Current Opinion on the Therapeutic Capacity of Taurine-Containing Halogen Derivatives in Infectious and Inflammatory Diseases.

COVID-19 Infection diseases Inflammation N-bromotaurine N-chlorotaurine Taurine bromamine Taurine chloramine Taurine derivatives

Journal

Advances in experimental medicine and biology
ISSN: 0065-2598
Titre abrégé: Adv Exp Med Biol
Pays: United States
ID NLM: 0121103

Informations de publication

Date de publication:
2022
Historique:
entrez: 26 7 2022
pubmed: 27 7 2022
medline: 29 7 2022
Statut: ppublish

Résumé

Taurine haloamines, N-chlorotaurine (NCT, TauCl), and N-bromotaurine (NBT, TauBr) are formed by a reaction between taurine and hypohalous acids, HOCl and HOBr, respectively. The major source of endogenous taurine haloamines is neutrophils. Both NCT and NBT share strong anti-inflammatory and microbicidal activities supported by an absence of microbial resistance. In the light of these properties, a number of clinical studies have been performed to document their effectiveness in treatment of bacterial, fungal, and viral infections. The administration of NCT and NBT has been limited to topical application, as they are decomposed upon systemic delivery. This review summarizes current knowledge concerning the therapeutic use of NCT and NBT mainly in various skin disorders such as non-healing wounds, acne vulgaris, herpes zoster, and psoriasis. Moreover, the beneficial effect of NCT inhalation in early stages of COVID-19 and other viral respiratory infections is discussed. And finally, we would like to suggest that NCT might be used to inhibit the development of the cytokine storm through its capacity to suppress the production of IL-6.

Identifiants

pubmed: 35882784
doi: 10.1007/978-3-030-93337-1_8
doi:

Substances chimiques

Anti-Inflammatory Agents 0
Halogens 0
Taurine 1EQV5MLY3D

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

83-98

Informations de copyright

© 2022. The Author(s), under exclusive license to Springer Nature Switzerland AG.

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Auteurs

Janusz Marcinkiewicz (J)

Department of Immunology, Jagiellonian University Medical College, Krakow, Poland. janusz.marcinkiewicz@uj.edu.pl.

Markus Nagl (M)

Department of Hygiene, Microbiology and Public Health, Institute of Hygiene and Medical Microbiology, Medical University of Innsbruck, Innsbruck, Austria.

Anthony Kyriakopoulos (A)

Nasco AD Biotechnology Laboratory, Piraeus, Greece.

Maria Walczewska (M)

Department of Immunology, Jagiellonian University Medical College, Krakow, Poland.

Magdalena Skóra (M)

Department of Infection Control and Mycology Chair of Microbiology, Jagiellonian University Medical College, Krakow, Poland.

Paulina Skalska (P)

Department of Immunology, Jagiellonian University Medical College, Krakow, Poland.

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