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10.1016/S1474-4422(20)30308-2

http://scihub22266oqcxt.onion/10.1016/S1474-4422(20)30308-2
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33031735!7535629!33031735
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suck abstract from ncbi


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pmid33031735      Lancet+Neurol 2020 ; 19 (11): 919-929
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  • Neuropathology of patients with COVID-19 in Germany: a post-mortem case series #MMPMID33031735
  • Matschke J; Lutgehetmann M; Hagel C; Sperhake JP; Schroder AS; Edler C; Mushumba H; Fitzek A; Allweiss L; Dandri M; Dottermusch M; Heinemann A; Pfefferle S; Schwabenland M; Sumner Magruder D; Bonn S; Prinz M; Gerloff C; Puschel K; Krasemann S; Aepfelbacher M; Glatzel M
  • Lancet Neurol 2020[Nov]; 19 (11): 919-929 PMID33031735show ga
  • BACKGROUND: Prominent clinical symptoms of COVID-19 include CNS manifestations. However, it is unclear whether severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of COVID-19, gains access to the CNS and whether it causes neuropathological changes. We investigated the brain tissue of patients who died from COVID-19 for glial responses, inflammatory changes, and the presence of SARS-CoV-2 in the CNS. METHODS: In this post-mortem case series, we investigated the neuropathological features in the brains of patients who died between March 13 and April 24, 2020, in Hamburg, Germany. Inclusion criteria comprised a positive test for SARS-CoV-2 by quantitative RT-PCR (qRT-PCR) and availability of adequate samples. We did a neuropathological workup including histological staining and immunohistochemical staining for activated astrocytes, activated microglia, and cytotoxic T lymphocytes in the olfactory bulb, basal ganglia, brainstem, and cerebellum. Additionally, we investigated the presence and localisation of SARS-CoV-2 by qRT-PCR and by immunohistochemistry in selected patients and brain regions. FINDINGS: 43 patients were included in our study. Patients died in hospitals, nursing homes, or at home, and were aged between 51 years and 94 years (median 76 years [IQR 70-86]). We detected fresh territorial ischaemic lesions in six (14%) patients. 37 (86%) patients had astrogliosis in all assessed regions. Activation of microglia and infiltration by cytotoxic T lymphocytes was most pronounced in the brainstem and cerebellum, and meningeal cytotoxic T lymphocyte infiltration was seen in 34 (79%) patients. SARS-CoV-2 could be detected in the brains of 21 (53%) of 40 examined patients, with SARS-CoV-2 viral proteins found in cranial nerves originating from the lower brainstem and in isolated cells of the brainstem. The presence of SARS-CoV-2 in the CNS was not associated with the severity of neuropathological changes. INTERPRETATION: In general, neuropathological changes in patients with COVID-19 seem to be mild, with pronounced neuroinflammatory changes in the brainstem being the most common finding. There was no evidence for CNS damage directly caused by SARS-CoV-2. The generalisability of these findings needs to be validated in future studies as the number of cases and availability of clinical data were low and no age-matched and sex-matched controls were included. FUNDING: German Research Foundation, Federal State of Hamburg, EU (eRARE), German Center for Infection Research (DZIF).
  • |Aged[MESH]
  • |Aged, 80 and over[MESH]
  • |Autopsy/methods[MESH]
  • |Betacoronavirus/*isolation & purification[MESH]
  • |Brain/*pathology/*virology[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/epidemiology/genetics/*pathology[MESH]
  • |Female[MESH]
  • |Germany/epidemiology[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Neuropathology[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/epidemiology/genetics/*pathology[MESH]
  • |SARS-CoV-2[MESH]


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