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Vaccines, Vaccine Allocation and Vaccine Research

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Overview

Vaccination is one of the most effective ways to minimize suffering and death from influenza. Research efforts have led to the development of a vaccine for one of the two known strains of the H5N1 influenza virus in humans.

The U.S. Government is working to expand domestic influenza vaccine production capacity to be able to produce pandemic influenza vaccines for the entire population within six months of a pandemic declaration. However, at the beginning of a pandemic, the scarcity of pre-pandemic and pandemic influenza vaccine will require that the limited supply be allocated or prioritized for distribution and administration.

The government has developed Guidance on Allocating and Targeting Pandemic Influenza Vaccine (PDF - 1.83 MB) which provides strong guidance to states, territories, and tribes for the allocation of limited supplies of vaccine, and describes the scientific and ethical framework for how this guidance was developed.

A tiered allocation for vaccines in severe pandemics is recommended with the following objectives considered to be the most important:

  • protect those who are essential to the pandemic response and provide care for persons who are ill;
  • Protect those who maintain essential community services;
  • Protect children;
  • Protect workers who are at greater risk of infection as a result of their job, and
  • Protect those who maintain homeland and national security.

Because there will likely be a limited supply of vaccine, research is underway to develop adjuvants. An adjuvant is a substance that is added to a vaccine to improve the immune system's production of antibodies, which is the desired response to vaccines. The successful addition of an adjuvant means that a given supply of vaccine can be used to treat more people.

 Vaccines

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 Vaccine Allocation

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 Vaccine Research

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 Clinical Trials

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 Adjuvants

  • NIAID Taps Chiron to Develop Vaccine Against H9N2 Avian Influenza
    The biotech company Chiron is testing a proprietary adjuvant called MF59 under contract to the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health (NIH) under the U.S. Department of Health and Human Services.

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