Research Topics
| Mattia BonsignoriSummaryAffiliation: Duke University Medical Center Country: USA Publications
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Detail Information
Publications
Antibody-dependent cellular cytotoxicity-mediating antibodies from an HIV-1 vaccine efficacy trial target multiple epitopes and preferentially use the VH1 gene familyMattia Bonsignori
Duke University Medical Center, Durham, North Carolina, USA
J Virol 86:11521-32. 2012..The polyclonality and low mutation frequency of these VH1 antibodies reveal fundamental differences in the regulation and maturation of these ADCC-mediating responses compared to VH1 bNAbs...
HIV-1 antibodies from infection and vaccination: insights for guiding vaccine designMattia Bonsignori
Duke Human Vaccine Institute, Duke University Medical Center, Durham, NC 27710, USA
Trends Microbiol 20:532-9. 2012..Strategies are being developed for the analysis of infection and vaccine candidate-induced antibodies, their gene usage, and their maturation pathways such that this information can be used to attempt to guide rational vaccine design...
Two distinct broadly neutralizing antibody specificities of different clonal lineages in a single HIV-1-infected donor: implications for vaccine designMattia Bonsignori
Duke Human Vaccine Institute, Durham, North Carolina, USA
J Virol 86:4688-92. 2012..These data provide proof of concept for an HIV-1 vaccine that aims to elicit bnAbs of multiple specificities...
HIV-1 envelope induces memory B cell responses that correlate with plasma antibody levels after envelope gp120 protein vaccination or HIV-1 infectionMattia Bonsignori
Duke Human Vaccine Institute, Duke University Medical Center, Durham, NC 27710, USA
J Immunol 183:2708-17. 2009..The inability to generate high titers of long-lived anti-envelope Abs is a major hurdle to overcome for the development of a successful HIV-1 vaccine...
Analysis of a clonal lineage of HIV-1 envelope V2/V3 conformational epitope-specific broadly neutralizing antibodies and their inferred unmutated common ancestorsMattia Bonsignori
Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA
J Virol 85:9998-10009. 2011..Thus, E.A244, B.9021, and AE.CM243 Envs are three potential immunogen candidates for studies aimed at defining strategies to induce V2/V3 conformational epitope-specific antibodies...
Vaccine induction of antibodies against a structurally heterogeneous site of immune pressure within HIV-1 envelope protein variable regions 1 and 2Hua Xin Liao
Duke Human Vaccine Institute, Duke University Medical Center, Durham, NC 27710, USA
Immunity 38:176-86. 2013..Variation may signal sites of HIV-1 envelope vulnerability, providing vaccine designers with new options...
Antigenicity and immunogenicity of RV144 vaccine AIDSVAX clade E envelope immunogen is enhanced by a gp120 N-terminal deletionS Munir Alam
Duke Human Vaccine Institute, Duke University Medical Center, Durham, North Carolina, USA
J Virol 87:1554-68. 2013..These results demonstrate that deletion of N-terminal residues in the RV144 A244 gp120 immunogen improves both envelope antigenicity and immunogenicity...
Magnitude and breadth of the neutralizing antibody response in the RV144 and Vax003 HIV-1 vaccine efficacy trialsDavid C Montefiori
Department of Surgery, Duke University Medical Center, Durham, North Carolina 27710, USA
J Infect Dis 206:431-41. 2012..No protection was observed in Thai injection drug users who received AIDSVAX B/E alone (Vax003 trial). We compared the neutralizing antibody response in these 2 trials...
