IDRI Makes Its Adjuvant Available to Increase Global Supply of Pandemic Vaccines
Posted on: Thursday, 11 June 2009, 14:21 CDT
Adjuvants are a major component of a global strategy against the newly declared swine flu pandemic
"As stressed by Dr. Chan at today's press conference, there is a real urgency to address the needs of developing countries for adequate supplies of swine flu pandemic vaccines. She rightly urged for global solidarity to ensure that no one would be left behind," said Dr.
IDRI's soluble-emulsion (SE) adjuvant was shown in pre-clinical studies to increase the immune response induced by a flu antigen. Importantly, while using decreasing amounts of antigen, the immune response to the adjuvanted flu vaccine remained higher than with the same vaccine without adjuvant.(1) As a result of the immune boost provided by the SE adjuvant, a smaller dose of flu antigen would be required for the vaccine to stimulate a protective immune response against the disease. This "antigen-sparing" activity would allow the production of more vaccine doses that could protect many more people against pandemic influenza.
In addition, IDRI's SE adjuvant was recently evaluated in a clinical trial of a seasonal flu vaccine through collaboration with its biotech partner Immune Design Corp. Preliminary data show that in healthy adult and elderly volunteers the adjuvanted vaccine candidate was well-tolerated and had a safety profile comparable to the standard seasonal flu vaccine.(1)
The major global public threat posed by new A (H1N1) flu strain demands seamless coordination among vaccine manufacturers, governments, and global health authorities to manage the supply of vaccines and to ensure there are enough doses for everyone, including those who live in the poorest countries. IDRI, with its history of public-private partnerships and international collaborations, is well positioned to effectively team up with those organizations involved in the development of pandemic influenza vaccines.
IDRI's SE adjuvant is similar in composition to adjuvant formulations currently used in pandemic influenza vaccines by large pharmaceutical companies, but which are not easily accessible to developing country manufacturers. Data collected to date with IDRI's SE adjuvant are comparable to results reported with these proprietary adjuvants. It is expected that "antigen-sparing" would also be observed when combining IDRI's adjuvant with a pandemic A (H1N1) vaccine antigen.
"IDRI's adjuvant expertise is unique in the not-for-profit sector and probably also unique for a U.S.-based organization," continued Dr. Reed. "To ensure access to the adjuvant as quickly as possible, we are actively exploring ways to increase our adjuvant production capacity in the U.S. as well as mechanisms to transfer our adjuvant technology and manufacturing know-how to vaccine manufacturers worldwide."
About IDRI's adjuvants
Adjuvants are compounds used to improve the body's immune response to vaccines. Adjuvant technology is proving invaluable in the development of serious diseases for which vaccines are not currently available, including malaria and HIV.
Adjuvants are a key research component of IDRI's malaria, tuberculosis, leishmaniasis and leprosy vaccine development programs with the support of leading institutions such as the Bill and Melinda Gates Foundation and the National Institutes of Health (NIH).
IDRI has already transferred some of its adjuvants to the Instituto Butantan in
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(1) Data on file
SOURCE Infectious Disease Research Institute
Source: PR Newswire
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