Evidence map›Paper›PMID 38353210›Full record

ArticleAnnals of medicine2024

Dual role for microbial short-chain fatty acids in modifying SIV disease trajectory following anti-α4β7 antibody administration.

Samuel D Johnson, Nageswara Pilli, Jianshi Yu, Lindsey A Knight, Maureen A Kane, Siddappa N Byrareddy

Open access · goldAbstract read
In one paragraph

Article in Annals of medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Samuel D JohnsonDepartment of Pathology and Microbiology, University of NE Medical Center, Omaha, NE, USA.ORCID 0000-0002-9978-6968
Nageswara PilliDepartment of Pharmaceutical Sciences, University of MD School of Pharmacy, Baltimore, MD, USA.
Jianshi YuDepartment of Pharmaceutical Sciences, University of MD School of Pharmacy, Baltimore, MD, USA.
Lindsey A KnightDepartment of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, USA.
Maureen A KaneDepartment of Pharmaceutical Sciences, University of MD School of Pharmacy, Baltimore, MD, USA.ORCID 0000-0002-5525-9170
Siddappa N ByrareddyDepartment of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, USA.ORCID 0000-0002-6889-4640
University of Maryland, Baltimore · USUniversity of Nebraska Medical Center · US

Funding

Nonhuman Primate Reagent ResourceU24AI126683 · NIAID · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Diogo Magnani · 2016 to 2026
$20.1M
Resource CoreP40OD028116 · OD · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI Diogo Magnani · 2020 to 2026
$5.9M
Limiting HIV establishment and maintenace by preserving intestinal immunityR01AI129745 · NIAID · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BYRAREDDY, SIDDAPPA N, PAIARDINI, MIRKO · 2017 to 2020
$3.3M
Neuroimmunology of Disease Training ProgramT32NS105594 · NINDS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI Aditya N Bade, Howard E Gendelman · 2018 to 2026
$1.4M
Targeting gut-brain axis to eliminate CNS reservoirsR21MH113455 · NIMH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI BYRAREDDY, SIDDAPPA N · 2017 to 2018
$414k
NIAID NIH HHS R01 AI129745NIAID NIH HHS U24 AI126683NIH HHS P40 OD028116NIMH NIH HHS R21 MH113455NINDS NIH HHS T32 NS105594
6 · The paper itself

Abstract

backgroundHuman Immunodeficiency Virus (HIV)/Simian Immunodeficiency Virus (SIV) infection is associated with significant gut damage, similar to that observed in patients with inflammatory bowel disease (IBD). This pathology includes loss of epithelial integrity, microbial translocation, dysbiosis, and resultant chronic immune activation. Additionally, the levels of all- MATERIALS AND

methodsTo determine whether the microbiome contributes to gut homeostasis after anti-α4β7 antibody administered to SIV-infected rhesus macaques, faecal SCFA concentrations were determined, 16S rRNA sequencing was performed, plasma viral loads were determined, plasma retinoids were measured longitudinally, and gut retinoid synthesis/response gene expression was quantified.

resultsOur results suggest that anti-α4β7 antibody facilitates the return of retinoid metabolism to baseline levels after SIV infection. Furthermore, faecal SCFAs were shown to be associated with retinoid synthesis gene expression and rebound viral loads after therapy interruption.

conclusionsTaken together, these data demonstrate the therapeutic advantages of anti-α4β7 antibody administration during HIV/SIV infection and that the efficacy of anti-α4β7 antibody may depend on microbiome composition and SCFA generation.

Indexed as

HIV InfectionsSimian Immunodeficiency VirusAnimalsHumansIntegrinsMacaca mulattaRetinoidsRNA, Ribosomal, 16SIntegrinsRetinoidsRNA, Ribosomal, 16S16S rRNAAnti-α4β7 antibodiesgutretinoic acidshort-chain fatty acid (SCFA)SIV

Identifiers

PMID38353210
PMCPMC10868432
OpenAlexW4391822266

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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.