Once in the lymph nodes, these vaccines can stimulate production of huge numbers of T
cells against the vaccine target.
Not exact matches
Vaccines depend on them, and scientists are even employing the
cells to stir up immunity
against cancer
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.
Flu
vaccines are designed to prevent infection by eliciting antibodies
against HA, which the virus uses to break into
cells lining the airways.
The
vaccine caused the mice to create antibodies
against neuraminidase, a flu protein that lets newly born virus particles escape from infected
cells.
The
vaccine also induced a sharp rise in CD4 T -
cells, whose job is to mobilize the antibody response and other immune elements
against viral infections.
Rewinding skin
cells back to their origins in the womb could provide a powerful new
vaccine against multiple types of cancer.
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.
Vaccine Protection of Chimpanzees
Against Challenge with HIV -1-Infected Peripheral Blood Mononuclear
Cells
Vaccine - mediated protection of nonhuman primates
against low doses of
cell - free HIV - 1, HIV - 2, or simian immunodeficiency virus (SIV) has been demonstrated.
Currently, seasonal flu
vaccines are designed to induce high levels of protective antibodies
against hemagglutinin (HA), a protein found on the surface of the influenza virus that enables the virus to enter a human
cell and initiate infection.
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.
cruzi T
cell immunity, and booster immunization would be an effective strategy to maintain or enhance the
vaccine - induced protective immunity
against T. cruzi infection and Chagas disease.»
Thus, in principle, a successful
vaccine has to stimulate the first B
cells in this lineage and then coax them along a fairly narrow evolutionary path until they have changed enough to provide effective protection
against HIV.
Instead of working through antibody - mediated immunity, Liang says successful prophylactic
vaccines against the virus might have to work through
cell - mediated immunity, which means immune
cells are taught to attack infected
cells.
Learning what they contribute to
cell structure, permeability, membrane biogenesis and so on is important in
vaccine research because antibodies
against protein antigens can disable the protein's function.»
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.
«Developing a new vaccination strategy
against AIDS: The type of
vaccine administered and the activation of the body's own immune
cells influence the
vaccine protection.»
However, a new study of children from Sweden and Finland shows that the
vaccine increased neither the risk of developing autoantibodies
against insulin - producing beta
cells nor the occurrence of type 1 diabetes.
Purdue scientists identify an intestinal
cell protein that could lead to a
vaccine against Listeria, a bacterium that causes food poisoning.
Up until now, efforts in generating a
vaccine against TB have been mainly focused on T
cells (
cells from the adaptive arm of our immune response with memory capacity), with very disappointing outcomes in both pre-clinical as well as clinical trials.
The researchers, therefore, wanted to study whether the
vaccine also increased the risk of developing autoantibodies
against beta
cells in the pancreas and the occurrence of type 1 diabetes.
This result, effectively a method for blocking the spread of alphaviruses between
cells, is one that could eventually lead to a single
vaccine that protects
against multiple viruses.
A therapeutic
vaccine would not be intended to prevent the disease but rather to help patients» immune systems mobilize
against the cancer
cells, without recourse to surgery or radiation.
Significant advances also have been made in understanding T -
cell responses that may be important to
vaccine - induced immunity
against HIV.
A human
vaccine against malaria has faltered in the face of the sophisticated life cycle of Plasmodium falciparum, the one -
celled parasite responsible for the most severe form of the disease.
It included a 1994 report from the Institute of Medicine that said it was biologically plausible for a
vaccine to «induce... an autoimmune response... by nonspecific activation of the T
cells directed
against myelin proteins.»
The researchers found that the personal
vaccine induced a focused T
cell response
against several tumor neoantigens, beyond what is normally seen in response to existing immunotherapies.
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.
So if you received a
vaccine for varicella, for instance, you will have T
cells that will protect you for life
against chickenpox.
The assay will be validated
against clinical outcomes in human
vaccine studies (correlates of protection such as neutralising antibodies or
vaccine - induced protection in human challenge models, or exploratory correlates such as multifunctional Th1
cells).
As demonstrated by the breadth of clinical trial involvement shown above, CCIR members are testing the utility of immune checkpoint blockade in lymphoma (shown by Dr. Allison to be effective
against melanoma), genetic engineering in
cell therapy (e.g., CD19, CXCR2, TGF - β DNR), and TLR agonists or IL - 2 in
vaccine formulations as well as some novel combination therapies, such as the infusion of tumor - reactive lymphocytes from HLA - matched donors who were vaccinated with a lymphoma idiotype.
'» In all patients who were vaccinated, his team found tumor - targeting T
cells, and he noted that in addition to augmenting pre-existing T
cell responses, the
vaccine also stimulated new T
cell responses
against tumors.
Cancer
vaccines are designed to stimulate an immune response
against tumor - specific or tumor - associated antigens, encouraging the immune system to attack cancer
cells bearing these antigens.
[13] AN1792 was an active
vaccine, with Aβ aggregates as the antigen, and the meningoencephalitis is postulated to have been the result of the
vaccine having roused a T -
cell response
against Aβ along with the necessary B -
cell response, leading to a Th1 - biased inflammatory attack centralized on sites in the brain with local Aβ deposits.
«IL - 28B is a key regulator of B - and T -
Cell vaccine responses
against influenza» by Adrian Egli et al. published in PLOS Pathogens on Thursday 11 December 2014.
A new study demonstrates that it is possible to vaccinate patients with MDS
against a decitabine - induced antigen and that the level of induced expression is sufficient to trigger cytotoxicity in patient - derived
vaccine - induced T
cells.
The clinical consortium is led by AFFiRiS itself, and in addition to the PD booster trial, it is now recruiting for a separate Phase I trial of the α - synuclein
vaccine against MSA, a synucleinopathy differentiated from PD or LBD based on the
cell populations affected, the regional concentration of AS neuropathology, and the spectrum of movement and other symptoms.
The study relates to a particular type of
vaccine (killed)
against a particular virus, influenza, though the findings might hold true for other killed
vaccines and for those
vaccines consisting only of proteins produced by GM in bacteria, yeast or insect
cells,
against diseases such as hepatitis B (HBV) and human papilloma virus (HPV, the causative agent of cervical cancer).
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.
Therapeutic
vaccines are designed to elicit an immune response
against tumor - specific or tumor - associated antigens, encouraging the immune system to attack cancer
cells bearing these antigens.
Similar to these projects, IDRI's subunit tuberculosis
vaccine, ID93, also utilizes adjuvants that induce a
cell - mediated immune response, which is required for protection
against M. tuberculosis infection in low dose aerosol models of TB.
Therapeutic cancer
vaccines are designed to elicit an immune response
against tumor - specific or tumor - associated antigens, encouraging the immune system to attack cancer
cells bearing these antigens.
One is that there is no interaction between antibody - mediated immunity and T
cell immunity (which we know is an oversimplification), and that the future universal
vaccines do not actually protect
against infection (this does seem a rather radical assumption).
2000 Johns Hopkins Cancer Center researchers develop a pancreatic cancer
vaccine and prove it activates immune
cells against pancreatic tumor
cells.
Publication in
Cell Demonstrates Moderna's Zika mRNA
Vaccine Prevents In Utero Transmission of Zika Virus in Mice, Protects
Against Zika - Related Congenital Damage
Bird R.C., Deinnocentes P., Lenz S., Thacker E.E., Curiel D.T., Smith B.F., An allogeneic hybrid -
cell fusion
vaccine against canine mammary cancer.