Evidence map›Paper›PMID 27183217›Full record

ArticleNature medicine2016

Impact of pre-adapted HIV transmission.

Jonathan M Carlson, Victor Y Du, Nico Pfeifer, Anju Bansal, Vincent Y F Tan, Karen Power, Chanson J Brumme, Anat Kreimer, Charles E DeZiel, Nicolo Fusi and 20 more

Abstract read
In one paragraph

Article in Nature medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing 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

77 citing papers in PubMed.

  1. Trial
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  14. Article
  15. Cytokine Storm Syndrome as a Manifestation of Primary HIV Infection.Advances in experimental medicine and biology · 2024
    Review
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors.

Jonathan M CarlsonMicrosoft Research, Redmond, Washington, USA.ORCID 0000-0001-6618-3653
Victor Y DuDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Nico PfeiferMicrosoft Research, Redmond, Washington, USA.
Anju BansalDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Vincent Y F TanMicrosoft Research, Redmond, Washington, USA.
Karen PowerRagon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts, USA.
Chanson J BrummeBritish Columbia Centre for Excellence in HIV/AIDS, Vancouver, British Columbia, Canada.
Anat KreimerMicrosoft Research, Redmond, Washington, USA.
Charles E DeZielMicrosoft Research, Redmond, Washington, USA.
Nicolo FusiMicrosoft Research, Redmond, Washington, USA.ORCID 0000-0002-4102-0169
Malinda SchaeferEmory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA.
Mark A BrockmanBritish Columbia Centre for Excellence in HIV/AIDS, Vancouver, British Columbia, Canada.
Jill GilmourInternational AIDS Vaccine Initiative, New York, New York, USA.
Matt A PriceInternational AIDS Vaccine Initiative, New York, New York, USA.
William KilembeRwanda-Zambia HIV Research Group, Zambia-Emory HIV Research Project, Lusaka, Zambia.
Richard HaubrichGilead Sciences, Foster City, California, USA.
Mina JohnInstitute for Immunology and Infectious Diseases, Murdoch University, Murdoch, Western Australia, Australia.
Simon MallalInstitute for Immunology and Infectious Diseases, Murdoch University, Murdoch, Western Australia, Australia.
Roger ShapiroHarvard T.H. Chan School of Public Health, Harvard University, Boston, Massachusetts, USA.
John FraterNuffield Department of Clinical Medicine, University of Oxford, Oxford, UK.
P Richard HarriganBritish Columbia Centre for Excellence in HIV/AIDS, Vancouver, British Columbia, Canada.
Thumbi Ndung'uRagon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts, USA.
Susan AllenRwanda-Zambia HIV Research Group, Zambia-Emory HIV Research Project, Lusaka, Zambia.
David HeckermanMicrosoft Research, Redmond, Washington, USA.
John SidneyDivision of Vaccine Discovery, La Jolla Institute for Allergy and Immunology, La Jolla, California, USA.
Todd M AllenRagon Institute of Massachusetts General Hospital, Massachusetts Institute of Technology and Harvard University, Cambridge, Massachusetts, USA.
Philip J R GoulderHIV Pathogenesis Programme, the Doris Duke Medical Research Institute, University of KwaZulu-Natal, Durban, South Africa.
Zabrina L BrummeBritish Columbia Centre for Excellence in HIV/AIDS, Vancouver, British Columbia, Canada.
Eric HunterEmory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia, USA.ORCID 0000-0002-4273-8631
Paul A GoepfertDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Funding

LOC: HIV Vaccine Trials NetworkUM1AI068614 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Dan H. Barouch, Lawrence Corey · 2011 to 2026
$1175.6M
Leadership and Operations Center (LOC), AIDS Clinical Trials Group (ACTG); LOC 1/UM1AI068636 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Joseph J Eron, RAJESH T GANDHI · 2011 to 2026
$1073.1M
SDMC: HIV Vaccine Trials NetworkUM1AI068635 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Peter B. Gilbert, Yunda Huang · 2011 to 2026
$385.9M
Statistical and Data Management Center (SDMC), AIDS Clinical Trials Group (ACTG)UM1AI068634 · NIAID · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Marlene Ann Cooper, Michael David Hughes · 2011 to 2026
$246.6M
Yerkes National Primate Research Center Role of type-I IFN in regulating COVID-19 induced inflammation and pathogenesisP51OD011132 · OD · EMORY UNIVERSITY · PI Joon Sup Lee · 2012 to 2026
$167.0M
AIDS Clinical Trials Group NetworkU01AI068636 · NIAID · SOCIAL AND SCIENTIFIC SYSTEMS, INC. · PI KURITZKES, DANIEL R. · 2006 to 2010
$147.1M
Virology CoreP30AI027767 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OLAF KUTSCH · 1988 to 2026
$84.1M
Virology and Molecular Biomarkers CoreP30AI050409 · NIAID · EMORY UNIVERSITY · PI Carlos del Rio · 2002 to 2026
$74.0M
Tennessee CFAR: Implementation of Culturally Responsive Trauma-Informed Care with Youth with HIV in Memphis, TNP30AI110527 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI John Koethe · 2015 to 2026
$27.5M
CTL and HIV Polymorphisms in Heterosexual TransmissionR01AI064060 · NIAID · EMORY UNIVERSITY · PI GOEPFERT, PAUL A., HUNTER, ERIC · 2005 to 2019
$21.7M
Recognition of HIV-1 by Innate Immunity Receptors during Primary InfectionP01AI074415 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI ALLEN, TODD M · 2008 to 2013
$17.3M
Virologic Correlates of Heterosexual TransmissionR37AI051231 · NIAID · EMORY UNIVERSITY · PI HUNTER, ERIC · 2008 to 2017
$9.6M
Howard Hughes Medical InstituteMedical Research Council MR/L006588/1NIAID NIH HHS P01 AI074415NIAID NIH HHS P30 AI027767NIAID NIH HHS P30 AI050409NIAID NIH HHS P30 AI110527NIAID NIH HHS R01 AI046995NIAID NIH HHS R01 AI064060NIAID NIH HHS R01 AI071906NIAID NIH HHS R01 AI112566NIAID NIH HHS R37 AI051231NIAID NIH HHS R56 AI098551NIAID NIH HHS U01 AI066454NIAID NIH HHS U01 AI068636NIAID NIH HHS UM1 AI068614NIAID NIH HHS UM1 AI068634NIAID NIH HHS UM1 AI068635NIH HHS P51 OD011132Wellcome TrustWellcome Trust WT104748MA
6 · The paper itself

Abstract

Human leukocyte antigen class I (HLA)-restricted CD8(+) T lymphocyte (CTL) responses are crucial to HIV-1 control. Although HIV can evade these responses, the longer-term impact of viral escape mutants remains unclear, as these variants can also reduce intrinsic viral fitness. To address this, we here developed a metric to determine the degree of HIV adaptation to an HLA profile. We demonstrate that transmission of viruses that are pre-adapted to the HLA molecules expressed in the recipient is associated with impaired immunogenicity, elevated viral load and accelerated CD4(+) T cell decline. Furthermore, the extent of pre-adaptation among circulating viruses explains much of the variation in outcomes attributed to the expression of certain HLA alleles. Thus, viral pre-adaptation exploits 'holes' in the immune response. Accounting for these holes may be key for vaccine strategies seeking to elicit functional responses from viral variants, and to HIV cure strategies that require broad CTL responses to achieve successful eradication of HIV reservoirs.

Indexed as

Adaptation, PhysiologicalAfrica, SouthernAIDS VaccinesBritish ColumbiaCD4 Lymphocyte CountCD8-Positive T-LymphocytesCohort StudiesEvolution, MolecularHistocompatibility Antigens Class IHIV-1HIV InfectionsHumansImmune EvasionImmunity, CellularLinear ModelsModels, ImmunologicalAIDS VaccinesHistocompatibility Antigens Class IReceptors, Antigen, T-Cell

Identifiers

PMID27183217
PMCPMC4899163

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Registered trials

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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.