Not exact matches
Flu
vaccines are
designed to prevent infection
by eliciting antibodies against HA, which the virus uses to break into cells lining the airways.
These findings improve understanding of the mechanisms that make flu outbreaks so difficult to prevent, and inform efforts to
design more effective flu
vaccines that are less easily thwarted
by continual mutation.
The HPV
vaccine - specific educational brochure,
designed to motivate parents to start the series, had mixed results
by race / ethnicity.
Scientists say that the new
design may eliminate the problems with the failed 2002
vaccine (manufactured
by Elan Corporation, an Ireland - based drug company).
By better understanding how antigen presentation is translated into long - term immunity, immunologists can inform the
design of simpler
vaccines.
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.
Equipped with this deeper understanding, researchers are trying to make allergy
vaccines safer and more effective
by designing them to micromanage the allergic immune response.
By customizing the RNA sequences, the researchers can
design vaccines that produce nearly any protein they want.
The
vaccine is
designed to be delivered
by intramuscular injection, making it easy to administer.
According to Malo, «public health interventions
designed to increase HPV
vaccine recommendation for males should focus on increasing recommendations
by family practitioners and also identifying and supporting innovators and early adopters who may help diffuse HPV vaccination guidelines and encourage later adopters to support the recommendations.»
«This helps us understand that process, and it opens up the window to targeting these cells
by designing vaccines that prevent autoimmunity.»
«Our
vaccine was made possible
by combining a wide range of biomedical expertise that thrives in Boston and Cambridge,» said Mooney, who specializes in the
design of biomaterials for tissue engineering and drug delivery.
Led
by University of Texas Austin researcher Dr Steve Bellan, and in collaboration with the U.S. Centers for Disease Control and Prevention (CDC), the study on the
design of CDC's
vaccine trial in Sierra Leone is published in The Lancet Infectious Diseases.
«Uncovering the process
by which neutralizing antibodies develop is critical to HIV
vaccine design,» said Elise Landais, Senior Research Scientist with IAVI and lead author of the study.
Inspired
by the earlier work, Deborah Fuller from the University of Washington in Seattle, USA, who is interested in developing influenza drugs and
vaccines, teamed up with David Baker, also at the University of Washington, who is an expert in computational protein
design.
«This will allow us to
design better inhibitors or
vaccines that block invasion
by targeting multiple steps at the same time.»
Led
by scientists at the International AIDS
Vaccine Initiative (IAVI) and The Scripps Research Institute (TSRI), the results offer important insight into a potential AIDS vaccine
Vaccine Initiative (IAVI) and The Scripps Research Institute (TSRI), the results offer important insight into a potential AIDS
vaccine vaccine design.
«This is good news for
vaccine design,» says O'Connor, whose work is funded
by the National Institutes of Health.
Historically, many
vaccines have been
designed to evoke an antibody response
by B cells following innoculation with weakened or dead pathogens.
More to the point,
by genetically stripping dengue virus of its ability to bind 14 -3-3 epsilon, Gack has generated a crippled virus that can elicit a strong human immune response, providing a framework for rational
vaccine design against emerging infectious diseases.
More importantly, Gack found that avian, swine, and human flu viruses block TRIM25 to evade immune defense
by RIG - I, unraveling a molecular target for the
design of antiviral drugs and
vaccines.
This approach will also elucidate mechanisms of anti-body mediated protection from infection
by HIV - that are highly likely to inform
vaccine design.
Historically, many
vaccines have been
designed to evoke an antibody response
by B cells following inoculation with weakened or dead pathogens.
We also carry a product called «VacciShield,» an evidence - based supplement
designed by a naturopathic physician for the purpose of reducing
vaccine reactions.
With a new properly
designed facility, our
vaccine clinics could essentially double
by providing 30,000 affordable vaccinations each year — which will keep pets healthy and compliant with the law.
Zoetis discovers, develops and manufactures a diverse portfolio of animal health medicines and
vaccines, complemented
by diagnostic products, genetic tests, biodevices and a range of services, which are
designed to meet the real - world needs of veterinarians and the livestock farmers and companion animal owners they support.
Animal Friends» Clinic Services Program consists of three core components each uniquely
designed to support a targeted population
by offering pets high - quality, low - cost spay / neuter,
vaccines and wellness services.
A
vaccine is
designed to trigger an immune response within the pet's immune system to help the body to recognize and appropriately respond to future infections caused
by disease.
Thankfully there is a
vaccine, which we carry,
designed to protect against disease caused
by the CIV H3N2 strain.
VANGUARD ® crLyme is a multivalent
vaccine which contains an OspA protein and a single OspC protein that is composed of antigenic material from seven common types of OspC found in Lyme - infected dogs in the U.S. 1 Its uniquely targeted
design helps provide a broad spectrum of coverage while delivering a low - reactive
vaccine by minimizing the amount of extraneous proteins administered to the dog.
About Vanguard crLyme Vanguard crLyme is a next - generation multivalent
vaccine which contains outer surface protein A (OspA) protein and a single OspC protein that is composed of antigenic material from seven common types of OspC found in Lyme - infected dogs in the U.S. 1 Its uniquely targeted
design helps provide a broad spectrum of coverage while delivering a low - reactive
vaccine by minimizing the amount of extraneous proteins administered to the dog.
Guided
by the Behavioral
Vaccine Theory of prevention, this study uses a no - control group
design to examine intervention variables that predict favorable changes in depressive symptoms at the six - to - eight week follow - up in at - risk adolescents who participated in a primary care, Internet - based prevention program.