Evidence map›Paper›PMID 28983013›Full record

ArticleThe Journal of experimental medicine2017

Role of HIV-specific CD8

Ellen M Leitman, Christina F Thobakgale, Emily Adland, M Azim Ansari, Jayna Raghwani, Andrew J Prendergast, Gareth Tudor-Williams, Photini Kiepiela, Joris Hemelaar, Jacqui Brener and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

23 citing papers in PubMed, 35 citations in OpenAlex.

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  8. Long-term non-progression and risk factors for disease progression among children living with HIV in Botswana and Uganda: A retrospective cohort study.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2024
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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

23 authors at 14 institutions in 5 countries.

Ellen M LeitmanDepartment of Paediatrics, University of Oxford, Oxford, England, UK.
Christina F ThobakgaleHIV Pathogenesis Programme, Doris Duke Medical Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Emily AdlandDepartment of Paediatrics, University of Oxford, Oxford, England, UK.
M Azim AnsariOxford Martin School, University of Oxford, Oxford, England, UK.
Jayna RaghwaniDepartment of Zoology, University of Oxford, Oxford, England, UK.ORCID http://orcid.org/0000-0001-8538-4995
Andrew J PrendergastBlizard Institute, Queen Mary University of London, London, England, UK.
Gareth Tudor-WilliamsDivision of Medicine, Department of Paediatrics, Imperial College London, London, England, UK.
Photini KiepielaMedical Research Council, Durban, South Africa.ORCID http://orcid.org/0000-0003-2563-7617
Joris HemelaarNuffield Department of Obstetrics and Gynaecology, University of Oxford, John Radcliffe Hospital, Oxford, England, UK.
Jacqui BrenerDepartment of Paediatrics, University of Oxford, Oxford, England, UK.ORCID http://orcid.org/0000-0002-6528-6471
Ming-Han TsaiDepartment of Paediatrics, University of Oxford, Oxford, England, UK.
Masahiko MoriDepartment of Paediatrics, University of Oxford, Oxford, England, UK.
Lynn RiddellNorthampton Healthcare NHS Foundation Trust, Cliftonville, England, UK.
Graz LuzziBuckinghampshire Healthcare NHS Foundation Trust, High Wycombe, England, UK.
Pieter JoostePaediatric Department, Kimberley Hospital, Northern Cape, South Africa.ORCID http://orcid.org/0000-0002-8635-2255
Thumbi Ndung'uHIV Pathogenesis Programme, Doris Duke Medical Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Bruce D WalkerHIV Pathogenesis Programme, Doris Duke Medical Research Institute, University of KwaZulu-Natal, Durban, South Africa.ORCID http://orcid.org/0000-0001-6122-9245
Oliver G PybusDepartment of Zoology, University of Oxford, Oxford, England, UK.
Paul KellamKymab Ltd., Babraham Research Campus, Babraham, England, UK.ORCID http://orcid.org/0000-0003-3166-4734
Vivek NaranbhaiRagon Institute of MGH, MIT, and Harvard, Cambridge, MA.
Philippa C MatthewsDepartment of Infectious Diseases and Microbiology, Oxford University Hospitals NHS Trust, John Radcliffe Hospital, Oxford, England, UK.ORCID http://orcid.org/0000-0002-4036-4269
Astrid GallWellcome Trust Sanger Institute, Hinxton, England, UK.
Philip J R GoulderDepartment of Paediatrics, University of Oxford, Oxford, England, UK philip.goulder@paediatrics.ox.ac.uk.ORCID http://orcid.org/0000-0002-9842-4674
University of Oxford · GBRagon Institute of MGH, MIT and Harvard · USBuckinghamshire Healthcare NHS Trust · GBCentre for the AIDS Programme of Research in South Africa · ZAImperial College London · GBJohn Radcliffe Hospital · GBKimberley Hospital · ZAKymab (United Kingdom) · GBNorthamptonshire Healthcare NHS Foundation Trust · GBQueen Mary University of London · GBSouth African Medical Research Council · ZAUniversity of KwaZulu-Natal · ZAUniversity of the Witwatersrand · ZAWellcome Sanger Institute · GB

Funding

Wellcome Trust 098051
6 · The paper itself

Abstract

Recent studies have suggested greater HIV cure potential among infected children than adults. A major obstacle to HIV eradication in adults is that the viral reservoir is largely comprised of HIV-specific cytotoxic T lymphocyte (CTL) escape variants. We here evaluate the potential for CTL in HIV-infected slow-progressor children to play an effective role in "shock-and-kill" cure strategies. Two distinct subgroups of children were identified on the basis of viral load. Unexpectedly, in both groups, as in adults, HIV-specific CTL drove the selection of escape variants across a range of epitopes within the first weeks of infection. However, in HIV-infected children, but not adults, de novo autologous variant-specific CTL responses were generated, enabling the pediatric immune system to "corner" the virus. Thus, even when escape variants are selected in early infection, the capacity in children to generate variant-specific anti-HIV CTL responses maintains the potential for CTL to contribute to effective shock-and-kill cure strategies in pediatric HIV infection.

Indexed as

AdultCD8-Positive T-LymphocytesChildChild, PreschoolEpitopes, T-Lymphocytegag Gene Products, Human Immunodeficiency VirusHIV-1HIV InfectionsHLA AntigensHost-Pathogen InteractionsHumansImmune EvasionInterferon-gammaT-Lymphocytes, CytotoxicViral LoadEpitopes, T-Lymphocytegag Gene Products, Human Immunodeficiency VirusHLA AntigensInterferon-gamma

Identifiers

PMID28983013
PMCPMC5679167
OpenAlexW2761902165

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.