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HER2-Specific CAR T-Cell Therapy Active in Progressive Glioblastoma – Cancer Network

Posted: April 20, 2017 at 8:44 pm

Administration of autologous HER2-specific chimeric antigen receptor (CAR)-modified virus specific T Cells (VSTs) was safe and had clinical benefit for some patients with progressive glioblastoma, a disease with limited effective therapeutic options.

Results of a small phase I study of this monotherapy were published in JAMA Oncology, by Nabil Ahmed, MD, MPH, of Baylor College of Medicine in Houston, and colleagues.

CAR T-cell therapies are an attractive strategy to improve the outcomes for patients with glioblastoma, they wrote. In our study, we infused HER2-CAR VSTs intravenously because T cells can travel to the brain after intravenous injections, as evidenced by clinical responses after the infusion of tumor-infiltrating lymphocytes for melanoma brain metastasis and by detection of CD19-CAR T cells in the cerebrospinal fluid of patients with B-precursor leukemia.

The study included 17 patients with progressive HER2-positive glioblastoma (10 patients aged 18 or older; 7 patients younger than 18). Patients were given one or more infusions of autologous VSTs specific for cytomegalovirus, Epstein-Barr virus, or adenovirus and genetically modified to express HER2-CARs. Six patients were given multiple infusions.

Infusions were well tolerated with no dose limiting toxicities presenting. Two patients had grade 2 seizures and/or headaches, which the researchers wrote were probably related to the T-cell infusion.

Although HER2-CAR VSTs did not expand, they were detected in the peripheral blood for up to 12 months after the infusion.

Although we did not observe an expansion of HER2-CAR VSTs in the peripheral blood, T cells could have expanded at glioblastoma sites. At 6 weeks after T-cell infusion, the MRI scans of patients 3, 7, 10, 16, and 17 showed an increase in peritumoral edema, the researchers wrote. Although these patients were classified as having a progressive disease, it is likely that the imaging changes for some of these patients were due to inflammatory responses, indicative of local T-cell expansion, especially since these patients survived for more than 6 months.

Only 16 of the 17 patients were evaluable for response. Patients underwent brain MRI 6 weeks after T-cell infusion. One patient had a partial response for longer than 9 months and seven patients had stable disease for between 8 weeks to 29 months. Three patients with stable disease are alive without any evidence of progression from 24 to 29 months of follow-up. Eight patients progressed after the infusion.

The median overall survival was 11.1 months from the first T-cell infusion and 24.5 months from diagnosis.

The researchers noted that the inclusion of children in the study, who have a better prognosis than adults, may have affected the results; however, there was no significant difference between the survival probability for children and that for adults in this clinical study.

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PolarityTE (COOL) Signs Manufacturing Agreement with Cell Therapy and Regenerative Medicine – StreetInsider.com

Posted: April 20, 2017 at 8:44 pm

News and research before you hear about it on CNBC and others. Claim your 2-week free trial to StreetInsider Premium here.

PolarityTE, Inc. (NASDAQ: COOL) announces the signing of a manufacturing agreement with Cell Therapy and Regenerative Medicine at the University of Utah School of Medicine. CTRM is the established manufacturer of hematopoietic stem cell transplants for renowned institutions of the Salt Lake region such as the Huntsman Cancer Institute and Primary Children's Hospital. In addition, CTRM manufactures a variety of regenerative medicine products, is FACT accredited, and has technical expertise in current Good Tissue Practice (cGTP) and current Good Manufacturing Practice (cGMP).

Denver Lough, MD, PhD, Chairman and CEO, stated, "This agreement with CTRM should provide PolarityTE with rapid clinical translation of the promising products we are developing, and takes us one step closer to achieving our goal of clinical application of our launch product, SkinTE. As we prepare for market entry in 2018, our established relationship with CTRM creates a springboard for the anticipated scale-up to address the large burn and chronic wound markets, with the pursuit of our own independent manufacturing facility. Plans are solidifying for a unique solution to both commercial and emergent relief manufacturing of SkinTE and future Polarity products. Our goal is not only to meet demand, but also to be able to deliver promptly around the globe when urgent response is needed."

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Novartis CAR-T Cell Therapy Receives FDA Breakthrough … – Pharmaceutical Processing

Posted: April 20, 2017 at 8:44 pm

Novartis CAR-T cell therapy CTL019 receives FDA Breakthrough Therapy designation for treatment of adult patients with r/r DLBCL.

Novartis announced that the U.S. Food and Drug Administration (FDA) has granted Breakthrough Therapy designation to CTL019, an investigational chimeric antigen receptor T cell (CAR-T) therapy, for the treatment of adult patients with relapsed and refractory (r/r) diffuse large B-cell lymphoma (DLBCL), who have failed two or more prior therapies.

This is the second indication for which CTL019 has received this designation; the first being for the treatment of r/r B-cell acute lymphoblastic leukemia (ALL) in pediatric and young adult patients.

"At Novartis, we are eager to unlock the full potential of CTL019, including the potential to help patients with r/r DLBCL," said Vas Narasimhan, Global Head of Drug Development and Chief Medical Officer, Novartis. "We look forward to working closely with the FDA to help bring this potential new treatment option to patients as soon as possible."

CAR-T cell therapy is different from typical small molecule or biologic therapies currently on the market because it is manufactured for each individual patient. During the treatment process, T cells are drawn from a patient's blood and reprogrammed in the laboratory to create T cells that are genetically coded to hunt the patient's cancer cells and other B-cells expressing a particular antigen.

CTL019 was first developed by the University of Pennsylvania (Penn). In 2012, Novartis and Penn entered into a global collaboration to further research, develop and then commercialize CAR-T cell therapies, including CTL019, for the investigational treatment of cancers. Through the collaboration, Novartis holds the worldwide rights to CARs developed with Penn for all cancer indications.

In March 2017, Novartis announced that the FDA accepted the company's Biologics License Application filing and granted priority review for CTL019 in the treatment of r/r pediatric and young adult patients with B-cell ALL.

The Breakthrough Therapy designation is based on data from the multi-center phase II JULIET study (NCT02445248), which is evaluating the efficacy and safety of CTL019 in adult patients with r/r DLBCL. JULIET is the second global CAR-T trial, following the Novartis ELIANA study (NCT02435849) investigating CTL019 in r/r B-cell ALL. Findings from JULIET are expected to be presented at an upcoming medical congress.

"We are encouraged by the FDA's recognition in the potential of CTL019 for this indication, which follows our promising studies of this therapy for ALL and the FDA filing by Novartis in pediatric and young adult ALL that received priority review," said the Penn team's leader, Carl June, M.D., director of the Center for Cellular Immunotherapies in the Perelman School of Medicine at the University of Pennsylvania. "Work with our collaborators at trial sites across the world is paving a path to bring personalized cell therapies to more patients with these devastating blood cancers."

According to FDA guidelines, treatments that receive Breakthrough Therapy designation are those that treat a serious or life threatening disease or condition and demonstrate a substantial improvement over existing therapies on one or more clinically significant endpoints based on preliminary clinical evidence. The designation also indicates that the agency will expedite the development and review of CTL019 in adults with r/r DLBCL.

This marks the 14thBreakthrough Therapy designation for Novartis since the FDA initiated the program in 2013, underscoring an emphasis to develop innovative treatments in disease areas with significant unmet need.

DLBCL is the most common form of lymphoma and accounts for approximately 30 percent of all non-Hodgkin lymphoma cases1. Ten to 15 percent of DLBCL patients fail to respond to initial therapy or relapse within three months of treatment, and an additional 20 to 25 percent relapse after initial response to therapy2.

Because CTL019 is an investigational therapy, the safety and efficacy profile has not yet been established. Access to investigational therapies is available only through carefully controlled and monitored clinical trials. These trials are designed to better understand the potential benefits and risks of the therapy. Because of the uncertainty of clinical trials, there is no guarantee that CTL019 will ever be commercially available anywhere in the world. ____________________________________________________

References:

1 American Society of Clinical Oncology. Lymphoma - Non-Hodgkin: Subtypes (Dec. 2016 revision).http://www.cancer.net/cancer-types/lymphoma-non-hodgkin/subtypes. Accessed March 2017.

2 Sehn, L. Paramount prognostic factors that guide therapeutic strategies in diffuse large B-cell lymphoma. Hematology, December 2012; 1; 402-409.

(Source: GlobeNewswire)

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Diabetes control tied to heart stent outcomes – WHTC

Posted: April 20, 2017 at 8:43 pm

Thursday, April 20, 2017 5:03 p.m. EDT

By Will Boggs MD

(Reuters Health) - For people with type 2 diabetes, maintaining good blood sugar control in the years after receiving a coronary artery stent is associated with a lower risk of heart attack and stroke, according to a recent study.

Although intensive glucose control had no benefit on the rate of major cardiovascular events in previous studies, our data suggest that strict glucose control after PCI (heart catheterization) can improve long-term clinical outcomes in diabetic patients, Dr. Joo-Yong Hahn from Samsung Medical Center in Seoul told Reuters Health.

Heart disease is the major cause of death among people with type 2 diabetes, Hahns team writes in Circulation: Cardiovascular Interventions. Although intensive blood sugar control is known to reduce damage to tiny blood vessels that are involved in many of the nerve and circulatory effects of diabetes, its not clear if the same is true for major arteries such as the ones that carry blood to the heart.

The researchers studied 980 patients with type 2 diabetes who had undergone percutaneous cardiac intervention (PCI) to clear a blocked coronary artery and place a supportive mesh tube known as a stent. Hahns team followed the patients health for up to seven years.

They looked at long-term blood sugar control using a measurement known as hemoglobin A1c (HbA1c or A1C), and used it to compare the patients risks of death, heart attack, repeat catheterizations and stroke over the study period.

The researchers defined good control as an A1C score below 7.0 and poor control as A1C of 7.0 or higher. Then they matched patients according to other risk factors and ended up with 322 pairs of patients for comparison.

In the overall group of 980 patients, the risk of all bad outcomes was 25 percent lower with good blood glucose control than with poor blood glucose control.

In the matched comparison, some 37 percent of patients with poor control had bad outcomes (heart attack, stroke, and so on) over the next seven years, versus less than 28 percent of patients with good control. Most of the difference in bad outcomes between the groups resulted from a higher rate of repeat stenting in the group with poor blood glucose control.

PCI is not the end of treatment for coronary artery disease, Hahn said by email. Optimal medical treatment, including glycemic control, is a cornerstone therapy after PCI, he said.

The effects of glucose control in type 2 diabetes may differ according to patient characteristics, such as recent cardiovascular events, baseline glycemic control status and duration of diabetes, Hahn added.

The researchers write that more study is needed before they can conclude strict glucose control after stenting will improve long-term clinical outcomes in people with diabetes.

Its important to underscore the message of good glycemic control, said Dr. Azfar G. Zaman from Newcastle University in the UK. He was not involved in the study but has done similar research. In patients with PCI there is evidence to support better outcomes and need for fewer interventions, Zaman said by email.

This is a single center study with limited numbers, but the findings support data from other studies, he noted.

SOURCE: http://bit.ly/2pjU0al Circulation: Cardiovascular Interventions, online April 3, 2017.

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Good 4 You: Mental fitness for diabetes – WOAI

Posted: April 20, 2017 at 8:43 pm

by Delaine Mathieu, News 4 San Antonio

Good 4 You: Mental fitness for diabetes

There's a unique new therapy group in San Antonio designed to help people living with diabetes cope with the disease. It's called Mental Fitness for Diabetes. The goal of the program is to help treat mental side-effects that come along with diabetes. "I remember when I was diagnosed with diabetes," said Sarah Villegas. "March 31 for 2016. So, it's been a year."

The 71-year-old registered nurse was completely surprised when she was diagnosed with type two diabetes. "When the doctor came in and showed me my lab results," she explained. "I looked at the paper and I said, are you kidding me?"

Villegas lost seventeen pounds and got her condition under control. When she heard about this new mental fitness group, she was pleasantly surprised. "Never in my 49 years as a registered nurse -- to combine diabetes, a major chronic illness with a major mental health illness, which is chronic, and put them together -- that is an awesome concept," she said.

Valerie Moczgemba, with Alamo Wellness Group, will be running the sessions. "A lot of times, people who have been diagnosed with diabetes experience depression anxiety," she said. "There also may be anger or irritability. She said they'll be focusing on disease management and how mental health symptoms play into disease management.

Villegas says it's high time a treatment like this is made available for people with diabetes. "It cannot be ignored," she said. "We need to address their physical health issues as well as the mental issues. They both go hand-in-hand."

April 30th is the last day to register. If you're interested in signing up, go to alamowellnessgroup.com.

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Researchers discover technique that could lead to diabetes cure – FOX 29

Posted: April 20, 2017 at 8:43 pm

by Zack Hedrick, Fox San Antonio

Researchers discover technique that could lead to diabetes cure

SAN ANTONIO Doctors in San Antonio have made a breakthrough discovery which could mean a potential cure for people with diabetes.

Tom Mathieu is a fanatical bike rider.

He believes he's pedaled more than 20,000 miles since he began riding in his early thirties.

He started riding because of a condition he was diagnosed with as a teenager.

Doctors told me it'd be a miracle that you see 60," said Mathieu.

Mathieu is a type 1 diabetic and his doctors tell him his body produces zero insulin.

He and his doctors believe his bike riding has helped keep his diabetes in check.

Well I'm 73 and I've had [diabetes] since I was 14," said Mathieu.

Researchers at UT Health San Antonio have discovered a strategy that could mean a cure.

It's a game changer, said Dr. Bruno Doiron. It change drastically the life of a patient that's diabetic."

Using a technique called gene transfer, doctors can alter other cells so they start to secrete insulin but only in response to sugar.

"Im using already what's naturally in your body," said Dr. Doiron.

The University Health System says diabetes is the 4th leading cause of death in Bexar County.

Mathieu calls the potential therapy revolutionary.

He says diabetes is a condition that requires discipline, but says this discovery would give a lot of freedom back to people dealing with diabetes.

People won't be burdened by what diabetes causes and then the cost of those causes, said Mathieu. I think it's miraculous."

Doctors say the therapy has cured diabetes in mice for one year without any side effects, which has never been done.

The goal is to conduct large-animal studies and human clinical trials in the next three to five years.

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Family members of diabetes patients plead for law to limit … – Las Vegas Review-Journal

Posted: April 20, 2017 at 8:43 pm

CARSON CITY Patients and family members of those who suffer from diabetes shared stories of struggle and heartbreak Wednesday and urged support for a bill to rein in the escalating costs of diabetes medication.

Bonnie Sedich knows the pain all too well. Four of her five children were diagnosed with juvenile diabetes. There was no family history. Two children died when in adulthood. Two others live with the disease.

One son, Jeffrey, was diagnosed at age 3. His body was found in a rural California region in 1981, a bottle of insulin by his side. He died at 19.

Another daughter, Elizabeth, was diagnosed when she was 8. She died in November at 51 of complications from the disease. Over the years, the cost of her drugs skyrocketed from about $10 a bottle to more than $300. Toward the end, she was paying more than $2,100 a month if she could afford it, Sedich said.

If you cant afford your diabetes medications then you just suffer and die, Sedich said.

She and others spoke at a press conference to urge support for Senate Bill 265. Sponsored by state Sen. Yvanna Cancela, D-Las Vegas, the bill would establish a list of insulin-related diabetic products to be treated as essential medications. It also would create a refund when insulin costs exceed the medical consumer price index.

The bill would require drug makers to divulge how prices are set, including the cost of medications, as well as amounts spent on marketing and research. It would set registration and reporting requirements on pharmaceutical sales representatives.

Diabetes is a serious disease that affects people for a lifetime, Cancela said. Medical costs are twice as high for people with diabetes.

Deadly and common

Diabetes is the eighth-leading cause of death in Nevada, where 12.4 percent of adults have the disease and 38 percent are pre-diabetic, she said.

Senate Majority Leader Aaron Ford, D-Las Vegas, is one of those who have been determined to be pre-diabetic. He said he received he diagnosis about a year ago.

Diabetes has become one of the largest public health crises in our time, and the medication to treat this disease must be affordable and accessible, he said. In this time of crisis, we have to come together.

Keyonna Lawrence said she was diagnosed as diabetic three years ago. A personal care assistant, she tries to control the disease through diet, and she stretches mediations when she can afford it by taking a half-dose.

My biggest fear is my 11-year-old son is going to wake up, say, Mom? and Moms as cold as ice, Lawrence said.

SB265 was granted an exemption and waiver from deadlines and remains pending in the Senate.

Contact Sandra Chereb at schereb@reviewjournal.com or 775-461-3821. Follow @SandraChereb on Twitter.

Sen. Yvanna Cancela, sponsor of Senate Bill 265, said diabetes care cost Nevadans about $2.4 billiion annually in medical costs.

Over the last 20 years, vials of the most commonn insulin products have gone from $17 to $138; and $21 to $255.

According to the American Diabetes Association, 281,355 people in Nevada, or 12.4 percent of the adult population, have diabetes. Another 787,000, or 38.5 percent of the adult population are pre-diabetic with blood glucose levels higher than normal.

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Is Annual Eye Exam a Must for Type 1 Diabetes? – WebMD

Posted: April 20, 2017 at 8:43 pm

By Alan Mozes

HealthDay Reporter

WEDNESDAY, April 19, 2017 (HealthDay News) -- People with type 1 diabetes face the risk of developing a disease that can cause blindness, so treatment guidelines have long called for annual eye exams.

But new research suggests this one-size-fits-all advice is costly and ineffective, because people with a low risk may need less-frequent screenings while people at high risk may need to be seen more often.

Diabetic retinopathy can damage the light-sensitive tissue at the back of the eye and trigger full vision loss, the researchers explained. Screening can catch this disease before irreparable damage is done, but not every person with diabetes faces the same risk.

"For example, patients with no or minimal eye changes and good blood sugar levels might not need their next examination for another four years," said study author Dr. David Nathan.

"On the other hand, if the patient already has developing eye disease and their blood sugar control has not been in the recommended range, they might need a repeat examination in as soon as three months," he added.

Nathan is the director of the Diabetes Center and Clinical Research Center at Massachusetts General Hospital, in Boston.

Current guidelines suggest getting an annual eye screening within three to five years of a type 1 diabetes diagnosis. People with type 1 diabetes cannot produce any insulin.

To assess that advice, the investigators focused on type 1 diabetics (aged 13 to 39) who had enrolled in a large, national diabetes trial between 1983 and 1989.

The latest analysis involved 24,000 eye exams conducted over 30 years among roughly 1,400 people with type 1 diabetes.

Retinal photographs were taken every six months until 1993, and then -- in a follow-up study -- once every four years until 2012. The study participants' vision, advanced retinopathy status and general diabetes history were tracked for an average of nearly 29 years.

The researchers determined that those participants who had an average blood sugar level of 6 percent, but no signs of retinopathy, could forgo the annual screening in favor of just one exam every four years. Similar people with mild retinopathy should be screened once every three years, the team concluded.

By contrast, those with severe or moderate retinopathy would do well to get screened every three to six months, respectively, the study authors reported.

People with higher blood sugar levels (8 to 10 percent) might also need to be screened more often, the researchers cautioned.

On average, the new recommendations for people with type 1 diabetes would likely cut the need for eye exams in half over a two-decade period. That would translate into an overall savings of $1 billion, while ensuring that those facing the highest risk got more timely treatment, the researchers said.

The findings were published in the April 20 issue of the New England Journal of Medicine.

Nathan described the results as "definitive." However, he said the jury is still out as to "whether the individualized frequency of eye examinations will be implemented by physicians" and followed by people with type 1 diabetes.

"The risk is that physicians may find it easier to schedule an annual eye examination compared with the new individualized schedule, which may be more difficult for physicians and patients to remember," he acknowledged.

"However, most physicians and ophthalmology offices use computer programs -- including reminder programs -- for scheduling, so we think that this potential barrier should not be a substantial obstacle," Nathan added.

Courtney Cochran, senior manager of media relations for the American Diabetes Association (ADA), noted that the ADA issued updated guidelines for retinopathy screenings in February.

The new recommendations now state that people with type 1 diabetes should start annual screenings within five years of their diabetes diagnosis. But those who remain free of retinopathy for a year or two may "consider" the option of less-frequent exams.

However, the ADA also said that if and when "any level" of retinopathy is detected, annual screenings are a must, while those with progressing retinopathy will require even more frequent screenings.

Dr. Jamie Rosenberg, who wrote an editorial that accompanied the study, suggested the new recommendations reflect "a trend toward reducing unnecessary screening for eye diseases."

"The upside to this new screening protocol would be significant money saved for the health care system, in addition to time saved for both patients and doctors," said Rosenberg, who is an associate professor of clinical ophthalmology and visual sciences at the Albert Einstein College of Medicine, in New York City.

Individualized schedules will make tracking patients more difficult, Rosenberg agreed. But, "this new screening protocol has great potential if adherence to the examination schedule could be assured."

WebMD News from HealthDay

SOURCES: David Nathan, M.D., director, Diabetes Center and Clinical Research Center, Massachusetts General Hospital, and professor, medicine, Harvard Medical School, Boston; Jamie Rosenberg, M.D., associate professor, clinical ophthalmology & visual sciences, and associate professor, clinical pediatrics, Albert Einstein College of Medicine, and attending physician, Montefiore Health System, New York City; Courtney Cochran, senior manager, media relations, American Diabetes Association; April 20, 2017, New England Journal of Medicine

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Young minds meet new technology at STEM-focused after-school program – USC News

Posted: April 19, 2017 at 6:44 pm

La Bella Saunders gasped as she steppedtoward the giant fuchsia nucleus floating in front of her. She giggled as she reached out toward two oblong, orange mitochondria and an electric blue ball of protein, then lowered her head to look through a small pore one of dozens of openings in the nucleus to spy the DNAinside.

Saunders, a fifth-grader at Foshay Learning Center near USCs University Park Campus, was exploring human biology using a virtual-reality headset that put her inside a cell.

The experience was part of a Young Scientists Program (YSP) after-school workshop on emerging technologies, held March 22 at the school. YSP is a STEM (science, technology, engineering and math) learning initiative hosted through theJoint Educational Project (JEP) of the USC Dornsife College of Letters, Arts and Sciences.

In addition to exploring virtual and augmented reality, the 25 fourth- and fifth-grade participants experienced 3-D printing and drones many for the first time.

We chose these three fields because they are key elements in todays newly emerging technologies, said JEP STEM Program Manager Dieuwertje DJ Kast, who organized the workshop.

I want to show the YSP students what is possible and introduce them to potential careers that could spring from what theyre learning about today, she said. I also want to help level the playing field by giving them the opportunity to get exposure to this technology now, while theyre young.

Students spent 20 minutes at differentstations learning aboutthe three emerging technologies. YSP teaching assistants were on hand to ensure the youngsters had fun while also understanding the underlying science.

At the 3-D printing station, students designed objects in a virtual space using the 3D Slash computer program. This gave them firsthand experience of how architects and engineers, who work with 3-D concepts, think and design. Thanks to local 3-D printing company Deezmakers, students were able to observe printers in action. They watchedintentlyas their teachers and YSP staff were scanned by the Deezmaker selfie setup, which printed out tiny 3-D models.

At the drone station, students sawprofessional drone pilot Roee Fung fly a selection of four quadcopter drones. They grinned for the camera as a tiny, remote control aircraft snapped aerial drone selfies of them as it hovered overhead.

After watching the aerial drones, 10-year-old Maurice Stepter focused on building a fan-driven drone car of his own using a plastic lunch box, wheels, a propeller and a tiny battery-driven motor. It was the fourth-graders first time attending a YSP event.

When I got here it was like, Whoa, this is cool, and that made me want to stay.

Maurice Stepter

Some teachers were encouraging me to come along today so I did, and when I got here it was like, Whoa, this is cool, and that made me want to stay, he said.

Four stations were dedicated to VRand augmented reality, including the Into the Cell experience, a VR project built by Smart Sparrow Inc. and presented by Jessica Swann and Joe Tamer from Arizona State Universitys Center for Education Through eXploration. Students also got to experience a virtual safari, a roller coaster ride and a dive to the depths of the ocean, thanks to WeLens, which donated 50 cardboard VR headsets for students to take home.

Students learned about erosion by playing with the Deezmakers augmented reality sandbox, which changes the color of sand according to its depth. That allowed YSP staff to explain topographical maps by giving students hands-on experience with creating their own landscapes.

At another station, YSP teaching assistant Michelle Huber, a senior majoring in environmental studies at USC Dornsife, was helping students create holograms by cutting and folding transparencies into a trapezoidal shape and placing them on top of a smartphone inside a black box. As the phone played a video of a blue jellyfish, the images were reflected in the trapezoid, creating a hologram.

Working with YSP helped Huber realize that she wants to pursue a career in teaching. I want to go into education because I have really enjoyed programs like this one that involve teaching young kids, she said.

Saunders was impressed with the YSP workshop.I learned all about cells and how drones can help save people by showing firefighters the places they need to put out fires, she said.

Kast emphasized the importance of YSP workshops in introducing students to STEM and helping them advance on the path that will allow them to turn their career dreams into reality.

These workshops are extremely valuable because they really show students whats possible, she said, whether that involves careers, experiences or opportunities.

Jasmine Tigolo, Saunders teacher at Foshay, agreed, saying she was delighted to be able to offer YSP to her students.

This is the sort of up-to-date technology they need to know in order to be able to compete in the outside world, she said, so exposing them to something while theyre this young is phenomenal.

More stories about: Community Outreach, Joint Educational Project, Virtual Reality

Experts and peers in their respective fields agree: These Trojans are changing the world.

With the help of USC undergrads, fourth- and fifth-graders take part in a skills-shaping event hosted by the Joint Educational Project.

Students learn to write code, design games and control robots at a computer science workshop.

The Joint Educational Project curriculum brings in a weatherman to talk with youngsters about meteorology.

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3D-printed Patch Can Help Mend a ‘Broken’ Heart – Technology Networks

Posted: April 19, 2017 at 6:43 pm


Technology Networks
3D-printed Patch Can Help Mend a 'Broken' Heart
Technology Networks
In this study, researchers from the University of Minnesota-Twin Cities, University of Wisconsin-Madison, and University of Alabama-Birmingham used laser-based 3D-bioprinting techniques to incorporate stem cells derived from adult human heart cells on ...

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