Immunity Profiling of COVID-19 Infection, Dynamic Variations of Lymphocyte Subsets, a Comparative Analysis on Four Different Groups
Autor: | Donatello Iacobone, Rita Laforgia, Angelo Cefalo, Luigi Vimercati, Francesco Inchingolo, Giancarla Pricolo, Pietro Distratis, Davide Palazzo, Felice Lorusso, Antonella Prudenzano, Van Hung Pham, Ciro Gargiulo Isacco, Kieu C. D. Nguyen, Sergey K. Aityan, Gianna Dipalma, Giuseppe Mancusi Materi, Angela Pezzolla, Orazio Catucci, Antonio Scarano, Diego Tomassone, Felice Amatulli, Alessio Danilo Inchingolo, Patrizia D’Errico, Rita Lazzaro, Mario Giosuè Balzanelli |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Microbiology (medical)
medicine.medical_specialty Cellular immunity Coronavirus disease 2019 (COVID-19) QH301-705.5 Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) broncho-alveolar lavage fluid (BALF) coronavirus cellular immunity CD38 Microbiology Gastroenterology Article Immunity Virology Internal medicine medicine Biology (General) Respiratory system business.industry SARS-CoV-2 humoral response medicine.disease Pneumonia business Lymphocyte subsets |
Zdroj: | Microorganisms; Volume 9; Issue 10; Pages: 2036 Microorganisms Microorganisms, Vol 9, Iss 2036, p 2036 (2021) |
ISSN: | 2076-2607 |
DOI: | 10.3390/microorganisms9102036 |
Popis: | Background: A novel coronavirus (SARS-CoV-2)-induced pneumonia (COVID-19) emerged in December 2019 in China, spreading worldwide. The aim of the present investigation was to evaluate the immunological response and the clinical subset of peripheral lymphocyte subset alteration in COVID-19 infection. Methods: the study was conducted on four different clinical groups (n = 4; total n = 138). Each individual was assigned to different groups based on specific criteria evaluated at the admission such as fever, dyspnea, arterial blood gas analysis (ABG), oral-nasopharyngeal swab/RT-PCR, and thoracic CT-scan. Treatment was performed only after blood samples were collected from each patient (PP and PP) at day 1. The blood samples were analyzed and tested the same day (CBC and Flowcytometry). The positive–positive group (PP n = 45; F = 18/ M = 27; median age = 62.33), comprised individuals affected by COVID-19 who showed fever, dyspnea (ABG = pO2 < 60), confirmed positive by oral-nasopharyngeal swab/RT-PCR and with CT-scan showing ground-glass opacities. The negative–positive (NP; n = 37; F = 11/M = 26; median age = 75.94) or “COVID-like” group comprised individuals with fever and dyspnea (ABG = pO2 < 60), who tested negative to nasopharyngeal swab/RT-PCR, with CT-scans showing ground-glass opacities in the lungs. The negative–affected group (NA; n = 40; F = 14/M = 26; median age = 58.5) included individuals negative to COVID-19 (RT-PCR) but affected by different chronic respiratory diseases (the CT-scans didn’t show ground-glass opacities). Finally, the negative–negative group (NN; n = 16; F = 14/M = 2) included healthy patients (NN; n = 16; median age = 42.62). Data and findings were collected and compared. Results: Lymphocytes (%) cells showed a decline in COVID-19 patients. The subsets showed a significant association with the inflammatory status in COVID-19, especially with regard to increased neutrophils, T-killer, T-active, T-suppressor, and T-CD8+CD38+ in individuals belong to the either COVID-19 and Covid-like NP group. Conclusions: Peripheral lymphocyte subset alteration was associated with the clinical characteristics and progression of COVID-19. The level of sub-set cells T-lymphocytes (either high or low) and B-lymphocytes could be used as an independent predictor for COVID-19 severity and treatment efficacy. |
Databáze: | OpenAIRE |
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