ELENI DIMITRA PAPANAGNOU

Dr. ELENI DIMITRA PAPANAGNOU

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Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 April 2021 in Blood
Verified
Journal Article
Open access
PDF file
Evangelos TerposEvangelos Terpos
Evangelos Terpos
Ioannis TrougakosIoannis Trougakos
Ioannis Trougakos
MGMaria Gavriatopoulou
Maria Gavriatopoulou
IPIoannis Papassotiriou
Ioannis Papassotiriou
ASAimilia Sklirou
Aimilia Sklirou
Meletios-Athanasios DimopoulosMeletios-Athanasios Dimopoulos
Meletios-Athanasios Dimopoulos
Evangelos Terpos, Ioannis P Trougakos, Maria Gavriatopoulou, Ioannis Papassotiriou, Aimilia D Sklirou, Ioannis Ntanasis-Stathopoulos, Eleni-Dimitra Dimitra Papa

1 September 2021 in Journal of Imaging
Verified
Journal Article
Open access
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KKKleoniki Keklikoglou
Kleoniki Keklikoglou
CAChristos Arvanitidis
Christos Arvanitidis
GCGiorgos Chatzigeorgiou
Giorgos Chatzigeorgiou
Eva ChatzinikolaouEva Chatzinikolaou
Eva Chatzinikolaou
EKEfstratios Karagiannidis
Efstratios Karagiannidis
AVAngeliki Vogiatzi
Angeliki Vogiatzi
Several imaging techniques are used in biological and biomedical studies. Micro-computed tomography (micro-CT) is a non-destructive imaging technique that allows the rapid digitisation of internal and external structures of a sample in three dimensions and with great resolution. In this review, the strengths and weaknesses of some common imaging techniques applied in biological and biomedical fields, such as optical microscopy, confocal laser scanning microscopy, and scanning electron microscopy, are presented and compared with the micro-CT technique through five use cases. Finally, the ability of micro-CT to create non-destructively 3D anatomical and morphological data in sub-micron resolution and the necessity to develop complementary methods with other imaging techniques, in order to overcome limitations caused by each technique, is emphasised.

21 September 2020 in Life
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Journal Article
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OTOurania Tsitsilonis
Ourania Tsitsilonis
Dimitrios ParaskevisDimitrios Paraskevis
Dimitrios Paraskevis
Evi S. LianidouEvi S. Lianidou
Evi S. Lianidou
VPVassilios Pierros
Vassilios Pierros
AAAthanasios Akalestos
Athanasios Akalestos
Meletios-Athanasios DimopoulosMeletios-Athanasios Dimopoulos
Meletios-Athanasios Dimopoulos
Due to early implementation of public health measures, Greece had low number of SARS-CoV-2 infections and COVID-19 severe incidents in hospitalized patients. The National and Kapodistrian University of Athens (ΝΚUA), especially its health-care/medical personnel, has been actively involved in the first line of state responses to COVID-19. To estimate the prevalence of antibodies (Igs) against SARS-CoV-2 among NKUA members, we designed a five consecutive monthly serosurvey among randomly selected NKUA consenting volunteers. Here, we present the results from the first 2500 plasma samples collected during June–July 2020. Twenty-five donors were tested positive for anti-SARS-CoV-2 Igs; thus, the overall seroprevalence was 1.00%. The weighted overall seroprevalence was 0.93% (95% CI: 0.27, 2.09) and varied between males [1.05% (95% CI: 0.18, 2.92)] and females [0.84% (95% CI: 0.13, 2.49)], age-groups and different categories (higher in participants from the School of Health Sciences and in scientific affiliates/faculty members/laboratory assistants), but no statistical differences were detected. Although focused on the specific population of NKUA members, our study shows that the prevalence of anti-SARS-CoV-2 Igs for the period June–July 2020 remained low and provides knowledge of public health importance for the NKUA members. Given that approximately one in three infections was asymptomatic, continuous monitoring of the progression of the pandemic by assessing Ig seroprevalence is needed.

15 February 2021 in Leukemia
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Journal Article
Closed access
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EKEfstathios Kastritis
Efstathios Kastritis
ALAgeliki Laina
Ageliki Laina
GGGeorgios Georgiopoulos
Georgios Georgiopoulos
MGMaria Gavriatopoulou
Maria Gavriatopoulou
EPELENI DIMITRA PAPANAGNOU
ELENI DIMITRA PAPANAGNOU
Meletios-Athanasios DimopoulosMeletios-Athanasios Dimopoulos
Meletios-Athanasios Dimopoulos

19 October 2022 in Aging Cell
Verified
Journal Article
Open access
EPELENI DIMITRA PAPANAGNOU
ELENI DIMITRA PAPANAGNOU
SGSentiljana Gumeni
Sentiljana Gumeni
ASAimilia Sklirou
Aimilia Sklirou
ARAlexandra Rafeletou
Alexandra Rafeletou
Evangelos TerposEvangelos Terpos
Evangelos Terpos
Ioannis TrougakosIoannis Trougakos
Ioannis Trougakos
The ubiquitin–proteasome pathway and its functional interplay with other proteostatic and/or mitostatic modules are crucial for cell viability, especially in post‐mitotic cells like cardiomyocytes, which are constantly exposed to proteotoxic, metabolic, and mechanical stress. Consistently, treatment of multiple myeloma patients with therapeutic proteasome inhibitors may induce cardiac failure; yet the effects promoted by heart‐targeted proteasome dysfunction are not completely understood. We report here that heart‐targeted proteasome knockdown in the fly experimental model results in increased proteome instability and defective mitostasis, leading to disrupted cardiac activity, systemic toxicity, and reduced longevity. These phenotypes were partially rescued by either heart targeted‐ or by dietary restriction‐mediated activation of autophagy. Supportively, activation of autophagy by Rapamycin or Metformin administration in flies treated with proteasome inhibitors reduced proteome instability, partially restored mitochondrial function, mitigated cardiotoxicity, and improved flies' longevity. These findings suggest that autophagic inducers represent a novel promising intervention against proteasome inhibitor‐induced cardiovascular complications.

12 October 2021 in Life
Verified
Journal Article
Open access
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Evangelos TerposEvangelos Terpos
Evangelos Terpos
Vangelis D. KaralisVangelis D. Karalis
Vangelis D. Karalis
Ioannis Ntanasis-StathopoulosIoannis Ntanasis-Stathopoulos
Ioannis Ntanasis-Stathopoulos
MGMaria Gavriatopoulou
Maria Gavriatopoulou
SGSentiljana Gumeni
Sentiljana Gumeni
Meletios-Athanasios DimopoulosMeletios-Athanasios Dimopoulos
Meletios-Athanasios Dimopoulos
Elucidating long-term immunity following COVID-19 vaccination is essential for decision-making regarding booster shots. The aim of this study was to investigate the kinetics of neutralizing antibodies (Nabs) against SARS-CoV-2 up to six months after the second vaccination dose with the BNT162b2 mRNA vaccine. Nabs levels were measured on days 1 (before the first vaccine shot), 8, 22 (before the second shot), 36, 50, and 3 and 6 months after the second vaccination (NCT04743388). Three hundred and eight healthy individuals without malignant disease were included in this study. At six months, 2.59% of the participants had a Nabs value less than 30%, while 11.9% had Nabs values of less than 50%. Importantly, 58% of the subjects had Nabs values of more than 75%. Nabs were initially eliminated at a relatively slow rate, but after three months their elimination was 5.7 times higher. Older age was inversely associated with Nabs levels at all examined timepoints. Interestingly, a population modeling analysis estimated that half of the subjects will have Nabs values less than 73.8% and 64.6% at 9 and 12 months, respectively, post vaccination completion. In conclusion, we found a persistent but declining anti-SARS-CoV-2 humoral immunity at six months following full vaccination with BNT162b2 in healthy individuals, which was more pronounced among older persons. These data may inform the public health policies regarding the prioritization of booster vaccine shots.