A survey of type I interferons from a marsupial and monotreme: implications for the evolution of the type I interferon gene family in mammals

Cytokine ◽  
2003 ◽  
Vol 21 (3) ◽  
pp. 105-119 ◽  
Author(s):  
G Harrison
2015 ◽  
Vol 74 (Suppl 2) ◽  
pp. 893.3-893
Author(s):  
J.A. Enciso-Moreno ◽  
J.E. Castañeda-Delgado ◽  
N. Macias-Segura ◽  
D. Santiago-Algarra ◽  
J.D. Castillo-Ortiz ◽  
...  

2021 ◽  
Author(s):  
Magen E. Francis ◽  
Una Goncin ◽  
Andrea Kroeker ◽  
Cynthia Swan ◽  
Robyn Ralph ◽  
...  

AbstractCOVID-19 (coronavirus disease 2019) caused SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) infection is a disease affecting several organ systems. A model that captures all clinical symptoms of COVID-19 as well as long-haulers disease is needed. We investigated the host responses associated with infection in several major organ systems including the respiratory tract, the heart, and the kidneys after SARS-CoV-2 infection in Syrian hamsters. We found significant increases in inflammatory cytokines (IL-6, IL-1beta, and TNF) and type II interferons whereas type I interferons were inhibited. Examination of extrapulmonary tissue indicated inflammation in the kidney, liver, and heart which also lacked type I interferon upregulation. Histologically, the heart had evidence of mycarditis and microthrombi while the kidney had tubular inflammation. These results give insight into the multiorgan disease experienced by people with COVID-19 and possibly the prolonged disease in people with post-acute sequelae of SARS-CoV-2 (PASC).


2019 ◽  
Vol 18 (4) ◽  
pp. 393-398 ◽  
Author(s):  
Michelle Remião Ugolini-Lopes ◽  
Giovana Tardin Torrezan ◽  
Ana Paula Rossi Gândara ◽  
Eloisa Helena Ribeiro Olivieri ◽  
Iana Souza Nascimento ◽  
...  

2005 ◽  
Vol 19 (4) ◽  
pp. e12-e13
Author(s):  
Alicia Collado-Hidalgo ◽  
Caroline Y. Sung ◽  
Steve W. Cole

Genomics ◽  
1998 ◽  
Vol 47 (2) ◽  
pp. 217-229 ◽  
Author(s):  
Pamela L. Strissel ◽  
Hadas Arad Dann ◽  
Helen M. Pomykala ◽  
Manuel O. Diaz ◽  
Janet D. Rowley ◽  
...  

BMJ Open ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. e036563
Author(s):  
Edward R Hammond ◽  
Raj Tummala ◽  
Anna Berglind ◽  
Farhat Syed ◽  
Xia Wang ◽  
...  

IntroductionThe Systemic Lupus Erythematosus (SLE) Prospective Observational Cohort Study (SPOCS) aims to describe the disease course of SLE and its association with type I interferon gene signature (IFNGS) status.Methods and analysisSPOCS is an international, multicentre, prospective, observational cohort study designed to follow patients through biannual study visits during a 3-year observation period. Patients ≥18 years old with a physician diagnosis that meets the American College of Rheumatology or Systemic Lupus International Collaborating Clinics SLE classification criteria will be included. SPOCS will comprehensively analyse clinical features, disease progression and treatment, SLE outcomes, health status assessments and quality of life, and healthcare resource utilisation of patients with moderate to severe SLE. A four-gene test will be used to measure IFNGS status; scores will be compared with a pre-established cut-off. Patients will be stratified by low or high IFNGS expression levels. Enrolment began in June 2017, and study completion is expected in 2022. The total number of anticipated patients was initially planned for 1500 patients and was amended to 900 patients owing to slow accrual of eligible patients.Ethics and disseminationThe ethics committee/institutional review board/independent ethics committee at each study site approved the SPOCS protocol prior to study initiation (protocol number: D3461R00001, version 3.0, 26 June 2019). Study findings will be disseminated through peer-reviewed publications and presentations at scientific meetings.Trial registration numberNCT03189875.


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