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Published on: September 14, 2011
Effect of human newborn BCG immunization on monocyte viability and function at 3 months of age
R L Sepulveda1, S Arredondo, E Rodriguez
1National Institute of Respiratory Diseases and Thoracic Surgery, University of Chile Medical School, Santiago, Chile.
Insights
Bacille Calmette-Guérin (BCG) vaccination boosts infant monocyte viability and mycobacteria uptake but does not improve killing ability in the absence of T-cells. This impacts understanding of BCG
Area of Science:
- Immunology
- Microbiology
- Vaccinology
Background:
- Bacille Calmette-Guérin (BCG) vaccination is a primary tool against tuberculosis.
- BCG's immune response involves T-cell immunity and monocyte activation.
- The impact of BCG on innate monocyte-macrophage function requires further elucidation.
Purpose of the Study:
- To investigate if newborn BCG immunization enhances the innate capacity of monocyte-macrophages.
- To assess the ability of cultured monocyte-macrophages to ingest and kill virulent mycobacteria.
- To determine these effects in the absence of lymphocytes.
Main Methods:
- Cultured monocyte-macrophages from BCG-immunized infants, non-immunized infants, and BCG-immunized adults were used.
- Cells were incubated with Mycobacterium tuberculosis.
- Monocyte-macrophage viability, cell counts, and intracellular bacillary load were assessed over time.
Main Results:
- BCG-immunized infants and adults showed significantly higher monocyte-macrophage viability after 7 days.
- Uptake of M. tuberculosis by monocytes was significantly increased in BCG-immunized groups.
- No enhanced killing of intracellular M. tuberculosis was observed in BCG-immunized individuals.
Conclusions:
- BCG vaccination enhances monocyte viability and mycobacteria uptake.
- The enhanced innate response does not translate to improved mycobacterial killing in vitro without lymphocytes.
- Findings suggest BCG's effect on innate immunity is complex and context-dependent.
Setting:
Immune response induced by BCG vaccination seems to reflect the development of T-cell immunity and monocyte activation. Participants were recruited from a large prospective study in infants from a suburb in Santiago, Chile.
Objective:
To determine whether newborn BCG immunization changes the innate ability of cultured monocyte-macrophages to ingest and kill virulent mycobacteria in the absence of lymphocytes.
Design:
The study population consisted of 15 three-month-old, tuberculin-positive infants immunized with BCG (Japanese) at birth, 13 randomly-selected, age-matched tuberculin-nonreactive infants in whom BCG immunization was postponed until one year of age, and five BCG-immunized, tuberculin-reactive adults. Adherent cells were cultured for 48 h. Monocyte-macrophage viability and number and viability of intracellular Mycobacterium tuberculosis bacilli were assessed after an additional 2 h and 4 and 7 days of incubation.
Results:
There was no difference in the mean number of adherent cells present after 48 h among the three study groups. Adherent cells from BCG-immunized infants and adults had a significantly higher viability after 7 days in culture than adherent cells from non-immunized infants. The percentage of cells ingesting M. tuberculosis and the number of bacilli per cell after 2 h and 4 days was significantly higher in immunized infants and adults than in non-immunized infants. However, there was no evidence for increased killing of mycobacteria by cells from immunized infants and adults.
Conclusion:
These results suggest that BCG vaccination increases monocyte viability and the uptake of M. tuberculosis without enhancing the ability to kill ingested M. tuberculosis in the absence of lymphocytes.
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