Kinetics of maternal antibodies against rubella and varicella in infants

E Leuridan1, N Hens, V Hutse

  • 1Centre for Evaluation of Vaccination, Vaccine and Infectious Disease Institute, Faculty of Medicine, University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Antwerp, Belgium. elke.leuridan@ua.ac.be

Vaccine
|June 19, 2010
PubMed

Insights

Maternal antibodies for rubella and varicella wane in infants within 2-3 months. This passive immunity duration leaves infants vulnerable to both diseases in early life.

Area of Science:

  • Immunology
  • Pediatrics
  • Infectious Diseases

Background:

  • Maternal antibodies provide crucial early protection for infants.
  • Understanding the decay kinetics of these antibodies is vital for assessing infant susceptibility to vaccine-preventable and endemic diseases.

Purpose of the Study:

  • To longitudinally analyze the decay of maternal rubella IgG and varicella IgG antibodies in infants.
  • To determine the duration of passive immunity conferred by maternal antibodies against rubella and varicella.

Main Methods:

  • Longitudinal study of 213 mother-infant pairs in Belgium.
  • Blood sampling at 7 time points from pregnancy week 36 to 12 months postpartum.
  • Enzyme-linked immunosorbent assay (ELISA) for quantifying anti-rubella IgG and anti-varicella IgG.
  • Generalized exponential model applied to analyze antibody decay.

Main Results:

  • The mean duration of passive immunity was 2.1 months for rubella antibodies.
  • The mean duration of passive immunity was 2.4 months for varicella antibodies.
  • Infants become susceptible to rubella and varicella at a young age.

Conclusions:

  • Maternal antibody decay leads to a limited window of passive immunity in infants.
  • Infants are susceptible to rubella and varicella during the first few months of life.
  • This highlights the importance of timely vaccination strategies for both diseases.

Related Concept Videos

Development of Immunocompetence01:22

Development of Immunocompetence

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...
Respiratory Syncytial Virus Disease01:29

Respiratory Syncytial Virus Disease

Human respiratory syncytial virus (RSV) is a widespread pathogen that primarily targets infants and young children but also poses a serious health risk to elderly and immunocompromised individuals. Belonging to the Pneumoviridae family, RSV is a negative-sense, single-stranded RNA virus within the Pneumovirus genus. Its global health burden is significant, with millions of cases annually resulting in hospitalizations and mortality, particularly in resource-limited settings. Although most...
Rh Blood Group01:19

Rh Blood Group

The Rhesus (Rh) antigen is crucial in determining blood groups and ensuring compatibility during blood transfusions.
Transcytosis of IgG01:15

Transcytosis of IgG

Transcytosis is the process in which molecules are internalized by endocytosis, transported across the cell, and released through exocytosis from the opposite end of the cell. Molecules such as insulin, immunoglobulins, and certain nutrients are transferred through the recycling endosomes by recycling and transcytosis.
IgG molecules from a mother undergo transcytosis starting around 13 weeks of gestation. The amount of IgG transferred and entering the fetal blood circulation increases with...
Chickenpox01:20

Chickenpox

Chickenpox is an acute, highly contagious disease caused by the varicella-zoster virus (VZV), a double-stranded DNA virus belonging to the Herpesviridae family. Its transmission occurs primarily through the inhalation of respiratory droplets or direct contact with vesicular fluid from skin lesions. The incubation period typically ranges from 10 to 21 days, during which the virus replicates and disseminates through sequential phases within the host. Although generally self-limiting in children,...