Immunisation against an organism whose target is an important
component of the immune system presents particular difficulties.
In addition, HIV has already been shown to be perhaps the most variable virus yet discovered, and HIV-2 differs greatly from all HIV-1 isolates. So far, efforts to immunise against the virus have concentrated on the use of cloned gp120 because all strains of virus so far tested use gp120 to bind to the CD4 molecule, implying that a part of the envelope is similar in all strains. In experimental animals gp120 does induce a neutralising antibody response to the virus but restricted to the immunising strain of virus (type specific immunity) and these neutralising sera do not provide reliable protection against virus challenge in vivo in animal experiments. More recently it has been shown that gp120 and its anchor gp41 exist in the viral envelope as a trimer of heterodimers. Because of this and because gp120 is heavily glycosylated, much of the antibody response is to the variable V2 and V3 loops. Furthermore, primary isolates have been shown to be less susceptible to neutralisation than the tissue culture-adapted strains, from which the recombinant gp120 used as immunogen in most experiments derives. Thus new immunogens are needed to raise broadly reactive neutralising antibody and a variety of oligomeric and deglycosylated forms of gp120, lacking the V2 and V3 loops, are being tried.
High levels of CTL are seen in the early stages of HIV infection and the demonstration of CTL escape mutants suggests that they play a role in controlling the virus. That individuals exposed to HIV but with no evidence of infection exhibit CTL responses, reinforces the view that this type of response is important in protection. An effective vaccine might therefore contain components able to stimulate both neutralising antibody, CD4 T-cells and strong CTL responses.
A key factor in generating immune responses is the way in which the antigens are presented to the immune system. For the generation of effective CTL responses attenuated live viruses are effective and attenuated (nef deleted) simian immunodeficiency virus (SIV) has been shown able to protect monkeys against challenge with virulent virus. While such a strategy is unlikely to be used in humans because of worries about the safety of such a virus, it suggests that live viral vectors may be an effective means of immunising against HIV. HIV genes have been inserted into several possible vectors (vaccinia, canary pox, adenovirus) and a number of phase 1 trials are in progress. Alternate means of delivery capable of inducing both antibody and cellular immunity, such as peptides or proteins in novel adjuvants, naked DNA, or the use of different methods of antigen administration in sequence (prime/boost regimes) are under active investigation.
In addition, HIV has already been shown to be perhaps the most variable virus yet discovered, and HIV-2 differs greatly from all HIV-1 isolates. So far, efforts to immunise against the virus have concentrated on the use of cloned gp120 because all strains of virus so far tested use gp120 to bind to the CD4 molecule, implying that a part of the envelope is similar in all strains. In experimental animals gp120 does induce a neutralising antibody response to the virus but restricted to the immunising strain of virus (type specific immunity) and these neutralising sera do not provide reliable protection against virus challenge in vivo in animal experiments. More recently it has been shown that gp120 and its anchor gp41 exist in the viral envelope as a trimer of heterodimers. Because of this and because gp120 is heavily glycosylated, much of the antibody response is to the variable V2 and V3 loops. Furthermore, primary isolates have been shown to be less susceptible to neutralisation than the tissue culture-adapted strains, from which the recombinant gp120 used as immunogen in most experiments derives. Thus new immunogens are needed to raise broadly reactive neutralising antibody and a variety of oligomeric and deglycosylated forms of gp120, lacking the V2 and V3 loops, are being tried.
High levels of CTL are seen in the early stages of HIV infection and the demonstration of CTL escape mutants suggests that they play a role in controlling the virus. That individuals exposed to HIV but with no evidence of infection exhibit CTL responses, reinforces the view that this type of response is important in protection. An effective vaccine might therefore contain components able to stimulate both neutralising antibody, CD4 T-cells and strong CTL responses.
A key factor in generating immune responses is the way in which the antigens are presented to the immune system. For the generation of effective CTL responses attenuated live viruses are effective and attenuated (nef deleted) simian immunodeficiency virus (SIV) has been shown able to protect monkeys against challenge with virulent virus. While such a strategy is unlikely to be used in humans because of worries about the safety of such a virus, it suggests that live viral vectors may be an effective means of immunising against HIV. HIV genes have been inserted into several possible vectors (vaccinia, canary pox, adenovirus) and a number of phase 1 trials are in progress. Alternate means of delivery capable of inducing both antibody and cellular immunity, such as peptides or proteins in novel adjuvants, naked DNA, or the use of different methods of antigen administration in sequence (prime/boost regimes) are under active investigation.
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