Wassermann test
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The Wassermann test is a complement-fixation (Complement system) antibody test for syphilis, named after the bacteriologist August von Wassermann.
Method
A sample of blood or cerebrospinal fluid is taken and introduced to the antigen - cardiolipin extracted from bovine muscle or heart. Syphilis-specific antibodies (reagines) react with the lipid - the Wassermann reaction of antiphospholipid antibodies (APAs). The intensity of the reaction (1, 2, 3, or 4) indicates the severity of the condition.
Uncertainty
The reaction is not actually specific to syphilis and will produce a positive reaction to other diseases, including malaria, tuberculosis, and numerous other diseases. It is possible for an infected individual to produce no reaction and for a successfully treated individual to continue to produce a reaction (called Wassermann fast or fixed).
Development and refinement
The antibody test was developed by Wassermann and Albert Neisser at the Robert Koch Institute for Infectious Diseases in 1906.[1][1] The test was a growth from the work of Jules Jean Baptiste Vincent Bordet and Octave Gengou on complementing-fixation reaction, published in 1901, and the positive reaction is sometimes called the Bordet-Gengou-Wassermann reaction or Bordet-Wassermann reaction.
The Wassermann test has been refined - Kahn test, Kolmer test - and it is rarely used today. Replacement tests (VDRL test, Rapid plasma reagent (RPR test), initially based on flocculation techniques (Hinton), have been shown to produce far fewer false positive results. Indeed the "biologic false positives" of modern tests usually indicate a serious alternate condition, often an autoimmune disease.
References
External links
nl:Wassermannreactie
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

