|
In an initial step towards the development of a new vaccine to prevent
tuberculosis, the The global scale of the AIDS epidemicholocaust prompted
EpiVax, a Rhode Island vaccine design firm and the Brown University's
TB/HIV Research Laboratory to provide HIV researchers free access to their
valuable informatics tool, EpiMatrix, on the world wide web at http://tbhiv.biomed.brown.edu/.
Using Epimatrix, rResearchers will be able to screenanalyze any of 40,000
published protein sequences of the chameleon-like HIV-1 virus, including
tens of thousands of sequences from HIV-1 strains afflicting African and
Indian populations, for putative epitopes.
Epitopes, short fragments derived from HIV proteins, contain the minimum
information necessary to turn on the immune system and form a crucial
link between infected Antigen Presenting Cells (APCs) and the T-Cells
which form the core of the human cell mediated immune system. Response
to any vaccine is based on recognition of epitopes contained within those
vaccines by the host (animal or human) immune system. Most vaccines contain
a great deal of additional information that may not be necessary to achieve
the desired result. Stripping vaccines down to the bare essentials, the
epitopes, makes it possible to build and test vaccines faster, while also
permitting researchers to "stuff" more vaccine information into the vaccines
that they are building. EpiMatrix, a bioinformatics tool that identifies
epitopes, was developed by De Groot and coworkers at the TB/HIV Research
lab, Brown University, and licensed to EpiVax, Inc. in August 1999. In
collaborative studies carried out this year by the TB/HIV Research lab
and by researchers at the CDC, T cells derived from healthy HIV infected
individuals have been shown to respond to HIV-1 epitopes selected by EpiMatrix.
Dr. Anne De Groot, HIV physician and founder of the vaccine design firm,
stated "providing this valuable tool to HIV/AIDS vaccine researchers will
accelerate the pace of AIDS vaccine development." She and EpiVax CIO Bill
Martin have supported the development of the EpiVax/ TB/HIV Research Lab
HIV analysis website vaccine project from profits earned from vaccine
design contracts with large vaccine corporations. De Groot is also director
of the TB/HIV Research Lab at Brown University, which recently won a $150,000
HIV vaccine Innovation Award from the NIH to support further development
of the HIV vaccine. Asked whether providing her tool would undermine her
own efforts to develop an AIDS vaccine, De Groot stated " the point is
to contribute to the development of an AIDS vaccine - if someone else
makes it faster, using our tools, we will still be proud of our contribution.
We want to help stop the AIDS holocaust, by any means possible."
Sequella Global Tuberculosis Foundation has named William R. Jacobs, Jr.,
Professor at Albert Einstein College of Medicine of Yeshiva University
and Investigator of the Howard Hughes Medical Institute, , as one of 13
researchers to the Core Scientist Program of its Tuberculosis Vaccine
Collaboration (TBVC) program. Acting as a focused research team, these
core scientists will help to guide the Foundation as it supports new and
innovative tuberculosis vaccine development. "What we are trying to do
in the Core Scientist Program is to accelerate the transition of experimental
vaccines from the research bench to the clinic. The three major areas
addressed by this program are clinical trial site development, new tools
for vaccine assessment in clinical trials, and research supporting the
eventual clinical evaluation of candidate tuberculosis vaccines," says
Carol Nacy, Ph.D., President of the Foundation. "Our goal is not just
the research, but an actual vaccine." Jacobs
The EpiVax / TB/HIV Research Lab HIV analysis website provides information
on potential epitopes, or short fragments derived from HIV proteins, that
train T cells, the body's primary immune defense against the virus, to
respond to the threat of HIV infection. Response to any vaccine is based
on recognition of epitopes contained within those vaccines by the host
(animal or human) immune system. Most vaccines contain a great deal of
additional information that may not be necessary to achieve the desired
result. Stripping vaccines down to the bare essentials, the epitopes,
makes it possible to build and test vaccines faster, while also permitting
researchers to "stuff" more vaccine information into the vaccines that
they are building. EpiMatrix, a bioinformatics tool that identifies epitopes,
the minimum amount of information necessary to turn on the immune system,
was developed by De Groot and coworkers at the TB/HIV Research lab, Brown
University, and licensed to EpiVax, Inc. in August 1999. In collaborative
studies carried out this year by the TB/HIV Research lab and by researchers
at the CDC, T cells derived from healthy HIV infected individuals have
been shown to respond to HIV-1 epitopes selected by EpiMatrix.
De Groot and Martin reiterated one of their company's core values in making
this announcement. "We do projects that have inherent human value. AIDS
is decimating populations in countries that have no funds to pay for vaccines.
Providing access to this website may contribute to the development of
a vaccine that saves millions of human lives."
The website can be accessed at http://tbhiv.biomed.brown.edu/ http://tbhiv.biomed.brown.edu/
Access to the website is unrestricted, although registration is requested
for use.has been selected along with Barry Bloom, Dean of the Harvard
School of Public Health, for their proposal to develop live attenuated
strains of Mycobacterium tuberculosis for use in new vaccines. Currently,
the only tuberculosis vaccine available is based on an attentuated strain
of a related bacterium, Mycobacterium bovis. Although this vaccine does
provide protection against severe and fatal forms of tuberculosis in children,
its efficacy in adults is questionable. Their research within the Core
Scientist Program will focus on genetic manipulation of the bacteria in
order to create a strain of M. tuberculosis that does not cause disease
and can be used as a vaccine.
Once thought to be under control and nearly eradicated in industrialized
countries, tuberculosis continues to be a threat in all countries because
of increasing drug resistance. It is estimated that nearly a third of
the world's population, approximately 2 billion people, are infected with
Mycobacterium tuberculosis, the bacterium that causes the disease. About
10% of these individuals will develop active tuberculosis disease within
their lifetime. The antibiotics and the vaccine currently used to treat
and prevent this disease are antiquated and have limited effectiveness.
The Core
Scientists Program is the first step in the Foundation's TBVC, an international
program designed to coordinate and facilitate the development of a vaccine.
The scientists represent a variety of scientific, engineering and public
health disciplines that are necessary to create a successful vaccine.
Later this year the Foundation will begin accepting investigator-initiated
grant applications in its Vaccine Innovation Program, designed to fund
novel tuberculosis vaccine research.
Founded in 1997, the Sequella Global Tuberculosis Foundation is a non-profit
organization devoted to providing resources, facilities and expertise
to assist tuberculosis researchers across the world to move their discoveries
in basic science through the laboratory, into the clinic and out to health
care workers. It is funded by a number of corporate and philanthropic
sources including a generous grant from the Bill and Melinda Gates Foundation.
The TBVC core scientists are: Marcel A. Behr, MD, Assistant Professor,
McGill University Health Centre, Montreal William Bishai, MD, Ph.D., Assistant
Professor, Johns Hopkins University, Baltimore Barry R. Bloom, Ph.D.,
Dean, Harvard School of Public Health Anne S. De Groot, MD, CEO, EpiVax,
Inc., Providence, Rhode Island Wafaa El Sadr, MD, MPH, Professor of Clinical
Medicine, Columbia University, New York William R. Jacobs, Jr., Ph.D.,
Professor, Albert Einstein College of Medicine, New York Gilla Kaplan,
Ph.D., Associate Professor, The Rockefeller University, New York Douglas
B. Lowrie, Ph.D., St. Georges Hospital, London John D. McKinney, Ph.D.,
Assistant Professor, The Rockefeller University, New York Boris V. Nikonenko,
Ph.D., Sequella, Inc., Rockville, Maryland Erwin Schurr, Ph.D., Associate
Professor, McGill University Center for Study of Host Resistance, Montreal
David R. Sherman, Ph.D., Assistant Professor, University of Washington
School of Public Health and Community Medicine, Seattle Zena Stein, M.A.,
MBBCh, Professor, Columbia University, New York
|