Zika virus restriction of host antioxidant response is mediated by intracellular NS1 and reveals its ability to upregulate Bach1 expression DOI Creative Commons
Grégorie Lebeau,

Daed El Safadi,

Mathilde Hoarau

и другие.

Biochemical and Biophysical Research Communications, Год журнала: 2023, Номер 690, С. 149312 - 149312

Опубликована: Ноя. 23, 2023

Язык: Английский

The biology and function of extracellular vesicles in immune response and immunity DOI
Raghu Kalluri

Immunity, Год журнала: 2024, Номер 57(8), С. 1752 - 1768

Опубликована: Авг. 1, 2024

Язык: Английский

Процитировано

34

Role of extracellular vesicles in the pathogenesis of mosquito-borne flaviviruses that impact public health DOI Creative Commons
Pedro Pablo Martínez-Rojas,

Verónica Monroy-Martínez,

Blanca H. Ruíz-Ordaz

и другие.

Journal of Biomedical Science, Год журнала: 2025, Номер 32(1)

Опубликована: Янв. 4, 2025

Abstract Mosquito-borne flaviviruses represent a public health challenge due to the high-rate endemic infections, severe clinical outcomes, and potential risk of emerging global outbreaks. Flavivirus disease pathogenesis converges on cellular factors from vectors hosts, their interactions are still unclear. Exosomes microparticles extracellular vesicles released cells that mediate intercellular communication necessary for maintaining homeostasis; however, they have been shown be involved in establishment progression. This review focuses roles mosquito-borne flavivirus diseases: how contribute viral cycle completion, cell-to-cell transmission, responses such as inflammation, immune suppression, evasion, well use biomarkers or therapeutics (antiviral vaccines). We highlight current findings concerning functionality different models dengue virus, Zika yellow fever Japanese encephalitis West Nile virus infections diseases. The available evidence suggests diverse functions between constituting novel effectors understanding pathogenic mechanisms flaviviral

Язык: Английский

Процитировано

1

Zika virus modulates mitochondrial dynamics, mitophagy, and mitochondria-derived vesicles to facilitate viral replication in trophoblast cells DOI Creative Commons
Jae Kwan Lee, Ok Sarah Shin

Frontiers in Immunology, Год журнала: 2023, Номер 14

Опубликована: Сен. 14, 2023

Zika virus (ZIKV) remains a global public health threat with the potential risk of future outbreak. Since viral infections are known to exploit mitochondria-mediated cellular processes, we investigated effects ZIKV infection in trophoblast cells terms different mitochondrial quality control pathways that govern integrity and function. Here demonstrate (PRVABC59) JEG-3 manipulates dynamics, mitophagy, formation mitochondria-derived vesicles (MDVs). Specifically, nonstructural protein 4A (NS4A) translocates mitochondria, triggers fission suppresses associated antiviral (MAVS)-mediated type I interferon (IFN) response. Furthermore, proteomics profiling small extracellular (sEVs) revealed an enrichment proteins sEVs secreted by ZIKV-infected cells, suggesting MDV may also be another mechanism manipulated during placental infection. Altogether, our findings highlight mechanisms as host immune evasion utilized at placenta suppress response facilitate

Язык: Английский

Процитировано

22

Exosome-Mediated Antigen Delivery: Unveiling Novel Strategies in Viral Infection Control and Vaccine Design DOI Creative Commons

Daed El Safadi,

Alexandre Mokhtari,

Morgane Krejbich

и другие.

Vaccines, Год журнала: 2024, Номер 12(3), С. 280 - 280

Опубликована: Март 7, 2024

Exosomes are small subtypes of extracellular vesicles (EVs) naturally released by different types cells into their environment. Their physiological roles appear to be multiple, yet many aspects biological activities remain understood. These can transport and deliver a variety cargoes may serve as unconventional secretory vesicles. Thus, they play crucial role important vectors for intercellular communication the maintenance homeostasis. Exosome production content vary under several stresses or modifications in cell microenvironment, influencing cellular responses stimulating immunity. During infectious processes, exosomes described double-edged swords, displaying both beneficial detrimental effects. Owing tractability, analysis EVs from multiple biofluids has become booming tool monitoring various pathologies, cancerous origins. In this review, we present an overview exosome features discuss particular ambiguous functions contexts. We then focus on properties diagnostic therapeutic tools. regard, explore capacity vectorize immunogenic viral antigens function mounting adaptive immune responses. As provide interesting platforms antigen presentation, further review available data engineering, which enables peptides interest exposed at surface. light all these data, emerging promising avenues vaccine strategies.

Язык: Английский

Процитировано

8

Viral Components Trafficking with(in) Extracellular Vesicles DOI Creative Commons

Félix Rey-Cadilhac,

Florian Rachenne,

Dorothée Missé

и другие.

Viruses, Год журнала: 2023, Номер 15(12), С. 2333 - 2333

Опубликована: Ноя. 28, 2023

The global public health burden exerted by viruses partially stems from viruses’ ability to subdue host cells into creating an environment that promotes their multiplication (i.e., pro-viral). It has been discovered alter cell physiology transferring viral material through extracellular vesicles (EVs), which serve as vehicles for intercellular communication. Here, we aim provide a conceptual framework of all possible EV-virus associations and resulting functions in infection output. First, describe the different materials potentially associated with EVs reporting can harbor entire virions, proteins nucleic acids. We also delineate mechanisms underlying internalization these components EVs. Second, potential fate EV-associated cargo detailing how EV circulate target naive once secreted. Finally, itemize pro-viral strategies Trojan horse strategy, alternative mode transmission, expansion cellular tropism, pre-emptive alteration immunity decoy. With this overview, stimulate research on interactions.

Язык: Английский

Процитировано

11

A non-structural protein 1 substitution of dengue virus enhances viral replication by interfering with the antiviral signaling pathway DOI Creative Commons

Hée J,

Dayna Cheng,

Yu‐Hong Chen

и другие.

Journal of Biomedical Science, Год журнала: 2025, Номер 32(1)

Опубликована: Фев. 20, 2025

Abstract Background The largest dengue virus 2 (DENV2) outbreak occurred in Taiwan 2015, resulting many fatalities. We therefore aim to identify crucial genetic variations which determine the virulence of 2015 strains. Methods compared DENV2 sequences pre-2015 sequences. Reverse genetics (rg) viruses with substitutions were produced and viral growth kinetics investigated. treated A549 cells interferon (IFN) interferon-stimulated genes (ISGs) expression STAT1 phosphorylation rg infection plasmid transfection systems. IFN pro-inflammatory cytokines levels measured upon DENV using ELISA. Results rgNS1-K272R mutant showed faster replication IFN-I producing wildtype (WT) virus. revealed that NS1-K272R substitution contributed higher soluble NS1 secretion evade antiviral response by suppressing ISGs NS1-WT. Infection induced through activation canonical nuclear factor-kappa B (NF-κB) signaling pathway. Conclusions Our results amino acid affects ability immune evasion, may contribute since 1990s.

Язык: Английский

Процитировано

0

Extracellular Vesicles in Flaviviridae Pathogenesis: Their Roles in Viral Transmission, Immune Evasion, and Inflammation DOI Open Access
Anastasia Latanova, В. Л. Карпов, Elizaveta Starodubova

и другие.

International Journal of Molecular Sciences, Год журнала: 2024, Номер 25(4), С. 2144 - 2144

Опубликована: Фев. 10, 2024

The members of the Flaviviridae family are becoming an emerging threat for public health, causing increasing number infections each year and requiring effective treatment. consequences these can be severe include liver inflammation with subsequent carcinogenesis, endothelial damage hemorrhage, neuroinflammation, and, in some cases, death. mechanisms pathogenesis being actively investigated, but there still many gaps their understanding. Extracellular vesicles may play important roles mechanisms, therefore, this topic deserves detailed research. Recent data have revealed involvement extracellular steps such as transmission, immune evasion, inflammation, which is critical disease establishment. This review covers recent papers on includes examples clinical applications accumulated data.

Язык: Английский

Процитировано

3

Subcapsular sinus macrophages maximize germinal center development in non-draining lymph nodes during blood-borne viral infection DOI
Cynthia C. Aguilar, Anurag Kalia, Morgan Brisse

и другие.

Science Immunology, Год журнала: 2024, Номер 9(93)

Опубликована: Март 8, 2024

Lymph node (LN) germinal centers (GCs) are critical sites for B cell activation and differentiation. GCs develop after specialized CD169 + macrophages residing in LN sinuses filter antigens (Ags) from the lymph relay these Ags into proximal follicles. Many viruses, however, first reach LNs through blood during viremia (virus blood), rather than drainage infected tissue. How capture viral Ag to allow GC development is not known. Here, we followed Zika virus (ZIKV) dissemination mice subsequent formation both tissue–draining non-draining LNs. From footpad, ZIKV initially disseminated two chains, infecting leading formation. Despite rapid viremia, were several days. Non-draining infection correlated with virus-induced vascular leakage neutralization of permeability reduced macrophage attrition. Depletion significantly decreased cells nodes. Thus, although inefficiently captured directly blood, proceeded similarly draining sinus macrophages. Together, our findings reveal a conserved pathway allowing activate antiviral distal tissue blood-borne infection.

Язык: Английский

Процитировано

3

Infection-Simulator, Immunostimulatory and Immunomodulatory Effects of Interferons I and III in Biological Systems: A New Era in Vaccinology and Therapeutics Possible? DOI Open Access
Theodor-Nicolae Carp,

Michael Metoudi,

Vanshika Ojha

и другие.

Опубликована: Июль 10, 2024

The severe acquired respiratory coronavirus–2 (SARS–CoV-2) infection has initiated both acute and chronic COVID–19 disease between 2020 2023, currently evolving with other homologous prior coronavirus strains of the Nidoviridae order, which encompasses prevalent alpha/ beta coronaviruses, but also Middle East Respiratory Syndrome (MERS-CoV) SARS-CoV-1, recent SARS–CoV–2 variants, increasing demands for effective immunogens therapeutic approaches that will reduce global burden further from SARS–CoV-2 affected individuals may experience post sequelae (PASC) or “Long COVID”. Following a worldwide programme prophylactic vaccination, there is still dilemma in efforts to find early would treat novel SARS-CoV-2 variants prevent future epidemics pandemics within host human animal populations, where zoonotic cross species transfer naturally occurs. Concerns about viral immune escape intersect at specific point; gained evolutionary ability several viruses co–infect compete against previous scientific advances since 1796 remain undetected asymptomatic during stages progressing symptomatic via double methylation 5' end eukaryotic DNA RNA-based genomes, 7-MeGpppA2’-O-Me cap, its capping process performed by activated 2’ - O Methyltransferase (MTase) enzyme, complex two non-structural proteins (NSPs) joined together through an activation (NSP10/16) N7-Methyltransferase (N7-MTase/NSP14), respectively. Moreover, it was discovered polymorphic translate NSP1, prevents various Pattern Recognition Receptors (PRRs), consequently, detection Pathogen-Associated Molecular Patterns (PAMPs) Damage-Associated (DAMPs) alike. NSP1 silences important interferon-encoding genes (INGs) interferon-stimulated (ISGs), signalled paracrine manner neighbouring cells, induces apoptosis inducing effect “trace erase” making as immunologically “invisible” possible initial, key replication distribution, all such mechanisms occurring independently cause. Another NSP NSP14, plays functional roles are independent each other; produce new genetic material purpose maintaining validity genome well, not just methyl group 5’ genome. Other NSPs share role 10, 14 16 directly suppressing PRRs ISGs, help virus self-camouflaging first- second-line immunity, thereby often severely impacting quality produced adaptive responses. outcome phenomena sharp decrease Type I III interferons' (IFNs) rate synthesis usually occur affect homeostatic cellular pathways, resulting induced apoptosis. Nonetheless, effects microbial evasion development carcinogenic pathologies widely known. In short, developed proportionate response responses, relying on gaps mostly situated natural system their molecular self-camouflaging. Scientists numerous treatment generally showed good success rates fewer risks adverse events, present COVID-19 research should be taken into consideration whilst filtering most appropriate solutions. For example, administration recombinant interferons nasal mucosa layer, mediators anti–viral activity, can simulate intracellular stimulate activity timely manner, training innate cells develop appropriately adequate B T cells. example could involve lymphocytes low dose IFNs possibly III, insertion lymphatic system, alongside additional recruitment plasmacytoid dendritic (pDCs) interferon “factories”, management. It might focusing offering information genetics protein structure pathogen, rather than first-line faster, excessively increases specificity, reach level brings opportunity evolve previously-developed mechanisms. until community realises this potentially crucial aspect large proportions world population probably continue face serious diseases over coming decades, evidenced dengue fever more recently, monkeypox avian flu. Of note, been indicated IFN / display significant immunising, clinical onset-attenuating many evoked diseases, well number oncological diseases.

Язык: Английский

Процитировано

3

A game of hide-and-seek: how extracellular vesicles evade the immune system DOI Creative Commons
Bartika Ghoshal, Siddharth Jhunjhunwala

Drug Delivery and Translational Research, Год журнала: 2025, Номер unknown

Опубликована: Янв. 22, 2025

Язык: Английский

Процитировано

0