Evidence map›Paper›PMID 26297764›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

Decreased T Follicular Regulatory Cell/T Follicular Helper Cell (TFH) in Simian Immunodeficiency Virus-Infected Rhesus Macaques May Contribute to Accumulation of TFH in Chronic Infection.

Ankita Chowdhury, Perla Mariana Del Rio Estrada, Perla Maria Estrada Del Rio, Greg K Tharp, Ronald P Trible, Rama R Amara, Ann Chahroudi, Gustavo Reyes-Teran, Steven E Bosinger, Guido Silvestri

Erratum issuedAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. 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 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 82 citations in OpenAlex.

  1. The Hitchhiker Guide to CD4Frontiers in immunology · 2021
    Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Regulatory T Cell Plasticity and Stability and Autoimmune Diseases.Clinical reviews in allergy & immunology · 2020
    Review
  14. Follicular regulatory T cells: a novel target for immunotherapy?Clinical & translational immunology · 2020
    Review
  15. Article
  16. Article
  17. Programmed Death-1 Restrains the Germinal Center in Type 1 Diabetes.Journal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  18. Regulatory roles of IL-10-producing human follicular T cells.The Journal of experimental medicine · 2019
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Ankita ChowdhuryEmory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA30329;
Perla Mariana Del Rio EstradaEmory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA30329; Departamento de Investigación en Enfermedades Infecciosas, Instituto Nacional de Enfermedades Respiratorias, "Ismael Cosio Villegas," Tlapan, Sección XVI, 14080 City of Mexico Federal District, Mexico; and.
Perla Maria Estrada Del RioEmory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA30329; Departamento de Investigación en Enfermedades Infecciosas, Instituto Nacional de Enfermedades Respiratorias, "Ismael Cosio Villegas," Tlapan, Sección XVI, 14080 City of Mexico Federal District, Mexico; and.
Greg K TharpEmory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA30329;
Ronald P TribleEmory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA30329;
Rama R AmaraEmory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA30329;
Ann ChahroudiEmory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA30329; Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30329.
Gustavo Reyes-TeranDepartamento de Investigación en Enfermedades Infecciosas, Instituto Nacional de Enfermedades Respiratorias, "Ismael Cosio Villegas," Tlapan, Sección XVI, 14080 City of Mexico Federal District, Mexico; and.
Steven E BosingerEmory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA30329;
Guido SilvestriEmory Vaccine Center, Yerkes National Primate Research Center, Emory University, Atlanta, GA30329; gsilves@emory.edu.
Atlanta VA Medical Center · USEmory University · USInstituto Nacional de Enfermedades Respiratorias · MX

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
Role of Follicular T Helper Cells In Enhancing Humoral Immunity and ProtectionU19AI096187 · NIAID · EMORY UNIVERSITY · PI DERDEYN, CYNTHIA ANN · 2011 to 2015
$26.5M
Atlanta Pediatric Scholars ProgramK12HD072245 · NICHD · EMORY UNIVERSITY · PI Shari Barkin · 2012 to 2026
$5.5M
NCRR NIH HHS P51 RR000165NCRR NIH HHS RR000165NIAID NIH HHS P30 AI050409NIAID NIH HHS U19 AI096187NICHD NIH HHS K12 HD072245NIH HHS OD011132NIH HHS P51 OD011132
6 · The paper itself

Abstract

T follicular helper cells (TFH) are critical for the development and maintenance of germinal center (GC) and humoral immune responses. During chronic HIV/SIV infection, TFH accumulate, possibly as a result of Ag persistence. The HIV/SIV-associated TFH expansion may also reflect lack of regulation by suppressive follicular regulatory CD4(+) T cells (TFR). TFR are natural regulatory T cells (TREG) that migrate into the follicle and, similar to TFH, upregulate CXCR5, Bcl-6, and PD1. In this study, we identified TFR as CD4(+)CD25(+)FOXP3(+)CXCR5(+)PD1(hi)Bcl-6(+) within lymph nodes of rhesus macaques (RM) and confirmed their localization within the GC by immunohistochemistry. RNA sequencing showed that TFR exhibit a distinct transcriptional profile with shared features of both TFH and TREG, including intermediate expression of FOXP3, Bcl-6, PRDM1, IL-10, and IL-21. In healthy, SIV-uninfected RM, we observed a negative correlation between frequencies of TFR and both TFH and GC B cells, as well as levels of CD4(+) T cell proliferation. Post SIV infection, the TFR/TFH ratio was reduced with no change in the frequency of TREG or TFR within the total CD4(+) T cell pool. Finally, we examined whether higher levels of direct virus infection of TFR were responsible for their relative depletion post SIV infection. We found that TFH, TFR, and TREG sorted from SIV-infected RM harbor comparable levels of cell-associated viral DNA. Our data suggest that TFR may contribute to the regulation and proliferation of TFH and GC B cells in vivo and that a decreased TFR/TFH ratio in chronic SIV infection may lead to unchecked expansion of both TFH and GC B cells.

Indexed as

AnimalsBase SequenceB-LymphocytesCell ProliferationFemaleForkhead Transcription FactorsGerminal CenterImmunity, HumoralInterleukin-10Interleukin-21InterleukinsLymphocyte CountMacaca mulattaProto-Oncogene Proteins c-bcl-6Repressor ProteinsSequence Analysis, RNAForkhead Transcription FactorsInterleukin-10Interleukin-21InterleukinsProto-Oncogene Proteins c-bcl-6Repressor Proteins

Identifiers

PMID26297764
PMCPMC4575868
OpenAlexW2111038995

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.