Abstract:
SIV infection of macaques has been developed as a model for AIDS resulting from HIV infection of humans. By analogy with HIV, it is likely that the envelope protein of SIV will play an important role in eliciting neutralising, and possibly protective, responses. It is therefore important to define epitopes within the SIV glycoproteins gp120 and gp41 that can induce neutralising antibodies when presented to the immune system as hybrid Ty virus-like particles (Ty-VLPs). We therefore decided to use this system to scan SIV gp120 and gp41 for neutralising determinants. Overlapping DNA fragments encoding SIV gp120 and gp41 were inserted into Ty-VLP vectors and the resulting fusion proteins assembled into particles. The purified hybrid Ty-VLPs have been used to immunise mice and the sera are being tested for their reactivity against both conformational and linear epitopes of gp120 and gp41. Previous studies by Kent et al have demonstrated that the V2 region of gp120 reacts with neutralising monoclonal antibodies. These antibodies also recognise hybrid Ty-VLPs carrying the V1 and V2 regions of gp120. Immunogenicity studies with these Ty-VLPs indicate that these particles elicit antibodies that recognise gp120 and gp 160 by both ELISA and Western blot analysis. Further investigations into the ability of these sera to induce neutralising antibodies are underway.
Keywords: Animal Antibodies, Viral/ANALYSIS Antibody Formation Blotting, Western Enzyme-Linked Immunosorbent Assay Epitopes/ANALYSIS/IMMUNOLOGY Gene Products, env/*IMMUNOLOGY HIV Envelope Protein gp120/*IMMUNOLOGY Mice Neutralization Tests Protein Conformation Recombinant Fusion Proteins/IMMUNOLOGY SIV/*IMMUNOLOGY Vaccines, Synthetic/*IMMUNOLOGY Viral Vaccines/*IMMUNOLOGY ABSTRACT 930630
M9361055
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