Malaria vaccines: immunogen selection and epitope mapping [Review]. Vaccine 1998;6:183-7.

(15.) Voller A, Huldt G, Thors C, Engvall E. New serological test for malaria antibodies. Br Med J 1975;1:659-61.

(16.) Ljungstrom I, Engvall E, Ruitenberg EJ. Proceedings: ELISA, enzyme-linked immunosorbent assay-a new technique for sero-diagnosis of trichinosis. Parasitology 1974;69:xxiv.

(17.) Engvall E. Quantitative enzyme immunoassay (ELISA) in microbiology. Med Biol 1977;55:193-200.

(18.) Seppala M, Rutanen EM, Heikinheimo M, Jalanko H, Engvall E. Detection of trophoblastic tumour activity by pregnancy-specific R1 glycoprotein. Int J Cancer 1978;21:265-7.

(19.) Sipponen P, Ruoslahti E, Vuento M, Engvall E, Stenman U. CEA and CEA-like activity in gastric cancer. Acta Hepatogastroenterol (Stung) 1976;13:276-9.

(20.) Uotila M, Ruoslathi E, Envall E. Two-site sandwich enzyme immunoassay with monoclonal antibodies to human alphafetoprotein. J Immunol Methods 1981;42:11-5.

(21.) Engvall E, Wewer UM. The new frontier in muscular dystrophy research: booster genes. FASEB J 2003;17:1579-84.

(22.) Catt K, Tregear GW. Solid-phase radioimmunoassay in antibody-coated tubes. Science 1967;158:1570-2.

(23.) Schuurs AHWM, van Weemen BK. Enzyme-immunoassay: a powerful analytical tool [Review]. J Immunoassay 1980;1:229-49.

(24.) van Weemen BK, Schuurs AHWM. Immunoassay using antibody-enzyme conjugates. FEBS Lett 1974;43:215-8.

(25.) Bosch AMG, van Hell H, Brands JAM, van Weemen BK, Schuurs AHWM. Methods for the determination of total estrogens (TE) and human placental lactogen (HPL) in plasma of pregnant women by enzyme-immunoassay. Clin Chem 1975;21:1009.

(26.) Wolters G, Kuijpers LPC, Kacaki J, Schuurs AHWM. Enzyme-immunoassay for HbsAg. Lancet 1976;11:690.

(27.) van der Waart M, Snelting A, Cichy J, Wolters G, Schuurs AHWM. Enzyme-immunoassay in diagnosis of hepatitis with emphasis on the detection of "e" antigen (HbeAg). J Med Virol 1978;3:43-9.

Diagnostics Consultancy Desk, 5631 AH 44, Eindhoven, The Netherlands. Fax 31-40-290-8621; e-mail
COPYRIGHT 2005 American Association for Clinical Chemistry, Inc.
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2005 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:History
Author:Lequin, Rudolf M.
Publication:Clinical Chemistry
Date:Dec 1, 2005
Previous Article:SDF1-3'A gene polymorphism is associated with chronic myeloproliferative disease and thrombotic events.
Next Article:Use of an automated method improves the yield and quality of cell-free fetal DNA extracted from maternal plasma.

Related Articles
Automated immunoassay systems: a new frontier.
HIV testing: an update.
Rapid field immunoassay for detecting antibody to Sin Nombre virus in deer mice.
45. Immuno-PCR--highly sensitive protein detection: results of the detection of native mistletoe lectin in human serum samples.
CISBIO Bioassays Launches Chromoa(TM) Chromogranin A ELISA Kit.
Perspective on the historical note on EIA/ELISA by Dr. R.M. Lequin.
The rise of EIA/ELISA.
Abbreviated direct and indirect ELISAs: a new and simple format.
Electrochemical enzyme immunoassay for serum prostate-specific antigen at low concentrations.
Evaluation of the tacrolimus II microparticle enzyme immunoassay (MEIA II) in liver and renal transplant recipients.

Terms of use | Copyright © 2018 Farlex, Inc. | Feedback | For webmasters