Differential Immune Checkpoint and Ig-like V-Type Receptor Profiles in COVID-19: Associations with Severity and Treatment
Identifying patients' immune system status has become critical to managing SARS-CoV-2 infection and avoiding the appearance of secondary infections during a hospital stay. Despite the high volume of research, robust severity and outcome markers are still lacking in COVID-19. We recruited 87 COV...
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Veröffentlicht in: | Journal of clinical medicine 2022-06, Vol.11 (12), p.3287 |
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creator | Lozano-Rodríguez, Roberto Terrón-Arcos, Verónica López, Raúl Martín-Gutiérrez, Juan Martín-Quirós, Alejandro Maroun-Eid, Charbel Del Val, Elena Muñoz Cañada-Illana, Carlos Pascual Iglesias, Alejandro Quiroga, Jaime Valentín Montalbán-Hernández, Karla Casalvilla-Dueñas, José Carlos García-Garrido, Miguel A Del Balzo-Castillo, Álvaro Peinado-Quesada, María A Gómez-Lage, Laura Herrero-Benito, Carmen G Butler, Ray Avendaño-Ortiz, José López-Collazo, Eduardo |
description | Identifying patients' immune system status has become critical to managing SARS-CoV-2 infection and avoiding the appearance of secondary infections during a hospital stay. Despite the high volume of research, robust severity and outcome markers are still lacking in COVID-19. We recruited 87 COVID-19 patients and analyzed, by unbiased automated software, 356 parameters at baseline emergency department admission including: high depth immune phenotyping and immune checkpoint expression by spectral flow cytometry, cytokines and other soluble molecules in plasma as well as routine clinical variables. We identified 69 baseline alterations in the expression of immune checkpoints, Ig-like V type receptors and other immune population markers associated with severity (O
requirement). Thirty-four changes in these markers/populations were associated with secondary infection appearance. In addition, through a longitudinal sample collection, we described the changes which take place in the immune system of COVID-19 patients during secondary infections and in response to corticosteroid treatment. Our study provides information about immune checkpoint molecules and other less-studied receptors with Ig-like V-type domains such as CD108, CD226, HVEM (CD270), B7H3 (CD276), B7H5 (VISTA) and GITR (CD357), defining these as novel interesting molecules in severe and corticosteroids-treated acute infections. |
doi_str_mv | 10.3390/jcm11123287 |
format | Article |
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requirement). Thirty-four changes in these markers/populations were associated with secondary infection appearance. In addition, through a longitudinal sample collection, we described the changes which take place in the immune system of COVID-19 patients during secondary infections and in response to corticosteroid treatment. Our study provides information about immune checkpoint molecules and other less-studied receptors with Ig-like V-type domains such as CD108, CD226, HVEM (CD270), B7H3 (CD276), B7H5 (VISTA) and GITR (CD357), defining these as novel interesting molecules in severe and corticosteroids-treated acute infections.</description><identifier>ISSN: 2077-0383</identifier><identifier>EISSN: 2077-0383</identifier><identifier>DOI: 10.3390/jcm11123287</identifier><identifier>PMID: 35743356</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Bacterial infections ; Chemokines ; Clinical medicine ; Coronaviruses ; COVID-19 ; Cytokines ; Immune system ; Immunology ; Infections ; Ligands ; Monoclonal antibodies ; Normal distribution ; Pandemics ; Patients ; Plasma ; Sample size ; Severe acute respiratory syndrome coronavirus 2 ; Software ; Steroids ; Thrombosis</subject><ispartof>Journal of clinical medicine, 2022-06, Vol.11 (12), p.3287</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c409t-1ee70f261714071fbda073634f7cb4feb394e604ff33cbea4a41792c98f8406c3</citedby><cites>FETCH-LOGICAL-c409t-1ee70f261714071fbda073634f7cb4feb394e604ff33cbea4a41792c98f8406c3</cites><orcidid>0000-0002-2214-5441 ; 0000-0002-1612-103X ; 0000-0002-2847-3673 ; 0000-0001-6460-0708 ; 0000-0003-0093-9707</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225268/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225268/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35743356$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lozano-Rodríguez, Roberto</creatorcontrib><creatorcontrib>Terrón-Arcos, Verónica</creatorcontrib><creatorcontrib>López, Raúl</creatorcontrib><creatorcontrib>Martín-Gutiérrez, Juan</creatorcontrib><creatorcontrib>Martín-Quirós, Alejandro</creatorcontrib><creatorcontrib>Maroun-Eid, Charbel</creatorcontrib><creatorcontrib>Del Val, Elena Muñoz</creatorcontrib><creatorcontrib>Cañada-Illana, Carlos</creatorcontrib><creatorcontrib>Pascual Iglesias, Alejandro</creatorcontrib><creatorcontrib>Quiroga, Jaime Valentín</creatorcontrib><creatorcontrib>Montalbán-Hernández, Karla</creatorcontrib><creatorcontrib>Casalvilla-Dueñas, José Carlos</creatorcontrib><creatorcontrib>García-Garrido, Miguel A</creatorcontrib><creatorcontrib>Del Balzo-Castillo, Álvaro</creatorcontrib><creatorcontrib>Peinado-Quesada, María A</creatorcontrib><creatorcontrib>Gómez-Lage, Laura</creatorcontrib><creatorcontrib>Herrero-Benito, Carmen</creatorcontrib><creatorcontrib>G Butler, Ray</creatorcontrib><creatorcontrib>Avendaño-Ortiz, José</creatorcontrib><creatorcontrib>López-Collazo, Eduardo</creatorcontrib><title>Differential Immune Checkpoint and Ig-like V-Type Receptor Profiles in COVID-19: Associations with Severity and Treatment</title><title>Journal of clinical medicine</title><addtitle>J Clin Med</addtitle><description>Identifying patients' immune system status has become critical to managing SARS-CoV-2 infection and avoiding the appearance of secondary infections during a hospital stay. Despite the high volume of research, robust severity and outcome markers are still lacking in COVID-19. We recruited 87 COVID-19 patients and analyzed, by unbiased automated software, 356 parameters at baseline emergency department admission including: high depth immune phenotyping and immune checkpoint expression by spectral flow cytometry, cytokines and other soluble molecules in plasma as well as routine clinical variables. We identified 69 baseline alterations in the expression of immune checkpoints, Ig-like V type receptors and other immune population markers associated with severity (O
requirement). Thirty-four changes in these markers/populations were associated with secondary infection appearance. In addition, through a longitudinal sample collection, we described the changes which take place in the immune system of COVID-19 patients during secondary infections and in response to corticosteroid treatment. 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requirement). Thirty-four changes in these markers/populations were associated with secondary infection appearance. In addition, through a longitudinal sample collection, we described the changes which take place in the immune system of COVID-19 patients during secondary infections and in response to corticosteroid treatment. Our study provides information about immune checkpoint molecules and other less-studied receptors with Ig-like V-type domains such as CD108, CD226, HVEM (CD270), B7H3 (CD276), B7H5 (VISTA) and GITR (CD357), defining these as novel interesting molecules in severe and corticosteroids-treated acute infections.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35743356</pmid><doi>10.3390/jcm11123287</doi><orcidid>https://orcid.org/0000-0002-2214-5441</orcidid><orcidid>https://orcid.org/0000-0002-1612-103X</orcidid><orcidid>https://orcid.org/0000-0002-2847-3673</orcidid><orcidid>https://orcid.org/0000-0001-6460-0708</orcidid><orcidid>https://orcid.org/0000-0003-0093-9707</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Bacterial infections Chemokines Clinical medicine Coronaviruses COVID-19 Cytokines Immune system Immunology Infections Ligands Monoclonal antibodies Normal distribution Pandemics Patients Plasma Sample size Severe acute respiratory syndrome coronavirus 2 Software Steroids Thrombosis |
title | Differential Immune Checkpoint and Ig-like V-Type Receptor Profiles in COVID-19: Associations with Severity and Treatment |
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