In a process called cellular reprogramming, researchers at Icahn School of Medicine at Mount Sinai have taken mature
blood cells from patients with myelodysplastic syndrome (MDS) and reprogrammed them back into iPSCs to study the genetic origins of this rare blood cancer.
The results of the empirical study show a clear distinction between the damage to the white
blood cells from patients with cancer, with pre-cancerous conditions and from healthy patients.
Not exact matches
Consider: Last year alone, the FDA approved two treatments,
from Novartis and Gilead, that literally reengineer
patients» immune T -
cells to target and destroy
blood cancers.
This new kind of approach to fighting
blood cancers is truly personalized; immune T -
cells are extracted
from patients, genetically tinkered to home in on an destroy cancerous
cells, multiplied in a lab, and then jolted back into the
patient's body within about two weeks.
In
blood samples
from these
patients, the researchers found an increase in the percentage of gamma delta T
cells, similar to what they observed in mice, which remained stable over years.
Users simply collect a
blood sample
from a
patient, feed it into the device, and retrieve any purified tumor
cells a few hours later.
They isolated
blood cells from HIV - positive
patients on antiretroviral therapy and at different stages of disease progression, as well as
cells from non-infected individuals.
In contrast, PD - L1 blockade increased the capacity of Treg
cells to multiply (and hence their overall numbers), but only in
cells from patients with viremia, i.e. those that had detectable virus in their
blood.
The Porteus team started with human stem
cells from the
blood of
patients with sickle
cell disease, corrected the gene mutation using CRISPR and then concentrated the human stem
cells so that 90 percent carried the corrected sickle
cell gene.
Another approach might be to selectively remove CD11b leukocytes
from the
blood circulation so that they are not available to adhere to the
blood - nerve barrier endothelial
cells in
patient's nerves.
Researchers analyzed peripheral
blood mononuclear
cells from a total of 18 children and adolescents in three matched groups: bipolar
patients, unaffected offspring of bipolar parents and children of parents with no history of psychiatric disorders.
Lu's team will extract immune
cells called T
cells from the
blood of the enrolled
patients, and then use CRISPR — Cas9 technology — which pairs a molecular guide able to identify specific genetic sequences on a chromosome with an enzyme that can snip the chromosome at that spot — to knock out a gene in the
cells.
These techniques include: human tissue created by reprogramming
cells from people with the relevant disease (dubbed «
patient in a dish»); «body on a chip» devices, where human tissue samples on a silicon chip are linked by a circulating
blood substitute; many computer modelling approaches, such as virtual organs, virtual
patients and virtual clinical trials; and microdosing studies, where tiny doses of drugs given to volunteers allow scientists to study their metabolism in humans, safely and with unsurpassed accuracy.
Researchers at Dana - Farber / Boston Children's Cancer and
Blood Disorders Center report promising outcomes
from a clinical trial with
patients with a rare form of bone marrow failure who received a hematopoietic stem
cell transplant (HSCT) after pre-treatment with immunosuppressive drugs only.
By introducing caerulein to the pancreas we were able to generate new beta
cells — the
cells that produce insulin — potentially freeing
patients from daily doses of insulin to manage their
blood - sugar levels.»
From a simple
blood draw, the test reads the DNA of the
patient's immune repertoire to find the immune
cell barcodes associated with the cancer.
Researchers are developing many different versions of CAR - T
cell therapies, but the basic premise is the same: Doctors remove a
patient's T
cells (immune system
cells that attack invaders)
from a
blood sample and genetically modify them to produce artificial proteins on their surfaces.
Fat
cells cultured
from the body mass index of a morbidly obese
patient cause multiple myeloma
cells to anchor to a much greater extent than normal
cells and produce a significantly larger number of
blood vessels to sustain the cancer
cells.
The researchers then took naïve immune
cells — which transform into different types based on the invaders they encounter —
from the
blood of healthy individuals and exposed them to bacteria in the guts of MS
patients.
The plan is to extract
blood - forming stem
cells from a
patient's bone marrow and correct as many copies of the mutated gene as possible.
They will have to address side effects such as the flulike symptoms and the kidney failure that occurred in one
patient due to all the dead
cells the body had to cleanse
from the
blood.
Next, the team exposed immature immune
cells from the
blood of healthy people to the bacteria found in the guts of MS
patients.
In DBA, a mutation prevents a
patient's bone marrow
from producing normal quantities of red
blood cells, resulting in severe, sometimes life - threatening anemia.
By taking the age of
patients»
blood cells into account, the researchers» model, when tested in more than 200 diabetic
patients, reduced the error rate
from one in three
patients with the standard
blood test to an error rate of one in 10.
In new research, scientists reprogrammed skin
cells from patients with rare
blood disorders into iPSCs, highlighting the great promise of these
cells in advancing understanding of those challenging diseases — and eventually in treating them.
Researchers can create iPSCs
from a
patient's
blood or skin
cells, and use these
patient - specific
cells to study diseases or even create new tissues that could be transplanted back into the
patient as therapy.
«Compared to
blood from the same
patients, the inflamed joint immune
cells were much less sensitive to active vitamin D.
Another key finding of the research was that the impact of vitamin D on inflammatory disease can not be predicted using
cells from healthy individuals or even
from the
blood of
patients with inflammation as
cells from the disease tissue are very different.
In this study, researchers took
cells from patients with
blood cancer MDS and turned them into stem
cells to study the deletions of human chromosome 7 often associated with this disease.
Blood vessels grown
from a person's own
cells may soon help kidney dialysis
patients.
Seven years after Moore's initial therapy, Golde asked his
patient to sign a contract relinquishing his rights and those of his heirs to any
cell lines or products derived
from his
blood or tissues (Moore's spleen had been removed in the course of his treatment).
Now a team of researchers in China has developed a new microfluidic chip that can quickly and efficiently segregate and capture live circulating tumor
cells (CTCs)
from a
patient's
blood, with potential applications for cancer screenings and treatment assessments.
Current genome sequencing techniques involve the chemical disintegration of samples of red
blood cells from infected
patients to obtain parasite DNA, which are then sequenced.
«FDG PET shows tumor DNA levels in
blood are linked to NSCLC aggressiveness: Insights derived
from FDG PET could improve treatment selection for
patients with advanced non-small
cell lung cancer.»
To make the vaccine, cancer
cells are harvested
from a tumor after surgery and stripped of their proteins; then those proteins are cultured with dendritic
cells, a subclass of white
blood cells, drawn
from the
patient's
blood.
He did, however, publish a paper last year documenting a study in which he infused three cancer
patients with white
blood cells from young donors who had been injected with G - CSF.
A study combining tumor
cells from patients with breast cancer with a laboratory model of
blood vessel lining provides the most compelling evidence so far that a specific trio of
cells is required for the spread of breast cancer.
The researchers
from UC Berkeley, UC San Francisco Benioff Children's Hospital Oakland Research Institute (CHORI) and the University of Utah School of Medicine hope to re-infuse
patients with the edited stem
cells and alleviate symptoms of the disease, which primarily afflicts those of African descent and leads to anemia, painful
blood blockages and early death.
The researchers also analyzed specific immune
cells called cytotoxic T
cells isolated
from the
patients»
blood and found increases in biomarkers indicative of immune activation.
Stem
cell source: Obtained
from skin or
blood cells of
patients.
Analyzing white
blood cells from 934
patients and 1,698 healthy controls, they found BRCA1 methylation among 6.4 % of
patients diagnosed with ovarian cancer, contrasting 4.2 % among controls.
Next, T
cells — the immune system's foot soldiers — are harvested
from the
patient's
blood and infected with the virus, which rewrites their genetic code to recognize and destroy cancer
cells.
In recent studies of cancer
patients who received a bone marrow transplant, genes
from the marrow's white
blood cells were found in the
patient's tumor
cells.
The SC3 tool was then used to analyse single -
cell RNA - sequence data
from two
patients diagnosed with myeloproliferative neoplasm (MPN)
blood cancers.
HSCT is effectively used today as a form of «replacement» therapy for
patients with hard - to - treat
blood cancers, providing healthy
cells from either the
patient (autologous transplantation) or
from a donor (allogeneic transplantation) to better equip
patients to fight the disease on their own.
He is pioneering a new treatment for autoimmune disorders, one in which
patients» immune systems are suppressed and then replaced with an infusion of their own immune stem
cells, filtered out
from their
blood.
Cheng, an assistant professor of medicine in hematology / oncology at Feinberg, provided the
cell lines and NanoFlare targets the researchers used to model
blood samples taken
from breast cancer
patients.
Further searching turned up retroviral particles, which could kill white
blood cells and which also reacted with antibodies
from infected
patients.
In a comprehensive and complex molecular study of
blood samples
from Ebola
patients in Sierra Leone, published in
Cell Host and Microbe, a scientific team led by the University of Wisconsin - Madison has identified signatures of Ebola virus disease that may aid in future treatment efforts.
Abatacept, when added to the standard drug regimen used to prevent GvHD, reduced the occurrence of acute, grade III - IV GvHD
from 32 to 3 percent in pediatric and adult
patients who underwent mismatched unrelated donor stem
cell transplants to treat advanced cancer and other
blood disorders.