Evidence map›Paper›PMID 30778076›Full record

ArticleNature communications2019

Adenosine deaminase-1 delineates human follicular helper T cell function and is altered with HIV.

Virginie Tardif, Roshell Muir, Rafael Cubas, Marita Chakhtoura, Peter Wilkinson, Talibah Metcalf, Rana Herro, Elias K Haddad

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

27 citing papers in PubMed, 29 citations in OpenAlex.

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  17. Catalytically active holo Homo sapiens adenosine deaminase I adopts a closed conformation.Acta crystallographica. Section D, Structural biology · 2022
    Article
  18. Generation of a Retargeted OncolyticInternational journal of molecular sciences · 2021
    Article
  19. Article
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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

8 authors at 3 institutions in 1 country.

Virginie TardifDepartment of Medicine, Division of Infectious Diseases and HIV Medicine, Drexel University, Philadelphia, 19102, PA, USA.
Roshell MuirDepartment of Medicine, Division of Infectious Diseases and HIV Medicine, Drexel University, Philadelphia, 19102, PA, USA.
Rafael CubasGenentech, San Francisco, 94080, CA, USA.
Marita ChakhtouraDepartment of Medicine, Division of Infectious Diseases and HIV Medicine, Drexel University, Philadelphia, 19102, PA, USA.
Peter WilkinsonDepartment of Pathology, Case Western Reserve University, Cleveland, OH, 44106, USA.
Talibah MetcalfDepartment of Medicine, Division of Infectious Diseases and HIV Medicine, Drexel University, Philadelphia, 19102, PA, USA.
Rana HerroLa Jolla Institute for Allergy and Immunology, San Diego, 92037, CA, USA.
Elias K HaddadDepartment of Medicine, Division of Infectious Diseases and HIV Medicine, Drexel University, Philadelphia, 19102, PA, USA. elias.elhaddad@drexelmed.edu.
Drexel University · USCase Western Reserve University · USLa Jolla Institute for Immunology · US

Funding

Investigating the impact of helminth infection on microbioma composition and innate immunity generated during HepB vaccination. U19AI128910 · NIAID · DREXEL UNIVERSITY · PI HADDAD, ELIAS K · 2017 to 2021
$7.0M
Boosting anti-HIV immunity through manipulation of Tfh function.R01AI106482 · NIAID · VGTI FLORIDA · PI HADDAD, ELIAS K · 2013 to 2017
$2.8M
NIAID NIH HHS R01 AI106482NIAID NIH HHS U19 AI128910
6 · The paper itself

Abstract

Follicular helper T cells (Tfh) play critical roles instructing, and initiating T-cell dependent antibody responses. The underlying mechanisms that enhance their function is therefore critical for vaccine development. Here we apply gene array analysis identifying adenosine deaminase (ADA) as a key molecule that delineates a human Tfh helper program in proliferating circulating Tfh (cTfh) cells and Germinal Centers Tfh (GC-Tfh). ADA-1 expression and enzymatic activity are increased in efficient cTfh2-17/GC-Tfh cells. Exogenous ADA-1 enhances less efficient cTfh1 and pro-follicular Tfh PD-1+ CXCR5+ cells to provide B cell help, while pharmacological inhibition of ADA-1 activity impedes cTfh2-17/GC-Tfh function and diminished antibody response. Mechanistically, ADA-1 controls the Tfh program by influencing IL6/IL-2 production, controlling CD26 extracellular expression and could balance signals through adenosine receptors. Interestingly, dysfunctional Tfh from HIV infected-individual fail to regulate the ADA pathway. Thus, ADA-1 regulates human Tfh and represents a potential target for development of vaccine strategy.

Indexed as

Adenosine DeaminaseAdenylyl CyclasesB-LymphocytesCoculture TechniquesDipeptidyl Peptidase 4Germinal CenterHIV InfectionsHumansInterleukin-2Interleukin-6T-Lymphocytes, Helper-InducerADA protein, humanAdenosine DeaminaseAdenylyl CyclasesDipeptidyl Peptidase 4DPP4 protein, humanIL2 protein, humanIL6 protein, humanInterleukin-2Interleukin-6

Identifiers

PMID30778076
PMCPMC6379489
OpenAlexW2914153814

What OpenQuestion holds

Textmetadata
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.