Evidence map›Paper›PMID 27401039›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2016

Elimination of Latently HIV-infected Cells from Antiretroviral Therapy-suppressed Subjects by Engineered Immune-mobilizing T-cell Receptors.

Hongbing Yang, Sandrine Buisson, Giovanna Bossi, Zoë Wallace, Gemma Hancock, Chun So, Rebecca Ashfield, Annelise Vuidepot, Tara Mahon, Peter Molloy and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.6field-weighted citation impact, top 7% of its field
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

34 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  6. Review
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  8. Article
  9. An HLA-E-targeted TCR bispecific molecule redirects T cell immunity against Mycobacterium tuberculosis.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Instability of the HLA-E peptidome of HIV presents a major barrier to therapeutic targeting.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  11. Tebentafusp: a first-in-class treatment for metastatic uveal melanoma.Therapeutic advances in medical oncology · 2023
    Review
  12. Article
  13. Article
  14. Article
  15. The reservoir of latent HIV.Frontiers in cellular and infection microbiology · 2022
    Review
  16. Review
  17. Article
  18. [Clinical cure strategy for hepatitis B: immunomodulatory therapy].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2020
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 1 country.

Hongbing YangNuffield Department of Medicine & Oxford NIHR Biomedical Research Centre, University of Oxford, Oxford, UK.
Sandrine BuissonImmunocore Ltd, Abingdon, Oxfordshire, UK.
Giovanna BossiImmunocore Ltd, Abingdon, Oxfordshire, UK.
Zoë WallaceNuffield Department of Medicine & Oxford NIHR Biomedical Research Centre, University of Oxford, Oxford, UK.
Gemma HancockNuffield Department of Medicine & Oxford NIHR Biomedical Research Centre, University of Oxford, Oxford, UK.
Chun SoNuffield Department of Medicine & Oxford NIHR Biomedical Research Centre, University of Oxford, Oxford, UK.
Rebecca AshfieldImmunocore Ltd, Abingdon, Oxfordshire, UK.
Annelise VuidepotImmunocore Ltd, Abingdon, Oxfordshire, UK.
Tara MahonImmunocore Ltd, Abingdon, Oxfordshire, UK.
Peter MolloyImmunocore Ltd, Abingdon, Oxfordshire, UK.
Joanne OatesImmunocore Ltd, Abingdon, Oxfordshire, UK.
Samantha J PastonImmunocore Ltd, Abingdon, Oxfordshire, UK.
Milos AleksicImmunocore Ltd, Abingdon, Oxfordshire, UK.
Namir J HassanImmunocore Ltd, Abingdon, Oxfordshire, UK.
Bent K JakobsenImmunocore Ltd, Abingdon, Oxfordshire, UK.
Lucy DorrellNuffield Department of Medicine & Oxford NIHR Biomedical Research Centre, University of Oxford, Oxford, UK. Electronic address: lucy.dorrell@ndm.ox.ac.uk.
Immunocore (United Kingdom) · GBOxford BioMedica (United Kingdom) · GBUniversity of Oxford · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Persistence of human immunodeficiency virus (HIV) in a latent state in long-lived CD4+ T-cells is a major barrier to eradication. Latency-reversing agents that induce direct or immune-mediated cell death upon reactivation of HIV are a possible solution. However, clearance of reactivated cells may require immunotherapeutic agents that are fine-tuned to detect viral antigens when expressed at low levels. We tested the antiviral efficacy of immune-mobilizing monoclonal T-cell receptors against viruses (ImmTAVs), bispecific molecules that redirect CD8+ T-cells to kill HIV-infected CD4+ T-cells. T-cell receptors specific for an immunodominant Gag epitope, SL9, and its escape variants were engineered to achieve supraphysiological affinity and fused to a humanised CD3-specific single chain antibody fragment. Ex vivo polyclonal CD8+ T-cells were efficiently redirected by immune-mobilising monoclonal T-cell receptors against viruses to eliminate CD4+ T-cells from human histocompatibility leukocyte antigen (HLA)-A*0201-positive antiretroviral therapy-treated patients after reactivation of inducible HIV in vitro. The efficiency of infected cell elimination correlated with HIV Gag expression. Immune-mobilising monoclonal T-cell receptors against viruses have potential as a therapy to facilitate clearance of reactivated HIV reservoir cells.

Indexed as

Antibodies, MonoclonalAntiretroviral Therapy, Highly ActiveCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell LineHIV-1HIV AntibodiesHIV InfectionsHumansReceptors, Antigen, T-CellVirus LatencyAntibodies, MonoclonalHIV AntibodiesReceptors, Antigen, T-Cell

Identifiers

PMID27401039
PMCPMC5154472
OpenAlexW2432068972

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

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.