Cococcia S, Lenti MV, Santacroce G, Achilli G, Borrelli de Andreis F, Di Sabatino A. Liver-spleen axis dysfunction in COVID-19. World J Gastroenterol 2021; 27(35): 5919-5931 [PMID: 34629809 DOI: 10.3748/wjg.v27.i35.5919]
Corresponding Author of This Article
Marco Vincenzo Lenti, MD, Academic Research, Research Assistant Professor, First Department of Internal Medicine, San Matteo Hospital Foundation, University of Pavia, Viale Golgi 19, Pavia 27100, Italy. marco.lenti@unipv.it
Research Domain of This Article
Gastroenterology & Hepatology
Article-Type of This Article
Minireviews
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No cases of severe liver injury in this cohort. Liver involvement was generally mild and, although correlated to a higher need of ICU care, not associated to higher mortality
ACE2 expression on tissue-resident CD169+ macrophages in spleen; viral NP antigen found in ACE2+ cells in spleen; direct damage of spleen tissue (lymph follicle depletion, splenic nodule atrophy, lymphocyte reduction, etc.)
Decrease in spleen cell composition with decrease in lymphocyte components, white pulp atrophied, lymphoid follicles decreased or absent, increase in red pulp to white pulp ratio
Lymphoid hypoplasia in 100%, red pulp haemorrhages in 60%, splenitis in 40%, extramedullary haematopoiesis in 50%, endothelial changes in 80%, vasculitis and arterial thrombus in 20%
Loss of spleen germinal centres due to depletion of Bcl-6+ germinal centre B cells and Bcl-6+ germinal centre T follicular helper cells, resulting in a dysregulated humoral immune response
Citation: Cococcia S, Lenti MV, Santacroce G, Achilli G, Borrelli de Andreis F, Di Sabatino A. Liver-spleen axis dysfunction in COVID-19. World J Gastroenterol 2021; 27(35): 5919-5931