A T - cell marker panel that can identify subsets of tumor - associated T - cells allows scientists to identify and target subpopulations of T - cells playing unique roles
in the immune response against a tumor.
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.
C. novyi is really a two - pronged weapon
against cancer: It germinates
in tumors and releases cancer - killing enzymes, and it may also trigger an
immune response similar to Coley's Toxin.
Principal Investigator John Morris, MD, clinical co-leader of the Molecular Therapeutics and Diagnosis Program for the CCC, co-leader of the UC Cancer Institute's Comprehensive Lung Cancer Program, professor
in the division of hematology oncology at the UC College of Medicine and UC Health medical oncologist, says a number of antitumor vaccines have shown promise for causing
immune responses against tumor antigens to improve patient outcomes.
Now, scientists have modified Salmonella bacteria to trigger a particularly powerful
immune response against human cancer cells implanted
in mice, shrinking the
tumors and — for the first time — preventing them from metastasizing.
They used the gene - editing CRISPR / Cas9 technique to sift the genomes of melanoma cells for changes that made
tumors resistant to being killed by
immune T cells, which are the main actors
in the
immune system
response against infections and cancer cells.
These types of engineered
tumors are much more difficult to treat than human
tumors implanted
in mice, because they suppress the
immune response against them.
In 2008, he joined the group of Caetano Reis e Sousa at the Cancer Research UK (CRUK) London Research Institute and later joined the Francis Crick Institute, where he was awarded Marie Curie and EMBO long - term postdoctoral fellowships to investigate innate
immune receptors and signaling pathways that trigger dendritic cell activation and drive T - cell
responses against viruses or
tumors.
In experiments in animals, researchers from the University of Michigan Medical School showed that adding rapamycin to an immunotherapy approach strengthened the immune response against brain tumor cell
In experiments
in animals, researchers from the University of Michigan Medical School showed that adding rapamycin to an immunotherapy approach strengthened the immune response against brain tumor cell
in animals, researchers from the University of Michigan Medical School showed that adding rapamycin to an immunotherapy approach strengthened the
immune response against brain
tumor cells.
While much recent research has not been published
in this area, there is actually a long history of studies that show: (1) there is a significant number of antigens shared between
tumors and embryonic tissues (called «oncofetal antigens») and, consequently, antibodies made
against tumors can also recognize embryonic tissues, and vice versa; (2) pregnancy confers some immunity
against cancer (accompanied by antibody production
against oncofetal antigens), not only
against its occurrence but also
against its growth; (3) similar to pregnancy, an
immune response against cancer can be generated by vaccinating animals with embryonic tissues.
In different contexts, viruses appear capable of attacking tumors in a number of different ways — by directly infecting them, by releasing tumor proteins that trigger a broad immune response against the cancer, and by damaging the blood supply tumors need to surviv
In different contexts, viruses appear capable of attacking
tumors in a number of different ways — by directly infecting them, by releasing tumor proteins that trigger a broad immune response against the cancer, and by damaging the blood supply tumors need to surviv
in a number of different ways — by directly infecting them, by releasing
tumor proteins that trigger a broad
immune response against the cancer, and by damaging the blood supply
tumors need to survive.
She is registred to the National Order of Biologists
in the province of Palermo; collaboration
in research project from 2012 to 2015 at the Department of Biopathology and Biotechnology, University of Palermo, focusing the study on the identification of molecules capable to modulate intracellular metabolic pathways for the prevention and treatment of infectious,
tumor and degenerative disease,
in collaboration with Prof. Angela Santoni, University of Rome; collaboration
in research project
in 2011 at the hospital «Villa Sofia Cervello» of Palermo to study methods can cure the genetic defect that causes thalassemia through genetic engineering; she studies different mechanisms of the differentiation and the activation of human gammadelta T cells as effector cells of the
immune response against cancer and infectious diseases; she investigates about the identification and development of biomarkers of resistance and susceptibility to Mycobacterium tuberculosis infection; Valentina Orlando has published 13 papers
in peer reviewed journals and 3 comunications at national and international congress.
The TCGA analysis showed
tumors with PTEN loss
in the background of BRCA1 / 2 deficiency had lower levels of cytolytic
immune molecules and
immune - activating pathways that would normally drive
immune responses against tumors.
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.
Also, CMB305 was well tolerated, and generated a strong and broad anti-NY-ESO-1
immune response in > 50 % of the patients, including evidence of antigen spreading — the induction of an
immune response against other
tumor antigens not targeted by CMB305.
Induction of
immune responses in patients with b - cell lymphoma
against the surface - immunoglobulin idiotype expressed by their
tumors