Not exact matches
«The discovery of this special class of
cells that sit right
at the nerve endings where HSV - 2 is released into skin is changing how we think about HSV - 2 and possible
vaccines,» said Corey.
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.
«The best explanation for what we are seeing is that frequently, after exposure to HIV, a few
cells in the genital tract are infected, without establishment of a systemic infection,» says senior investigator Eric Hunter, PhD, professor of pathology and laboratory medicine
at Emory University School of Medicine, Emory
Vaccine Center, and Yerkes National Primate Research Center.
At the centre of the theory is the plausible, if unlikely, speculation that a direct forerunner of HIV contaminated monkey
cells that were used to grow polio virus for the
vaccines.
The 9vHPV
vaccine was also highly effective
at reducing the risk of having HPV 31/33/45 / 52 / 58 - associated cervical
cell abnormalities, biopsies, and definitive therapies.
They believe a
vaccine that stimulates the body to produce more of these
cells could be effective
at preventing flu viruses, including new strains that cross into humans from birds and pigs, from causing serious disease.
Based
at the Wistar Institute in Philadelphia, he was a gifted young scientist who reasoned that fetal
cells derived from a normal pregnancy would be a virus - free and safe alternative for
vaccine development.
Protein chemist Michael Way,
cell biologist Sally Cudmore, and their colleagues
at the European Molecular Biology Laboratory in Heidelberg and
at the Pasteur Institute in Paris have found that vaccinia — a virus used in smallpox
vaccines — surfs through
cells on piles of actin, one of the basic structural proteins in the cellular skeleton.
A
vaccine under development prevents adhesion proteins
at the tips of spaghettilike pili on UTI - causing bacteria (left) from latching onto host
cells.
The study included 124 newly diagnosed patients
at 25 clinical trial sites in the U.S. Two - thirds of the patients were treated with ICT - 107, an experimental
vaccine based on immune system
cells called dendritic
cells that were exposed to six synthetic proteins, or antigens, known to be involved in GBM development.
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.
Now a team of engineers
at MIT has developed a new way to deliver such
vaccines directly to the lymph nodes, where huge populations of immune
cells reside: These
vaccines hitch a ride to the lymph nodes by latching on to the protein albumin, found in the bloodstream.
Dr. Levine directs the Clinical
Cell and Vaccine Production Facility (CVPF), which develops, manufactures, and tests novel cell and gene therapies in clinical trials at Penn and collaborating instituti
Cell and
Vaccine Production Facility (CVPF), which develops, manufactures, and tests novel
cell and gene therapies in clinical trials at Penn and collaborating instituti
cell and gene therapies in clinical trials
at Penn and collaborating institutions.
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.
«The idea basically is that a
vaccine should induce antibodies T
cells immune response, that would neutralise HIV in all of its forms,» explains Ulrich Fruth,
vaccine development and evaluation team leader
at the World Health Organisation, in Geneva, Switzerland.
In his look
at the wider benefits of
vaccines, Michael Brooks describes type 1 and type 2 helper T -
cells as...
«Although right now we are focusing on developing a cancer
vaccine, in the future we could be able to manipulate which type of dendritic
cells or other types of immune
cells are recruited to the 3D scaffold by using different kinds of cytokines released from the MSRs,» said co-lead author Aileen Li, a graduate student pursuing her Ph.D. in bioengineering
at Harvard SEAS.
The researchers are now looking
at how ICOS signals can be altered to diminish autoimmune disorders and augmented for more effective
vaccine development, and are beginning research on how ICOS signaling may benefit Chimeric Antigen Receptor - T
cell (CAR - T) therapies, which involves engineering of patient's own immune
cells to recognize and attack their cancers.
In his look
at the wider benefits of
vaccines, Michael Brooks describes type 1 and type 2 helper T -
cells as competitive, with levels of one going down as the other goes up (17 August, p 38).
But Nabel noticed that this modified adenovirus alone stimulated rapid antibody production, and even produced a T -
cell response, although
at a lower level than the DNA
vaccine.
The new technique, pioneered by Wilson and fellow researchers
at the Emory University School of Medicine in Atlanta, saves time by using antibodies produced by so - called B
cells (white blood
cells that produce and then ferry them to infection sites to battle invading germs) in response to
vaccines instead of to actual infections.
While this approach has had some clinical success, in most cases, the immune response resulting from dendritic
cell vaccines is short - lived and not robust enough to keep tumors
at bay over the long run.
Reported in the January 16, 2015 issue of the journal Science, the new findings provide a cautionary tale for the development of
vaccines aimed
at eliciting robust CD4 T
cell immunity against chronic infections, including HIV.
In the June issue of the journal
Vaccine, Christopher Blyth
at the University of Western Australia and colleagues found that Fluvax (but not other flu
vaccines) triggered the release of high levels of cytokines in blood
cells isolated from the children who had febrile seizures.
In their report published in Cancer Immunology Research, a team from the
Vaccine and Immunotherapy Center (VIC)
at Massachusetts General Hospital (MGH) describes how adding AMD3100 (plerixafor)-- previously approved for the stimulation of stem
cell production prior to bone marrow transplantation — to their investigational drug VIC - 008 more than doubled the animals» survival time.
Cancer
vaccines, engineered to continue to train T
cells to mount a strong immune response against your cancer, also haven't been very effective
at mounting a strong fight, says He, and likely one weak point is the lack of strong receptors.
The
vaccine was aimed
at generating responses to the neoantigens from T
cells of two kinds — CD8 + killer
cells and CD4 + helper
cells.
«Our findings support PfSEA - 1 as a potential
vaccine candidate, and we are confident that by partnering with our colleagues
at the National Institutes of Health and other researchers focused on
vaccines to prevent the parasites from entering red blood
cells, we can approach the parasite from all angles, which could help us develop a truly effective
vaccine to prevent this infectious disease that kills millions of children every year.»
Dr. Nina Bhardwaj is the director of immunotherapy and the medical director of the
Vaccine and
Cell Therapy Core facility
at the Icahn School of Medicine
at Mount Sinai.
Now as an Assistant Professor in Medicine
at Harvard Medical School, Daniel uses membrane structure and function as a means to define B
cell antigen recognition and inform
vaccine design.
At the end of his talk, Coukos turned his attention to a dendritic
cell vaccine approach in combination with a VEGF - targeting antibody and chemotherapy.
There is evidence that this might cause chronic inflammation in the gut, Petri said, coming from work by Evan Newell of Stanford University and colleagues who looked
at peripheral blood mononuclear
cells in three year old children who had received the oral polio
vaccine in the first months of their life.
Potential correlates of TCR diversity under evaluation include the cytokine milieu and T
cell activation state present
at birth and the early responses to birth
vaccines.
The full paper that this statement is in response to can be found
at: Niederberger et al. 2018 Safety and efficacy of immunotherapy with the recombinant B -
cell epitope — based grass pollen
vaccine BM32.
Similarly, MVA - p53
vaccine is targeted
at the p53 protein, a tumor suppressor that contols how
cells divide and replicate.
«Identifying specific biomarkers of latently infected
cells is considered as the «holy grail» in the HIV eradication field,» said lead corresponding author Luis J. Montaner, D.V.M., D.Phil., director of the HIV - 1 Immunopathogenesis Unit
at The Wistar Institute
Vaccine & Immunotherapy Center.
Inventors
at MUSC have identified a unique human CD4 + T
cell population that expresses high levels of surface CD26, termed CD26high T
cells, which mediate durable antitumor immunity in vivo, and have immediate clinical relevance for designing new
vaccines and cellular therapies.
A
vaccine should tip the balance of this contest in favor of the immune system by increasing the numbers of CD4 + and CD8 +
cells that are poised to swing into action if HIV gains entry to the body
at some point in the future.
Through long - established collaborations in Durban and Kimberley, these studies in particular seek to define: the immune responses that are effective in control of HIV infection; the impact of HLA - mediated selection pressure on HIV
at the individual and population level; the mechanisms of HIV non-pathogenicity; the nature and consequences of ontogeny of the virus - specific immune response; and finally the prospects for interventions including antiretroviral therapy, alone or in combination with broadly neutralising antibodies and / or T -
cell vaccines, to achieve HIV eradication.
1994 saw her as Head of the Department of Transplantation Immunology
at the CLB, in Amsterdam, and in 1999 she became Head of the department of the Immunology of the Laboratory of
Vaccine Research of the National Institute of Public Health and Environmental Protection (RIVM), in Bilthoven, where her research activities focused on defining immunological correlates of protection on the T and B
cell level after natural infection and vaccination.
Researchers compared NK
cells at the protein and transcript level in samples provided by healthy donors, volunteers with chronic HIV infection and healthy recipients of an HIV
vaccine.
The most famous, oldest, and most commonly used immortal
cell line, dubbed HeLa, originated in a tumor sample taken from an African - American woman, Henrietta Lacks, who is the subject of the recent book The Immortal Life of Henrietta Lacks.9 The tumor
cells, harvested
at Johns Hopkins Hospital, gave rise to the eponymous HeLa
cell line which researchers have used continuously since her death in 1951 for numerous experiments, including Jonas Salk's development of the polio
vaccine.
The Heart for Companion Animal Research
at Colorado State College has shown that cats vaccinated with FVRCP
vaccines grown on Crandell - Rees Feline Kidney (CRFK)
cell traces can develop antibodies to renal (kidney) proteins, and that cats hypersensitized to CRFK
cell lysates can develop interstitial nephritis.
We have now improved the generation of this
vaccine by generating canine specific feeder
cells that are moderately more efficient
at inducing canine B
cells to grow from PBMCs.
Studies
at Purdue University showed that canine
vaccines grown in calf serum caused antibodies to be made to many calf proteins including red blood
cells; thyroid; DNA; connective tissue proteins such as collagen, fibronectin, laminin, albumin, transferrin; and others.
At some point, the distemper
vaccine was grown on cat kidney
cells... from cats infected with FPV.