Boosted Pro-Inflammatory Activity in Human PBMCs by Lipopolysaccharide and SARS-CoV-2 Spike Protein Is Regulated by α-1 Antitrypsin

For the treatment of severe COVID-19, supplementation with human plasma-purified α-1 antitrypsin (AAT) to patients is currently considered. AAT inhibits host proteases that facilitate viral entry and possesses broad anti-inflammatory and immunomodulatory activities. Researchers have demonstrated tha...

Full description

Bibliographic Details
Main Authors: Srinu Tumpara, Anna R. Gründing, Kokilavani Sivaraman, Sabine Wrenger, Beata Olejnicka, Tobias Welte, Maria J. Wurm, Paco Pino, Divor Kiseljak, Florian M. Wurm, Sabina Janciauskiene
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:International Journal of Molecular Sciences
Subjects:
LPS
AAT
Online Access:https://www.mdpi.com/1422-0067/22/15/7941
id doaj-381b24cc03dd491d94d7b6dacb501463
record_format Article
spelling doaj-381b24cc03dd491d94d7b6dacb5014632021-08-06T15:24:50ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-07-01227941794110.3390/ijms22157941Boosted Pro-Inflammatory Activity in Human PBMCs by Lipopolysaccharide and SARS-CoV-2 Spike Protein Is Regulated by α-1 AntitrypsinSrinu Tumpara0Anna R. Gründing1Kokilavani Sivaraman2Sabine Wrenger3Beata Olejnicka4Tobias Welte5Maria J. Wurm6Paco Pino7Divor Kiseljak8Florian M. Wurm9Sabina Janciauskiene10Department of Respiratory Medicine, Member of the German Center for Lung Research (DZL), Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), Hannover Medical School, 30625 Hannover, GermanyDepartment of Respiratory Medicine, Member of the German Center for Lung Research (DZL), Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), Hannover Medical School, 30625 Hannover, GermanyDepartment of Respiratory Medicine, Member of the German Center for Lung Research (DZL), Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), Hannover Medical School, 30625 Hannover, GermanyDepartment of Respiratory Medicine, Member of the German Center for Lung Research (DZL), Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), Hannover Medical School, 30625 Hannover, GermanyDepartment of Respiratory Medicine, Member of the German Center for Lung Research (DZL), Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), Hannover Medical School, 30625 Hannover, GermanyDepartment of Respiratory Medicine, Member of the German Center for Lung Research (DZL), Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), Hannover Medical School, 30625 Hannover, GermanyExcellGene SA, 1970 Monthey, SwitzerlandExcellGene SA, 1970 Monthey, SwitzerlandÉcole Polytechnique Fédérale de Lausanne, Faculty of Life Sciences, 1015 Lausanne, SwitzerlandExcellGene SA, 1970 Monthey, SwitzerlandDepartment of Respiratory Medicine, Member of the German Center for Lung Research (DZL), Biomedical Research in Endstage and Obstructive Lung Disease Hannover (BREATH), Hannover Medical School, 30625 Hannover, GermanyFor the treatment of severe COVID-19, supplementation with human plasma-purified α-1 antitrypsin (AAT) to patients is currently considered. AAT inhibits host proteases that facilitate viral entry and possesses broad anti-inflammatory and immunomodulatory activities. Researchers have demonstrated that an interaction between SARS-CoV-2 spike protein (S) and lipopolysaccharides (LPS) enhances pro-inflammatory responses in vitro and in vivo. Hence, we wanted to understand the potential anti-inflammatory activities of plasma-derived and recombinant AAT (recAAT) in a model of human total peripheral blood mononuclear cells (PBMCs) exposed to a combination of CHO expressed trimeric spike protein and LPS, ex vivo. We confirmed that cytokine production was enhanced in PBMCs within six hours when low levels of LPS were combined with purified spike proteins (“spike”). In the presence of 0.5 mg/mL recAAT, however, LPS/spike-induced TNF-α and IL-1β mRNA expression and protein release were significantly inhibited (by about 46–50%) relative to LPS/spike alone. Although without statistical significance, recAAT also reduced production of IL-6 and IL-8. Notably, under the same experimental conditions, the plasma-derived AAT preparation Respreeza (used in native and oxidized forms) did not show significant effects. Our findings imply that an early pro-inflammatory activation of human PBMCs is better controlled by the recombinant version of AAT than the human plasma-derived AAT used here. Considering the increasing clinical interest in AAT therapy as useful to ameliorate the hyper-inflammation seen during COVID-19 infection, different AAT preparations require careful evaluation.https://www.mdpi.com/1422-0067/22/15/7941COVID-19spikeLPSAATPBMCsinflammation
collection DOAJ
language English
format Article
sources DOAJ
author Srinu Tumpara
Anna R. Gründing
Kokilavani Sivaraman
Sabine Wrenger
Beata Olejnicka
Tobias Welte
Maria J. Wurm
Paco Pino
Divor Kiseljak
Florian M. Wurm
Sabina Janciauskiene
spellingShingle Srinu Tumpara
Anna R. Gründing
Kokilavani Sivaraman
Sabine Wrenger
Beata Olejnicka
Tobias Welte
Maria J. Wurm
Paco Pino
Divor Kiseljak
Florian M. Wurm
Sabina Janciauskiene
Boosted Pro-Inflammatory Activity in Human PBMCs by Lipopolysaccharide and SARS-CoV-2 Spike Protein Is Regulated by α-1 Antitrypsin
International Journal of Molecular Sciences
COVID-19
spike
LPS
AAT
PBMCs
inflammation
author_facet Srinu Tumpara
Anna R. Gründing
Kokilavani Sivaraman
Sabine Wrenger
Beata Olejnicka
Tobias Welte
Maria J. Wurm
Paco Pino
Divor Kiseljak
Florian M. Wurm
Sabina Janciauskiene
author_sort Srinu Tumpara
title Boosted Pro-Inflammatory Activity in Human PBMCs by Lipopolysaccharide and SARS-CoV-2 Spike Protein Is Regulated by α-1 Antitrypsin
title_short Boosted Pro-Inflammatory Activity in Human PBMCs by Lipopolysaccharide and SARS-CoV-2 Spike Protein Is Regulated by α-1 Antitrypsin
title_full Boosted Pro-Inflammatory Activity in Human PBMCs by Lipopolysaccharide and SARS-CoV-2 Spike Protein Is Regulated by α-1 Antitrypsin
title_fullStr Boosted Pro-Inflammatory Activity in Human PBMCs by Lipopolysaccharide and SARS-CoV-2 Spike Protein Is Regulated by α-1 Antitrypsin
title_full_unstemmed Boosted Pro-Inflammatory Activity in Human PBMCs by Lipopolysaccharide and SARS-CoV-2 Spike Protein Is Regulated by α-1 Antitrypsin
title_sort boosted pro-inflammatory activity in human pbmcs by lipopolysaccharide and sars-cov-2 spike protein is regulated by α-1 antitrypsin
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-07-01
description For the treatment of severe COVID-19, supplementation with human plasma-purified α-1 antitrypsin (AAT) to patients is currently considered. AAT inhibits host proteases that facilitate viral entry and possesses broad anti-inflammatory and immunomodulatory activities. Researchers have demonstrated that an interaction between SARS-CoV-2 spike protein (S) and lipopolysaccharides (LPS) enhances pro-inflammatory responses in vitro and in vivo. Hence, we wanted to understand the potential anti-inflammatory activities of plasma-derived and recombinant AAT (recAAT) in a model of human total peripheral blood mononuclear cells (PBMCs) exposed to a combination of CHO expressed trimeric spike protein and LPS, ex vivo. We confirmed that cytokine production was enhanced in PBMCs within six hours when low levels of LPS were combined with purified spike proteins (“spike”). In the presence of 0.5 mg/mL recAAT, however, LPS/spike-induced TNF-α and IL-1β mRNA expression and protein release were significantly inhibited (by about 46–50%) relative to LPS/spike alone. Although without statistical significance, recAAT also reduced production of IL-6 and IL-8. Notably, under the same experimental conditions, the plasma-derived AAT preparation Respreeza (used in native and oxidized forms) did not show significant effects. Our findings imply that an early pro-inflammatory activation of human PBMCs is better controlled by the recombinant version of AAT than the human plasma-derived AAT used here. Considering the increasing clinical interest in AAT therapy as useful to ameliorate the hyper-inflammation seen during COVID-19 infection, different AAT preparations require careful evaluation.
topic COVID-19
spike
LPS
AAT
PBMCs
inflammation
url https://www.mdpi.com/1422-0067/22/15/7941
work_keys_str_mv AT srinutumpara boostedproinflammatoryactivityinhumanpbmcsbylipopolysaccharideandsarscov2spikeproteinisregulatedbya1antitrypsin
AT annargrunding boostedproinflammatoryactivityinhumanpbmcsbylipopolysaccharideandsarscov2spikeproteinisregulatedbya1antitrypsin
AT kokilavanisivaraman boostedproinflammatoryactivityinhumanpbmcsbylipopolysaccharideandsarscov2spikeproteinisregulatedbya1antitrypsin
AT sabinewrenger boostedproinflammatoryactivityinhumanpbmcsbylipopolysaccharideandsarscov2spikeproteinisregulatedbya1antitrypsin
AT beataolejnicka boostedproinflammatoryactivityinhumanpbmcsbylipopolysaccharideandsarscov2spikeproteinisregulatedbya1antitrypsin
AT tobiaswelte boostedproinflammatoryactivityinhumanpbmcsbylipopolysaccharideandsarscov2spikeproteinisregulatedbya1antitrypsin
AT mariajwurm boostedproinflammatoryactivityinhumanpbmcsbylipopolysaccharideandsarscov2spikeproteinisregulatedbya1antitrypsin
AT pacopino boostedproinflammatoryactivityinhumanpbmcsbylipopolysaccharideandsarscov2spikeproteinisregulatedbya1antitrypsin
AT divorkiseljak boostedproinflammatoryactivityinhumanpbmcsbylipopolysaccharideandsarscov2spikeproteinisregulatedbya1antitrypsin
AT florianmwurm boostedproinflammatoryactivityinhumanpbmcsbylipopolysaccharideandsarscov2spikeproteinisregulatedbya1antitrypsin
AT sabinajanciauskiene boostedproinflammatoryactivityinhumanpbmcsbylipopolysaccharideandsarscov2spikeproteinisregulatedbya1antitrypsin
_version_ 1721218364195471360