AIDS in the Third World: how to stop the HIV infection?

E De Clercq
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Abstract

Of the 38.6 million people living with HIV/AIDS globally, almost 25 million (65%) live in sub-Saharan Africa. Preventive strategies and measures fall short, often simply because they are not available or are largely male-controlled. A preventive HIV vaccine is still far away; hence the drive to develop alternative prevention technologies, such as microbicides and oral pre-exposure prophylaxis, that could be female controlled. There are, at present, twenty-two anti-HIV drugs which have been formally licensed for clinical use in the treatment of HIV infections (AIDS): zidovudine, didanosine, zalcitabine, stavudine, lamivudine, abacavir, emtricitabine, tenofovir, nevirapine, delavirdine, efavirenz, saquinavir, ritonavir, indinavir, nelfinavir, amprenavir, lopinavir, atazanavir, fosamprenavir, tipranavir, darunavir and enfuvirtide. These compounds, in combination, form the basis of HAART (highly active antiretroviral therapy), which has led to the development of a single daily pill existing of the combination of tenofovir disoproxil fumarate, emtricitabine and efavirenz, which has to be taken orally once daily for the treatment of AIDS. Beyond development of new drugs and clinical evaluation of existing medications, several companies within the pharmaceutical industry have established innovative policies that provide HIV medications at affordable prices in the least-developed countries. Reduced pricing is not alone a solution, and thus companies are actively working in partnership with the World Health Organization and other multinational groups to address roadblocks such as complex registration and procurement systems. Even in this period of successful anti-HIV therapy via HAART, a growing number of patients is cycling through the various remaining therapeutic options and are increasingly becoming dependent of the availability of newly developed anti-HIV agents. It is of concern that existing and future therapies will have to be effective against newly evolving (including drug-resistant) HIV variants in patients who currently face many years, if not decades, of chronic anti-HIV drug treatment. In spite of continuous long-term interventions to promote safer sexual behaviour, HIV prevalence is high and still rising in many parts of the world. The face of the epidemic is now black, female, young and poor..., and female controlled methods are urgently needed. Female controlled methods such as microbicides and cervical barrier methods provide hopeful perspectives when condom use is low due to social, cultural and/or economic factors, but, after all, the oral administration of a single daily pill would seem the most convenient way to prevent HIV infection, as its protective activity may be independent of the route of viral transmission.

第三世界的艾滋病:如何阻止艾滋病毒感染?
在全球3860万艾滋病毒/艾滋病感染者中,近2500万(65%)生活在撒哈拉以南非洲。预防战略和措施不足,往往仅仅是因为无法获得或主要由男性控制。预防性艾滋病毒疫苗仍然遥遥无期;因此,推动开发可由女性控制的替代预防技术,例如杀微生物剂和口服暴露前预防。目前,有22种抗艾滋病毒药物已被正式许可用于临床治疗艾滋病毒感染(艾滋病):齐多夫定、二达苷、扎西他滨、他夫定、拉米夫定、阿巴卡韦、恩曲西他滨、替诺福韦、奈韦拉平、德拉韦定、依非韦伦、沙奎那韦、利托那韦、因地那韦、奈非那韦、安普雷那韦、洛匹那韦、阿他那韦、福samprenavir、替那韦、达那韦和恩福韦肽。这些化合物结合在一起构成了高效抗逆转录病毒疗法的基础,这种疗法导致了一种由富马酸替诺福韦二氧吡酯、恩曲他滨和依非韦伦组成的每日单一药丸的发展,这种药丸必须每天口服一次,以治疗艾滋病。除了开发新药和对现有药物进行临床评价之外,制药业的几家公司还制定了创新政策,在最不发达国家以可负担的价格提供艾滋病毒药物。降低价格并不是唯一的解决办法,因此,各公司正积极与世界卫生组织和其他跨国集团合作,以解决诸如复杂的登记和采购系统等障碍。即使在通过HAART成功进行抗艾滋病毒治疗的这一时期,越来越多的患者正在循环使用各种剩余的治疗方案,并且越来越依赖于新开发的抗艾滋病毒药物的可用性。令人担忧的是,现有和未来的治疗方法必须对目前面临多年(如果不是几十年)慢性抗艾滋病毒药物治疗的新发展(包括耐药)艾滋病毒变体有效。尽管不断采取长期干预措施促进更安全的性行为,但在世界许多地方,艾滋病毒流行率很高,而且仍在上升。这一流行病的面孔现在是黑人、女性、年轻人和穷人……,并且迫切需要女性控制的方法。当由于社会、文化和/或经济因素,避孕套的使用率较低时,女性控制的方法,如杀微生物剂和宫颈屏障方法提供了希望,但毕竟,每天口服一粒药丸似乎是预防艾滋病毒感染最方便的方法,因为其保护作用可能与病毒传播途径无关。
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