|
|||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||
|
PROLOGUEImplementation: Vaccine Promise And PitfallsParents worldwide, frightened by reports of a possible link between the measles-mumps-rubella (MMR) vaccine and autism, refuse to have their children vaccinated, leaving them unprotected against deadly diseases and threatening to disrupt the "herd immunity" that protects entire societies. Commercial vaccine manufacturers have focused on the lucrative "travelers market" for enteric disease but have neglected the specific needs of the developing world, where 5,500 children die each day as a result of such illnesses. In October 2004 reports surfaced that Chiron, which manufactures half the U.S. supply of influenza vaccine, cannot ensure the safety of the vaccine produced in its Liverpool facility, sparking fears of a global pandemic. The preceding vignettes illustrate the delicate balance that policymakers must maintain for science and technology to fully realize their promise in keeping infectious diseases in check. The papers in this section describe how countries have grappled with balancing the available science with their economic, political, and regulatory processes. First, Patricia Danzon and her colleagues focus on economic impediments to vaccine production and implementation in industrialized markets. Their prime example is the flu vaccine, for which high fixed costs, uncertain returns, a single or limited number of producers, and the high cost of compliance with regulations contributed to the U.S. flu vaccine shortage of 2004. Next, Julia Milstien and colleagues focus on the risk/benefit ratios used by many industrialized countries in evaluating vaccines for their populations and for developing countries. They charge that the regulatory and programmatic decisions that protect industrialized countries have led to a dangerous rigidity in global vaccine practices. The next group of papers examine the U.S. and U.K. experiences more closely. James Colgrove and Ronald Bayer (and Richard Epsteins Perspective) highlight the two countries varying experiences with the MMR vaccine, which caused political and social upheaval in the United Kingdom but not in the United States. Next, David Salisburys paper and Gary Freeds Perspective depict in greater detail the differences in operation, procurement, and implementation of vaccines in the United Kingdom. Finally, Sarah Landry and Carole Heilman illuminate the advances in immunology and biotechnology that hold great promise for vaccine development. Research on new, safer, and more stable delivery systems for vaccines is taking place, including edible vaccines grown in potatoes. Landry and Heilmans paper is a clarion call for countries to reevaluate their regulatory and economic policies regarding vaccines. As the research moves forward, it will have little impact on global health if we cannot find the political will to implement the discoveries.
| |||||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||||