Early corticosteroid treatment enhances recovery from SARS-CoV-2 induced loss of smell in hamster
Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved..
Among the numerous long COVID symptoms, olfactory dysfunction persists in ∼10 % of patients suffering from SARS-CoV-2 induced anosmia. Among the few potential therapies, corticoid treatment has been used for its anti-inflammatory effect with mixed success in patients. In this study, we explored its impact using hamster as an animal model. SARS-CoV-2 infected hamsters lose their smell abilities and this loss is correlated with damage of the olfactory epithelium and persistent presence of innate immunity cells. We started a dexamethasone treatment 2 days post infection, when olfaction was already impacted, until 11 days post infection when it started to recover. We observed an improvement of olfactory capacities in the animals treated with corticoid compared to those treated with vehicle. This recovery was not related to differences in the remaining damage to the olfactory epithelium, which was similar in both groups. This improvement was however correlated with a reduced inflammation in the olfactory epithelium with a local increase of the mature olfactory neuron population. Surprisingly, at 11 days post infection, we observed an increased and disorganized presence of immature olfactory neurons, especially in persistent inflammatory zones of the epithelium. This unusual population of immature olfactory neurons coincided with a strong increase of olfactory epithelium proliferation in both groups. Our results indicate that persistent inflammation of the olfactory epithelium following SARS-CoV-2 infection may alter the extent and speed of regeneration of the olfactory neuron population, and that corticoid treatment is effective to limit inflammation and improve olfaction recovery following SARS-CoV-2 infection.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2024 |
---|---|
Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:118 |
---|---|
Enthalten in: |
Brain, behavior, and immunity - 118(2024) vom: 15. Apr., Seite 78-89 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Merle-Nguyen, Laetitia [VerfasserIn] |
---|
Links: |
---|
Themen: |
Adrenal Cortex Hormones |
---|
Anmerkungen: |
Date Completed 10.04.2024 Date Revised 10.04.2024 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1016/j.bbi.2024.02.020 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM368579069 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM368579069 | ||
003 | DE-627 | ||
005 | 20240410232528.0 | ||
007 | cr uuu---uuuuu | ||
008 | 240218s2024 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.bbi.2024.02.020 |2 doi | |
028 | 5 | 2 | |a pubmed24n1371.xml |
035 | |a (DE-627)NLM368579069 | ||
035 | |a (NLM)38367845 | ||
035 | |a (PII)S0889-1591(24)00256-3 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Merle-Nguyen, Laetitia |e verfasserin |4 aut | |
245 | 1 | 0 | |a Early corticosteroid treatment enhances recovery from SARS-CoV-2 induced loss of smell in hamster |
264 | 1 | |c 2024 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 10.04.2024 | ||
500 | |a Date Revised 10.04.2024 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved. | ||
520 | |a Among the numerous long COVID symptoms, olfactory dysfunction persists in ∼10 % of patients suffering from SARS-CoV-2 induced anosmia. Among the few potential therapies, corticoid treatment has been used for its anti-inflammatory effect with mixed success in patients. In this study, we explored its impact using hamster as an animal model. SARS-CoV-2 infected hamsters lose their smell abilities and this loss is correlated with damage of the olfactory epithelium and persistent presence of innate immunity cells. We started a dexamethasone treatment 2 days post infection, when olfaction was already impacted, until 11 days post infection when it started to recover. We observed an improvement of olfactory capacities in the animals treated with corticoid compared to those treated with vehicle. This recovery was not related to differences in the remaining damage to the olfactory epithelium, which was similar in both groups. This improvement was however correlated with a reduced inflammation in the olfactory epithelium with a local increase of the mature olfactory neuron population. Surprisingly, at 11 days post infection, we observed an increased and disorganized presence of immature olfactory neurons, especially in persistent inflammatory zones of the epithelium. This unusual population of immature olfactory neurons coincided with a strong increase of olfactory epithelium proliferation in both groups. Our results indicate that persistent inflammation of the olfactory epithelium following SARS-CoV-2 infection may alter the extent and speed of regeneration of the olfactory neuron population, and that corticoid treatment is effective to limit inflammation and improve olfaction recovery following SARS-CoV-2 infection | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Anosmia | |
650 | 4 | |a Dexamethasone | |
650 | 4 | |a Nasal cavity | |
650 | 4 | |a Olfaction | |
650 | 4 | |a Olfactory | |
650 | 4 | |a Respiratory virus | |
650 | 4 | |a Smell | |
650 | 7 | |a Adrenal Cortex Hormones |2 NLM | |
700 | 1 | |a Ando-Grard, Ophélie |e verfasserin |4 aut | |
700 | 1 | |a Bourgon, Clara |e verfasserin |4 aut | |
700 | 1 | |a St Albin, Audrey |e verfasserin |4 aut | |
700 | 1 | |a Jacquelin, Juliette |e verfasserin |4 aut | |
700 | 1 | |a Klonjkowski, Bernard |e verfasserin |4 aut | |
700 | 1 | |a Le Poder, Sophie |e verfasserin |4 aut | |
700 | 1 | |a Meunier, Nicolas |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Brain, behavior, and immunity |d 1992 |g 118(2024) vom: 15. Apr., Seite 78-89 |w (DE-627)NLM012962538 |x 1090-2139 |7 nnns |
773 | 1 | 8 | |g volume:118 |g year:2024 |g day:15 |g month:04 |g pages:78-89 |
856 | 4 | 0 | |u http://dx.doi.org/10.1016/j.bbi.2024.02.020 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 118 |j 2024 |b 15 |c 04 |h 78-89 |