Flow Cytometric Analysis of Lymphocyte Subsets of Covid-19 Patients from A Single Centre in Turkey

Authors : Tuğrul ELVERDİ, Abdülkadir ERÇALIŞKAN, Rıdvan KARAALİ, İlker İnanç BALKAN, Deniz ÖZMEN, Ayşe SALİHOĞLU, Birgül METE, Ahmet Emre EŞKAZAN, Zafer BAŞLAR, Fehmi TABAK, Muhlis Cem AR

Pages : 534-541

Doi:10.31067/acusaglik.1335196

View : 53 | Download : 56

Publication Date : 2023-10-01

Article Type : Research Paper

Abstract :Purpose: Lymphocyte counts have been shown to negatively correlate with the severity in Covid-19. The aim of this study is to analyse the distribution of lymphocyte subsets in response to SARS-CoV-2 infection and its relation to the severity of the disease. Methods: Blood samples were obtained from 67 consecutive patients between April 2020 and July 2020. Data on other laboratory parameters, and clinical course were collected retrospectively from patient files and patients were defined to have as severe or non-severe insert ignore into journalissuearticles values(mild/moderate); disease. Leukocyte subsets to be studied were identified by using flow cytometric analysis insert ignore into journalissuearticles values(Beckman Coulter Navios Ex V2.0);. Patients were allocated into 3 groups based on the day of blood sample collection: Days 0-7, 8-14 and >14 as Group I, Group II and Group III, respectively. In 10 of 67 patients an additional analysis was done 7-10 days after the initial sampling. Results: A total of 67 patients insert ignore into journalissuearticles values(30 female, 37 male); with a median age of 57 were evaluated. Lower total lymphocyte, CD3 positive, CD4 positive and B-cell counts were identified in severe infection compared to non-severe infection group which were also correlated with high serum CRP, D-dimer and ferritin levels. NK and monocyte counts were not different between the two groups. Activation markers CD38 and HLA-DR on CD4 and CD8 positive lymphocytes also were not different in either group. Conclusion: CD3 and CD4 lymphopenia were lower in accordance with previous studies and were associated with severe disease. The expectancy of high activation markers was not met. Future studies with detailed subgroup analyses at different time-points will shed more light on our general knowledge of the immune response to COVID-19.
Keywords : FLOW CYTOMETRY, COVID 19, IMMUNE PROFILE, LYMPHOCYTE SUBSETS, MONOCYTES