Therefore, we will continue to generate CD40 - B
cell vaccines using freshly irradiated feeder cells.
Not exact matches
«The holy grail is to target a piece of the virus by antibody or t
cell,» Tom Evans, the CEO of a company called Vaccitech that is working on a universal
vaccine they hope can be
used to treat all strains of influenza A, told National Geographic.
While other papers have examined these mutations
using expensive and time - consuming experiments on live ferrets and laboratory
cell cultures, Deem and Melia Bonomo
used the pEpitope method to rapidly calculate how much the egg - passage mutations would decrease
vaccine efficacy in humans.
And a new analysis of the STEP trial, published last November in Proceedings of the National Academy of Sciences USA, provides a warning that the very vectors (adenoviruses, which are also employed in other
vaccine development work)
used to distribute the inactive HIV strains can actually make the immune system more vulnerable to infection by recruiting susceptible T
cells to mucous membranes, where they are more likely to be infected during sexual activity.
Not all
vaccines are produced
using the same antiquated system; for example, the HPV
vaccine known as Gardasil, which was approved by the FDA in 2006, is made in yeast
cells.
The so - called STEP trial, sponsored by pharmaceutical giant Merck & Co. and the federally funded HIV
Vaccine Trials Network (HVTN), was the first to test the idea of stimulating the immune system's killer T
cells to hunt for the virus more aggressively, in this case
using a weakened form of the cold virus to carry three genes from HIV.
The older
vaccine, DTP,
used whole
cells of the pertussis bacterium but had more dramatic side effects, often causing high fevers and sometimes fever - induced seizures.
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.
Davis will
use his findings to figure out a way to match specific immune
cells to
vaccine response.
Flu
vaccines are designed to prevent infection by eliciting antibodies against HA, which the virus
uses to break into
cells lining the airways.
We are looking for the proteins that make the tumour
cells different to the host devils that they infect and then
use these «tumour specific» proteins to design a
vaccine that will save the devil from extinction.
For their research, Pekosz and his team,
using human nasal tract
cells, studied the weakened strain of the flu virus that is
used in the nasal spray
vaccine and compared its behavior with that of the flu virus itself.
Using the findings from this study, the team has designed
vaccine immunogens to selectively trigger the cooperating antibody - producing B
cells to cooperate to make broadly neutralizing antibodies in a manner that mimics broadly neutralizing antibody development in natural HIV infection.
Fact: The WI - 38 and MRC - 5
cell lines, derived from two fetuses that were aborted, respectively, in 1962 in Sweden and in 1966 in the United Kingdom, are
used to produce the following
vaccines, all licensed and marketed in the United States:
In 1967 and 1968, Yugoslavia conducted a mass polio vaccination campaign
using polio virus propagated in WI - 38
cells; Sweden and Switzerland had already run trials of the same
vaccine.
(In seeming contradiction, the report goes on to state, one page later, that «11 [current
vaccines]... are produced
using historic, fetal - derived
cell lines.»)
Currently, most influenza
vaccines in the United States are produced
using chicken eggs, while a few are made in
cell culture or by
using recombinant DNA technologies.
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.
Early
vaccines also
used cells from other animals.
He wonders whether it's not vaccinia, the virus
used to induce smallpox resistance, but some other component of the
vaccine that's prompting inflammation, perhaps bovine
cells from the manufacturing process.
The company
uses cells to grow the virus for the
vaccine and claims that this «shows significant time saving» over traditional production with eggs.
And a new analysis of the stopped STEP trial, published online Monday in Proceedings in the National Academy of Sciences, provides a warning that the very vectors (adenoviruses, which are also employed in other
vaccine development)
used to distribute the inactive HIV strains can actually prime the immune system to be infected by recruiting susceptible T
cells to mucous membranes, where they are more likely to be infected during sexual activity.
Sun is currently conducting collaborative research with hydrogels for applications and efficiency with anticancer drugs screening and delivery, stem
cells and wound healing, as well as being
used in
vaccines for H1N1 influenza and animal diseases, such as the porcine reproductive and respiratory syndrome virus, or PRRS.
Others tackle bigger issues, such as drug and
vaccine safety and the
use of stem
cells for drug discovery.
Researchers
used IL - 15 to develop a whole tumor
cell vaccine to target breast (TS / A) and prostate (TRAMP - C2) cancer
cells in animal models; results showed that tumor
cells stopped growing after the
vaccine was introduced and that beneficial effects were enhanced further when IL - 15Rα was co-produced by the
vaccine cells.
But in truth, most (26 of 28
vaccines currently licensed for human
use) stimulate primarily a B -
cell or antibody response, which in many cases is sufficient.
The
vaccine contains DNA much like the virus
uses to encode a protein for
cell entry.
To develop subunit
vaccines for other diseases, scientists have tried targeting them to lymph nodes
using nanoparticles to deliver them, or tagging them with antibodies specific to immune
cells in the lymph nodes.
Instead, the
vaccines use killed autologous tumor
cells from the patient to activate the immune system.
These
vaccines have been
used in combination with chemotherapy to provide a one - two punch to pancreatic cancer
cells.
«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.
«
Vaccine used to treat cervical precancers triggers immune
cell response.»
Two types of
vaccines were
used for the study: one constructed with genetically engineered DNA molecules that teach immune system
cells to recognize premalignant
cells expressing HPV16 E7 proteins, and one that is a non-infectious, engineered virus that targets and kills precancerous
cells marked by HPV16 and HPV18 E6 and E7 proteins.
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.
Instead of stirring up powerful T
cells through an injected amyloid
vaccine, they
used a nasal spray containing two drugs that provoke a less robust but more manageable immune response.
But the CDC's Martin notes that the United States will probably never
use the whole
cell vaccine again because of concerns about its possible side effects.
Kirschstein worked on another aspect of
vaccine safety, doing «very prominent» early research on another virus, simian virus 40, which contaminated some of the monkey
cells used to grow poliovirus for the Salk
vaccine, says Singer, who later joined the same field.
The
vaccine sets off an immune response
using a piece of a protein, called PR1 peptide, found on the surface of leukemia
cells.
Now Joseph Wu of Stanford University, California, and his team have found that stem
cells can be
used as a
vaccine to help the immune system recognise such change.
Current
vaccines activate T
cells and thus the CD40 receptor by
using purified bacterial proteins attached to a number of different polysaccharides.
An alternative approach is to persuade the immune system to attack tumours,
using vaccines, biological therapies such as alpha interferon or interleukin 2 and genetically altered white blood
cells.
After constructing the first synthetic bacterial
cell and the first minimal bacterial
cell, JCVI scientists are
using the groundbreaking techniques
used in these milestones to construct synthetic flu
vaccines, develop unique new sources of insulin, and more efficient means to produce algae - based biofuels.
Since T
cells can only recognize neoantigens that are «presented» to them by HLA molecules of the immune system, a key step in making the
vaccine is
using computer algorithms to predict which neoantigen peptides will bind strongly to the HLA molecules for recognition by T
cells.
By contrast, the neoantigen
vaccine is custom - made for each patient
using antigens produced by mutations unique to the patient's cancer and only present on cancer
cells, thus bypassing the nature immune tolerance process.
Once developed, the assays will be
used to analyse in vitro cytokine and chemokine induction, e.g. to compare different versions of a
vaccine, or the same
vaccine produced in different host
cells, or different batches of a
vaccine to demonstrate batch - to - batch reproducibility.
Identification of optimal
vaccine formulations and administration routes for the induction of CD8 + T -
cell responses (SSI): The induction of suitable CD8 + T -
cell responses following vaccination usually requires the
use of live viral vectors.
These same models are
used to develop new anti-cancer
vaccines based on long peptide or DNA vaccination targeting the antigen to antigen presenting
cells.
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.
The technology also improves
cell culture systems
used to produce therapeutic proteins,
vaccines, and gene therapy vectors.
Tanyi said he is eager to explore whether the dendritic -
cell vaccine might also be
used as a first - line treatment for women who are newly diagnosed with ovarian cancer.