Bone marrow haematopoiesis in patients with COVID-19

被引:0
|
作者
Marques-Maggio, Ewerton [1 ,2 ]
Maccio, Umberto [1 ]
Marx, Alexandra [3 ]
Galli, Serena [4 ]
Schwab, Nathalie
Frank, Angela
Hamelin, Baptiste
Varga, Zsuzsanna [1 ]
Nombela-Arrieta, Cesar [4 ]
Mertz, Kirsten D. [5 ]
Theocharides, Alexandre P. A. [4 ,6 ]
Koelzer, Viktor H. [1 ,7 ]
机构
[1] Univ Zurich, Univ Hosp Zurich, Dept Pathol & Mol Pathol, Zurich, Switzerland
[2] Med Pathol Zent Zurich, Zurich, Switzerland
[3] Klin Innere Med, Stadtspital Zurich Waid, Zurich, Switzerland
[4] Univ Zurich, Univ Hosp Zurich, Dept Med Oncol & Hematol, Zurich, Switzerland
[5] Cantonal Hosp Baselland, Inst Pathol, Liestal, Switzerland
[6] Univ Zurich, Univ Hosp, Dept Med Oncol & Hematol, Ramistr 100, CH-8091 Zurich, Switzerland
[7] Univ Zurich, Univ Hosp, Dept Pathol & Mol Pathol, Schmelzbergstr 12, CH-8091 Zurich, Switzerland
关键词
autopsy; COVID-19; haematology; pathology; SARS-CoV-2;
D O I
10.1111/his.14969
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
AimsSevere acute respiratory syndrome coronavirus type 2 (SARS-CoV-2) infection broadly affects organ homeostasis, including the haematopoietic system. Autopsy studies are a crucial tool for investigation of organ-specific pathologies. Here we perform an in-depth analysis of the impact of severe coronavirus disease 2019 (COVID-19) on bone marrow haematopoiesis in correlation with clinical and laboratory parameters. Methods and resultsTwenty-eight autopsy cases and five controls from two academic centres were included in the study. We performed a comprehensive analysis of bone marrow pathology and microenvironment features with clinical and laboratory parameters and assessed SARS-CoV-2 infection of the bone marrow by quantitative polymerase chain reaction (qPCR) analysis. In COVID-19 patients, bone marrow specimens showed a left-shifted myelopoiesis (19 of 28, 64%), increased myeloid-erythroid ratio (eight of 28, 28%), increased megakaryopoiesis (six of 28, 21%) and lymphocytosis (four of 28, 14%). Strikingly, a high proportion of COVID-19 specimens showed erythrophagocytosis (15 of 28, 54%) and the presence of siderophages (11 of 15, 73%) compared to control cases (none of five, 0%). Clinically, erythrophagocytosis correlated with lower haemoglobin levels and was more frequently observed in patients from the second wave. Analysis of the immune environment showed a strong increase in CD68+ macrophages (16 of 28, 57%) and a borderline lymphocytosis (five of 28, 18%). The stromal microenvironment showed oedema (two of 28, 7%) and severe capillary congestion (one of 28, 4%) in isolated cases. No stromal fibrosis or microvascular thrombosis was found. While all cases had confirmed positive testing of SARS-CoV-2 in the respiratory system, SARS-CoV-2 was not detected in the bone marrow by high-sensitivity PCR, suggesting that SARS-CoV-2 does not commonly replicate in the haematopoietic microenvironment. ConclusionsSARS-CoV-2 infection indirectly impacts the haematological compartment and the bone marrow immune environment. Erythrophagocytosis is frequent and associated with lower haemoglobin levels in patients with severe COVID-19.
引用
收藏
页码:582 / 590
页数:9
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