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April, 2022

No. 107 (4)

2020 Impact Factor: 9.941 Submission > Acceptance: 80 days

The GPIbα intracellular tail - role in transducing VWF- and collagen/GPVI-mediated signaling

The GPIbα-VWF A1 domain interaction is essential for platelet tethering under high shear. Synergy between GPIbα and GPVI signaling machineries has been suggested previously, however its molecular mechanism remains unclear. Generation of a novel GPIbα transgenic mouse allowed the authors of this study to identify a new role for the intracellular tail of GPIbα in transducing both VWF-GPIbα and collagen-GPVI signaling events in platelets.

Adela Constantinescu-Bercu et al.


Comparative analysis of ChAdOx1 nCoV-19 and Ad26.COV2.S SARS-CoV-2 vector vaccines

This study analyzed the ChAdOx1 nCoV-19 (AstraZeneca) and Ad26.COV2.S (Johnson & Johnson) vaccines. ChAdOx1 nCoV-19 contains significant amounts of host cell protein impurities, including functionally active proteasomes, and adenoviral proteins. A much smaller amount of impurities was found in Ad26.COV2.S. These differences in impurities together with EDTA-induced capillary leakage might contribute to the higher incidence rate of vaccine-induced immune thrombotic thrombocytopenia associated with ChAdOx1 nCoV-19.

Stephan Michalik et al.


Brain injury pathophysiology study by a multimodal approach in children with sickle cell anemia with no intra or extra cranial arteriopathy

This study investigated 59 patients with sickle cell anemia by a multimodal approach and found that those with silent cerebral infarcts (SCI) had a distinctive profile characterized by decreased blood pressure, impaired blood rheology, increased P-selectin levels, and marked anemia. Magnetic resonance imaging and arterial spin labeling were effective screening tools for SCI. Early treatment targeting hemolysis, anemia and endothelial dysfunction should reduce the risk of this under diagnosed and serious complication.

Valentine Brousse et al.

Case Report

VEXAS syndrome in a female patient with constitutional 45,X (Turner syndrome)

VEXAS syndrome is a newly defined autoinflammatory disorder that arises from somatic mutations affecting UBA1. This gene lies on the X-chromosome, making VEXAS an X-linked syndrome affecting only males. This case report describes the occurrence of VEXAS in a female with Turner syndrome. It is important to be alert to the presence of disorders that result in the inactivation of the X-chromosome when assessing female patients with a possible X-linked disorder, such as VEXAS syndrome.

Ryan J. Stubbins et al.

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