Evidence map›Paper›PMID 28133802›Full record

ReviewImmunological reviews2017

Antibody-virus co-evolution in HIV infection: paths for HIV vaccine development.

Mattia Bonsignori, Hua-Xin Liao, Feng Gao, Wilton B Williams, S Munir Alam, David C Montefiori, Barton F Haynes

Abstract readReview
In one paragraph

Review in Immunological reviews, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

128 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Under the Radar: Immune Evasion, Pathogenesis and Control of HIV Infection.International journal of molecular sciences · 2025
    Review
  8. Article
  9. Article
  10. Activation of CXCR3Journal of virology · 2025
    Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. The CH1 domain influences the expression and antigen sensing of the HIV-specific CH31 IgM-BCR and IgG-BCR.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

68 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Mattia BonsignoriDepartment of Medicine, Duke University School of Medicine, Durham, NC, USA.
Hua-Xin LiaoDepartment of Medicine, Duke University School of Medicine, Durham, NC, USA.
Feng GaoDepartment of Medicine, Duke University School of Medicine, Durham, NC, USA.
Wilton B WilliamsDepartment of Medicine, Duke University School of Medicine, Durham, NC, USA.
S Munir AlamDepartment of Medicine, Duke University School of Medicine, Durham, NC, USA.
David C MontefioriDuke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, USA.
Barton F HaynesDepartment of Medicine, Duke University School of Medicine, Durham, NC, USA.

Funding

Virus biology scientific research support componentUM1AI100645 · NIAID · DUKE UNIVERSITY · PI MCMICHAEL, ANDREW JAMES · 2012 to 2018
$204.7M
NIAID NIH HHS UM1 AI100645
6 · The paper itself

Abstract

Induction of HIV-1 broadly neutralizing antibodies (bnAbs) to date has only been observed in the setting of HIV-1 infection, and then only years after HIV transmission. Thus, the concept has emerged that one path to induction of bnAbs is to define the viral and immunologic events that occur during HIV-1 infection, and then to mimic those events with a vaccine formulation. This concept has led to efforts to map both virus and antibody events that occur from the time of HIV-1 transmission to development of bnAbs. This work has revealed that a virus-antibody "arms race" occurs in which a HIV-1 transmitted/founder (TF) Env induces autologous neutralizing antibodies that can not only neutralize the TF virus but also can select virus escape mutants that in turn select affinity-matured neutralizing antibodies. From these studies has come a picture of bnAb development that has led to new insights in host-pathogen interactions and, as well, led to insight into immunologic mechanisms of control of bnAb development. Here, we review the progress to date in elucidating bnAb B cell lineages in HIV-1 infection, discuss new research leading to understanding the immunologic mechanisms of bnAb induction, and address issues relevant to the use of this information for the design of new HIV-1 sequential envelope vaccine candidates.

Indexed as

AIDS VaccinesAnimalsAntibodies, NeutralizingBiological EvolutionHIV-1HIV AntibodiesHIV AntigensHIV InfectionsHost-Pathogen InteractionsHumansImmune EvasionMutationAIDS VaccinesAntibodies, NeutralizingHIV AntibodiesHIV Antigensco-evolutionHIV neutralizationHIV vaccine

Identifiers

PMID28133802
PMCPMC5302796

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.