HIV preventive vaccines. Progress to date
- PMID: 8586027
- DOI: 10.2165/00003495-199550050-00003
HIV preventive vaccines. Progress to date
Abstract
The major conceptual problem for HIV vaccine development has been the lack of information on immune responses known to correlate with protection against HIV infection in humans. In this regard, studies on the natural history of HIV infection and AIDS, especially of people with apparent resistance to HIV infection and of patients with HIV infection who have long term survival without disease progression, may provide important information for vaccine development. In addition, a major concern for the development of broadly effective vaccines has been the extensive genetic variability which is characteristic of HIV. In spite of these unknowns, the first generation of HIV candidate vaccines has been developed and evaluated. HIV candidate vaccines based on the subunit recombinant envelope concept (gp120 or gp160) have been shown to protect chimpanzees from HIV infection on challenge, and have now been evaluated in humans in phase I and phase II trials. These products are well tolerated, and capable of inducing neutralising antibodies, but not cytotoxic T lymphocytes. A second vaccine concept, currently in phase I trials, is based on live recombinant vectors, especially using poxvirus vectors followed by boosting with subunit recombinant envelope vaccines. This concept is theoretically very attractive because preliminary data suggest that these vaccines induce both humoral and cell-mediated immunity. However, no published information is available on the ability of live recombinant vector vaccines to protect chimpanzees from HIV infection. The next step in HIV vaccine development is to proceed carefully to expanded phase II and phase III trials to assess the protective efficacy of these candidate vaccines in humans. These trials will be extremely complex from the logistical, scientific and ethical points of view, and will require close collaboration between clinical, basic science and behavioural researchers, national and international organisations, and the pharmaceutical industry.
Similar articles
-
HIV gp120 vaccine - VaxGen: AIDSVAX, AIDSVAX B/B, AIDSVAX B/E, HIV gp120 vaccine - Genentech, HIV gp120 vaccine AIDSVAX - VaxGen, HIV vaccine AIDSVAX - VaxGen.Drugs R D. 2003;4(4):249-53. doi: 10.2165/00126839-200304040-00007. Drugs R D. 2003. PMID: 12848591
-
Vaccines and vaccine strategies against HIV.Curr Drug Targets. 2004 Jan;5(1):71-88. doi: 10.2174/1389450043490686. Curr Drug Targets. 2004. PMID: 14738219 Review.
-
[The quest for an HIV vaccine].Bull Acad Natl Med. 2005 May;189(5):831-44; discussion 844. Bull Acad Natl Med. 2005. PMID: 16433455 Review. French.
-
Obstacles and progress toward development of a preventive HIV vaccine.J Int Assoc Physicians AIDS Care. 1997 Aug;3(8):28-34. J Int Assoc Physicians AIDS Care. 1997. PMID: 11364630
-
An HIV vaccine: how and when?Bull World Health Organ. 2001;79(12):1133-7. Bull World Health Organ. 2001. PMID: 11799445 Free PMC article.
Cited by
-
Characterization of a virtually full-length human immunodeficiency virus type 1 genome of a prevalent intersubtype (C/B') recombinant strain in China.J Virol. 2000 Dec;74(23):11367-76. doi: 10.1128/jvi.74.23.11367-11376.2000. J Virol. 2000. PMID: 11070037 Free PMC article.
-
Cytotoxic T-lymphocyte cross-reactivity among different human immunodeficiency virus type 1 clades: implications for vaccine development.J Virol. 1997 Nov;71(11):8615-23. doi: 10.1128/JVI.71.11.8615-8623.1997. J Virol. 1997. PMID: 9343219 Free PMC article.
-
Current concepts in human immunodeficiency virus infection and AIDS.Clin Diagn Lab Immunol. 1999 May;6(3):295-305. doi: 10.1128/CDLI.6.3.295-305.1999. Clin Diagn Lab Immunol. 1999. PMID: 10225826 Free PMC article. Review. No abstract available.
-
A comprehensive panel of near-full-length clones and reference sequences for non-subtype B isolates of human immunodeficiency virus type 1.J Virol. 1998 Jul;72(7):5680-98. doi: 10.1128/JVI.72.7.5680-5698.1998. J Virol. 1998. PMID: 9621027 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical