Evidence map›Paper›PMID 28159893›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Dynamics of SIV-specific CXCR5+ CD8 T cells during chronic SIV infection.

Geetha H Mylvaganam, Daniel Rios, Hadia M Abdelaal, Smita Iyer, Gregory Tharp, Maud Mavigner, Sakeenah Hicks, Ann Chahroudi, Rafi Ahmed, Steven E Bosinger and 4 more

Erratum issuedAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
10.3field-weighted citation impact, top 1% 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

89 citing papers in PubMed, 122 citations in OpenAlex.

  1. C-X-C chemokine receptor type 5World journal of gastroenterology · 2025
    Trial
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  4. Trial
  5. Article
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  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. An angel or a devil? Current view on the role of CD8Journal of translational medicine · 2024
    Review
  14. Cytolytic CD8Science immunology · 2023
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 2 institutions in 2 countries.

Geetha H MylvaganamDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322.
Daniel RiosDepartment of Pathology, Emory University School of Medicine, Atlanta, GA 30322.
Hadia M AbdelaalDepartment of Veterinary and Biomedical Sciences, University of Minnesota, Saint Paul, MN 55108.
Smita IyerDivision of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA 30329.
Gregory TharpDivision of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA 30329.
Maud MavignerDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322.
Sakeenah HicksDivision of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA 30329.
Ann ChahroudiDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322.
Rafi AhmedDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322; ramara@emory.edu vvelu@emory.edu rahmed@emory.edu.
Steven E BosingerDivision of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA 30329.
Ifor R WilliamsDepartment of Pathology, Emory University School of Medicine, Atlanta, GA 30322.
Pamela J SkinnerDepartment of Veterinary and Biomedical Sciences, University of Minnesota, Saint Paul, MN 55108.
Vijayakumar VeluDivision of Microbiology and Immunology, Emory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA 30329; ramara@emory.edu vvelu@emory.edu rahmed@emory.edu.
Rama R AmaraDepartment of Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA 30322; ramara@emory.edu vvelu@emory.edu rahmed@emory.edu.ORCID 0000-0002-6309-6797
Emory University · USUniversity of Minnesota · US

Funding

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
YNPRC NHP CLINICAL MEDICINE RESIDENCY PROGRAM - SUPPLEMENTP51RR000165 · NCRR · EMORY UNIVERSITY · PI ALTMAN, JOHN DAVID · 1985 to 2011
$114.0M
Virology and Molecular Biomarkers CoreP30AI050409 · NIAID · EMORY UNIVERSITY · PI Carlos del Rio · 2002 to 2026
$74.0M
Targeting mTOR to Enhance Immunogenicity and Efficacy of HIV VaccinesP01AI088575 · NIAID · EMORY UNIVERSITY · PI AMARA, RAMA RAO · 2010 to 2013
$11.4M
Preclinical Studies and T cell ResponsesU19AI109633 · NIAID · EMORY UNIVERSITY · PI AMARA, RAMA RAO · 2014 to 2018
$10.2M
Targeting PD-1 Pathway for Functional Cure of AIDSR37AI112787 · NIAID · EMORY UNIVERSITY · PI AMARA, RAMA RAO · 2014 to 2023
$9.2M
SPF Breeding Colonies at the Yerkes NPRCU24OD011023 · OD · EMORY UNIVERSITY · PI COHEN, JOYCE KIMBERLY · 2012 to 2017
$8.2M
Mechanisms Underlying Persistent Lentivirus Replication in Follicular T CellsR01AI096966 · NIAID · UNIVERSITY OF COLORADO DENVER · PI CONNICK, ELIZABETH, SKINNER, PAMELA J · 2013 to 2017
$4.2M
NCRR NIH HHS P51 RR000165NIAID NIH HHS P01 AI088575NIAID NIH HHS P30 AI050409NIAID NIH HHS R01 AI096966NIAID NIH HHS R37 AI112787NIAID NIH HHS U19 AI109633NIH HHS P51 OD011132NIH HHS U24 OD011023
6 · The paper itself

Abstract

A significant challenge to HIV eradication is the elimination of viral reservoirs in germinal center (GC) T follicular helper (Tfh) cells. However, GCs are considered to be immune privileged for antiviral CD8 T cells. Here, we show a population of simian immunodeficiency virus (SIV)-specific CD8 T cells express CXCR5 (C-X-C chemokine receptor type 5, a chemokine receptor required for homing to GCs) and expand in lymph nodes (LNs) following pathogenic SIV infection in a cohort of vaccinated macaques. This expansion was greater in animals that exhibited superior control of SIV. The CXCR5+ SIV-specific CD8 T cells demonstrated enhanced polyfunctionality, restricted expansion of antigen-pulsed Tfh cells in vitro

Indexed as

AnimalsCD8-Positive T-LymphocytesChronic DiseaseGerminal CenterMacaca mulattaMaleReceptors, CXCR5Simian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusReceptors, CXCR5CXCR5+CD8+ T cellsfollicular CD8 T cellsHIVlymphoid folliclesSIV

Identifiers

PMID28159893
PMCPMC5338410
OpenAlexW2583644004

What OpenQuestion holds

Textmetadata
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.