Evidence map›Paper›PMID 21283794›Full record

ArticlePloS one2011

Dynamics of viral evolution and CTL responses in HIV-1 infection.

Yi Liu, John P McNevin, Sarah Holte, M Juliana McElrath, James I Mullins

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

46 citing papers in PubMed, 69 citations in OpenAlex.

  1. Trial
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  8. Review
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  10. Article
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  12. Article
  13. Phylogenetic approach to recover integration dates of latent HIV sequences within-host.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  14. Quarter Century of Anti-HIV CAR T Cells.Current HIV/AIDS reports · 2018
    Review
  15. Article
  16. Article
  17. Article
  18. Engineering HIV-Resistant, Anti-HIV Chimeric Antigen Receptor T Cells.Molecular therapy : the journal of the American Society of Gene Therapy · 2017
    Article
  19. Article
  20. Article
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

5 authors at 3 institutions in 1 country.

Yi LiuDepartment of Microbiology, University of Washington School of Medicine, Seattle, Washington, United States of America.
John P McNevin
Sarah Holte
M Juliana McElrath
James I Mullins
Cancer Research Center · USUniversity of Washington · USFred Hutch Cancer Center · US

Funding

University of Washington/Fred Hutch Center for AIDS ResearchP30AI027757 · NIAID · UNIVERSITY OF WASHINGTON · PI Kenneth Sherr · 1988 to 2026
$104.9M
ZIPRASIDONE IN NORMAL HEPATIC FUNCTION SUBJECTS &IN HEPATIC DYSFUCTIN SUBJECTSM01RR000037 · NCRR · UNIVERSITY OF WASHINGTON · PI MCDONALD, RUTH C · 1985 to 2007
$33.8M
Viral Determinants of HIV-1 Transmission in African HeterosexualsP01AI057005 · NIAID · UNIVERSITY OF WASHINGTON · PI COREY, LAWRENCE · 2003 to 2014
$20.5M
Mathematical and Experimental Models for HIV DynamicsR01AI055343 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI HOLTE, SARAH E · 2003 to 2007
$1.7M
NCRR NIH HHS M01 RR000037NCRR NIH HHS M01-RR-00037NIAID NIH HHS P01 AI057005NIAID NIH HHS P01 AI57005NIAID NIH HHS P30 AI027757NIAID NIH HHS P30 AI27757NIAID NIH HHS R01 AI055343
6 · The paper itself

Abstract

Improved understanding of the dynamics of host immune responses and viral evolution is critical for effective HIV-1 vaccine design. We comprehensively analyzed Cytotoxic T-lymphocyte (CTL)-viral epitope dynamics in an antiretroviral therapy-naïve subject over the first four years of HIV-1 infection. We found that CTL responses developed sequentially and required constant antigenic stimulation for maintenance. CTL responses exerting strong selective pressure emerged early and led to rapid escape, proliferated rapidly and were predominant during acute/early infection. Although CTL responses to a few persistent epitopes developed over the first two months of infection, they proliferated slowly. As CTL epitopes were replaced by mutational variants, the corresponding responses immediately declined, most rapidly in the cases of strongly selected epitopes. CTL recognition of epitope variants, via cross-reactivity and de novo responses, was common throughout the period of study. Our data demonstrate that HIV-specific CTL responses, especially in the critical acute/early stage, were focused on regions that are prone to escape. Failure of CTL responses to strongly target functional or structurally critical regions of the virus, as well as the sequential cascade of CTL responses, followed closely by viral escape and decline of the corresponding responses, likely contribute to a lack of sustainable viral suppression. Focusing early and rapidly proliferating CTL on persistent epitopes may be essential for durable viral control in HIV-1 infection.

Indexed as

Biological EvolutionEpitopes, T-LymphocyteHIV-1HIV InfectionsHumansImmune EvasionMutationT-Lymphocytes, CytotoxicEpitopes, T-Lymphocyte

Identifiers

PMID21283794
PMCPMC3024315
OpenAlexW2167155055

What OpenQuestion holds

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LicenceCC BY
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.