Abstract
In 1985 the enzyme-linked immunosorbent assay (ELISA) to detect antibody to the human immunodeficiency virus (HIV) was licensed by the Food and Drug Administration. Used in conjunction with appropriate confirmatory tests such as the Western blot, it was now possible to identify individuals who had been infected with this virus. The use of these tests was immediately and universally adopted by blood banks in this country. However, their use in the clinical setting was limited by a number of unanswered questions raised by clinicians, advocacy groups, and public health officials. These issues are nearing resolution, and it is now time to place HIV testing in wider clinical use.
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© 1989 Medical Society of the State of New York
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Dehovitz, J.A., Landesman, S.H. (1989). Human immunodeficiency virus antibody testing: Time for clinicians to use it. In: Imperato, P.J. (eds) Acquired Immunodeficiency Syndrome. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-0807-2_29
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DOI: https://doi.org/10.1007/978-1-4613-0807-2_29
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