Serotype replacement in disease after pneumococcal vaccination

Abstract

Vaccination with heptavalent pneumococcal conjugate vaccine (PCV7) has significantly reduced the burden of pneumococcal disease and has had an important public health benefit. Because this vaccine targets only seven of the more than 92 pneumococcal serotypes, concerns have been raised that non-vaccine serotypes (NVTs) could increase in prevalence and reduce the benefits of vaccination. Indeed, among asymptomatic carriers, the prevalence of NVTs has increased substantially, and consequently, there has been little or no net change in the bacterial carriage prevalence. In many populations, pneumococcal disease caused by NVT has increased, but in most cases this increase has been less than the increase in NVT carriage. We review the evidence for serotype replacement in carriage and disease, and address the surveillance biases that might affect these findings. We then discuss possible reasons for the discrepancy between near-complete replacement in carriage and partial replacement for disease, including differences in invasiveness between vaccine serotypes. We contend that the magnitude of serotype replacement in disease can be attributed, in part, to a combination of lower invasiveness of the replacing serotypes, biases in the pre-vaccine carriage data (unmasking), and biases in the disease surveillance systems that could underestimate the true amount of replacement. We conclude by discussing the future potential for serotype replacement in disease and the need for continuing surveillance.

Conflict of interest statement

Conflicts of Interest: DMW declares no conflicts. RM is a member of the Scientific Advisory Board of Genocea Biosciences. ML has accepted honoraria or consulting fees from Pfizer and Novartis.

Copyright © 2011 Elsevier Ltd. All rights reserved.

Figures

Figure

Timing of the increase in the incidence of non-vaccine serotypes relative to vaccine introduction in select studies that report serotype replacement. Light grey bars indicate pre-vaccine era, medium-grey bars indicate the period of vaccine introduction or low coverage, and the dark grey bars indicate widespread vaccination. The values represent the incidence in each year divided by the mean pre-PCV7 incidence, as indicated by the shaded bars and table 1. The data from the U.S., Spain, and England represent changes in all non-vaccine serotypes, and the data from the Norway study is just serotype 19A. There was no net increase among NVTs in Norway as of 2008.