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Published on: December 19, 2020
Immunohistochemical and Morphometric Analysis of Lung Tissue in Fatal COVID-19
Ioana-Andreea Gheban-Roșca1,2, Bogdan-Alexandru Gheban3,4, Bogdan Pop5,6
1Department of Medical Informatics and Biostatistics, Iuliu Hațieganu University of Medicine and Pharmacy, 400349 Cluj-Napoca, Romania.
Abstract:
The primary targets of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in the lungs are type I pneumocytes, macrophages, and endothelial cells. We aimed to identify lung cells targeted by SARS-CoV-2 using viral nucleocapsid protein staining and morphometric features on patients with fatal COVID-19. We conducted a retrospective analysis of fifty-one autopsy cases of individuals who tested positive for SARS-CoV-2. Demographic and clinical information were collected from forensic reports, and lung tissue was examined for microscopic lesions and the presence of specific cell types. Half of the evaluated cohort were older than 71 years, and the majority were male (74.5%). In total, 24 patients presented diffuse alveolar damage (DAD), and 50.9% had comorbidities (56.9% obesity, 33.3% hypertension, 15.7% diabetes mellitus). Immunohistochemical analysis showed a similar pattern of infected macrophages, infected type I pneumocytes, and endothelial cells, regardless of the presence of DAD (p > 0.5). The immunohistochemical reactivity score (IRS) was predominantly moderate but without significant differences between patients with and without DAD (p = 0.633 IRS for type I pneumocytes, p = 0.773 IRS for macrophage, and p = 0.737 for IRS endothelium). The nucleus/cytoplasm ratio shows lower values in patients with DAD (median: 0.29 vs. 0.35), but the difference only reaches a tendency for statistical significance (p = 0.083). Our study confirms the presence of infected macrophages, type I pneumocytes, and endothelial cells with a similar pattern in patients with and without diffuse alveolar damage.
Insights
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infects type I pneumocytes, macrophages, and endothelial cells in the lungs. This pattern of infection remains consistent in patients with and without diffuse alveolar damage (DAD).
Area of Science:
- Pathology
- Virology
- Pulmonology
Background:
- Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is known to target lung cells.
- Understanding specific cellular targets is crucial for comprehending COVID-19 pathogenesis.
Purpose of the Study:
- To identify lung cells targeted by SARS-CoV-2 in fatal COVID-19 cases.
- To analyze the pattern of SARS-CoV-2 infection in relation to diffuse alveolar damage (DAD).
Main Methods:
- Retrospective analysis of 51 autopsy cases of SARS-CoV-2 positive individuals.
- Immunohistochemical staining for viral nucleocapsid protein.
- Morphometric analysis of lung tissue, including nucleus/cytoplasm ratio.
Main Results:
- Infected macrophages, type I pneumocytes, and endothelial cells were identified.
- The pattern of infected cells was similar in patients with and without DAD.
- No significant differences in immunohistochemical reactivity scores (IRS) were observed between groups.
Conclusions:
- The study confirms macrophages, type I pneumocytes, and endothelial cells as primary SARS-CoV-2 targets in the lungs.
- Cellular tropism of SARS-CoV-2 is consistent across patients with and without DAD.
- Morphometric changes showed a tendency towards significance in patients with DAD.

