Evidence map›Paper›PMID 32675558›Full record

ArticleAIDS (London, England)2020

Changes in gastrointestinal microbial communities influence HIV-specific CD8+ T-cell responsiveness to immune checkpoint blockade.

Ivo N SahBandar, Glen M Chew, Michael J Corley, Alina P S Pang, Naoky Tsai, Nancy Hanks, Vedbar S Khadka, Nichole R Klatt, Tiffany Hensley-McBain, Ma Somsouk and 4 more

Open access · greenAbstract read
In one paragraph

Article in AIDS (London, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 53% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Review
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

14 authors at 4 institutions in 1 country.

Ivo N SahBandarDepartment of Tropical Medicine.
Glen M ChewDepartment of Tropical Medicine.
Michael J CorleyDepartment of Native Hawaiian Health.
Alina P S PangDepartment of Native Hawaiian Health.
Naoky TsaiHawaii Center for AIDS.
Nancy HanksHawaii Center for AIDS.
Vedbar S KhadkaDepartment of Biostatistics and Quantitative Health Science, John A. Burns School of Medicine, University of Hawaii, Honolulu, Hawaii.
Nichole R KlattDepartment of Pharmaceutics, University of Washington, Seattle, Washington.
Tiffany Hensley-McBainDepartment of Pharmaceutics, University of Washington, Seattle, Washington.
Ma SomsoukDivision of Gastroenterology, Department of Medicine, Zuckerberg San Francisco General Hospital, University of California, San Francisco, California.
Ivan Vujkovic-CvijinMetaorganism Immunity Section, National Institute of Allergy & Infectious Disease, National Institutes of Health, Bethesda, Maryland, USA.
Dominic C ChowHawaii Center for AIDS.
Cecilia M ShikumaHawaii Center for AIDS.
Lishomwa C NdhlovuDepartment of Tropical Medicine.
University of Washington · USAIDS United · USUniversity of California, San Francisco · USUniversity of Hawaiʻi at Mānoa · US

Funding

University of Washington/Fred Hutch Center for AIDS ResearchP30AI027757 · NIAID · UNIVERSITY OF WASHINGTON · PI EDWIN ROBERTO ORELLANA · 1988 to 2026
$104.9M
Tracking and EvaluationU54GM104944 · NIGMS · UNIVERSITY OF NEVADA LAS VEGAS · PI MARCHAND, GWEN · 2013 to 2023
$39.6M
Impact of Cannabis on Inflammation and Viral Persistence in Treated HIV/SIVDP1DA037979 · NIDA · UNIVERSITY OF WASHINGTON · PI KLATT, NICHOLE ROSE · 2015 to 2019
$4.3M
Targeting novel pathways to enhance gastrointestinal integrity during HIV infectionR01DK112254 · NIDDK · UNIVERSITY OF WASHINGTON · PI BURGENER, ADAM, KLATT, NICHOLE ROSE · 2017 to 2021
$1.8M
The role of epigenetic transcriptional memory in monocyte-macrophage cells and cardiovascular disease riskK01HL140271 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI CORLEY, MICHAEL JAY · 2018 to 2022
$788k
Reversal of Adaptive Immune Dysfunction in Shock and Kill HIV Cure StrategiesR21AI122393 · NIAID · UNIVERSITY OF HAWAII AT MANOA · PI NDHLOVU, LISHOMWA C · 2016 to 2017
$471k
Fecal microbial transplantation to reduce HIV-associated inflammationR21DK104664 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SOMSOUK, MA · 2015 to 2016
$436k
Modulating Tim-3 to control HIV infectionR56AI083112 · NIAID · UNIVERSITY OF HAWAII AT MANOA · PI NDHLOVU, LISHOMWA C · 2010 to 2010
$377k
NHLBI NIH HHS K01 HL140271NIAID NIH HHS P30 AI027757NIAID NIH HHS R21 AI122393NIAID NIH HHS R56 AI083112NIDA NIH HHS DP1 DA037979NIDDK NIH HHS R01 DK112254NIDDK NIH HHS R21 DK104664NIGMS NIH HHS U54 GM104944
6 · The paper itself

Abstract

objectivesThe aim of this study was to examine the relationship between gut microbial communities in HIV-infected individuals on suppressive antiretroviral therapy (cART), and the peripheral HIV-Gag-specific CD8 T-cell responses before and after ex-vivo immune checkpoint blockade (ICB).

designThirty-four HIV-seropositive, 10 HIV-seronegative and 12 HIV-seropositive receiving faecal microbiota transplant (FMT) participants were included. Gut microbial communities, peripheral and gut associated negative checkpoint receptors (NCRs) and peripheral effector functions were assessed.

methodsBacterial 16s rRNA sequencing for gut microbiome study and flow-based assays for peripheral and gut NCR and their cognate ligand expression, including peripheral HIV-Gag-specific CD8 T-cell responses before and after ex-vivo anti-PD-L1 and anti-TIGIT ICB were performed.

resultsFusobacteria abundance was significantly higher in HIV-infected donors compared to uninfected controls. In HIV-infected participants receiving Fusobacteria-free FMT, Fusobacteria persisted up to 24 weeks in stool post FMT. PD-1 TIGIT and their ligands were expanded in mucosal vs. peripheral T cells and dendritic cells, respectively. PD-L1 and TIGIT blockade significantly increased the magnitude of peripheral anti-HIV-Gag-specific CD8 T-cell responses. Higher gut Fusobacteria abundance was associated with lower magnitude of peripheral IFN-γ+ HIV-Gag-specific CD8 T-cell responses following ICB.

conclusionThe gut colonization of Fusobacteria in HIV infection is persistent and may influence anti-HIV T-cell immunity to PD-1 or TIGIT blockade. Strategies modulating Fusobacteria colonization may elicit a favourable mucosal immune landscape to enhance the efficacy of ICB for HIV cure.

Indexed as

Gastrointestinal MicrobiomeAdultAgedAnti-HIV AgentsCD8-Positive T-LymphocytesFecal Microbiota TransplantationFemaleFusobacteriaHIV InfectionsHumansImmune Checkpoint InhibitorsMaleMiddle AgedRNA, Ribosomal, 16SSexual and Gender MinoritiesAnti-HIV AgentsImmune Checkpoint InhibitorsRNA, Ribosomal, 16S

Identifiers

PMID32675558
PMCPMC7371239
OpenAlexW3043222318

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Registered trials

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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.