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Published on: June 19, 2018
[Mechanisms of formation of post-vaccinal immune response in children immunized with APDT and ADT-M preparations]
Insights
Children immunized with APDT and ADT-M vaccines showed increased TLR2 and TLR4 expression and cytokine production in response to pertussis antigens, indicating robust immune responses. Antibody levels correlated with immune cell activity.
Area of Science:
- Immunology
- Vaccinology
- Microbiology
Background:
- Cell and humoral immunity are crucial for protection against infectious diseases like pertussis, diphtheria, and tetanus.
- Immunization with vaccines such as APDT and ADT-M aims to elicit protective immune responses.
- Understanding the innate immune mechanisms activated by these vaccines is essential for evaluating vaccine efficacy.
Purpose of the Study:
- To investigate the mechanisms of cell and humoral immunity formation against pertussis, diphtheria, and tetanus in children.
- To assess the expression of Toll-like receptors (TLR2 and TLR4) and cytokine production following immunization with APDT and ADT-M vaccines.
- To correlate immune responses with antibody levels against diphtheria, tetanus, and pertussis.
Main Methods:
- Studied 30 children (6-9 years) immunized with APDT and ADT-M vaccines.
- Determined TLR2 and TLR4 expression on mononuclear cells (MNC) stimulated with vaccine components and bacterial strains.
- Measured cytokine production (TNF-alpha, IL-1, IL-6) and antibody levels (anti-diphtheria, anti-tetanus, anti-pertussis) using EIA and PHA reactions.
Main Results:
- MNC exhibited increased TLR2 and TLR4 expression and cytokine production upon stimulation with APDT, ADT-M, and Bordetella pertussis 345.
- No significant response was observed when MNC were stimulated with Corynebacterium diphtheriae strains.
- Direct correlations were found between antibody levels against diphtheria and tetanus (R=0.486), and against pertussis and diphtheria (R=0.529).
Conclusions:
- The study highlights the role of TLR2 and TLR4 in mediating immune responses to pertussis components in vaccinated children.
- Cytokine profiles and TLR expression can serve as indicators of innate immunity status and post-vaccinal immunity intensity.
- These findings contribute to a better understanding of vaccine-induced immunity and immune system evaluation.
Aim:
Study the mechanisms of formation of cell and humoral immunity against pertussis, diphtheria and tetanus in children immunized with immunobiological preparations (APDT vaccine and ADT anatoxin).
Materials And Methods:
30 practically healthy children (6 - 9 years of age) immunized with APDT and ADT-M preparations had TLR2, TLR4 expression determined in mononuclear cells (MNC). Vaccine preparations (APDT, ADT-M, AD-M, AT) and Corynebacterium diphtheriae gravis tox+, C. diphtheriae mitis tox- and Bordetella pertussis 345 were used as ligands. Cytokine production was determined in EIA. Content of anti-diphtheria, anti-tetanus and anti-pertussis antibodies--by PHA reaction and EIA.
Results:
During stimulation with vaccines and B. pertussis 345 strain MNC were characterized by an increase (p < 0.05) of expression level of TLR2 and TLR4 and did not respond to stimulation with C. diphtheriae gravis tox+ and C. diphtheriae mitis tox- strains. Similar results were obtained during study of cytokine production (TNFalpha, IL-1, IL-6). A direct correlation between levels of antitoxic antibodies against diphtheria and tetanus (R = 0.486), antibacterial antibodies against pertussis and diphtheria was detected (R = 0.529).
Conclusion:
Analysis of cytokine production profile and determination of surface TLR expression can be used during evaluation of functional status of innate immunity cells and intensity of post-vaccinal immunity.
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