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Effect Of Therapeutic Hiv Vaccine On Cd4 Count And Viral Load Of Aids Patients: Hope For Care Of Hiv Infections.

机译:艾滋病毒治疗性疫苗对艾滋病患者Cd4计数和病毒载量的影响:希望为艾滋病毒感染提供护理。

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Previous efforts by great scientists were made to develop HIV vaccine using genetic engineering. There was no much success achieved. At our end live attenuated, killed or fragments of the virus was used as a vaccine. The vaccine was first produced in 1987 and used on thirty five (35) AIDS patients. The patients were monitored and followed up, using CD4 count, viral load and clinical parameters. Based on the above thirty five of them responded positively to the therapy. The result of this study had given hope for cure of HIV infection. Indroduction Since 1984, when DR Robert Gallo declared at the American national cancer institute (ANCL), the discovery of Human immune deficiency virus (HIV), the virus that cause Acquire immune deficiency syndrome (AIDS), the human existence has been attacked by the deadly diseases, with devastating effect (1,2,3). Report have it that as of 1998 AIDS has killed no fewer that 14 million people worldwide and over 40 million people were living with HIV. About seventy-five (75) percent of the people were living in the developing countries. The picture presently is gloomier in Africa where AIDS kills about 5, 000, and infects 11,000 every day ( 3,4,5).At present almost every family seams to be affected. It is believed that AIDS has killed more people than those killed in the wars of Africa combined (5). Cases of HIV/AIDS have now been reported in virtually all ages and every tribe and both sexes. Surveillance reports have shown that the rate of infection in Nigeria is spreading like wild fire (6). For instance the prevalence of the disease was 1.4% in 1992, rose to 3.8% in 1994. In 1997 4.1% of the adults in Nigeria were infected (4, 5, 6). According to United Nations program on AIDS report of 1998 approximately 590,000 Nigeria developed full blown AIDS by the end of 1997 (5). It was reported that more than 2.2 million Nigerians were infected with HIV in 1998 (5).In Nigeria and other developing countries where most of the HIV infected people reside, the vast majority of them could not afford anti retroviral drugs by the time of this research (1997-1998) there was accordingly, a growing census that the development of a safe, effective and cheap vaccine against HIV represents the world’s most urgent public priority.Unfortunately, it was taking much longer to develop such a vaccine than was anticipated back in 1983-84, when research on HIV began in earnest. The reasons for this may be as a result of the tremendous degree of anti-genic variability seen among different clinical isolates and subtypes of HIV. Another reason is the particular route of transmission used by HIV which will probably require that a vaccine elicit both mucosal and systemic immunity. It is against this background however that I developed this classical approach of using mainly the whole virus /life attenuated or killed vaccine, to stimulate specific anti-HIV cellular and humoral immune response. Attenuated vaccines have been widely used around the world to protect against other viral diseases, including rabies, small pox, polio, yellow fever, measles and mumps. In each case the immunity from the poorly replicating virus (vaccine) strains is able to clear the attenuated virus, the virus and to provide long-lasting immunity against re-infection by the same pathogen. However before this research there were no attenuated vaccines in use against disease caused by HIV. To use a vaccine as preventive one must be sure that it is avirulent. This concern is highlighted by findings that vaccinated newborn macaques with strains of SIV (Simian immune deficiency Virus) caused fatal immune disease (6,7). No one should try to down play either this problem or the fact that an attenuated HIV vaccine strains may be spread to the partners and vaccinated women to their babies.It would be wrong to argue that the development of live attenuated HIV vaccine is not associated with biological and ethical problem. That is the reason for using the vaccine only
机译:伟大的科学家先前做出的努力是利用基因工程开发HIV疫苗。没有太大的成就。在我们的最后,减毒,杀死或片段的活病毒被用作疫苗。该疫苗于1987年首次生产,已用于三十五(35)名艾滋病患者。使用CD4计数,病毒载量和临床参数对患者进行监测和随访。基于以上所述,其中三十五人对该疗法有积极的反应。这项研究的结果为治愈HIV感染提供了希望。引言自1984年罗伯特·加洛(Robert Roberto)博士在美国国家癌症研究所(ANCL)宣布发现人类免疫缺陷病毒(HIV)以来,该病毒引起了后天免疫缺陷综合症(AIDS),人类的生存受到了人类的攻击。致命的疾病,具有毁灭性的影响(1,2,3)。报告说,截止到1998年,艾滋病已经杀死了全世界1400万人,超过4000万人感染了艾滋病毒。大约百分之七十五(75)的人口生活在发展中国家。在非洲,目前的情况更为悲观,那里的艾滋病致死人数约为5,000,每天感染11,000(3、4、5)。目前几乎每个家庭都受到影响。人们认为,艾滋病造成的死亡人数比非洲战争中丧生的人数还要多(5)。现在几乎所有年龄段,每个部落以及男女都报告了艾滋病毒/艾滋病病例。监视报告显示,尼日利亚的感染率像野火一样在蔓延(6)。例如,该病的患病率在1992年为1.4%,在1994年升至3.8%。1997年,尼日利亚有4.1%的成年人被感染(4、5、6)。根据1998年联合国艾滋病规划署的报告,到1997年底,约有590,000尼日利亚发展为完全感染的艾滋病(5)。据报道,1998年有超过220万尼日利亚人感染了艾滋病毒(5)。在大多数艾滋病毒感染者所居住的尼日利亚和其他发展中国家,到那时,他们中的绝大多数人都买不起抗逆转录病毒药物。因此(1997-1998)的研究表明,开发一种安全,有效和廉价的抗HIV疫苗代表了世界上最紧迫的公共优先事项,不幸的是,开发这种疫苗花费的时间比预期的要长得多在1983-84年间,认真开展了关于艾滋病的研究。造成这种情况的原因可能是由于在不同的临床分离株和亚型的HIV之间看到了很大程度的抗原变异性。另一个原因是HIV使用的特殊传播途径,这可能需要疫苗同时引起粘膜和全身免疫。正是在这种背景下,我开发了这种经典方法,主要使用整个病毒/生命减毒或杀死的疫苗来刺激特定的抗HIV细胞和体液免疫反应。减毒疫苗已在世界范围内广泛用于预防其他病毒性疾病,包括狂犬病,天花,小儿麻痹症,黄热病,麻疹和腮腺炎。在每种情况下,来自复制能力较弱的病毒(疫苗)株的免疫力都能够清除减毒的病毒(该病毒)并提供针对相同病原体的再次感染的持久免疫力。但是,在进行这项研究之前,没有针对艾滋病毒引起的疾病的减毒疫苗。要使用预防疫苗,必须确保它是无毒的。接种猕猴SIV(Simian免疫缺陷病毒)的新生猕猴引起致命的免疫疾病的发现突显了这种担忧(6,7)。没有人应该淡化这个问题,也不要淡化HIV减毒疫苗株可能会传播给伴侣和已接种疫苗的妇女给婴儿的事实。认为活的HIV减毒疫苗的开发与感染无关生物和伦理问题。那就是只使用疫苗的原因

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