[Articles] Safety and immunogenicity of mRNA-based seasonal influenza vaccines formulated to include multiple A/H3N2 strains with or without the B/Yamagata strain in US adults aged 50–75 years: a phase 1/2, open-label, randomised trial

Di |2024-09-06T00:30:00+02:00Settembre 6th, 2024|Categorie: Coronavirus Lancet|

These data support the continued clinical development of mRNA-based next-generation seasonal influenza vaccines with broadened influenza A/H3N2 strain coverage.

[Articles] The evidence base for the optimal antibiotic treatment duration of upper and lower respiratory tract infections: an umbrella review

Di |2024-09-05T00:30:02+02:00Settembre 5th, 2024|Categorie: Coronavirus Lancet|

The available evidence for non-ICU CAP and AECOPD supports a short-course treatment duration of 5 days in patients who have clinically improved. Efforts of the scientific community should be directed at implementing this evidence in daily practice. Hig...

[Articles] Safety and immunogenicity of a live-attenuated chikungunya virus vaccine in endemic areas of Brazil: interim results of a double-blind, randomised, placebo-controlled phase 3 trial in adolescents

Di |2024-09-05T00:30:01+02:00Settembre 5th, 2024|Categorie: Coronavirus Lancet|

VLA1553 was generally safe and induced seroprotective titres in almost all vaccinated adolescents with favourable safety data in adolescents who were seropositive at baseline. The data support the use of VLA1553 for the prevention of disease caused by ...

[Comment] First immunogenicity and safety data on live chikungunya vaccine in an endemic area

Di |2024-09-05T00:30:01+02:00Settembre 5th, 2024|Categorie: Coronavirus Lancet|

Chikungunya virus causes an emerging mosquito-borne viral infection that is endemic to much of Latin America, Africa, and south and southeast Asia. Chikungunya is prone to 8–15 year cycles of temporary epidemic expansion, with the last global outbreak ...

[Articles] Effect of timing of casirivimab and imdevimab administration relative to mRNA-1273 COVID-19 vaccination on vaccine-induced SARS-CoV-2 neutralising antibody responses: a prospective, open-label, phase 2, randomised controlled trial

Di |2024-09-03T00:30:02+02:00Settembre 3rd, 2024|Categorie: Coronavirus Lancet|

Casirivimab and imdevimab administration before or at the time of COVID-19 vaccination reduced the elicitation of SARS-CoV-2 neutralising antibodies, but minimal effect was observed when vaccination occurred before mAb administration. Although the clin...

[Articles] Effect of timing of casirivimab and imdevimab administration relative to mRNA-1273 COVID-19 vaccination on vaccine-induced SARS-CoV-2 neutralising antibody responses: a prospective, open-label, phase 2, randomised controlled trial

Di |2024-09-03T00:30:02+02:00Settembre 3rd, 2024|Categorie: Coronavirus Lancet|

Casirivimab and imdevimab administration before or at the time of COVID-19 vaccination reduced the elicitation of SARS-CoV-2 neutralising antibodies, but minimal effect was observed when vaccination occurred before mAb administration. Although the clin...

[Correspondence] Limitations of mpox lateral flow tests in assessing orthopoxvirus immunity

Di |2024-09-03T00:30:01+02:00Settembre 3rd, 2024|Categorie: Coronavirus Lancet|

Monkeypox virus (MPXV) is a zoonotic virus and the causative agent of mpox (formerly known as monkeypox) disease1 previously limited to countries, such as Nigeria and the Democratic Republic of the Congo, except for occasional importations globally. Ho...

[Correspondence] Limitations of mpox lateral flow tests in assessing orthopoxvirus immunity

Di |2024-09-03T00:30:01+02:00Settembre 3rd, 2024|Categorie: Coronavirus Lancet|

Monkeypox virus (MPXV) is a zoonotic virus and the causative agent of mpox (formerly known as monkeypox) disease1 previously limited to countries, such as Nigeria and the Democratic Republic of the Congo, except for occasional importations globally. Ho...

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