Reduced immunogenicity of diphtheria and tetanus toxoids when combined with pertussis toxoid

Birger Trollfors1, John Taranger, Teresa Lagergård

  • 1Department of Pediatrics, Sahlgrenska University Hospital and Göteborg University, Göteborg, Sweden.

Insights

Adding pertussis toxoid to diphtheria and tetanus toxoids (DT) vaccines slightly reduces their immunogenicity. This finding is crucial for understanding vaccine efficacy and optimizing infant immunization schedules.

Area of Science:

  • Immunology
  • Vaccinology
  • Pediatric Infectious Diseases

Background:

  • Diphtheria and tetanus toxoids (DT) are crucial components of routine infant immunization.
  • The immunogenicity of combined vaccines can be influenced by the presence of additional antigens.
  • Understanding these interactions is vital for developing effective vaccine formulations.

Purpose of the Study:

  • To investigate the impact of pertussis toxoid on the immunogenicity of diphtheria and tetanus toxoids.
  • To evaluate antibody responses to DT vaccines administered with or without pertussis toxoid in infants.

Main Methods:

  • A double-blind efficacy trial of an acellular pertussis vaccine was conducted.
  • Infants received either DT or DT combined with pertussis toxoid at 3, 5, and 12 months.
  • Antibody concentrations for diphtheria and tetanus toxoids were measured at 1 month and 2 years post-vaccination.

Main Results:

  • Geometric mean concentrations of diphtheria and tetanus toxoids were significantly lower in infants who received the DT-pertussis toxoid combination compared to those who received DT alone.
  • This reduction in immunogenicity was observed both 1 month and 2 years after the third vaccine dose.
  • Specifically, antibody levels for diphtheria toxoid were 3.58 IU/mL vs 4.76 IU/mL at 1 month and 0.10 IU/mL vs 0.15 IU/mL at 2 years.
  • Tetanus toxoid levels were 2.66 IU/mL vs 4.42 IU/mL at 1 month and 0.18 IU/mL vs 0.38 IU/mL at 2 years.

Conclusions:

  • Pertussis toxoid exerts a small but statistically significant suppressive effect on the immunogenicity of co-administered diphtheria and tetanus toxoids.
  • These findings highlight potential antigenic competition within combined vaccines.
  • Further research may be warranted to optimize the formulation of combined vaccines to maximize immune responses against all target diseases.

Related Concept Videos

Diphtheria01:28

Diphtheria

Diphtheria is an acute, toxin-mediated infectious disease that primarily affects the upper respiratory tract. It is caused by Corynebacterium diphtheriae, a Gram-positive, pleomorphic rod that lacks spore-forming capability and exhibits a characteristic club-shaped morphology under microscopic examination. While C. diphtheriae can asymptomatically colonize mucosal surfaces, clinical disease manifests only when the bacterial strain is lysogenized by a specific β-corynephage. This phage...
Vaccinations01:51

Vaccinations

Overview
Cross-reactivity00:42

Cross-reactivity

Overview
Poliomyelitis01:17

Poliomyelitis

Poliomyelitis is caused by poliovirus, a small, non-enveloped, positive-sense RNA virus of the Picornaviridae family and Enterovirus genus. Transmission occurs primarily via the fecal-oral route, often through ingestion of contaminated water or food. The virus initially replicates in the oropharynx and intestinal mucosa, particularly in lymphoid tissues such as the tonsils, Peyer’s patches, and regional lymph nodes. Primary viremia follows, allowing dissemination throughout the body.In most...
Active versus Passive Immunity01:31

Active versus Passive Immunity

Immunity, along with the ability to limit pathogen growth to prevent significant body tissue damage, can be gained either by (1) actively developing an immune response within the individual after exposure to a pathogen or after getting vaccinated or (2) passively transferring immune components from an immune individual to one who is nonimmune. Both these forms of immunity can be found naturally and in medical practices.
Active Immunity
Active immunity refers to the resistance one develops...
Hypersensitivity Reactions: Delayed Hypersensitivity Reactions01:29

Hypersensitivity Reactions: Delayed Hypersensitivity Reactions

Delayed-Type Hypersensitivity (DTH), or Type IV hypersensitivity, is a cell-mediated immune response. It occurs when T cells, rather than antibodies, mediate a reaction to specific antigens. It is characterized by a delayed onset (1-2 days) and involves the recruitment of macrophages to the inflammation site.The initiation of a DTH response begins with the sensitization of T cells. During this phase, which lasts at least 1-2 weeks, antigen-specific T cells are activated, clonally expanded, and...