Globally, 36 lakh hospitalisations reported among children aged under five
A monoclonal antibody — a
protein created in a lab which mimics the work of a natural antibody — could be
highly effective in preventing severe respiratory syncytial virus (RSV), a
respiratory infection and major cause of serious illness in infants, according
to a research.
Findings of the study,
published in The Lancet Child and Adolescent Health journal, show that
injecting infants with the antibody ‘nirsevimab’ reduces risk of RSV-related
hospitalisations by 83 per cent and intensive care admissions by 81 per cent.
Infant immunisation
programmes could, therefore, help address the health and economic burden due to
RSV in the high-risk period following birth, a team of researchers from Canada
and the US said.
RSV is one of the leading
causes of serious respiratory ill-health in the early years of one’s life, and
is usually prevalent during early winter months. Globally, the condition is
estimated to cause 36 lakh hospitalisations a year among children aged under
five, according to the World Health Organisation.
Nirsevimab was approved
in 2023 by regulatory agencies, including the US’ Food and Drug Administration
and European Medicines Agency, after the lab-created antibody was found to be
safe and effective in clinical trials.
Through national
programmes, infants in high-income countries, such as in the US and European
Union, have been injected with nirsevimab.
The researchers said the
efficacy of nirsevimab seen in the controlled settings of a clinical trial may
not fully reflect how the lab-created antibody performs in real-world settings.
Real-world effectiveness studies are essential to evaluate the effectiveness of
nirsevimab across diverse infant populations and clinical settings, the team
added.
For this study, the
researchers analysed 27 previously published studies, which were conducted
during the RSV seasons of 2023-2024 across five countries — France, Italy,
Luxembourg, Spain and the US. The team mainly focused on infants aged under 12
months.
“Nirsevimab is highly
effective in preventing RSV-related outcomes in infants, with a pooled
real-world effectiveness of 83 per cent against hospitalisation, 81 per cent
against ICU admission and 75 per cent against LRTI (lower respiratory tract
infections),” the authors wrote.
The lab-created antibody
was also found to be more effective among infants aged over three months,
compared to those aged under three months.
The researchers noted
that nirsevimab is not a vaccine, despite being delivered as an injection.
A monoclonal
antibody is created in a lab to mimic how an antibody works, whereas a vaccine
empowers the body’s immune system to produce an immune response, which involves
creating antibodies, they said.
The
findings indicate that the benefits of nirsevimab seen in clinical trials could
be translated into real-world settings, potentially reducing the burden of RSV
disease among infants and use of healthcare resources, the authors said.
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