Evidence map›Paper›PMID 38355731›Full record

ArticleNature communications2024

TGF-β blockade drives a transitional effector phenotype in T cells reversing SIV latency and decreasing SIV reservoirs in vivo.

Jinhee Kim, Deepanwita Bose, Mariluz Araínga, Muhammad R Haque, Christine M Fennessey, Rachel A Caddell, Yanique Thomas, Douglas E Ferrell, Syed Ali, Emanuelle Grody and 9 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. 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 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 5 institutions in 1 country.

Jinhee KimDepartment of Medicine, Division of Infectious Diseases, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Deepanwita Bose *New Iberia Research Center, University of Louisiana at Lafayette, New Iberia, LA, USA.ORCID 0000-0003-4164-6556
Mariluz Araínga *New Iberia Research Center, University of Louisiana at Lafayette, New Iberia, LA, USA.
Muhammad R HaqueCell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Christine M FennesseyAIDS and Cancer Virus Program, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
Rachel A CaddellDivision of Immunology, Tulane National Primate Research Center, Covington, LA, USA.
Yanique ThomasCell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Douglas E FerrellNew Iberia Research Center, University of Louisiana at Lafayette, New Iberia, LA, USA.
Syed AliNew Iberia Research Center, University of Louisiana at Lafayette, New Iberia, LA, USA.
Emanuelle GrodyCell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Yogesh GoyalCell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.ORCID 0000-0003-3502-6465
Claudia CicalaLaboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
James ArthosLaboratory of Immunoregulation, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-6767-4267
Brandon F KeeleAIDS and Cancer Virus Program, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.ORCID 0000-0002-2381-1151
Monica VaccariDivision of Immunology, Tulane National Primate Research Center, Covington, LA, USA.ORCID 0000-0002-4514-2681
Ramon Lorenzo-RedondoDepartment of Medicine, Division of Infectious Diseases, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.ORCID 0000-0002-5462-9483
Thomas J HopeCell and Developmental Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.ORCID 0000-0001-7183-8319
Francois VillingerNew Iberia Research Center, University of Louisiana at Lafayette, New Iberia, LA, USA.
Elena MartinelliDepartment of Medicine, Division of Infectious Diseases, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA. elena.martinelli@northwestern.edu.ORCID 0000-0002-3416-9627
Northwestern University · USUniversity of Louisiana at Lafayette · USFrederick National Laboratory for Cancer Research · USNational Institutes of Health · USTulane University · US

Funding

WORK ORDER 126643 B539 EXPAND IC SUITE75N91019D00024 · NIAID · LEIDOS BIOMEDICAL RESEARCH, INC. · PI BRISCOE, LYNN · 2019 to 2025
$3932.6M
Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Devalingam Mahalingam · 1993 to 2026
$153.9M
Tulane NPRC SPF Sheltered Outdoor Enclosure ExpansionP51OD011104 · OD · TULANE UNIVERSITY OF LOUISIANA · PI L Lee HAMM · 2012 to 2026
$142.4M
Nonhuman Primate Reagent ResourceU24AI126683 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Diogo Magnani · 2016 to 2026
$20.1M
Unraveling the Mechanisms of HIV Persistence and ReboundP01AI169600 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Thomas Hope · 2022 to 2026
$9.3M
Role of myeloid cells in CNS and systemic reservoirs and reboundR01MH125778 · NIMH · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Thomas Hope, Ramon Lorenzo-Redondo · 2022 to 2026
$5.1M
Resource for Nonhuman Primate Immune ReagentsR24OD010947 · OD · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI VILLINGER, FRANCOIS J · 2012 to 2025
$4.9M
Turning off HIV White Noise: Switching from Long-Lived to Short-Lived ReservoirR01AI176599 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Elena Martinelli · 2023 to 2026
$4.7M
TGFBR1 Blockade as Novel Release and Kill HIV StrategyR56AI157822 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MARTINELLI, ELENA · 2021 to 2021
$787k
NCI NIH HHS 75N91019D00024NCI NIH HHS HHSN261201500003CNCI NIH HHS HHSN261201500003INCI NIH HHS P30 CA060553NIAID NIH HHS P01 AI169600NIAID NIH HHS R01 AI176599NIAID NIH HHS R56 AI157822NIAID NIH HHS U24 AI126683NIH HHS P51 OD011104NIH HHS R24 OD010947NIMH NIH HHS R01 MH125778ODCDC CDC HHS R24 OD010947
6 · The paper itself

Abstract

HIV-1 persistence during ART is due to the establishment of long-lived viral reservoirs in resting immune cells. Using an NHP model of barcoded SIVmac239 intravenous infection and therapeutic dosing of anti-TGFBR1 inhibitor galunisertib (LY2157299), we confirm the latency reversal properties of in vivo TGF-β blockade, decrease viral reservoirs and stimulate immune responses. Treatment of eight female, SIV-infected macaques on ART with four 2-weeks cycles of galunisertib leads to viral reactivation as indicated by plasma viral load and immunoPET/CT with a

Indexed as

Simian Acquired Immunodeficiency SyndromeSimian Immunodeficiency VirusAnimalsCD4-Positive T-LymphocytesFemaleLeukocytes, MononuclearTransforming Growth Factor betaViral LoadVirus ReplicationTransforming Growth Factor beta

Identifiers

PMID38355731
PMCPMC10867093
OpenAlexW4391820664

What OpenQuestion holds

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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.