Elucidating the Pivotal Immunomodulatory and Anti-Inflammatory Potentials of Chloroquine and Hydroxychloroquine

Chloroquine (CQ) and hydroxychloroquine (HCQ) are derivatives of 4-aminoquinoline compounds with over 60 years of safe clinical usage. CQ and HCQ are able to inhibit the production of cytokines such as interleukin- (IL-) 1, IL-2, IL-6, IL-17, and IL-22. Also, CQ and HCQ inhibit the production of int...

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Main Authors: Seidu A. Richard, Sylvanus Kampo, Maite Esquijarosa Hechavarria, Marian Sackey, Alexis D. B. Buunaaim, Eugene Dogkotenge Kuugbee, Thomas Winsum Anabah
Format: Article
Language:English
Published: Hindawi Limited 2020-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2020/4582612
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spelling doaj-e86b13b8f77d4ad5aab2b1f36c81f2222020-11-25T03:59:17ZengHindawi LimitedJournal of Immunology Research2314-88612314-71562020-01-01202010.1155/2020/45826124582612Elucidating the Pivotal Immunomodulatory and Anti-Inflammatory Potentials of Chloroquine and HydroxychloroquineSeidu A. Richard0Sylvanus Kampo1Maite Esquijarosa Hechavarria2Marian Sackey3Alexis D. B. Buunaaim4Eugene Dogkotenge Kuugbee5Thomas Winsum Anabah6Department of Medicine, Princefield University, P. O. Box MA128, Ho, West Africa, GhanaDepartment of Anesthesia and Critical Care, School of Medicine, University of Health and Allied Sciences, Ho, GhanaDepartment of Anesthesia and Critical Care, School of Medicine, University of Health and Allied Sciences, Ho, GhanaDepartment of Pharmacy, Ho Teaching Hospital, P.O. Box MA374, Ho, West Africa, GhanaDepartment of Surgery, School of Medicine and Health Science, University for Development Studies, Tamale, GhanaDepartment of Clinical Microbiology, School of Medicine and Health Science, University for Development Studies, Tamale, GhanaDepartment of Clinical Medicine, Habana Medical Services, Tamale, GhanaChloroquine (CQ) and hydroxychloroquine (HCQ) are derivatives of 4-aminoquinoline compounds with over 60 years of safe clinical usage. CQ and HCQ are able to inhibit the production of cytokines such as interleukin- (IL-) 1, IL-2, IL-6, IL-17, and IL-22. Also, CQ and HCQ inhibit the production of interferon- (IFN-) α and IFN-γ and/or tumor necrotizing factor- (TNF-) α. Furthermore, CQ blocks the production of prostaglandins (PGs) in the intact cell by inhibiting substrate accessibility of arachidonic acid necessary for the production of PGs. Moreover, CQ affects the stability between T-helper cell (Th) 1 and Th2 cytokine secretion by augmenting IL-10 production in peripheral blood mononuclear cells (PBMCs). Additionally, CQ is capable of blocking lipopolysaccharide- (LPS-) triggered stimulation of extracellular signal-modulated extracellular signal-regulated kinases 1/2 in human PBMCs. HCQ at clinical levels effectively blocks CpG-triggered class-switched memory B-cells from differentiating into plasmablasts as well as producing IgG. Also, HCQ inhibits cytokine generation from all the B-cell subsets. IgM memory B-cells exhibits the utmost cytokine production. Nevertheless, CQ triggers the production of reactive oxygen species. A rare, but serious, side effect of CQ or HCQ in nondiabetic patients is hypoglycaemia. Thus, in critically ill patients, CQ and HCQ are most likely to deplete all the energy stores of the body leaving the patient very weak and sicker. We advocate that, during clinical usage of CQ and HCQ in critically ill patients, it is very essential to strengthen the CQ or HCQ with glucose infusion. CQ and HCQ are thus potential inhibitors of the COVID-19 cytokine storm.http://dx.doi.org/10.1155/2020/4582612
collection DOAJ
language English
format Article
sources DOAJ
author Seidu A. Richard
Sylvanus Kampo
Maite Esquijarosa Hechavarria
Marian Sackey
Alexis D. B. Buunaaim
Eugene Dogkotenge Kuugbee
Thomas Winsum Anabah
spellingShingle Seidu A. Richard
Sylvanus Kampo
Maite Esquijarosa Hechavarria
Marian Sackey
Alexis D. B. Buunaaim
Eugene Dogkotenge Kuugbee
Thomas Winsum Anabah
Elucidating the Pivotal Immunomodulatory and Anti-Inflammatory Potentials of Chloroquine and Hydroxychloroquine
Journal of Immunology Research
author_facet Seidu A. Richard
Sylvanus Kampo
Maite Esquijarosa Hechavarria
Marian Sackey
Alexis D. B. Buunaaim
Eugene Dogkotenge Kuugbee
Thomas Winsum Anabah
author_sort Seidu A. Richard
title Elucidating the Pivotal Immunomodulatory and Anti-Inflammatory Potentials of Chloroquine and Hydroxychloroquine
title_short Elucidating the Pivotal Immunomodulatory and Anti-Inflammatory Potentials of Chloroquine and Hydroxychloroquine
title_full Elucidating the Pivotal Immunomodulatory and Anti-Inflammatory Potentials of Chloroquine and Hydroxychloroquine
title_fullStr Elucidating the Pivotal Immunomodulatory and Anti-Inflammatory Potentials of Chloroquine and Hydroxychloroquine
title_full_unstemmed Elucidating the Pivotal Immunomodulatory and Anti-Inflammatory Potentials of Chloroquine and Hydroxychloroquine
title_sort elucidating the pivotal immunomodulatory and anti-inflammatory potentials of chloroquine and hydroxychloroquine
publisher Hindawi Limited
series Journal of Immunology Research
issn 2314-8861
2314-7156
publishDate 2020-01-01
description Chloroquine (CQ) and hydroxychloroquine (HCQ) are derivatives of 4-aminoquinoline compounds with over 60 years of safe clinical usage. CQ and HCQ are able to inhibit the production of cytokines such as interleukin- (IL-) 1, IL-2, IL-6, IL-17, and IL-22. Also, CQ and HCQ inhibit the production of interferon- (IFN-) α and IFN-γ and/or tumor necrotizing factor- (TNF-) α. Furthermore, CQ blocks the production of prostaglandins (PGs) in the intact cell by inhibiting substrate accessibility of arachidonic acid necessary for the production of PGs. Moreover, CQ affects the stability between T-helper cell (Th) 1 and Th2 cytokine secretion by augmenting IL-10 production in peripheral blood mononuclear cells (PBMCs). Additionally, CQ is capable of blocking lipopolysaccharide- (LPS-) triggered stimulation of extracellular signal-modulated extracellular signal-regulated kinases 1/2 in human PBMCs. HCQ at clinical levels effectively blocks CpG-triggered class-switched memory B-cells from differentiating into plasmablasts as well as producing IgG. Also, HCQ inhibits cytokine generation from all the B-cell subsets. IgM memory B-cells exhibits the utmost cytokine production. Nevertheless, CQ triggers the production of reactive oxygen species. A rare, but serious, side effect of CQ or HCQ in nondiabetic patients is hypoglycaemia. Thus, in critically ill patients, CQ and HCQ are most likely to deplete all the energy stores of the body leaving the patient very weak and sicker. We advocate that, during clinical usage of CQ and HCQ in critically ill patients, it is very essential to strengthen the CQ or HCQ with glucose infusion. CQ and HCQ are thus potential inhibitors of the COVID-19 cytokine storm.
url http://dx.doi.org/10.1155/2020/4582612
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