Vaccines directed against HIV: preventive and therapeutic strategies.

AIDS clinical review Pub Date : 1993-01-01
J O Kahn, D L Birx
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Abstract

Vaccine therapy studies in HIV-seropositive volunteers over the next year should provide additional insights into whether different vaccine viral strains (LAI, IIIB, MN, SF2), different protein sources (whole virus particles, recombinant protein, peptides), different expression systems (baculovirus, mammalian), or different adjuvants (incomplete Freund's, MTP-PE, MF59, alum) generate significantly different immune responses at the cellular and humoral level. In addition, differences in the ability of each vaccine to induce humoral immune responses to epitopes in the constant regions vs. variable regions, contiguous or noncontiguous "conformational" epitopes, with high vs. low antibody affinity can be evaluated. The roles of antibody-dependent cellular cytotoxicity (ADCC), cellular recognition, nonspecific natural killing, and MHC-restricted cytotoxicity can also be explored. To date, the majority of the immunogens have proven to be safe. Many induce new humoral and cellular immune responses against HIV. The final important question remains, whether any of these vaccines used as therapeutic immunogens generate immune responses that induce an altered disease course with a prolonged asymptomatic period without immunodeficiency, whether vaccines can affect increased viral clearance, or decreased transmission/infectivity? There remains no in vitro assay known to correlate with lack of disease progression, no immune profile consistent with a prolonged asymptomatic period. The vaccine therapy trial researchers seek the answers to these important questions. No single research organization can begin to address all the possibilities, so the overall pace of exploration of this therapeutic concept is likely to be dictated by the level of cooperation between the many groups involved in these studies. Open collaboration between researchers and open exchange of reagents, immunogens for in vitro experiments, and sera will allow faster dissection of the many questions and issues raised in this chapter. Whether vaccine therapy proves to have a useful role in the treatment of HIV-1-induced disease, these studies will ultimately lead to the development of useful techniques and provide new insights into the nature of the immunological responses, as the investigation of vaccine therapy did over a century ago.

艾滋病毒疫苗:预防和治疗战略。
在接下来的一年里,对hiv血清阳性志愿者的疫苗治疗研究将提供更多的见解,以了解不同的疫苗病毒株(LAI, IIIB, MN, SF2),不同的蛋白质来源(全病毒颗粒,重组蛋白,肽),不同的表达系统(棒状病毒,哺乳动物)或不同的佐剂(不完全Freund's, MTP-PE, MF59,明胶)是否在细胞和体液水平上产生显著不同的免疫反应。此外,可以评估每种疫苗诱导对固定区与可变区、连续或非连续“构象”表位、高抗体亲和力与低抗体亲和力的体液免疫应答的能力差异。抗体依赖性细胞毒性(ADCC)、细胞识别、非特异性自然杀伤和mhc限制性细胞毒性的作用也可以探讨。迄今为止,大多数免疫原已被证明是安全的。许多诱导新的体液和细胞免疫应答HIV。最后一个重要的问题仍然存在,这些用作治疗性免疫原的疫苗是否会产生免疫反应,导致病程改变,并延长无免疫缺陷的无症状期,疫苗是否会增加病毒清除,或降低传播/传染性?目前还没有已知的与缺乏疾病进展相关的体外试验,也没有与延长无症状期相一致的免疫谱。疫苗治疗试验的研究人员寻求这些重要问题的答案。没有一个单一的研究机构可以开始解决所有的可能性,所以这个治疗概念的整体探索速度可能取决于参与这些研究的许多小组之间的合作水平。研究人员之间的开放合作和试剂、体外实验的免疫原和血清的开放交换将使本章提出的许多问题和问题得以更快地解剖。无论疫苗疗法是否被证明在治疗hiv -1诱导的疾病中具有有用的作用,这些研究最终将导致有用技术的发展,并提供对免疫反应性质的新见解,正如一个多世纪前对疫苗疗法的研究所做的那样。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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