Spark Therapeutics hopes to win U.S. approval in January 2018 for a gene therapy to cure a rare inherited form of blindness, while Novartis could get a U.S. go - ahead as early as next month for its gene - modified
cell therapy against leukaemia - a variation on standard gene therapy.
Not exact matches
On its own, this immune response had no immediate effect in the fight
against the utilized breast tumors, but in combination with the ADC it proved itself effective in attacking cancer
cells in mice, resulting in the complete cure of the majority of mice receiving the combination
therapy.
They then tried adoptive T
cell therapy (ACT), in which T
cells directed
against a tumor are infused into a patient.
Now a University of Colorado Cancer Center study published online ahead of print in the journal Oncogene offers compelling evidence explaining this failure and offering a possible strategy for the use of retinoic acid or other retinoids
against some breast cancers: Because early clinical trials are often offered to patients who have already tried other more established
therapies, breast cancer
cells may have been pushed past an important tipping point that offers retinoic acid resistance.
Antibodies and T
cells against the protein could cause the immune system to attack
cells carrying it, making gene
therapy ineffective.
Just as chemotherapy often requires several drugs to combat resistance in cancerous
cells, successful antimicrobial
therapy against some pathogens requires a combination of drugs.
Researchers at the Center for
Cell and Gene
Therapy at Baylor College of Medicine, Texas Children's Hospital and Houston Methodist have developed an alternative treatment in which virus - specific
cells protect patients
against severe, drug - resistant viral infections.
It showed effectiveness
against liver cancer in a phase II clinical trial and will move into a phase III trial later this year, David Kirn, an oncologist and the company's president and chief executive officer, said at a recent meeting of the American Society for Gene &
Cell Therapy in Washington, D.C..
The authors said their results, which they have made publicly available, constitute an invaluable resource to help clinicians predict which chemotherapies will be most effective
against tumor
cells with particular genetic mutations, and how to rationally combine
therapies to prevent cancers from developing resistance.
By viewing this fusion as another disease imposed onto tumor
cells, scientists could devise new
therapies against metastasis, the researchers say in the May Nature Reviews Cancer.
Using an experimental DNA - based
therapy, scientists might slow the self - destructive immune reaction
against insulin - making
cells that causes type 1 diabetes.
Therefore, the insights of Dr. Melendez and her colleagues may deepen our understanding of cancer and aid in the development of
therapies against malignant
cell growth.
For patients, down the road Dr. Ohashi envisions a new era of combined
therapies to simultaneously target and kill these suppressive
cells while augmenting the immune response
against cancer.
By tracking and understanding which host
cell pathways are manipulated by these T. gondii proteins, scientists can identify potential new targets to develop more effective
therapies against highly aggressive solid tumors.
Kole Roybal is the 2018 grand prize winner of the inaugural Sartorius & Science Prize for Regenerative Medicine &
Cell Therapy, for developing a new class of T cell immunotherapies that can be fine - tuned to better help the immune system recognize cancer and initiate precise therapeutic action against the dise
Cell Therapy, for developing a new class of T
cell immunotherapies that can be fine - tuned to better help the immune system recognize cancer and initiate precise therapeutic action against the dise
cell immunotherapies that can be fine - tuned to better help the immune system recognize cancer and initiate precise therapeutic action
against the disease.
They are examining every aspect of
cell function and
cell structure, looking for clusters of phenotypes that could label a patient's cancer so precisely that it could be linked to
therapies proven effective
against just that type.
«Given these results in
cells and mice, it may be worthwhile to consider that patients receiving, or who may receive, Amphotericin B - based
therapies be appropriately vaccinated
against influenza virus.
In the present study, the scientists demonstrated that the drug BI-97D6 increased cancer
cell death caused by mda - 7 / IL - 24, and it also helped defend
against resistance to the viral gene
therapy.
To harness the power of bacteriophages and develop effective
therapies against bacteria like C.diff, scientists need to know exactly how these viruses destroy bacterial
cell walls.
Cruse and Metcalfe tested their
therapy on mast
cells in vitro — where it eliminated activation of mast
cells by allergen — and
against allergic dermatitis in vivo, using a mouse model.
Experimental
therapies using T
cells taken from the bloodstream have not, however, worked very well
against solid tumors.
Therapies based on immune
cells, which target particular tumor molecules, are more specific, but they are not effective
against a variety of tumors.
Neoantigens are molecules on
cell's surfaces that are produced by DNA mutations that are present in cancer
cells but not in normal
cells, making neoantigens ideal targets for immune
therapy against cancer, say the scientists.
The safe use of a stem -
cell - based
therapy against brain metastasis would require preventing the engineered
cells from persisting within the brain, where they could affect normal tissue and possibly give rise to new tumors.
An international research team led by Université de Montréal medical professor Christopher Rudd, director of research in immunology and
cell therapy at Maisonneuve - Rosemont Hospital Research Centre, has identified a key new mechanism that regulates the ability of T -
cells of the immune system to react
against foreign antigens and cancer.
They also identified targets for potential
therapies: bolstering levels of either a particular chaperone or a growth factor in brain
cells can protect
against the toxic effects of misfolded proteins.
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.
It's only three patients on a low dose of
cells, but San Diego - based Poseida said the results — activity
against the cancer and no «cytokine storm» side effects that often come with CAR - T
therapy — were good enough to step up to the next dose.
He added: «Truly naive human ES
cell lines would not only help answer fundamental questions about how we are made, and be useful for drug screening and tissue
therapy, but they would also provide a benchmark
against which other types of stem
cells could be measured in terms of their effectiveness in stem
cell therapy and regenerative medicine.»
Dr. Semenza's research interests include the molecular mechanisms of oxygen homeostasis; gene and stem
cell therapy for ischemic cardiovascular disease; the role of HIF - 1 in cancer; and protection of the heart
against ischemia - reperfusion injury.
CAR T -
cell therapy was also named as the American Society of Clinical Oncology's Advance of the Year in its Clinical Cancer Advances 2018: ASCO's Annual Report on Progress
Against Cancer.
These
therapies use non-specific molecules that do not affect the cancer directly, but send signals that stimulate other
cells of the immune system to fight
against cancer
cells.
This new
therapy works well
against B -
cell acute lymphomblastic leukemia, a cancer of the blood system, which has led the U.S. Food and Drug Administration to expedite approval of the first CAR - T treatment for children and young adults.
New research into CAR - T
cell therapy has revealed crucial mechanisms that could help the immunotherapy technique, which is currently only effective
against blood cancers, be adapted for the treatment of brain tumors and other forms of solid cancers.
The
therapy, produced by Kite Pharma and owned by Gilead Sciences, is approved for use
against some types of large B -
cell lymphomas.
In contrast, increasing progranulin levels via gene
therapy effectively lowered amyloid beta levels, protecting
against cell toxicity and reversing the cognitive deficits typically seen in these Alzheimer's models.
This may be the first time a
therapy has been directed
against the disorganized nature of cancer
cells.»
Low - dose chemotherapy, radiation, or targeted
therapies given in combination with immune checkpoint blockade may prove to be an effective and efficient way to immunize the body
against tumor
cells,» says CRI Scientific Advisory Council associate director James P. Allison, Ph.D., who identified the first immune checkpoint blockade with his discovery in 1995 that the cytotoxic T lymphocyte antigen - 4 (CTLA - 4) receptor inhibited T
cell responses.
Through a joint UNC School of Medicine - NC State research project shows how to harvest lung stem
cells non-invasively and then multiply healthy
cells — a potentially powerful
therapy against inflammatory lung conditions.
Adults with advanced renal
cell carcinoma after targeted
therapy against vascular endothelial growth factor (VEGF)
Through a joint UNC School of Medicine - NC State research project shows how to harvest lung stem
cells non-invasively and then multiply healthy
cells — a potential powerful
therapy against inflammatory lung conditions.
Radiation
therapy can help extend the lives of affected dogs, but also is ineffective
against tumor
cells that have metastasized.
«We were banging our heads
against the wall and this stem
cell therapy was a last resort.»