tetano
Editor, Senior Moderator
iScience
. 2023 Jan 13;105972.
doi: 10.1016/j.isci.2023.105972. Online ahead of print.
SARS-CoV-2 variants induce distinct disease and impact in the bone marrow and thymus of mice
Rute Gonçalves[SUP] 1 [/SUP], Joana Couto[SUP] 1 [/SUP], Pedro Ferreirinha[SUP] 1 2 [/SUP], José Maria Costa[SUP] 1 3 [/SUP], Diogo Silvério[SUP] 1 4 [/SUP], Marta L Silva[SUP] 1 4 [/SUP], Ana Isabel Fernandes[SUP] 1 4 [/SUP], Pedro Madureira[SUP] 1 5 [/SUP], Nuno L Alves[SUP] 1 2 [/SUP], Sofia Lamas[SUP] 1 2 [/SUP], Margarida Saraiva[SUP] 1 2 [/SUP]
Affiliations
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has evolved to variants associated with milder disease. We employed the k18-hACE2 mouse model to study how differences in the course of infection by SARS-CoV-2 variants alpha, delta and omicron relate to tissue pathology and the immune response triggered. We documented a variant-specific pattern of infection severity, inducing discrete lung and blood immune responses and differentially impacting primary lymphoid organs. Infections with variants alpha and delta promoted bone marrow (BM) emergency myelopoiesis, with blood and lung neutrophilia . The defects in the BM hematopoietic compartment extended to the thymus, with the infection by the alpha variant provoking a marked thymic atrophy. Importantly, the changes in the immune responses correlated with the severity of infection. Our study provides a comprehensive platform to investigate the modulation of disease by SARS-CoV-2 variants and underscores the impact of this infection in the function of primary lymphoid organs.
Keywords: COVID-19; SARS-CoV-2; alpha variant; delta variant; immunology; k18-hACE2; lymphoid organs; omicron variant; pathogenesis; tissue pathology.
. 2023 Jan 13;105972.
doi: 10.1016/j.isci.2023.105972. Online ahead of print.
SARS-CoV-2 variants induce distinct disease and impact in the bone marrow and thymus of mice
Rute Gonçalves[SUP] 1 [/SUP], Joana Couto[SUP] 1 [/SUP], Pedro Ferreirinha[SUP] 1 2 [/SUP], José Maria Costa[SUP] 1 3 [/SUP], Diogo Silvério[SUP] 1 4 [/SUP], Marta L Silva[SUP] 1 4 [/SUP], Ana Isabel Fernandes[SUP] 1 4 [/SUP], Pedro Madureira[SUP] 1 5 [/SUP], Nuno L Alves[SUP] 1 2 [/SUP], Sofia Lamas[SUP] 1 2 [/SUP], Margarida Saraiva[SUP] 1 2 [/SUP]
Affiliations
- PMID: 36687317
- PMCID: PMC9838028
- DOI: 10.1016/j.isci.2023.105972
Abstract
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has evolved to variants associated with milder disease. We employed the k18-hACE2 mouse model to study how differences in the course of infection by SARS-CoV-2 variants alpha, delta and omicron relate to tissue pathology and the immune response triggered. We documented a variant-specific pattern of infection severity, inducing discrete lung and blood immune responses and differentially impacting primary lymphoid organs. Infections with variants alpha and delta promoted bone marrow (BM) emergency myelopoiesis, with blood and lung neutrophilia . The defects in the BM hematopoietic compartment extended to the thymus, with the infection by the alpha variant provoking a marked thymic atrophy. Importantly, the changes in the immune responses correlated with the severity of infection. Our study provides a comprehensive platform to investigate the modulation of disease by SARS-CoV-2 variants and underscores the impact of this infection in the function of primary lymphoid organs.
Keywords: COVID-19; SARS-CoV-2; alpha variant; delta variant; immunology; k18-hACE2; lymphoid organs; omicron variant; pathogenesis; tissue pathology.