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Probabilities of developing HIV-1 bNAb sequence features in uninfected and chronically infected individuals

Author

Listed:
  • Christoph Kreer

    (University of Cologne)

  • Cosimo Lupo

    (PSL University, Sorbonne Université, and Université Paris Cité
    Istituto Nazionale di Fisica Nucleare (INFN), Sezione di Roma I)

  • Meryem S. Ercanoglu

    (University of Cologne)

  • Lutz Gieselmann

    (University of Cologne
    German Center for Infection Research, Partner Site Bonn-Cologne)

  • Natanael Spisak

    (PSL University, Sorbonne Université, and Université Paris Cité)

  • Jan Grossbach

    (University of Cologne)

  • Maike Schlotz

    (University of Cologne)

  • Philipp Schommers

    (University of Cologne
    German Center for Infection Research, Partner Site Bonn-Cologne
    University of Cologne
    University of Cologne)

  • Henning Gruell

    (University of Cologne
    University of Cologne)

  • Leona Dold

    (University Hospital of Bonn
    German Center for Infection Research (DZIF), Partner Site Bonn-Cologne)

  • Andreas Beyer

    (University of Cologne
    University of Cologne)

  • Armita Nourmohammad

    (Max Planck Institute for Dynamics and Self-Organization
    University of Washington
    University of Washington
    University of Washington)

  • Thierry Mora

    (PSL University, Sorbonne Université, and Université Paris Cité)

  • Aleksandra M. Walczak

    (PSL University, Sorbonne Université, and Université Paris Cité)

  • Florian Klein

    (University of Cologne
    German Center for Infection Research, Partner Site Bonn-Cologne
    University of Cologne)

Abstract

HIV-1 broadly neutralizing antibodies (bNAbs) are able to suppress viremia and prevent infection. Their induction by vaccination is therefore a major goal. However, in contrast to antibodies that neutralize other pathogens, HIV-1-specific bNAbs frequently carry uncommon molecular characteristics that might prevent their induction. Here, we perform unbiased sequence analyses of B cell receptor repertoires from 57 uninfected and 46 chronically HIV-1- or HCV-infected individuals and learn probabilistic models to predict the likelihood of bNAb development. We formally show that lower probabilities for bNAbs are predictive of higher HIV-1 neutralization activity. Moreover, ranking bNAbs by their probabilities allows to identify highly potent antibodies with superior generation probabilities as preferential targets for vaccination approaches. Importantly, we find equal bNAb probabilities across infected and uninfected individuals. This implies that chronic infection is not a prerequisite for the generation of bNAbs, fostering the hope that HIV-1 vaccines can induce bNAb development in uninfected people.

Suggested Citation

  • Christoph Kreer & Cosimo Lupo & Meryem S. Ercanoglu & Lutz Gieselmann & Natanael Spisak & Jan Grossbach & Maike Schlotz & Philipp Schommers & Henning Gruell & Leona Dold & Andreas Beyer & Armita Nourm, 2023. "Probabilities of developing HIV-1 bNAb sequence features in uninfected and chronically infected individuals," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-42906-y
    DOI: 10.1038/s41467-023-42906-y
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