Evidence map›Paper›PMID 26983786›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2016

HIV-1-Specific CD8 T Cells Exhibit Limited Cross-Reactivity during Acute Infection.

Victor Y Du, Anju Bansal, Jonathan Carlson, Jesus F Salazar-Gonzalez, Maria G Salazar, Kristin Ladell, Stephanie Gras, Tracy M Josephs, Sonya L Heath, David A Price and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. CD8Immunity · 2021
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Lessons from acute HIV infection.Current opinion in HIV and AIDS · 2016
    Review
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

13 authors at 7 institutions in 4 countries.

Victor Y DuDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294;
Anju BansalDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294;ORCID http://orcid.org/0000-0003-1880-4093
Jonathan CarlsonMicrosoft Research, Redmond, WA 98052;ORCID http://orcid.org/0000-0001-6618-3653
Jesus F Salazar-GonzalezDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294;ORCID http://orcid.org/0000-0003-4626-6448
Maria G SalazarDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294;ORCID http://orcid.org/0000-0003-0823-7697
Kristin LadellInstitute of Infection and Immunity, Cardiff University School of Medicine, Cardiff CF14 4XN, United Kingdom;ORCID http://orcid.org/0000-0002-9856-2938
Stephanie GrasInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria 3800, Australia; Australian Research Council Centre of Excellence for Advanced Molecular Imaging, Monash University, Clayton, Victoria 3800, Australia;ORCID http://orcid.org/0000-0001-7416-038X
Tracy M JosephsInfection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria 3800, Australia;
Sonya L HeathDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294;ORCID http://orcid.org/0000-0002-3826-0954
David A PriceInstitute of Infection and Immunity, Cardiff University School of Medicine, Cardiff CF14 4XN, United Kingdom; Human Immunology Section, Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892; and.
Jamie RossjohnInstitute of Infection and Immunity, Cardiff University School of Medicine, Cardiff CF14 4XN, United Kingdom; Infection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, Victoria 3800, Australia; Australian Research Council Centre of Excellence for Advanced Molecular Imaging, Monash University, Clayton, Victoria 3800, Australia;
Eric HunterDepartment of Pathology and Laboratory Medicine, Emory University, Atlanta, GA 30329.ORCID http://orcid.org/0000-0002-4273-8631
Paul A GoepfertDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294; paulg@uab.edu.ORCID http://orcid.org/0000-0001-8441-5737
University of Alabama at Birmingham · USAustralian Research Council · AUDiscovery Institute · USEmory University · USInstitute of Infection and Immunity · CAMicrosoft (United States) · USNational Institutes of Health · US

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
CTL and HIV Polymorphisms in Heterosexual TransmissionR01AI064060 · NIAID · EMORY UNIVERSITY · PI GOEPFERT, PAUL A., HUNTER, ERIC · 2005 to 2019
$21.7M
A Rational Approach for HIV Vaccine T Cell Epitope SelectionR01AI112566 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GOEPFERT, PAUL A. · 2014 to 2017
$1.9M
Medical Research Council G0501963NCI NIH HHS P30 CA013148NIAID NIH HHS R01 AI064060NIAID NIH HHS R01 AI112566Wellcome Trust 059864Wellcome Trust 093053
6 · The paper itself

Abstract

Prior work has demonstrated that HIV-1-specific CD8 T cells can cross-recognize variant epitopes. However, most of these studies were performed in the context of chronic infection, where the presence of viral quasispecies makes it difficult to ascertain the true nature of the original antigenic stimulus. To overcome this limitation, we evaluated the extent of CD8 T cell cross-reactivity in patients with acute HIV-1 clade B infection. In each case, we determined the transmitted founder virus sequence to identify the autologous epitopes restricted by individual HLA class I molecules. Our data show that cross-reactive CD8 T cells are infrequent during the acute phase of HIV-1 infection. Moreover, in the uncommon instances where cross-reactive responses were detected, the variant epitopes were poorly recognized in cytotoxicity assays. Molecular analysis revealed that similar antigenic structures could be cross-recognized by identical CD8 T cell clonotypes mobilized in vivo, yet even subtle differences in a single TCR-accessible peptide residue were sufficient to disrupt variant-specific reactivity. These findings demonstrate that CD8 T cells are highly specific for autologous epitopes during acute HIV-1 infection. Polyvalent vaccines may therefore be required to provide optimal immune cover against this genetically labile pathogen.

Indexed as

CD8-Positive T-LymphocytesCell LineCross ReactionsCrystallography, X-RayEpitopes, T-LymphocyteHIV-1HIV InfectionsHLA-B27 AntigenHLA-B7 AntigenHumansEpitopes, T-LymphocyteHLA-B*07:02 antigenHLA-B*27:05 antigenHLA-B27 AntigenHLA-B7 Antigen

Identifiers

PMID26983786
PMCPMC4821763
OpenAlexW2310732710

What OpenQuestion holds

Textmetadata
LicenceTDM
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.