Evaluation of circulating leucocyte populations both in subjects with previous SARS-COV-2 infection and in healthy subjects after vaccination
Innate immune mechanisms are central players in response to the binding of pathogens to pattern-recognition receptors providing a crucial initial block on viral replication. Moreover, innate immune response mobilizes cells of the cellular-mediated immune system, which develop into effector cells tha...
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Published in | Journal of immunological methods Vol. 502; p. 113230 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
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Elsevier B.V
01.03.2022
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ISSN | 0022-1759 1872-7905 1872-7905 |
DOI | 10.1016/j.jim.2022.113230 |
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Abstract | Innate immune mechanisms are central players in response to the binding of pathogens to pattern-recognition receptors providing a crucial initial block on viral replication. Moreover, innate immune response mobilizes cells of the cellular-mediated immune system, which develop into effector cells that promote viral clearance. Here, we observed circulating leukocyte T cell response in healthy subjects, COVID-19 infected, and in healthy vaccinated subjects. We found a significant CD8+ T cells (p < 0,05) decrease and an augmented CD4+/CD8+ ratio (p < 0,05) in COVID-19 infected group compared with vaccinated subjects. In addition, healthy vaccinated subjects have a significant increased expression of CD8+ T cells, and a reduction of CD4+/CD8+ ratio with respect to subjects previously COVID-19 infected. Central Memory and Terminal Effector Memory cells (TEMRA) increased after vaccine but not among groups. |
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AbstractList | Innate immune mechanisms are central players in response to the binding of pathogens to pattern-recognition receptors providing a crucial initial block on viral replication. Moreover, innate immune response mobilizes cells of the cellular-mediated immune system, which develop into effector cells that promote viral clearance. Here, we observed circulating leukocyte T cell response in healthy subjects, COVID-19 infected, and in healthy vaccinated subjects. We found a significant CD8+ T cells (p < 0,05) decrease and an augmented CD4+/CD8+ ratio (p < 0,05) in COVID-19 infected group compared with vaccinated subjects. In addition, healthy vaccinated subjects have a significant increased expression of CD8+ T cells, and a reduction of CD4+/CD8+ ratio with respect to subjects previously COVID-19 infected. Central Memory and Terminal Effector Memory cells (TEMRA) increased after vaccine but not among groups.Innate immune mechanisms are central players in response to the binding of pathogens to pattern-recognition receptors providing a crucial initial block on viral replication. Moreover, innate immune response mobilizes cells of the cellular-mediated immune system, which develop into effector cells that promote viral clearance. Here, we observed circulating leukocyte T cell response in healthy subjects, COVID-19 infected, and in healthy vaccinated subjects. We found a significant CD8+ T cells (p < 0,05) decrease and an augmented CD4+/CD8+ ratio (p < 0,05) in COVID-19 infected group compared with vaccinated subjects. In addition, healthy vaccinated subjects have a significant increased expression of CD8+ T cells, and a reduction of CD4+/CD8+ ratio with respect to subjects previously COVID-19 infected. Central Memory and Terminal Effector Memory cells (TEMRA) increased after vaccine but not among groups. Innate immune mechanisms are central players in response to the binding of pathogens to pattern-recognition receptors providing a crucial initial block on viral replication. Moreover, innate immune response mobilizes cells of the cellular-mediated immune system, which develop into effector cells that promote viral clearance. Here, we observed circulating leukocyte T cell response in healthy subjects, COVID-19 infected, and in healthy vaccinated subjects. We found a significant CD8+ T cells (p < 0,05) decrease and an augmented CD4+/CD8+ ratio (p < 0,05) in COVID-19 infected group compared with vaccinated subjects. In addition, healthy vaccinated subjects have a significant increased expression of CD8+ T cells, and a reduction of CD4+/CD8+ ratio with respect to subjects previously COVID-19 infected. Central Memory and Terminal Effector Memory cells (TEMRA) increased after vaccine but not among groups. Innate immune mechanisms are central players in response to the binding of pathogens to pattern-recognition receptors providing a crucial initial block on viral replication. Moreover, innate immune response mobilizes cells of the cellular-mediated immune system, which develop into effector cells that promote viral clearance. Here, we observed circulating leukocyte T cell response in healthy subjects, COVID-19 infected, and in healthy vaccinated subjects. We found a significant CD8⁺ T cells (p < 0,05) decrease and an augmented CD4⁺/CD8⁺ ratio (p < 0,05) in COVID-19 infected group compared with vaccinated subjects. In addition, healthy vaccinated subjects have a significant increased expression of CD8⁺ T cells, and a reduction of CD4⁺/CD8⁺ ratio with respect to subjects previously COVID-19 infected. Central Memory and Terminal Effector Memory cells (TEMRA) increased after vaccine but not among groups. Innate immune mechanisms are central players in response to the binding of pathogens to pattern-recognition receptors providing a crucial initial block on viral replication. Moreover, innate immune response mobilizes cells of the cellular-mediated immune system, which develop into effector cells that promote viral clearance. Here, we observed circulating leukocyte T cell response in healthy subjects, COVID-19 infected, and in healthy vaccinated subjects. We found a significant CD8 T cells (p < 0,05) decrease and an augmented CD4 /CD8 ratio (p < 0,05) in COVID-19 infected group compared with vaccinated subjects. In addition, healthy vaccinated subjects have a significant increased expression of CD8 T cells, and a reduction of CD4 /CD8 ratio with respect to subjects previously COVID-19 infected. Central Memory and Terminal Effector Memory cells (TEMRA) increased after vaccine but not among groups. |
ArticleNumber | 113230 |
Author | Sansone, Annunziata Napoli, Claudio Moccia, Giusi Signoriello, Giuseppe Grimaldi, Vincenzo Benincasa, Giuditta |
Author_xml | – sequence: 1 givenname: Vincenzo surname: Grimaldi fullname: Grimaldi, Vincenzo email: vincenzo.grimaldi@policliniconapoli.it organization: U.O.C. Division of Clinical Immunology, Immunohematology, Transfusion Medicine and Transplant Immunology. Clinical Department of Internal Medicine and Specialistic Units, University of Campania "L. Vanvitelli", 80138 Naples, Italy – sequence: 2 givenname: Giuditta surname: Benincasa fullname: Benincasa, Giuditta organization: Department of Advanced Medical and Surgical Sciences (DAMSS), University of Campania "Luigi Vanvitelli", 80138 Naples, Italy – sequence: 3 givenname: Giusi surname: Moccia fullname: Moccia, Giusi organization: U.O.C. Division of Clinical Immunology, Immunohematology, Transfusion Medicine and Transplant Immunology. Clinical Department of Internal Medicine and Specialistic Units, University of Campania "L. Vanvitelli", 80138 Naples, Italy – sequence: 4 givenname: Annunziata surname: Sansone fullname: Sansone, Annunziata organization: U.O.C. Division of Clinical Immunology, Immunohematology, Transfusion Medicine and Transplant Immunology. Clinical Department of Internal Medicine and Specialistic Units, University of Campania "L. Vanvitelli", 80138 Naples, Italy – sequence: 5 givenname: Giuseppe surname: Signoriello fullname: Signoriello, Giuseppe organization: Statistical Unit, Department of Mental Health and Preventive Medicine, University of Campania "Luigi Vanvitelli", 80138 Naples, Italy – sequence: 6 givenname: Claudio surname: Napoli fullname: Napoli, Claudio organization: U.O.C. Division of Clinical Immunology, Immunohematology, Transfusion Medicine and Transplant Immunology. Clinical Department of Internal Medicine and Specialistic Units, University of Campania "L. Vanvitelli", 80138 Naples, Italy |
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Cites_doi | 10.4049/jimmunol.181.8.5490 10.1177/039463201202500211 10.1016/j.immuni.2008.02.014 10.1126/science.1155209 10.1172/JCI137244 10.1016/j.imlet.2021.01.001 10.1007/s12026-014-8534-z 10.1126/sciadv.abg4081 10.1016/j.archger.2020.104174 10.1093/infdis/jiaa150 10.1111/dom.14547 10.1038/s41467-020-17292-4 10.1002/cyto.a.24172 10.1038/s41577-020-0402-6 10.1038/nri3152 10.1080/07357907.2020.1742349 10.1038/s41590-021-01058-1 |
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Keywords | Flow cytometry characterization COVID-19 infection COVID-19 mRNA BNT162b2 (Pfizer-BioNTech) vaccine T cell immune response |
Language | English |
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Immunol. doi: 10.1038/s41590-021-01058-1 |
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SubjectTerms | Adult Aged Case-Control Studies CD4-CD8 Ratio CD4-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - immunology COVID-19 - blood COVID-19 - immunology COVID-19 - prevention & control COVID-19 - virology COVID-19 infection COVID-19 mRNA BNT162b2 (Pfizer-BioNTech) vaccine COVID-19 Vaccines - administration & dosage COVID-19 Vaccines - immunology Cross-Sectional Studies Female Flow cytometry characterization Healthy Volunteers Humans Immunity, Innate Immunogenicity, Vaccine Immunophenotyping innate immunity Male memory Memory T Cells - immunology Middle Aged SARS-CoV-2 - immunology Severe acute respiratory syndrome coronavirus 2 T cell immune response Technical Note Vaccination vaccines virus replication |
Title | Evaluation of circulating leucocyte populations both in subjects with previous SARS-COV-2 infection and in healthy subjects after vaccination |
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