ABSTRACT
Background: Lymphopenia is predictive of survival in patients with coronavirus disease 2019 (COVID-19). Objective: The aim of this study was to understand the cause of the lymphocyte count drop in severe forms of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Methods: Monocytic production of reactive oxygen species (ROSs) and T-cell apoptosis were measured by flow cytometry, DNA damage in PBMCs was measured by immunofluorescence, and angiotensin II (AngII) was measured by ELISA in patients infected with SARS-CoV-2 at admission to an intensive care unit (ICU) (n = 29) or not admitted to an ICU (n = 29) and in age- and sex-matched healthy controls. Results: We showed that the monocytes of certain patients with COVID-19 spontaneously released ROSs able to induce DNA damage and apoptosis in neighboring cells. Of note, high ROS production was predictive of death in ICU patients. Accordingly, in most patients, we observed the presence of DNA damage in up to 50% of their PBMCs and T-cell apoptosis. Moreover, the intensity of this DNA damage was linked to lymphopenia. SARS-CoV-2 is known to induce the internalization of its receptor, angiotensin-converting enzyme 2, which is a protease capable of catabolizing AngII. Accordingly, in certain patients with COVID-19 we observed high plasma levels of AngII. When looking for the stimulus responsible for their monocytic ROS production, we revealed that AngII triggers ROS production by monocytes via angiotensin receptor I. ROSs released by AngII-activated monocytes induced DNA damage and apoptosis in neighboring lymphocytes. Conclusion: We conclude that T-cell apoptosis provoked via DNA damage due to the release of monocytic ROSs could play a major role in COVID-19 pathogenesis.
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This research examined the influence of COVID-19 on the stock returns of the cross-border transportation industry by performing an event study on the cumulative abnormal return of cross-border transportation companies listed in Taiwan from December 2019 to February 2021. The purpose is to analyze whether the pandemic has a negative impact on the stock returns of the cross-border transportation industry. The empirical results indicate the cumulative abnormal return is indeed influenced by COVID-19, but the impact can be positive or negative at different time points. © 2022, The Author(s), under exclusive license to Springer Nature Switzerland AG.
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Background: The aim of this study was to identify the cause of lymphopenia, strongly predictive of survival in COVID-19. Methods: We recruited PCR-positive SARS-CoV-2-infected patients upon admission to Intensive Care Units (ICU, n = 29) and to the Infectious Diseases Department (non-ICU, n = 29) at Nîmes University Hospital, as well as age-and sex-matched healthy controls (HC). Their Angiotensin II plasma levels were measured by ELISA and their monocytic reactive oxygen species (ROS) production and T-cell apoptosis were measured by flow cytometry using dichloro-dihydro-fluorescein diacetate and fluorescent annexin V, respectively. DNA damage and double strand breaks were quantified in immunofluorescence using antibodies specific for-γ-H2AX and 53BP1, respectively. Results: The monocytes of certain COVID-19 patients spontaneously released ROS able to induce DNA damage and apoptosis in neighboring cells. High ROS production was predictive of death. Indeed, in most patients we observed the presence of DNA damage in up to 50% of their peripheral mononuclear blood cells, with double-strand DNA breaks, and T-cell apoptosis. The intensity of this DNA damage was linked to lymphopenia. SARS-CoV-2 is known to induce the internalization of its receptor, Angiotensin Converting Enzyme 2, a protease able to catabolize Angiotensin II. Accordingly, we observed high plasma levels of Angiotensin II in ROS-producing patients. In search of the stimulus responsible for their ability to release ROS, we unveiled that Angiotensin II triggers ROS production by monocytes via Angiotensin receptor I (AT1). ROS released by Angiotensin II-activated monocytes induced DNA damage and apoptosis in neighboring cells. Conclusion: Mononuclear cell apoptosis provoked via DNA damage due to the release of monocytic ROS could play a major role in COVID-19 pathogenesis, inasmuch as ROS are also known to trigger inflammatory cytokine production. Unveiling this new pathogenic pathway opens up new therapeutic possibilities for COVID-19 based on the early association of AT1 antagonists and antioxidants.
ABSTRACT
SARS-CoV-2 exploits the host cellular machinery for virus replication leading to the acute syndrome of coronavirus disease 2019 (COVID-19). Growing evidence suggests SARS-CoV-2 also exacerbates many chronic diseases, including cancers. As mutations on the spike protein (S) emerged as dominant variants that reduce vaccine efficacy, little is known about the relation between SARS-CoV-2 virus variants and cancers. Compared to the SARS-CoV-2 wild-type, the Gamma variant contains two additional NXT/S glycosylation motifs on the S protein. The hyperglycosylated S of Gamma variant is more stable, resulting in more significant epithelial-mesenchymal transition (EMT) potential. SARS-CoV-2 infection promoted NF-κB signaling activation and p65 nuclear translocation, inducing Snail expression. Pharmacologic inhibition of NF-κB activity by nature food compound, I3C suppressed viral replication and Gamma variant-mediated breast cancer metastasis, indicating that NF-κB inhibition can reduce chronic disease in COVID-19 patients. Our study revealed that the Gamma variant of SARS-CoV-2 activates NF-κB and, in turn, triggers the pro-survival function for cancer progression.
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Background: Wuhan, the epicenter of the coronavirus disease 2019 outbreak, was locked down on January 23, 2020. We aimed to investigate the barriers to the physical prevention, negative attitudes, and anxiety levels. Methods: A online cross-sectional survey was conducted with the people living in Wuhan between March 12th and 23rd, 2020. Results: Of a total of 2411 complete responses, the mean and standard deviation for the total physical prevention barriers score was 19.73 (standard deviation +/- 5.3;range 12-45) out of a possible score of 48. Using a cut-off score of 44 for the State-Trait Inventory score, 79.9% (95% confidence interval [CI]: 78.2-81.5) of the participants reported moderate to severe anxiety during the early phase of the outbreak, and 51.3% (95% CI 49.2-53.3) reported moderate to severe anxiety after the peak of coronavirus disease 2019 was over (during the study period). Comparing anxiety levels in the early phase of the outbreak and after the peak of the outbreak, 58.5% (95% CI 56.5-60.5) recorded a decreased anxiety. Females reported a higher likelihood of having decreased levels of anxiety than males (odds ratio = 1.78, 95% CI 1.48-2.14). Low negative attitudes score were associated with a higher decrease in anxiety (odds ratio = 1.59, 95% CI 1.33-1.89). Conclusions: The attitudinal barriers to prevention of transmission of coronavirus disease 2019 are more prominent than physical prevention barriers after the peak of corona virus disease 2019. High anxiety levels even after the peak warrant serious attention.
ABSTRACT
The engagement of human angiotensin-converting enzyme 2 (hACE2) and SARS-CoV-2 spike protein facilitate virus spread. Thus far, ACE2 and TMPRSS2 expression is correlated with the epithelial-mesenchymal transition (EMT) gene signature in lung cancer. However, the mechanism for SARS-CoV-2-induced EMT has not been thoroughly explored. Here, we showed that SARS-CoV-2 induces EMT phenotypic change and stemness in breast cancer cell model and subsequently identified Snail as a modulator for this regulation. The in-depth analysis identifies the spike protein (S), but not envelope (E), nucleocapsid (N), or membrane protein (M), of SARS-CoV-2 induces EMT marker changes. Suppression of Snail expression in these cells abrogates S protein-induced invasion, migration, stemness, and lung metastasis, suggesting that Snail is required for SARS-CoV-2-mediated aggressive phenotype in cancer. This study reveals an important oncogenic role of SARS-CoV-2 in triggering breast cancer metastasis through Snail upregulation.
ABSTRACT
Objective: To analysis the clinical characteristics of"recurrence"RNA positive patients with Coronavirus disease 2019 ï¼COVID-19ï¼ and compared with those without"recurrence". Methods: 98 patients with COVID-19 in Wuhan Jinyintan Hospital and designated treatment hospitals in Quanzhou were included in this study from February 2020 to April 2020. There were 55 males and 43 femalesï¼ aged from15 to 83 yearsï¼ with a median age of 57.5 yearsï¼ in which 20 cases were complicated with basic diseases. 15 of these patients had been diagnosed and hospitalized had been found as"recurrence"2019-nCoV RNA positive after discharge while the other 83 cases were all negative. The clinical classification of all patients was common type. Clinical data of the COVID-19 RNA"recurrence"patients were collectedï¼ and general situationsï¼ symptomsï¼ laboratory examinations and CT images were also observed and analyzed. The patients were divided into 2019-nCoV"recurrent"group and 2019-nCoV"non-recurrent"group. There are 10 males and 5 females in 2019-nCoV"recurrent"group while 45 males and 38 females in"non-recurrent"group ï¼χ²=0.800ï¼P=0.371ï¼. The age of 2019-nCoV"recurrent"group ï¼57±21ï¼ was higher than that of"non-recurrent"groupï¼53±17ï¼. 8 of 15 the COVID-19"recurrent"group patients and 12 of 83"non-recurrent"patients have basic diseases. IgG and IgM of 2019-nCoVï¼ IL-6ï¼ procalcitoninï¼ ESRï¼ CRPï¼ BNP and other serum biochemical index levels were measured and compared between groups. Results: ï¼1ï¼ The proportion of patients with common type of COVID-19 was 15.3% during 2-week medical observation after discharge. ï¼2ï¼ All of the 2019-nCoV"recurrent"patients were hospitalized due to COVID-19 RNA positiveï¼ when they were quarantined after discharged from hospital. All the patients with mild symptoms which were clarified as common typeï¼ including 5 cases of feverï¼ 6 cases of coughï¼ 5 cases of expectorationï¼ and 2 cases of slight shortness of breath. The time of symptoms appeared on ï¼5.73±2.82ï¼ days after discharge. ï¼3ï¼ The serum procalcitonin of all 2019-nCoV"recurrent"group patients were normalï¼all<0.05 ng/mlï¼. The BNP of"recurrent"group ï¼151±171ï¼ ng/Lï¼ was higher than that of"non-recurrent"group ï¼63±78ï¼ ng/L ï¼t = 3.207ï¼ P = 0.000ï¼. There was no significant difference in laboratory tests like leukocyte ï¼»ï¼6.17±2.4ï¼ and ï¼6.04±2.41ï¼×109/Lï¼½ï¼ lymphocyteï¼»ï¼1.59±0.52ï¼ and ï¼1.32±0.64ï¼×109/Lï¼½ï¼ CRP ï¼»ï¼12.54±28.20ï¼ and ï¼21.74±25.63ï¼mg/Lï¼½ï¼ ESR ï¼»ï¼31.07±28.72ï¼ and ï¼34.10±22.16ï¼mm/1 hï¼½ï¼ AST ï¼»ï¼24.73±9.15ï¼ and ï¼30.24±23.20ï¼U/Lï¼½ï¼ ALT ï¼»ï¼22.60±12.82ï¼ and ï¼36.47±34.12ï¼U/Lï¼ï¼ LDH ï¼»ï¼268±208ï¼ and ï¼270±164ï¼U/Lï¼½ï¼ D-dimer ï¼»ï¼0.60±0.50ï¼ and ï¼0.84±0.98ï¼µg/Lï¼½ï¼ ferritin ï¼»ï¼294±195ï¼ and ï¼395±319ï¼µg/Lï¼½ï¼ IL-6 ï¼»ï¼9.17±6.42ï¼ and ï¼14.28±17.74ï¼ng/Lï¼½ and BUN ï¼5.77±2.66ï¼ and ï¼4.74±2.81ï¼U/Lï¼½ between"recurrent"and"non-recurrent"groups ï¼all P>0.05ï¼. ï¼4ï¼ In"recurrent"groupï¼ ground glassï¼ exudative or solid lesions could be found in most of the chest CT performed on re-admission. Meanwhileï¼ fibrosis lesion was relatively rare. ï¼5ï¼ There were no secondary transmissions were found to be caused by the 2019-nCoV"recurrent"group patients. Conclusions: Most of the 2019-nCoV patients had underlying diseases and active lesions were still found in CT imagesï¼ so the possibility of virus replication may still exist. All"recurrent"patients had mild illness which may suggest that they were in recovery stage, and no evidence of transmission is found.
Subject(s)
COVID-19/diagnosis , RNA, Viral/analysis , Adolescent , Adult , Aged , Aged, 80 and over , China , Female , Humans , Male , Middle Aged , Recurrence , Retrospective Studies , SARS-CoV-2 , Young AdultABSTRACT
Background: The rapid outbreak of COVID-19 pandemic promptly changed people’s daily lives, influenced human interactions and economic activities and induced mental reactions. Objective: This review synthesized the evidence of correlation between demographic factors, social media exposure, stressors and anxiety and depression status in the early phase of COVID-19. Method: A systematically search included observational studies published before May15, 2020. We selected studies designed with valid measuring instruments of anxiety and depression. Result: 20 articles were included (19 cross-sectional) for review. People who were divorced/widowed, with poor self-rated health status, chronic illness and previous psychiatric illness had higher anxiety and depression prevalence. Higher COVID-19 awareness (including COVID-19 knowledge and precautionary measure) decreased anxiety and depression. The protective measures to reduce anxiety and depression levels included avoiding sharing meals, frequently washing hands and wearing mask. Economic loss, academic delay, influence of daily life, worrying and symptoms related to infection were stressors of anxiety and depression. There were lots of inconsistent results due to convenience sampling and diverse measuring instrument. Conclusion: Our review suggested that reliable information from health authorities, enhancing health literacies and prevention measures of general population can reduce anxiety and depression levels.