Non-specific immunological effects of selected routine childhood immunisations: systematic review
Rama Kandasamy1, Merryn Voysey2, Fiona McQuaid3
1Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Churchill Hospital, Oxford OX3 7LE, UK NIHR Oxford Biomedical Research Centre, Oxford, OX3 7LE, UK rama.kandasamy@paediatrics.ox.ac.uk.
Insights
Routine childhood vaccines like BCG and measles may have non-specific immunological effects. However, the evidence quality is low due to study limitations, preventing confident conclusions on their clinical importance.
Area of Science:
- Immunology
- Vaccinology
- Public Health
Background:
- Routine childhood vaccinations aim to elicit specific immune responses against targeted pathogens.
- Emerging evidence suggests that some vaccines may also induce broader, non-specific immunological effects.
- Understanding these non-specific effects is crucial for optimizing vaccine strategies and public health outcomes.
Purpose of the Study:
- To systematically identify and characterize non-specific immunological effects following routine childhood vaccinations.
- To review evidence for heterologous immune responses induced by vaccines such as BCG, measles, diphtheria, pertussis, and tetanus.
Main Methods:
- Systematic review of randomized controlled trials, cohort studies, and case-control studies.
- Searched Embase, PubMed, Cochrane Library, and Trip databases (1947-2014).
- Included human studies reporting non-specific effects; excluded studies using recombinant vaccines or reporting only specific outcomes.
Main Results:
- 77 studies met inclusion criteria; 48% involved BCG vaccination.
- High risk of bias was noted across all included studies.
- BCG vaccination showed a trend towards increased in vitro IFN-γ production.
- Measles vaccination was associated with increased lymphoproliferation to microbial antigens.
- Diphtheria-tetanus and diphtheria-tetanus-pertussis vaccines showed increased immunogenicity to heterologous antigens.
Conclusions:
- Heterogeneous study designs precluded meta-analysis, resulting in low-quality evidence.
- Some studies suggest consistent directions of effect for non-specific responses (e.g., BCG and measles vaccines).
- The current evidence lacks confidence regarding the nature, magnitude, timing, and clinical significance of non-specific effects.
Objective:
To identify and characterise non-specific immunological effects after routine childhood vaccines against BCG, measles, diphtheria, pertussis, and tetanus.
Design:
Systematic review of randomised controlled trials, cohort studies, and case-control studies.
Data Sources:
Embase, PubMed, Cochrane library, and Trip searched between 1947 and January 2014. Publications submitted by a panel of experts in the specialty were also included.
Eligibility Criteria For Selecting Studies:
All human studies reporting non-specific immunological effects after vaccination with standard childhood immunisations. Studies using recombinant vaccines, no vaccine at all, or reporting only vaccine specific outcomes were excluded. The primary aim was to systematically identify, assemble, and review all available studies and data on the possible non-specific or heterologous immunological effects of BCG; measles; mumps, measles, and rubella (MMR); diphtheria; tetanus; and pertussis vaccines.
Results:
The initial search yielded 11 168 references; 77 manuscripts met the inclusion criteria for data analysis. In most included studies (48%) BCG was the vaccine intervention. The final time point of outcome measurement was primarily performed (70%) between one and 12 months after vaccination. There was a high risk of bias in the included studies, with no single study rated low risk across all assessment criteria. A total of 143 different immunological variables were reported, which, in conjunction with differences in measurement units and summary statistics, created a high number of combinations thus precluding any meta-analysis. Studies that compared BCG vaccinated with unvaccinated groups showed a trend towards increased IFN-γ production in vitro in the vaccinated groups. Increases were also observed for IFN-γ measured after BCG vaccination in response to in vitro stimulation with microbial antigens from Candida albicans, tetanus toxoid, Staphylococcus aureas, lipopolysaccharide, and hepatitis B. Cohort studies of measles vaccination showed an increase in lymphoproliferation to microbial antigens from tetanus toxoid and C albicans Increases in immunogenicity to heterologous antigens were noted after diphtheria-tetanus (herpes simplex virus and polio antibody titres) and diphtheria-tetanus-pertussis (pneumococcus serotype 14 and polio neutralising responses) vaccination.
Conclusions:
The papers reporting non-specific immunological effects had heterogeneous study designs and could not be conventionally meta-analysed, providing a low level of evidence quality. Some studies, such as BCG vaccine studies examining in vitro IFN-γ responses and measles vaccine studies examining lymphoproliferation to microbial antigen stimulation, showed a consistent direction of effect suggestive of non-specific immunological effects. The quality of the evidence, however, does not provide confidence in the nature, magnitude, or timing of non-specific immunological effects after vaccination with BCG, diphtheria, pertussis, tetanus, or measles containing vaccines nor the clinical importance of the findings.
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