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Related Concept Videos

Development of Immunocompetence01:22

Development of Immunocompetence

305
The initiation of cell-mediated immunity can be observed as early as the third month of fetal growth, with active antibody-mediated immunity following approximately one month later.
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
305
siRNA - Small Interfering RNAs02:30

siRNA - Small Interfering RNAs

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Small interfering RNAs, or siRNAs, are short regulatory RNA molecules that can silence genes post-transcriptionally, as well as the transcriptional level in some cases. siRNAs are important for protecting cells against viral infections and silencing transposable genetic elements.
In the cytoplasm, siRNA is processed from a double-stranded RNA, which comes from either endogenous DNA transcription or exogenous sources like a virus. This double-stranded RNA is then cleaved by the...
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Related Experiment Video

Updated: Jun 28, 2025

Intravenous Injections in Neonatal Mice
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Balanced on the Biggest Wave: Nirsevimab for Newborns.

Christopher McPherson, Christine R Lockowitz, Jason G Newland

    Neonatal Network : NN
    |April 10, 2024
    PubMed
    Summary

    A new monoclonal antibody, nirsevimab, offers season-long protection against severe respiratory syncytial virus (RSV) disease in infants with a single dose. This advancement provides a more convenient and effective option for preventing infant hospitalizations due to RSV.

    Keywords:
    RSVimmunizationinfectionmonoclonal antibodiesnirsevimabpalivizumabrespiratory syncytial virus

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    Area of Science:

    • Pediatrics
    • Immunology
    • Virology

    Background:

    • Respiratory syncytial virus (RSV) is a major cause of infant hospitalizations in the US, affecting nearly all children by age two.
    • Severe RSV disease can lead to long-term health issues like asthma and delayed speech development.
    • Existing interventions like palivizumab are costly and require multiple doses, limiting their widespread use.

    Purpose of the Study:

    • To evaluate the efficacy and safety of nirsevimab, a novel monoclonal antibody, for preventing severe RSV disease in infants.
    • To assess the potential of nirsevimab as a single-dose, season-long preventative measure against RSV hospitalization.

    Main Methods:

    • Conducted four landmark randomized controlled trials involving healthy and high-risk infants (preterm and term).
    • Nirsevimab targets the RSV prefusion F protein's Ø antigenic site.
    • Monitored efficacy in reducing medically attended RSV disease and hospitalizations, alongside safety profiles.

    Main Results:

    • Nirsevimab significantly reduced the risk of medically attended RSV disease (NNT 14-24) and hospitalization (NNT 33-63).
    • A single dose provided protection for an entire 5-month RSV season.
    • Observed rare side effects, primarily mild rash and injection site reactions.

    Conclusions:

    • Nirsevimab is an effective and safe single-dose preventative therapy for severe RSV disease in infants.
    • Recent CDC recommendations support nirsevimab for infants younger than 8 months and high-risk infants aged 8-19 months.
    • Equitable distribution and multidisciplinary collaboration are crucial for successful implementation of nirsevimab therapy.