Phage-displayed mimotopes recognizing a biologically active anti-HIV-1 gp120 murine monoclonal antibody

Antibody-dependent cellular cytotoxicity (ADCC) is a host defense mechanism in which Fc receptor-bearing effector cells in combination with antigen-specific antibodies recognize and kill antigen-expressing target cells. The authors previously described a murine monoclonal antibody (MAb-ID6) that med...

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Veröffentlicht in:Journal of acquired immune deficiency syndromes (1999) 2002-10, Vol.31 (2), p.147-153
Hauptverfasser: GOMEZ-ROMAN, Victor Raul, CHUANHAI CAO, YUN BAI, SANTAMARIA, Hugo, ACERO, Gonzalo, MANOUTCHARIAN, Karen, WEINER, David B, UGEN, Kenneth E, GEVORKIAN, Goar
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Sprache:eng
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Zusammenfassung:Antibody-dependent cellular cytotoxicity (ADCC) is a host defense mechanism in which Fc receptor-bearing effector cells in combination with antigen-specific antibodies recognize and kill antigen-expressing target cells. The authors previously described a murine monoclonal antibody (MAb-ID6) that mediated ADCC activity against HIV-infected cells. It was demonstrated that the specificity of MAb-ID6 maps to the first 204 amino acids of gp120; however, the exact epitope was not identified. In the present work, by screening phage display libraries with MAb-ID6, the authors have mapped the corresponding epitope to amino acids 86-100 (HIV-1 gp120 sequence). This epitope lies within the C1 region of gp120 and is highly conserved among all subtypes and circulating recombinant forms of HIV-1. Thus, these phage mimotopes of C1 may serve as components of a vaccine for the induction of gp120-specific antibodies mimicking MAb-ID6.
ISSN:1525-4135
1944-7884
DOI:10.1097/00126334-200210010-00004