Such GOF studies are «crucial» for the selection of each year's candidate
vaccine viruses because they help WHO identify the riskiest strains in the wild, Schultz - Cherry said.
Not exact matches
Because the swine flu
virus was traced on the evolutionary tree to see how it mutated and thus develop a
vaccine that works against it.
Because the flu
vaccines don't contain live
viruses, you can't get the flu from the shot.
After all,
vaccines are effective
because they contain weak traces of the
viruses they protect against.
The scientists believe that
because they included eight mutations in their lab - made viral strain, it is unlikely the
virus will revert back to its original, more dangerous form (a common concern with any live -
virus vaccine).
The long - term persistence of CD8αα + T cells where initial infection occurs may explain why patients have asymptomatic recurrences of genital herpes
because these cells constantly recognize and eliminate the
virus, according to Jia Zhu, Ph.D., corresponding author, research assistant professor in Laboratory Medicine at the University of Washington and an affiliate investigator in the Fred Hutch
Vaccine and Infectious Disease Division.
Many
viruses do not undergo this change, so for those kinds of
vaccines there's no need for change
because they work very well.
Joy: Yeah, but the point is we have the technology now to sequence and manufacture
vaccines fairly quickly; and ideally they wouldn't be grown in eggs or whatever, right;
because what if it starts as a
virus in chickens or something, and we're screwed.
US pig farms try to control it with
vaccines, but these attempts are largely ineffective
because the
virus evolves too rapidly, changing the surface proteins targeted by the
vaccine while keeping its internal genes unchanged.
From a
vaccine - development perspective, it would be particularly troubling if the former ends up being the case
because it is hard to control immune response — especially when scientists are not sure what facet of the
virus may set off that cascade of action.
Remarkably, the researchers also found that blocking this protein in mice protected them from the lethal effects of dengue
virus infection, an important finding given that an effective
vaccine against dengue has remained elusive, partly
because there are four serotypes of the
virus that cause disease.
Because there are no
vaccines or cures for these
viruses there is an increased urgency of those in the public health sector to identify alternative strategies to manage the disease, of which an early warning system is included.
Some conservative groups oppose targeting preteens, arguing that
because the
virus is sexually transmitted, the
vaccine will encourage promiscuity.
Efforts to develop a
vaccine have been unsuccessful
because the
virus does not spend much time in the bloodstream, where most traditional
vaccines do their work.
Though many early
vaccines worked well, side effects were always a concern, sometimes
because the
virus was still infectious, sometimes
because proteins were present that triggered severe immune reactions.
Notably,
because no live
viruses are used in their manufacture, VLP
vaccines do not need to be produced under high - level biocontainment conditions.
«Our finding will not help develop a
vaccine because the focus is on innate immunity rather than the
virus,» Huang said.
You need less
virus in a live
vaccine because it replicates in the body, induces immunity in the gut where it is needed, and vaccinated children shed it in faeces and «vaccinate» their friends.
But this information is vital for scientists who are trying to design
vaccines to protect against sexual transmission
because inside cells, the
virus may go undetected by the immune system.
But the
vaccine has been known to cause occasional outbreaks, presumably
because the procedure used to kill the
virus is imperfect.
Because this research does not require replicating «live»
viruses, it does not need to be done in high - level containment facilities when developing
vaccines for highly pathogenic
viruses.
Because the flu
virus is constantly evolving in this way, the World Health Organisation meets twice a year to determine whether the strains of flu included in the
vaccine should be changed.
Kang's primary research focuses on designing and developing effective
vaccines against viral diseases such as influenza
virus and RSV, but he partnered with a university and research institutes in South Korea that wanted international collaborative projects to study if ginseng can be used to improve health and protect against disease
because of the potential benefit in fighting these
viruses.
«The quality of these naturally occurring human antibodies as biological drugs to treat the
virus infection is remarkable, and we are doubly encouraged
because they recognize multiple species of Ebola,» said immunologist James Crowe, Director of the Vanderbilt
Vaccine Center.
In contrast to many other
vaccines, influenza
vaccines need to be reformulated each year
because circulating influenza
viruses continuously evolve.
It was developed
because children given the triple
vaccine were mounting an immune response mainly to type 2
virus, not to 1 and 3.
A new HCV infection is effectively treated with direct - acting antiviral drugs, but the researchers say a preventive
vaccine is needed to control what they call an HCV pandemic
because as many as 50 percent of people infected are unaware that they carry the
virus, putting others at risk of infection.
Because Ebola is so deadly, creating a conventional
vaccine of inactivated whole
virus, or a live weakened strain is thought too far too dangerous.
WRAIR is moving forward with the purified inactivated
virus (PIV)
vaccine, called ZPIV,
because it builds on «a type of
vaccine that has been licensed before,» said Col. Stephen Thomas, an infectious disease Army physician and a vaccinologist specializing in flaviviruses, and the WRAIR Zika program lead.
Deeks and others believe the trial may have been partly successful
because the
vaccine contains HIV genes that code for «highly conserved» internal structures and enzymes that can not change much without harming the
virus.
Interest in
vaccine safety was very high
because of the infamous Cutter incident, which involved batches of the
vaccine containing inadequately inactivated
virus that gave polio to hundreds of children.
Because Ebola diagnostics and some therapeutics like
vaccines are based on the specific viral sequence, it is important for researchers to have the most up - to - date
virus genome sequence possible.
And even if they were more dangerous than common flu strains, it would not make any difference
because manufacturers kill the
virus as part of the
vaccine production process, notes the group.
He notes that the new study is especially relevant
because it worked in mammalian cells, which ultimately are a better way to grow the
virus than eggs: It's a faster production system and avoids mutations that occur when the
virus adapts to chicken eggs, which can compromise
vaccine effectiveness.
«Repeat vaccination with a different subtype would not be possible,» Palese admits,
because after the first vaccination, the animals will be immune to the Newcastle
virus, rendering the
vaccine useless.
The
vaccine has particular significance
because the regions where outbreaks of the two
viruses occur overlap, says Donald Black, head of the capripox
virus group at the Agricultural and Food Research Council's Institute for Animal Health.
According to Christopher Zimmerman, medical director of the New York City Health Department's Bureau of Immunization, the
virus spread quickly among children who were not fully vaccinated, including those whose parents put off the shots
because of concern about the autism -
vaccine link.
The DNA
vaccine for Zika
virus is more immunogenic and effective than other
vaccines because it can create memory responses, which inactivated
vaccines with killed
viruses fail to produce, Higgs said.
The DNA
vaccine also is safer
because it does not use attenuated
viruses to produce viral antigens.
Whitehead and the other researchers said that in the case of dengue, the testing was warranted
because they knew that the
vaccine appeared to be effective at preventing dengue 1, 3 and 4
viruses through previous testing but needed to learn more about its impact on dengue 2 before proceeding to larger trials that could take three to 10 years and cost tens of millions of dollars.
Human challenge trials like this one are an extremely efficient way for scientists to tell whether a particular
vaccine is effective, but they are rarely conducted
because of the ethical dilemma of the risk it places on volunteers who are purposely exposed to a
virus.
But
because these human strains frequently mutate to adapt to their new environment in eggs, the resulting
vaccine is often an imperfect match to the actual
virus that it is supposed to protect against.
«
Because viruses typically mutate during
vaccine production, manufacturers have to screen for mutations, and decide which ones can be tolerated and which ones can't,» Heaton said.
Because hemagglutinin also happens to be the part of the flu
vaccine that induces an immune response in people (it's the H in a
virus name like H5N1), each mutation renders the
vaccine less effective.
The
vaccines were evaluated for immunogenicity and efficacy; however,
because of the previous report of immunopathology on challenge of ferrets and nonhuman primates that had been vaccinated with a whole
virus adjuvanted
vaccine and mice that had been vaccinated with a VLP
vaccine, the primary orientation was to assess for immunopathology among animals in relation to type of
vaccine, dosage, serum antibody responses, and
virus infection.
A
vaccine has not worked, and likely never will,
because the
virus hides out deep in our bodies and stays there for life.
That's
because while women ages 20 to 24 do have the highest infection rates — nearly 45 % — women past that age may not have been exposed to every form of the
virus the
vaccine protects against.
This suggests that elder be superior to
vaccines in preventing flu,
because flu
vaccines are only effective against known strains of flu, whereas the
virus is continually mutating to new strains.»
This means that puppies that receive needless
vaccines not only suffer the risk of adverse events from the
vaccine, but they are more at risk of picking up any other
virus or bacterium that crosses their path
because their immune system has been overloaded by the
vaccine itself.
These two
viruses in combination with Bordetella bronchiseptica are the agents most often associated with kennel cough, however, other factors play an important role in disease (e.g. stress, dust, humidity, molds, mycoplasma, etc.), thus kennel cough is not a
vaccine preventable disease
because of the complex factors associated with this disease.