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1.
Clin Exp Nephrol ; 26(1): 54-58, 2022 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-34324086

RESUMO

INTRODUCTION: In this single-centre retrospective observational study, the 8-week safety and the efficiency of a single dose of BNT162b2 vaccine was studied in 83 HD patients. METHODS: All clinically stable adult ESRD patients on chronic HD for at least 4 weeks were screened for participation in the study. Exclusion criteria for enrollment in the study included a medical history of COVID-19 infection within the last 12 weeks or delivery of both vaccine doses less than 8 weeks apart from each other. The same patients during the 8-week period that preceded the vaccination served as controls of themselves. The vaccine was administered intramuscularly in the deltoid muscle, on a dialysis day, at least 30 min either pre- or post-dialysis. The primary end-point of the study was severe COVID-19 infection, and/or death due to COVID-19 pneumonitis. Furthermore, all vaccinated patients were scrutinized for any local or systemic reactions within the first 7 days post-vaccination. RESULTS: Amongst 113 adult HD patients in our Unit, in total 83 patients had the first 30 µg dose of the BNT162b2 vaccine and were considered eligible to be included in the study. The 8-week survival rate was 91% for the controls and 100% for the vaccine group. No life-threatening allergic reaction or other side-effect was observed post-vaccination. CONCLUSION: The BNT162b2 vaccine can be safely used in HD patients and seems to offer significant protection against the infection even after the first vaccine dose.


Assuntos
Vacina BNT162/administração & dosagem , COVID-19/prevenção & controle , Falência Renal Crônica/terapia , Diálise Renal , Adulto , Idoso , Idoso de 80 Anos ou mais , Vacina BNT162/efeitos adversos , COVID-19/diagnóstico , COVID-19/epidemiologia , Inglaterra/epidemiologia , Feminino , Humanos , Esquemas de Imunização , Incidência , Injeções Intramusculares , Falência Renal Crônica/diagnóstico , Falência Renal Crônica/epidemiologia , Masculino , Pessoa de Meia-Idade , Segurança do Paciente , Estudos Retrospectivos , Medição de Risco , Índice de Gravidade de Doença , Fatores de Tempo , Resultado do Tratamento , Adulto Jovem
2.
Proc Natl Acad Sci U S A ; 118(3)2021 01 19.
Artigo em Inglês | MEDLINE | ID: mdl-33446503

RESUMO

Almost 150 papers about brain lymphatics have been published in the last 150 years. Recently, the information in these papers has been synthesized into a picture of central nervous system (CNS) "glymphatics," but the fine structure of lymphatic elements in the human brain based on imaging specific markers of lymphatic endothelium has not been described. We used LYVE1 and PDPN antibodies to visualize lymphatic marker-positive cells (LMPCs) in postmortem human brain samples, meninges, cavernous sinus (cavum trigeminale), and cranial nerves and bolstered our findings with a VEGFR3 antibody. LMPCs were present in the perivascular space, the walls of small and large arteries and veins, the media of large vessels along smooth muscle cell membranes, and the vascular adventitia. Lymphatic marker staining was detected in the pia mater, in the arachnoid, in venous sinuses, and among the layers of the dura mater. There were many LMPCs in the perineurium and endoneurium of cranial nerves. Soluble waste may move from the brain parenchyma via perivascular and paravascular routes to the closest subarachnoid space and then travel along the dura mater and/or cranial nerves. Particulate waste products travel along the laminae of the dura mater toward the jugular fossa, lamina cribrosa, and perineurium of the cranial nerves to enter the cervical lymphatics. CD3-positive T cells appear to be in close proximity to LMPCs in perivascular/perineural spaces throughout the brain. Both immunostaining and qPCR confirmed the presence of adhesion molecules in the CNS known to be involved in T cell migration.


Assuntos
Encéfalo/metabolismo , Sistema Linfático/metabolismo , Glicoproteínas de Membrana/metabolismo , Receptor 3 de Fatores de Crescimento do Endotélio Vascular/genética , Proteínas de Transporte Vesicular/metabolismo , Idoso , Idoso de 80 Anos ou mais , Anticorpos/imunologia , Anticorpos/isolamento & purificação , Autopsia , Encéfalo/diagnóstico por imagem , Movimento Celular/genética , Sistema Nervoso Central/imunologia , Sistema Nervoso Central/metabolismo , Dura-Máter/diagnóstico por imagem , Dura-Máter/metabolismo , Endotélio Linfático/diagnóstico por imagem , Endotélio Linfático/metabolismo , Feminino , Sistema Glinfático/metabolismo , Humanos , Imuno-Histoquímica/métodos , Sistema Linfático/diagnóstico por imagem , Vasos Linfáticos/diagnóstico por imagem , Vasos Linfáticos/metabolismo , Masculino , Glicoproteínas de Membrana/isolamento & purificação , Espaço Subaracnóideo/diagnóstico por imagem , Espaço Subaracnóideo/metabolismo , Linfócitos T/imunologia , Proteínas de Transporte Vesicular/isolamento & purificação
3.
Forensic Sci Int ; 202(1-3): 86-92, 2010 Oct 10.
Artigo em Inglês | MEDLINE | ID: mdl-20483553

RESUMO

OBJECTIVE: To compare suicide registration in eight European countries and provide recommendations for quality improvement. METHOD: Qualitative data were collected from country experts using a structured questionnaire. RESULTS: Suicide registration was based on the medico-legal system in six countries and the coronial system in two. Differences not only between, but also within these two systems emerged. Several elements crucial to the consistency of suicide registration were identified. CONCLUSION: A precise model for recording suicides should include: an accurate legal inquiry and clarification of suicidal intent; obligatory forensic autopsy for injury deaths; reciprocal communication among authorities; electronic data transmission; final decision-makers' access to information; trained coders.


Assuntos
Médicos Legistas/organização & administração , Medicina Legal/organização & administração , Sistema de Registros , Suicídio/estatística & dados numéricos , Atestado de Óbito , Europa (Continente) , Humanos , Controle de Qualidade , Estatísticas Vitais
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