Evidence map›Paper›PMID 40514685›Full record

ArticleBiology direct2025

Autophagy is influenced by vitamin D

Rita Casetti, Fabiola Ciccosanti, Harpreet Kaur Lamsira, Carmela Pinnetti, Valentina Mazzotta, Serena Ciolfi, Alessandra Sacchi, Alessandra Amendola, Giuseppe Ippolito, Mauro Piacentini and 1 more

Abstract read
In one paragraph

Article in Biology direct, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

11 authors.

Rita Casetti *Department of Epidemiology, Preclinical Research and Advanced Diagnostics, National Institute for Infectious Diseases 'Lazzaro Spallanzani' - IRCCS, Rome, 00149, Italy.
Fabiola Ciccosanti *Department of Epidemiology, Preclinical Research and Advanced Diagnostics, National Institute for Infectious Diseases 'Lazzaro Spallanzani' - IRCCS, Rome, 00149, Italy.
Harpreet Kaur LamsiraDepartmental Faculty of Medicine, Saint Camillus International University of Health Sciences, Rome, 00131, Italy.
Carmela PinnettiClinical and Research Department, National Institute for Infectious Diseases 'Lazzaro Spallanzani'-IRCCS, Rome, 00149, Italy.
Valentina MazzottaClinical and Research Department, National Institute for Infectious Diseases 'Lazzaro Spallanzani'-IRCCS, Rome, 00149, Italy.
Serena CiolfiDepartment of Science, University of Roma Tre, Rome, 00146, Italy.
Alessandra SacchiDepartment of Science, University of Roma Tre, Rome, 00146, Italy.
Alessandra AmendolaLaboratory of Virology and Biosafety Laboratories, National Institute for Infectious Diseases 'Lazzaro Spallanzani'- IRCCS, Rome, 00149, Italy.
Giuseppe IppolitoDepartmental Faculty of Medicine, Saint Camillus International University of Health Sciences, Rome, 00131, Italy.
Mauro PiacentiniDepartment of Epidemiology, Preclinical Research and Advanced Diagnostics, National Institute for Infectious Diseases 'Lazzaro Spallanzani' - IRCCS, Rome, 00149, Italy.
Roberta NardacciDepartmental Faculty of Medicine, Saint Camillus International University of Health Sciences, Rome, 00131, Italy. roberta.nardacci@unicamillus.org.

Funding

European Union-Next Generation EU-NRRP M6C2-Investment 2.1 Enhancement and strengthening of biomedical research in the NHS" PNRR-MAD-2022-12375755European Union NextGenerationEU through the Italian Ministry of University and Research under PNRR-MAC2-II.3 project PE6 "Heal Italia" E83C22004670001Italian Ministry of University and Research, PRIN 2022YAW9B4, CUP: D53D23002000008Ministero della Salute Ricerca Corrente and Ricerca Finalizzata
6 · The paper itself

Abstract

backgroundAutophagy is the primary catabolic process responsible for degrading intracellular components and potentially harmful cytosolic entities by delivering them to lysosomes. Notably, this mechanism is crucial for controlling intracellular pathogens, with significant implications for both innate and adaptive immunity. In the context of HIV-1 infection, emerging evidence suggests that autophagy contributes to immune responses against the virus. Various compounds can modulate autophagy, among which vitamin D₃ is particularly effective due to its ability to prevent inflammation and slow HIV-1 disease progression. Indeed, vitamin D₃ contributes to regulating both innate and adaptive immunity, thereby modulating antiviral and antibacterial inflammatory responses. Importantly, vitamin D₃ deficiency is highly prevalent among people with HIV (PWH) and has been associated with an increased risk of severe disease progression.

resultsIn this study, we investigated the relationship between serum vitamin D₃ levels and the expression of autophagy markers in peripheral blood mononuclear cells from different categories of PWH: PWH under antiretroviral therapy (ART) with either normal vitamin D₃ levels or hypovitaminosis, and treatment-naïve PWH with either normal vitamin D₃ levels or hypovitaminosis. Our results show that low vitamin D₃ blood levels is associated with lower expression of the main factors involved in the autophagy mechanism, particularly in treatment-naïve PWH.

conclusionsOur findings suggest that normal blood level of vitamin D₃ may play a crucial role in promoting autophagy in PWH. The observed differences in autophagy-related protein expression between ART-treated and untreated individuals underscore the intricate relationship between vitamin D₃ levels, ART exposure, and autophagic regulation. This is a preliminary exploration of the effects of vitamin D₃ on autophagy in PWH. Further studies are needed to deepen and explore the interplay between vitamin D₃ and autophagy in greater depth. A better understanding of these mechanisms could help to develop novel therapeutic strategies aimed at mitigating immune depletion and chronic inflammation, ultimately improving clinical outcomes for individuals living with HIV.

Indexed as

AutophagyCholecalciferolHIV-1HIV InfectionsAdultFemaleHumansLeukocytes, MononuclearMaleMiddle AgedVitamin D DeficiencyCholecalciferolAMBRA1ARTATG5AutophagyBECN1HIV-1Vitamin D₃

Identifiers

PMID40514685
PMCPMC12164164

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LicenceCC BY
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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.