Within the past 50 to 100 years, HIV went from being maintained primarily, if not exclusively, in sooty mangebeys (HIV-2) and chimpanzees (HIV-1) to being the etiologic agent of a worldwide pandemic. AIDS was not recognized as a specific disease until 1980, and HIV was not identified as the etiological agent until 1983. Nevertheless, an estimated 16 million persons have died from AIDS worldwide with 50 million currently infected with AIDS.
The outbreak of AIDS and infections of HIV have dropped significantly in
lso has greatly increased the expense and complexity of providing optimal antiretroviral therapy" (Zepf, 2001, 1443). One problem with such drugs is that HIV can readily adapt and develop resistance to the most powerful and current antiviral agents. Further, the cost of such medications make them inaccessible to many individuals especially those in impoverished nations. Adding to the inaccessibility of such drugs is the fact that many pharmaceutical companies who own the patents on such drugs have high licensing and royalty fees. Therefore, even though such powerful new drugs have been shown to work, they are cost-prohibitive for many especially those in hardest hit regions. Recently GalxoSmithKline (GSK) waived rights to its royalties and granted a drug license to generics company Aspen in South Africa (Freeman, 2001, 12). The company has granted a temporary license to the South Africa company for the manufacture of zidovudine (Retrovir-AZT), lamivudine (Epivir-3TC) and Combivir (Freeman, 2001, 12). Thus, we can see that while these drugs have been very effective, their cost is prohibitive and access to them is limited. Further, HIV is very capable of evolving to a form that is resistant to the most powerful antiretrov
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