Filoviruses: Innate Immunity, Inflammatory Cell Death, and Cytokines.
ALRs
CLRs
NLRs
PANoptosis
PANoptosome
RIG-I
RLRs
RNA virus
TLRs
apoptosis
caspase
cell death
ebolavirus
filovirus
host–pathogen interactions
inflammasome
inflammation
innate immunity
interferon
marburgvirus
necroptosis
pattern recognition receptors
pyroptosis
Journal
Pathogens (Basel, Switzerland)
ISSN: 2076-0817
Titre abrégé: Pathogens
Pays: Switzerland
ID NLM: 101596317
Informations de publication
Date de publication:
23 Nov 2022
23 Nov 2022
Historique:
received:
04
10
2022
revised:
17
11
2022
accepted:
19
11
2022
entrez:
23
12
2022
pubmed:
24
12
2022
medline:
24
12
2022
Statut:
epublish
Résumé
Filoviruses are a group of single-stranded negative sense RNA viruses. The most well-known filoviruses that affect humans are ebolaviruses and marburgviruses. During infection, they can cause life-threatening symptoms such as inflammation, tissue damage, and hemorrhagic fever, with case fatality rates as high as 90%. The innate immune system is the first line of defense against pathogenic insults such as filoviruses. Pattern recognition receptors (PRRs), including toll-like receptors, retinoic acid-inducible gene-I-like receptors, C-type lectin receptors, AIM2-like receptors, and NOD-like receptors, detect pathogens and activate downstream signaling to induce the production of proinflammatory cytokines and interferons, alert the surrounding cells to the threat, and clear infected and damaged cells through innate immune cell death. However, filoviruses can modulate the host inflammatory response and innate immune cell death, causing an aberrant immune reaction. Here, we discuss how the innate immune system senses invading filoviruses and how these deadly pathogens interfere with the immune response. Furthermore, we highlight the experimental difficulties of studying filoviruses as well as the current state of filovirus-targeting therapeutics.
Identifiants
pubmed: 36558734
pii: pathogens11121400
doi: 10.3390/pathogens11121400
pmc: PMC9785368
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Subventions
Organisme : NCI NIH HHS
ID : R35 CA253095
Pays : United States
Organisme : NIH HHS
ID : AI101935
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI124346
Pays : United States
Organisme : NIAID NIH HHS
ID : R37 AI101935
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI160179
Pays : United States
Organisme : NIH HHS
ID : AR056296
Pays : United States
Organisme : NIH HHS
ID : AI124346
Pays : United States
Organisme : NIAMS NIH HHS
ID : R01 AR056296
Pays : United States
Organisme : NIH HHS
ID : CA253095
Pays : United States
Organisme : NIH HHS
ID : AI160179
Pays : United States
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