Meningococcal meningitis, a disease that sweeps across sub-Saharan
Africa
in an area called the meningitis belt, is losing its power to
inflict illness and death. Scientists from FDA made a critical
contribution in developing the technology needed to manufacture a
vaccine against this terrible disease, and at an affordable cost for
African nations like Burkina Faso, Chad, Ethiopia, and Niger.
Meningococcal meningitis can be deadly. It kills 10 percent of people
it infects within two days after they start showing symptoms. Although
an antimicrobial drug saves large numbers of infected individuals, about
10 percent die from the infection and about 10 percent to 20 percent of
survivors develop mental retardation, hearing loss, or seizures. In
Africa, most meningococcal disease is caused by the group A
meningococcus bacteria, and about half of its victims are working-age
adolescents and young adults. The disease results in very significant
human, social, and economic losses to the affected communities and
countries. Vaccination offers the best chance to prevent the disease and
epidemic meningitis. However, an existing vaccine didn’t work very
well.
Developing a Vaccine:
In 2001, the Bill & Melinda Gates Foundation agreed to fund the
Meningitis Vaccine Project (MVP)–a partnership between the World Health
Organization and PATH, a non-profit organization based in Seattle, WA
that works with collaborating groups to provide health care technologies
and strategies to areas of the world that have limited resources.
Dr. F. Marc LaForce led MVP’s effort to develop, test and license a
new type of vaccine against group A meningococcus bacteria, that could
protect people before an epidemic begins. The new vaccine, called a
conjugate, is a chain of sugars connected to a protein that the immune
system responds to very well. When MVP hit a hurdle during the
development stage, FDA stepped in. Drs. Robert Lee and Carl E. Frasch,
two researchers in the Office of Vaccines Research and Review in FDA’s Center for Biologics Evaluation and Research (CBER),
had developed an alternative conjugation technology that was more
efficient and less costly. Through a technology transfer agreement, FDA
provided the technology to MVP via PATH, with help from the National
Institutes of Health.
Scientists at CBER also developed reagents for evaluating the
vaccine’s performance and safety and developed methods to monitor the
manufacturing process. MVP had partnered with the Serum Institute of
India Limited, a developing-country vaccine manufacturer, to make the
new conjugated vaccine. In December 2003, two scientists from the Serum
Institute came to Drs. Lee and Frasch’s FDA laboratory to learn the
conjugation method to manufacture the vaccine.
After preclinical animal studies and a series of clinical trials in
people in India and Africa’s meningitis belt to assess its safety and
effectiveness, the new vaccine, MenAfriVac, was licensed in Dec. 2009 by
India for export to Africa. By June 2010, the WHO had prequalified the
vaccine for use in global immunization programs.
Launching the Vaccination Campaign:
MVP launched its vaccination campaign in Dec. 2010, beginning in
Burkina Faso and moving on to Mali and Niger and eventually Cameroon,
Chad and Nigeria. By the end of 2011, an estimated 55 million people had
been vaccinated with MenAfriVac at a cost of only 40 cents per dose.
The contribution of CBER researchers Carl Frasch and Robert Lee was
perhaps best summed up by MVP director Dr. LaForce in a news story about
their timely contribution of the conjugation technology that enabled
the development of MenAfriVac at a price that Africa could afford:
“These guys are heroes.”
FDA’s contributions to a major health care project in Africa
underscore the agency’s recognition that infectious diseases know no
borders. Protecting human health globally is linked to the agency’s core
mission of protecting human health in the United States.
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