Evidence map›Paper›PMID 22922258›Full record

ArticleThe Journal of clinical investigation2012

CD4 T follicular helper cell dynamics during SIV infection.

Constantinos Petrovas, Takuya Yamamoto, Michael Y Gerner, Kristin L Boswell, Kaska Wloka, Emily C Smith, David R Ambrozak, Netanya G Sandler, Katherina J Timmer, Xiaoyong Sun and 12 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 240 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
240citing papers in PubMed, 2 pooled it
14.0field-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

240 citing papers in PubMed, 2 syntheses or guidelines pooled it, 314 citations in OpenAlex.

  1. The Hitchhiker Guide to CD4Frontiers in immunology · 2021
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180 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 3 institutions in 1 country.

Constantinos PetrovasVaccine Research Center, NIAID, NIH, Bethesda, MD 20892, USA. petrovasc@mail.nih.gov
Takuya Yamamoto
Michael Y Gerner
Kristin L Boswell
Kaska Wloka
Emily C Smith
David R Ambrozak
Netanya G Sandler
Katherina J Timmer
Xiaoyong Sun
Li Pan
Amanda Poholek
Srinivas S Rao
Jason M Brenchley
S Munir Alam
Georgia D Tomaras
Mario Roederer
Daniel C Douek
Robert A Seder
Ronald N Germain
Elias K Haddad
Richard A Koup
National Institutes of Health · USVaccine & Gene Therapy Institute of Florida · USDuke University · US

Funding

Optimization Of HIV Specific Immune Responses In VivoZIAAI005016 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SEDER, ROBERT A · 2009 to 2018
$31.2M
Multiscale Analysis of Immune ResponsesZIAAI000545 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI GERMAIN, RONALD N · 2009 to 2025
$29.4M
Mechanisms of Immune Activation and Disease Progression in Animal ModelsZIAAI001029 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI BRENCHLEY, JASON · 2009 to 2025
$28.2M
Tfh and B cells in HIV/SIV pathogenesis and vaccinationZIAAI005015 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI KOUP, RICHARD A · 2009 to 2025
$24.1M
Intramural NIH HHS
6 · The paper itself

Abstract

CD4 T follicular helper (TFH) cells interact with and stimulate the generation of antigen-specific B cells. TFH cell interaction with B cells correlates with production of SIV-specific immunoglobulins. However, the fate of TFH cells and their participation in SIV-induced antibody production is not well understood. We investigated the phenotype, function, location, and molecular signature of TFH cells in rhesus macaques. Similar to their human counterparts, TFH cells in rhesus macaques represented a heterogeneous population with respect to cytokine function. In a highly differentiated subpopulation of TFH cells, characterized by CD150lo expression, production of Th1 cytokines was compromised while IL-4 production was augmented, and cells exhibited decreased survival, cycling, and trafficking capacity. TFH cells exhibited a distinct gene profile that was markedly altered by SIV infection. TFH cells were infected by SIV; yet, in some animals, these cells actually accumulated during chronic SIV infection. Generalized immune activation and increased IL-6 production helped drive TFH differentiation during SIV infection. Accumulation of TFH cells was associated with increased frequency of activated germinal center B cells and SIV-specific antibodies. Therefore, chronic SIV does not disturb the ability of TFH cells to help B cell maturation and production of SIV-specific immunoglobulins.

Indexed as

AnimalsAntibodies, ViralB-LymphocytesCD4 AntigensCell DeathCell ProliferationCytokinesGene ExpressionGerminal CenterHost-Pathogen InteractionsLymph NodesMacaca mulattaOligonucleotide Array Sequence AnalysisProto-Oncogene Proteins c-mafReceptors, LysosphingolipidSimian Acquired Immunodeficiency SyndromeAntibodies, ViralCD4 AntigensCytokinesProto-Oncogene Proteins c-mafReceptors, LysosphingolipidT-Box Domain ProteinsTranscription Factors

Identifiers

PMID22922258
PMCPMC3428091
OpenAlexW2147365530

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.