Transmissible
Treatment Proposed for HIV Could Target Superspreaders to
Curb Epidemic
March
17, 2011 -- Engineered, virus-like particles would hitch
a ride with HIV to reach high-risk populations that don't
seek or comply with medical treatment and are responsible
for a disproportionate share of the spread of disease, a
new model demonstrates
Biochemist Leor Weinberger and colleagues at the University
of California, San Diego and UCLA have proposed a fundamentally
new intervention for the HIV/AIDS epidemic based on engineered,
virus-like particles that could subdue HIV infection within
individual patients and spread to high-risk populations
that are difficult for public health workers to reach.
With a model that considers the effects of the proposed
treatment on several scales, from interference with HIV
in infected cells to viral loads in individual patients
to the prevalence of HIV in large populations, they determined
that the engineered particles could work in concert with
current treatments for HIV infection and lower the prevalence
of infection more effectively than current drugs or proposed
vaccines alone. Their findings will appear in the March
17 issue of PLoS Computational Biology.
"Dr. Weinberger's idea to use engineered virus-derived
particles to combat infectious diseases is truly provocative,"
said James Anderson, M.D., Ph.D., Director of the Division
of Program Coordination, Planning, and Strategic Initiatives.
Anderson oversees the NIH Common Fund, which supports a
series of exceptionally high impact, trans-NIH programs
including the NIH Director's New Innovator Award, which
Weinberger received in 2009.
The engineered particles, called therapeutic interfering
particles or TIPs, would persist for years in an individual
patient and could be packed with genes that disrupt the
functioning of HIV. Weinberger's team has succeeded in creating
functional prototypes in the lab.
"TIPs are molecular parasites that 'piggyback' on HIV
to spread between individuals," Weinberger said. The
engineered particles use the same outer envelope as HIV
but lack the genes for components of this structure and
the enzymes needed to assemble it. They can only replicate,
infect additional cells and transmit to new individuals
by stealing these elements from HIV. Until the host cell
is infected with HIV, TIPs remain dormant.
In an HIV-infected individual, TIPs would transmit to others
in the same ways as the natural virus - through unprotected
sex or shared needles, for example. That means TIPs would,
by design, penetrate high-risk populations that are responsible
for a disproportionate share of the spread of disease and
can be particularly difficult for public-health officials
to reach.
Using an epidemiological model, Weinberger and colleagues
compared the predicted effects of the treatment they propose
with current drug campaigns and hypothetical vaccines and
found that TIPs could be more effective.
An intervention using TIPs could lower the number of people
infected with HIV in sub-Saharan Africa to one thirtieth
the current level in about 30 years, they found. Optimistic
predictions for vaccine campaigns or currently available
antiretroviral therapy would lower the number of HIV-infected
people by less than one half the current level over the
same period of time.
TIPs wouldn't replace other therapies, Weinberger said,
"In part, we are arguing that TIPs could be used in
conjunction with current antiretroviral drug therapy or
vaccine campaigns, and could enhance the efficacy of these
campaigns at the population level."
Weinberger acknowledges that an infectious treatment raises
ethical concerns and is working with bioethicists to explore
the unique issues associated with any use of TIPs in more
detail.
He also points out that vaccines already in use can spread
from one person to another. People who receive the oral
polio vaccine, for example, "shed" the weakened
version of the virus that is the basis of the vaccine and
this can transmit immunity to other individuals. Public
health officials see this transmission as a benefit; it
is one reason why this form of polio vaccine was chosen
for the worldwide effort to eradicate the disease.
Investigator
affiliations: Department of Chemistry & Biochemistry and
Division of Infectious Diseases, University of California, San
Diego, La Jolla, CA; Department of Ecology and Evolutionary
Biology, University of California, Los Angeles, CA; Fogarty
International Center, National Institutes of Health, Bethesda,
MD.
3/22/11
V
Metzger, J Lloyd-Smith, and L Weinberger. Autonomous Targeting
of Infectious Superspreaders Using Engineered Transmissible
Therapies. PLoS Computational Biology 7(3): e1002015
(free
full text). 2011.
Other Source
University of California at San Diego. Transmissible treatment
proposed for HIV could target superspreaders to curb epidemic.
Press release. March 17, 2011.
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