Age-dependent preference in human antibody responses to Streptococcus pneumoniae polypeptide antigens

S Lifshitz1, R Dagan, M Shani-Sekler

  • 1Paediatric Infectious Disease Unit, Soroka University Medical Centre, Tel Aviv, Israel.

Insights

Children under 42 months show limited immune response to Streptococcus pneumoniae surface proteins, impacting their vulnerability. Antibody development and adhesion inhibition improve with age, reaching adult levels by 42 months.

Area of Science:

  • Immunology
  • Microbiology
  • Pediatrics

Background:

  • Children exhibit heightened susceptibility to Streptococcus pneumoniae infections.
  • The specific microbial virulence factors and host immune responses contributing to this vulnerability remain incompletely understood.
  • Streptococcus pneumoniae is a leading cause of bacterial pneumonia, meningitis, and sepsis in young children.

Purpose of the Study:

  • To analyze the humoral immune response to Streptococcus pneumoniae surface proteins in children and adults.
  • To evaluate the ability of antibodies to inhibit Streptococcus pneumoniae adhesion to epithelial cells.
  • To understand the developmental trajectory of the immune response to pneumococcal surface proteins in early childhood.

Main Methods:

  • Analysis of sera from healthy adults and longitudinally collected sera from children (18-42 months).
  • Western blot analysis to detect antibodies against separated Strep. pneumoniae surface proteins (lectin and non-lectin).
  • Epithelial cell adhesion inhibition assays to quantify the functional antibody response.

Main Results:

  • Adult sera recognized multiple Strep. pneumoniae surface proteins and inhibited adhesion by ~80%.
  • Children's sera showed age-dependent development of antibodies to previously unrecognized surface proteins.
  • Antibody response magnitude and adhesion inhibition increased significantly with age, reaching adult levels by 42 months.

Conclusions:

  • Repeated Streptococcus pneumoniae exposures are insufficient to elicit a robust immune response in 18-month-old children.
  • Immune immaturity, potentially due to inefficient T-cell-dependent B-cell responses or low protein immunogenicity, contributes to early childhood vulnerability.
  • The development of effective humoral immunity against Strep. pneumoniae surface proteins is a maturational process occurring after 18 months of age.

Related Concept Videos

Humoral Immune Responses01:36

Humoral Immune Responses

Overview
Antibody Structure01:10

Antibody Structure

Overview
Antibodies, also known as immunoglobulins (Ig), are essential players of the adaptive immune system. These antigen-binding proteins are produced by B cells and make up 20 percent of the total blood plasma by weight. In mammals, antibodies fall into five different classes, which each elicits a different biological response upon antigen binding.
The Y-Shaped Structure of Antibodies Consists of Four Polypeptide Chains
Antibodies consist of four polypeptide chains: two identical heavy...
Affinity and Avidity01:41

Affinity and Avidity

Overview
Antibody Structure and Classes01:25

Antibody Structure and Classes

Antibodies, also known as immunoglobulins, are produced by B cells in response to foreign substances, such as bacteria and viruses. These proteins are critical for recognizing and neutralizing these substances, protecting the body from potential harm.
The basic structure of an antibody consists of four protein chains: two identical heavy chains and two identical light chains. These chains are held together by disulfide bonds and other non-covalent interactions, forming a Y-shaped structure.
Immunological Memory01:23

Immunological Memory

Immunological memory, a pivotal pillar of the adaptive immune system, is responsible for the body's ability to remember and respond more swiftly and effectively to previously encountered pathogens. This remarkable feature is what makes vaccines so effective in preventing diseases.
What is Immunological Memory?
Immunological memory is an integral function of the immune system that allows it to recognize and react more rapidly and effectively to pathogens previously encountered. This feature is...
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...