Evidence map›Paper›PMID 42039437›Full record

ArticlebioRxiv : the preprint server for biology2026

Distinct prokaryotic gut microbiome and proviral-immune axes of pathophysiology in Sickle Cell Disease.

Zachary N Flamholz, Jennifer De Los Santos, Karen Ireland, Janine Keenan, Jacob S Kazmi, Aakash Mahant Mahant, Anayeli Correa, Paul S Frenette, Betsy C Herold, Deepa Manwani and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Zachary N FlamholzDepartment of Systems and Computational Biology, Albert Einstein College of Medicine; Bronx, New York, USA.
Jennifer De Los SantosDepartment of Pediatrics, Montefiore Health System and Albert Einstein College of Medicine; Bronx, New York, USA.
Karen IrelandDepartment of Pediatrics, Montefiore Health System and Albert Einstein College of Medicine; Bronx, New York, USA.
Janine KeenanDepartment of Pediatrics, Montefiore Health System and Albert Einstein College of Medicine; Bronx, New York, USA.
Jacob S KazmiDepartment of Cell Biology, Albert Einstein College of Medicine; Bronx, New York, USA.
Aakash Mahant MahantDepartment of Microbiology and Immunology, Albert Einstein College of Medicine; Bronx, New York, USA.
Anayeli CorreaDepartment of Microbiology and Immunology, Albert Einstein College of Medicine; Bronx, New York, USA.
Paul S FrenetteDepartment of Cell Biology, Albert Einstein College of Medicine; Bronx, New York, USA.
Betsy C HeroldDepartment of Pediatrics, Montefiore Health System and Albert Einstein College of Medicine; Bronx, New York, USA.ORCID 0000-0001-9974-0786
Deepa ManwaniDepartment of Pediatrics, Montefiore Health System and Albert Einstein College of Medicine; Bronx, New York, USA.
Libusha KellyDepartment of Systems and Computational Biology, Albert Einstein College of Medicine; Bronx, New York, USA.ORCID 0000-0002-7303-1022

Funding

Patient and Population Health Outcomes Research SWGP30AI124414 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Vinayaka R. Prasad · 2017 to 2026
$28.3M
In Vivo Sickle Cell Vasoocclusion: Adhesion MechanismsR01HL069438 · NHLBI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI KELLY, LIBUSHA · 2001 to 2024
$9.5M
Medical Scientist Training ProgramT32GM149364 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Myles H. Akabas · 2023 to 2026
$7.5M
Hiding in plain sight: integrating AI with targeted bench methods to discover and characterize viruses in the human bodyU01DE035632 · NIDCR · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Kathryn M Kauffman, Libusha Kelly · 2026 to 2026
$423k
NHLBI NIH HHS R01 HL069438NIAID NIH HHS P30 AI124414NIDCR NIH HHS U01 DE035632NIGMS NIH HHS T32 GM149364
6 · The paper itself

Abstract

Sickle cell disease (SCD) is a chronic, inherited condition rising across the globe. Prior studies revealed a direct link between the gut microbiome and disease micropathology via aged-like (ANs) neutrophils in mouse models. In SCD patients community-level shifts in the gut microbiome included decreases in diversity and the Firmicutes/Bacteroides (F:B) ratio, coupled to a loss of short chain fatty acid producing microbes and a shift to non-canonical butyrate production and aerobic fatty acid oxidation pathways. ANs and the proviral microbiome associate with multiple blood cytokines, while bacterial gut microbiome features largely do not. Prophages depleted of genes related to lysis, transcriptional regulation, and host takeover were enriched in SCD patient guts, pointing to domestication of these elements, and 25% of prophages were shared at high identity between study patients. In sum, we identify a viral-immune axis in SCD pathophysiology and targetable functional alterations to the gut microbiome in a heterogeneous chronic disease both affected by and effecting microbiome composition and function.

Identifiers

PMID42039437
PMCPMC13104962

What OpenQuestion holds

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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.