Epidemiological evidence for serotype‐independent acquired immunity to pneumococcal carriage
SM Granat, J Ollgren, E Herva, Z Mia… - The Journal of …, 2009 - academic.oup.com
SM Granat, J Ollgren, E Herva, Z Mia, K Auranen, PH Mäkelä
The Journal of infectious diseases, 2009•academic.oup.comBackground. Asymptomatic nasopharyngeal carriage is the main reservoir for transmission
of Streptococcus pneumoniae. The rate of both carriage and pneumococcal disease
decreases with age. To what extent these changes are the result of developing natural
immunity is currently a subject of debate. Objective. To study the hypothesis that previous
carriage induces serotype‐independent protective immunity to new colonization. Methods.
We compared the rates of pneumococcal acquisition for children with different previous …
of Streptococcus pneumoniae. The rate of both carriage and pneumococcal disease
decreases with age. To what extent these changes are the result of developing natural
immunity is currently a subject of debate. Objective. To study the hypothesis that previous
carriage induces serotype‐independent protective immunity to new colonization. Methods.
We compared the rates of pneumococcal acquisition for children with different previous …
Abstract
Background. Asymptomatic nasopharyngeal carriage is the main reservoir for transmission of Streptococcus pneumoniae. The rate of both carriage and pneumococcal disease decreases with age. To what extent these changes are the result of developing natural immunity is currently a subject of debate.
Objective. To study the hypothesis that previous carriage induces serotype‐independent protective immunity to new colonization.
Methods. We compared the rates of pneumococcal acquisition for children with different previous carriage histories. We identified 435 episodes of carriage during the first year of life in follow‐up data for 99 Bangladeshi children. Cox regression analysis was adjusted for serotype‐specific exposure within the family and other confounding factors.
Results. Previous pneumococcal carriage was associated with serotype‐independent protection from subsequent acquisition (hazard ratio, 0.60 [95% confidence interval, 0.39–0.90]), whereas recent serotype‐specific exposure within the family was associated with an 8‐fold increase in the rate of acquisition for that serotype.
Conclusion. Our findings are consistent with the hypothesis that serotype‐independent protective immunity is stimulated in young children by previous pneumococcal carriage and reduces the rate of new colonization. This immunity has the potential to modulate the development of carriage, irrespective of the colonizing serotype, and to do so starting early in infancy.
Oxford University Press