Not exact matches
Researchers at Oregon Health & Science University are currently looking for volunteers that can be tested during an upcoming clinical trial for a
vaccine that may cure
HIV, the virus that causes AIDS.
To fend off
HIV,
researchers introduced one
vaccine (ALVAC) to induce a T cell response — thereby alerting the immune system — and another (AIDSVAX) later to spur an antibody response.
Researchers for the past decade have focused on the T cell approach, based on studies showing that monkeys receiving such
vaccines against simian immunodeficiency virus, related to
HIV, lived longer or had lower viral levels than usual.
In collaboration with many
researchers (graduate students, postdocs, and faculty elsewhere), we have examined the role of cross-immunity on the evolution and dynamics of influenza; the impact of behavioral changes, long periods of infectiousness, variable infectivity, co-infections, prostitution, social networks, and
vaccine efficacy on
HIV dynamics; the role of exogenous re-infection, variable progression rates, vaccination, public transportation, close and casual contacts on tuberculosis dynamics and control; the impact of life - history vector dynamics on dengue epidemics; and on the identification of time - response scales for epidemics of foot and mouth disease.
Researchers hope that the insights they are gleaning from the structure will open new doors to drug and
vaccine intervention against
HIV.
Researchers from the University of Zurich and University Hospital Zurich now reveal which factors are responsible for the human body forming such broadly neutralizing
HIV antibodies, thereby opening new avenues for the development of an
HIV vaccine.
At the start,
researchers pinned their hopes on
vaccines designed to trigger production of antibodies against
HIV's surface protein.
Vaccine researchers typically start with antigens — in this case, pieces of
HIV — and then evaluate the antibodies they elicit.
La Jolla Institute scientist Shane Crotty, Ph.D., a respected
vaccine researcher and member of one of the nation's top AIDS
vaccine consortiums, showed that certain helper T cells are important for triggering a strong antibody response against
HIV, the virus that causes AIDS.
In an early - morning announcement today,
researchers reported that an experimental
HIV (human immunodeficiency virus)
vaccine effectively reduced the number of people who contracted the virus by nearly a third.
A 2007 clinical trial of a
vaccine made by Merck was stopped when
researchers found that, in fact, more people who received the active
vaccine (49) than the placebo (33) had contracted
HIV.
In Britain, in 1991,
researchers led by Jim Stott at the National Institute of Biological Standards and Control in north London, stunned their colleagues by announcing that they had apparently protected monkeys from infection with the monkey virus SIV — the simian equivalent of
HIV — with a
vaccine based simply on human T cells.
To fend off
HIV,
researchers introduced one
vaccine (ALVAC -
HIV) to induce a T cell response — thereby alerting the immune system — and another (AIDSVAX B / E) later to spur an antibody response.
The next step is a bigger trial where the
researchers will combine romidepsin activation of hidden
HIV with a vaccine (vacc - 4x) to strengthen the ability of killer T - cells to fight hiv vir
HIV with a
vaccine (vacc - 4x) to strengthen the ability of killer T - cells to fight
hiv vir
hiv virus.
An exception to this trend is Dong Pyou Han, a former Iowa State University (ISU) biomedical
researcher who last week was sentenced to prison for 57 months — almost 5 years — for falsifying results in
HIV vaccine studies he participated in while working under lab head Michael Cho, The Guardian reports.
The
researchers are planning to test this method to deliver
HIV vaccines in nonhuman primates, and they are also working on further developing cancer
vaccines, including one for lung cancer.
The study, published Aug. 13, 2014, in the journal Cell Host & Microbe, builds on previous work from
researchers at the Duke Human
Vaccine Institute that outlined a perplexing quality about
HIV: The antibodies that originally arise to fight the virus are ineffective.
By integrating the gp41 protein into the
vaccine,
researchers try to trigger the production of antibodies that would block the entrance of
HIV into human cells.
Researchers led by a team at Duke University identified these immunologic variations by studying blood samples collected from people living with
HIV by the NIAID - supported Center for
HIV / AIDS
Vaccine Immunology (CHAVI).
LONDON (Reuters)--
Researchers announced the launch of two big studies in Africa on Thursday to test a new
HIV vaccine and a long - acting injectable drug, fuelling hopes for better ways to protect against the virus that causes AIDS.
Of more than 50 therapeutic
vaccine trials so far, this is the first one that has bolstered the immune system in a «meaningful» way, says Steven Deeks, an
HIV / AIDS clinician and
researcher at the University of California, San Francisco, who is «cautiously optimistic» that the data will inspire others to study the approach.
HIV is finally revealing its weak spots to
researchers, bringing an effective
vaccine against AIDS closer to reality.
That's the question posed by
researchers in the journal BMC Immunology, who think that the
vaccine might have offered partial protection against
HIV.
This is why it is so difficult for humans to mount an effective immune response and why it is challenging for
researchers to develop
vaccines targeting the
HIV envelope proteins,» Dr. Blanchard says.
The
researchers administered a potential
vaccine consisting of two components to twelve rhesus monkeys that served as an animal model for the human
HIV infection.
For 30 years,
researchers have struggled to determine which immune responses best foil
HIV, information that has guided the design of AIDS
vaccines and other prevention approaches.
For decades,
researchers have been trying — unsuccessfully — to develop a
vaccine that spurs the body to attack
HIV.
But as
researchers turn to diseases that are more difficult to protect against, such as malaria or
HIV, they are setting their sights lower, aiming for
vaccines that prevent severe disease but not infection.
Although no
vaccine against
HIV exists, advances in prevention and treatment have led to a growing conviction among
researchers, public health officials, and politicians that the
HIV / AIDS epidemic can be brought to a halt with existing tools.
Early tests of a gp120
vaccine looked promising, but optimism faded by the early 1990s as
researchers learned the
vaccine only worked against strains of
HIV that had adapted to conditions in the laboratory.
Researchers at the University of Maryland and Duke University have designed a novel protein - sugar
vaccine candidate that, in an animal model, stimulated an immune response against sugars that form a protective shield around
HIV.
Next, the
researchers injected the protein - sugar
vaccine candidate into rabbits and found that the rabbits» immune systems produced antibodies that physically bound to gp120 found in four dominant strains of
HIV in circulation today.
Researchers have tried to create an
HIV vaccine targeting gp120, but had little success for two reasons.
The
researchers» next steps will be to conduct longer - term studies in combination with other
vaccine candidates, hone in on what areas of gp120 the antibodies are binding to and determine how they can increase the antibodies» effectiveness at neutralizing
HIV.
WITHIN a few weeks,
researchers in Bangkok will start injecting people with a genetically engineered
vaccine against
HIV.
The row over the Thai trials has been fuelled by an explosive mix of factors, including the pace at which the
HIV epidemic is growing in Asia, the future of the
vaccines industry, and domestic tensions in the US between AIDS
researchers, activists and politicians.
AIDS
researcher Jay Levy at the University of California at San Francisco finds the results encouraging, but notes that the
vaccines seemed to have no effect on the amount of virus in the bloodstream of people who contracted
HIV during the study.
Speakers include Wistar scientists and renowned guest
researchers who discuss topics such as cancer, aging,
vaccines, immune disorders and allergies,
HIV, and infectious diseases, all in an approachable way for a non-scientific audience.
Since coming to Fred Hutch, he has been working with Dr. Leo Stamatatos and other top
researchers on
HIV, but as his small, four - person lab grows, he wants to expand to include other infections for which a
vaccine doesn't exist.
Researchers from the U.S. Military
HIV Research Program at the Walter Reed Army Institute of Research (WRAIR) have found that an experimental heroin
vaccine induced antibodies that prevented the drug from crossing the blood - brain barrier in mice and rats.
In the new issue of IAVI Report we wrote about how
researchers at the AIDS
Vaccine 2010 conference in Atlanta discussed the limited window of opportunity for conducting clinical trials to test partially effective HIV prevention strategies, including HIV vaccine candidates and oral or topical antiretroviral pre-exposure prophylaxis (PrEP), in combi
Vaccine 2010 conference in Atlanta discussed the limited window of opportunity for conducting clinical trials to test partially effective
HIV prevention strategies, including
HIV vaccine candidates and oral or topical antiretroviral pre-exposure prophylaxis (PrEP), in combi
vaccine candidates and oral or topical antiretroviral pre-exposure prophylaxis (PrEP), in combination.
Researchers have long sought to develop an effective
HIV vaccine.
These results may provide new ways for
vaccine researchers to target
HIV and may influence the design of future
HIV vaccines.
After comparing the genetic strains of
HIV in
vaccine and placebo recipients,
researchers found that cellular immune responses generated by the
vaccine may have impacted the
HIV - 1 strains that established infections (breakthrough viruses).
The trials would be for proof of concept, to show whether
researchers can, for the first time in humans, stimulate the right B cells to start the process of making broadly neutralizing antibodies, long considered the «holy grail» of
HIV vaccine research because they defend against infection by a broad spectrum of
HIV strains.
Nearly 35 years after
HIV, the virus that causes AIDS, was discovered,
researchers at UNLV continue to forge ahead in the quest for prevention, education and a possible
vaccine or cure.
AIDS
vaccine researchers say they have some new clues to help focus their search for a safe and effective
vaccine against
HIV.
2012 — MHRP
Researchers awarded $ 5 million grant to fund research into a novel heroin /
HIV vaccine — The innovative dual -
vaccine model would concurrently address the entwined epidemics of heron abuse and
HIV and could provide considerable public health benefits.
Critically, such trials direct
researchers towards protective immune responses we will need to generate with
HIV vaccines that will help the body protect itself from this destructive, complicated and deadly disease.
Immune responses of patients could point way forward for future vaccines.In the latest study,
researchers involved with the trial at Mahidol University in Bangkok and the U.S. Military
HIV Research Program in Washington DC assembled a team to scour the blood of trial participants for immune indicators that differed between 41 people who received the
vaccine and contracted
HIV and 205 participants who did not become infected.