1. Human Immunodeficiency Virus Type 2 Infection in the United States
- Author
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J. Richard George, Thomas R. O'Brien, and Scott D. Holmberg
- Subjects
medicine.medical_specialty ,business.industry ,Transmission (medicine) ,Public health ,Human immunodeficiency virus (HIV) ,virus diseases ,General Medicine ,medicine.disease_cause ,medicine.disease ,Virology ,Virus ,Natural history ,Acquired immunodeficiency syndrome (AIDS) ,Environmental health ,Epidemiology ,Medicine ,Viral disease ,business - Abstract
WITHIN the past year, the US Food and Drug Administration (FDA) has licensed two combined human immunodeficiency virus type 1 (HIV-1)/human immunodeficiency virus type 2 (HIV-2) enzyme immunoassays (EIAs) for screening donated blood and plasma. The FDA has also mandated that by June 1, 1992, US blood centers must implement testing for antibodies to HIV-2 in addition to testing for antibodies to HIV-1. Implementation of this policy and reports of HIV-2—infected US residents have raised important public health and clinical questions about HIV-2 infection in the United States. This article summarizes current information regarding the epidemiology and diagnosis of HIV-2 infection and discusses public health considerations that arise from the presence of HIV-2 in the United States. BACKGROUND: WORLDWIDE DISTRIBUTION, TRANSMISSION, AND NATURAL HISTORY Infection with HIV-2 is endemic in many countries in West Africa, but generally much rarer elsewhere in the world. 1,2 The highest prevalence of HIV-2 infection
- Published
- 1992
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