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Stem Cells: A Case for the Use of Human Embryos in Scientific Research
Posted: June 4, 2022 at 2:39 am
ABSTRACT
Embryonic stem cells have immense medical potential. While both their acquisition for and use in research are fraught with controversy, arguments against their usage are rebutted by showing that embryonic stem cells are not equivalent to human lives. It is then argued that not using human embryos is unethical. Finally, an alternative to embryonic stem cells is presented.
Embryonic stem cells have the potential to cure nearly every disease and condition known to humanity. Stem cells are natures Transformers. They are small cells that can regenerate indefinitely, waiting to transform into a specialized cell type such as a brain cell, heart cell or blood cell [1]. Most stem cells form during the earliest stages of human development, immediately when an embryo is formed. These cells, known as embryonic stem cells (ESCs), eventually develop into every single type of cell in the body. As the embryo develops, adult stem cells (ASCs) replace these all-powerful embryonic stem cells. ASCs can only become a number of different cells within their potency. This limited application means an adult mesenchymal stem cell cannot become a neural cell.
By harnessing the unique ability of embryonic stem cells to transform into functional cells, scientists can develop treatments for a number of diseases and injuries, according to the California Institute for Regenerative Medicine, a private organization which awards grants for stem cell research [1]. For example, scientists at the Cleveland Clinic converted ESCs into heart muscle cells and injected them into patients who suffered from heart attacks. The cells continued to grow and helped the patients hearts recover [2].
With this enormous potential to cure devastating diseases, including heart failure, spinal cord injuries and Alzheimers disease, governments and research organizations have the moral imperative to support and encourage embryonic stem cell research. President Barack Obama signed an executive order in 2009 loosening federal funding restrictions on stem cell research, saying, We will aim for America to lead the world in the discoveries it one day may yield. [3]. The National Institute of Health and seven state governments, including California, Maryland and New York, followed Obamas lead by creating programs that offered over $5 billion in funding and other incentives to scientists and research institutions for stem cell research [4].
Scientists believe that harnessing the capability of embryonic stem cells will unlock the cure for countless diseases. I am very excited about embryonic stem cells, said Dr. Dieter Egli, professor of developmental cell biology at Columbia University. They will lead to unprecedented discoveries that will transform life. I have no doubt about it. [5]. The results thus far are inspiring. In 2016, Kris Boesen, a 21-year-old college student from Bakersfield, California, suffered a severe spinal cord injury in a car accident that left him paralyzed from the neck down. In a clinical trial conducted by Dr. Charles Liu at the University of Southern California Keck School of Medicine, Boesen was injected with 10 million embryonic stem cells that transformed into nerve cells [6]. Three months after the treatment, Boesen regained the use of his arms and hands. He could brush his teeth, operate a motorized wheelchair, and live more independently. All Ive wanted from the beginning was a fighting chance, he said. The power of stem cells made his wish possible [6].
Embryonic stem cell treatments may also cure type 1 diabetes. Type 1 diabetes, which affects 42 million worldwide, is an autoimmune disorder that results in the destruction of insulin-producing beta cells found in the pancreas [7]. ViaCyte, a company in San Diego, California, is developing an implant that contains replacement beta cells originating from embryonic stem cells [7]. The implant will preserve or replace the original beta cells to protect them from the patients immune system [7]. The company believes that if successful, this strategy will effectively cure type 1 diabetes. Patients with the disease will no longer have to closely monitor their blood sugar levels and inject insulin [7]. ViaCyte projects that an experimental version of this implant will become available by 2020 [7].
Ultimately, scientists believe they will grow complex organs using stem cells within the next decade [8]. Over 115,000 people in the United States need a life-saving organ donation, and an average of 20 people die every day due to the lack of available organs for transplant, according to the American Transplant Foundation [9]. Three-dimensional printing of entire organs derived from stem cells holds the most promise for solving the organ shortage crisis [8]. Researchers at the University of California, San Diego have successfully printed part of a functional liver [8]. While the printed liver is not ready for transplant, it still performs the functions of a normal liver. This has helped scientists reduce the need for often cruel and unethical animal testing. The scientists expose drugs to the printed liver and observe how it reacts. The livers response closely mimics that of a human beings and no living animals are harmed in the process [8].
Research using embryonic stems cells provides an unprecedented understanding of human development and the potential to cure devastating diseases. However, stem cell research has generated controversy among religious organizations such as the Catholic Church as well as the pro-life movement [3]. That is because scientists harvest stem cells from embryos donated by fertility clinics. Opponents of embryonicstem cell research equate the destruction of an embryo to the murder of an innocent human being [10]. Pope Benedict XVI said that harvesting stem cells is not only devoid of the light of God but is also devoid of humanity [3]. However, this view does not reflect a reasonable understanding and interpretation of basic biology. Researchers typically harvest embryonic stem cells from an embryo five days after fertilization [1]. At this stage, the entire embryo consists of less than 250 cells, smaller than the tip of a pin. Of these cells, only 30 are embryonic stem cells, which cannot perform any human function [11]. For comparison, an adult has more than 72 trillion cells, each with a specialized function [3]. Therefore, this microscopic blob of cells in no way represents human life.
With no functional cells, there exist no characteristics of a human being. Fundamentalist Christians believe that the presence or absence of a heartbeat signifies the beginning and end of a human life [10]. However, at this stage there is no heart, not even a single heart cell [10]. Some contend that brain activity, or the ability to feel, defines a human being. Michael Gazzaniga, president of the Cognitive Neuroscience Institute at the University of California, Santa Barbara, explains in his book,The Ethical Brain,that the fertilized egg is a clump of cells with no brain. [12]. There is no brain nor nerve cells that could allow this cellular object to interact with its environment [12]. The only uniquely human feature of embryonic cells at this stage is that they contain human DNA. This means that a 5-day-old human embryo is effectively no different than the Petri dishes of human cells that have grown in laboratories for decades with no controversy or opposition. Therefore, if the cluster of cells in the earliest stage of a human embryo is considered a human life, a growing plate of skin cells must also be considered human life. Few would claim that a Petri dish of human cells is morally equivalent to a living human or any other animal. Why, then, would a microscopic collection of embryonic cells have the same moral status as an adult human?
The status of the human embryo comes from itspotentialto turn into a fully grown human being. However, the potential of this entity to become an individual does not logically mean that it has the same status as an individual who can think and feel. If this were true, virtually every cell grown in a laboratory would be subject to the same controversy. This is because scientists have developed technology to convert an ordinary cell such as a skin cell into an embryo [10]. Although this requires a laboratory with special conditions, the normal development of a human being also requires special conditions in the womb of the mother. Therefore, almost any cell could be considered a potential individual, so it is illogical to conclude that a cluster of embryonic cells deserves a higher moral status.
Hundreds of thousands of embryos are destroyed each year in a process known as in vitro fertilization (IVF), a popular procedure that helps couples have children [13]. Society has an ethical obligation to use these discarded embryos to make medical advancements rather than simply throw them in the trash for misguided ideological and religious reasons as opponents of embryonic stem cell research desire.
With IVF, a fertility clinician harvests sperm and egg cells from the parents and creates an embryo in a laboratory before implanting it in the womans womb. However, creating and implanting a single embryo is expensive and often leads to unsuccessful implantation. Instead, the clinician typically creates an average of seven embryos and selects the healthiest few to implant [13].
This leaves several unused embryos for every one implanted. The couple can pay a fee to preserve the unused embryos by freezing them or can donate them to another family. Otherwise, they are slated for destruction [14]. A 2011 study in the Journal of the American Society for Reproductive Medicine found that 19 percent of the unused embryos are discarded and only 3 percent are donated for scientific research [14]. Many of these embryos could never grow into a living person given the chance because they are not healthy enough to survive past early stages of development [14]. If a human embryo is already destined for destruction or has no chance of survival, scientists have the ethical imperative to use these embryos to research and develop medical treatments that could save lives. The modern version of the Hippocratic oath states, I will apply, for the benefit of the sick, all measures which are required [to heal] [10]. Republican Senator Orrin Hatch of Utah supports the pro-life movement, which recognizes early embryos as human individuals. However, even he favors using the leftover embryos for the greater good. The morality of the situation dictates that these embryos, which are routinely discarded, be used to improve and save lives. The tragedy would be in not using these embryos to save lives when the alternative is that they would be discarded. [3]
Although scientists have used embryonic stem cells (ESCs) for promising treatments, they are not ideal, and scientists hope to eliminate the need for them. Primarily, ESCs come from an embryo with different DNA than the patient who will receive the treatment, meaning they are not autologous. ESCs are not necessarily compatible with everyone and could cause the immune system to reject the treatment [11]. The most promising alternative to ESCs are known as induced pluripotent stem cells. In 2008, scientists discovered a way to reprogram human skin cells to embryonic stem cells [15]. Scientists easily obtained these cells from a patients skin, converted them into the desired cell type, then transplanted them into the diseased organ without risk of immune rejection [15]. This eliminates any ethical concerns because no embryos are harvested or destroyed in the process. However, induced stem cells have their own risks. Recent studies have shown that they can begin growing out of control and turn into cancer [3]. Several of the first clinical trials with induced stem cells, including one aimed at curing blindness by regenerating a patients retinal cells, were halted because potentially cancerous mutations were detected [3].
Scientists believe that induced stem cells created in a laboratory will one day completely replace embryonic stem cells harvested from human embryos. However, the only way to create perfect replicas of ESCs is to thoroughly understand their structure and function. Scientists still do not completely understand how ESCs work. Why does a stem cell sometimes become a nerve cell, sometimes become a heart cell and other times regenerate to produce another stem cell? How can we tell a stem cell what type of cell to become? To develop a viable alternative to ESCs, scientists must first answer these questions with experiments on ESCs from human embryos. Therefore, extensive embryonic stem cell research today will eliminate the need for embryonic stem cells in the future.
The Biomedical Engineering Society Code of Ethics calls upon engineers to use their knowledge, skills, and abilities to enhance the safety, health and welfare of the public. [16] Stem cell research epitomizes this. Stem cells hold the cure for numerous diseases ranging from spinal cord injuries to organ failure and have the potential to transform modern medicine. Therefore, the donation of human embryos to scientific research falls within most conventional ethical frameworks and should be allowed with minimal restriction.
Because of widespread ignorance about the science behind stem cells, ill-informed opposition has prevented scientists from receiving the funding and support they need to save millions of lives. For example, George W. Bushs religious opposition to stem cell research resulted in a 2001 law severely limiting government funding for such research [3]. Although most opponents of stem cell research compare the destruction of a human embryo to the death of a living human, the biology of these early embryos is no more human than a plate of skin cells in a laboratory. Additionally, all embryos sacrificed for scientific research would otherwise be discarded and provide no benefit to society. If society better understood the process and potential of embryonic stem cell research, more people would surely support it.
Within the next decade, stem cells will likely provide simple cures for diseases that are currently untreatable, such as Alzheimers disease and organ failure [1]. As long as scientists receive support for embryonic stem cell research, stem cell therapies will become commonplace in clinics and hospitals around the world. Ultimately, the fate of this new medical technology lies in the hands of the public, who must support propositions that will continue to allow and expand the impact of embryonic stem cell research.
By Jonathan Sussman, Viterbi School of Engineering, University of Southern California
At the time of writing this paper, Jonathan Sussman was a senior at the University of Southern California studying biomedical engineering with an emphasis in biochemistry. He was an undergraduate research assistant in the Graham Lab investigating proteomics of cancer cells and was planning to attend an MD/PhD program.
[1] Stem Cell Information,Stem Cell Basics, 2016. [Online]. Available at:https://stemcells.nih.gov/info/basics/3.htm%5BAccessed 11 Oct. 2018].
[2] Cleveland Clinic, Stem Cell Therapy for Heart Disease | Cleveland Clinic, 2017. [Online]. Available at:https://my.clevelandclinic.org/health/diseases/17508-stem-cell-therapy-for-heart-disease%5BAccessed 14 Oct. 2018].
[3] B. Lo and L. Parham, Ethical Issues in Stem Cell Research,Endocrine Reviews, 30(3), pp.204-213, 2009.
[4] G. Gugliotta,Why Many States Now Have Stem Cell Research Programs, 2015. [Online]. Available at:http://www.governing.com/topics/health-human-services/last-decades-culture-wars-drove-some-states-to-fund-stem-cell-research.html%5BAccessed 14 Oct. 2018].
[5] D. Cyranoski,How human embryonic stem cells sparked a revolution,Nature Journal, 2018. [Online]. Available at:https://www.nature.com/articles/d41586-018-03268-4%5BAccessed 11 Oct. 2018].
[6] K. McCormack,Young man with spinal cord injury regains use of hands and arms after stem cell therapy, The Stem Cellar, 2016. [Online]. Available at:https://blog.cirm.ca.gov/2016/09/07/young-man-with-spinal-cord-injury-regains-use-of-hands-and-arms-after-stem-cell-therapy/%5BAccessed 11 Oct. 2018].
[7] A. Coghlan,First implants derived from stem cells to cure type 1 diabetes,New Scientist, 2017. [Online]. Available at:https://www.newscientist.com/article/2142976-first-implants-derived-from-stem-cells-to-cure-type-1-diabetes/%5BAccessed 11 Oct. 2018].
[8] C. Scott,University of California San Diegos 3D Printed Liver Tissue May Be the Closest Weve Gotten to a Real Printed Liver,3DPrint.com | The Voice of 3D Printing / Additive Manufacturing, 2018. [Online]. Available at:https://3dprint.com/118932/uc-san-diego-3d-printed-liver/%5BAccessed 11 Oct. 2018].
[9] American Transplant Foundation,Facts and Myths about Transplant. [Online]. Available at:https://www.americantransplantfoundation.org/about-transplant/facts-and-myths/%5BAccessed 11 Oct. 2018].
[10] A. Siegel, Ethics of Stem Cell Research,Stanford Encyclopedia of Philosophy, 2013. [Online]. Available at:https://plato.stanford.edu/entries/stem-cells/%5BAccessed 11 Oct. 2018].
[11] I. Hyun,Stem Cells The Hastings Center,The Hastings Center, 2018. [Online]. Available at:https://www.thehastingscenter.org/briefingbook/stem-cells/%5BAccessed 11 Oct. 2018].
[12] M. Gazzaniga,The Ethical Brain,New York: Harper Perennial, 2006.
[13] M. Bilger,Shocking Report Shows 2.5 Million Human Beings Created for IVF Have Been Killed | LifeNews.com,LifeNews, 2016. [Online]. Available at:https://www.lifenews.com/2016/12/06/shocking-report-shows-2-5-million-human-beings-created-for-ivf-have-been-killed/%5BAccessed 11 Oct. 2018].
[14] Harvard Gazette, Stem cell lines created from discarded IVF embryos, 2008. [Online]. Available at:https://news.harvard.edu/gazette/story/2008/01/stem-cell-lines-created-from-discarded-ivf-embryos/%5BAccessed 11 Oct. 2018].
[15] K. Murray,Could we make babies from only skin cells?, CNN, 2017. [Online]. Available at:https://www.cnn.com/2017/02/09/health/embryo-skin-cell-ivg/index.html%5BAccessed 11 Oct. 2018].
[16] Biomedical Engineering Society,Biomedical Engineering Society Code of Ethics, 2004. [Online]. Available at:https://www.bmes.org/files/CodeEthics04.pdf%5BAccessed 11 Oct. 2018].
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Stem Cells: A Case for the Use of Human Embryos in Scientific Research
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Regenerative Medicine Market To Grow At A CAGR Of 11.27% By 2027, Due To Advancements In Cell Biology, Genomics Research, And Gene-Editing Technology…
Posted: June 4, 2022 at 2:39 am
According to a new report published by Grand View Research, Recent advancements in biological therapies have resulted in a gradual shift in preference toward personalized medicinal strategies over the conventional treatment approach. This has resulted in rising R&D activities in the regenerative medicine arena for the development of novel regenerative therapies.
Regenerative Medicine Industry Overview
The global regenerative medicine market size was valued at USD 27.29 billion in 2020 and is expected to reach USD 57.08 billion by 2027, growing at a CAGR of 11.27% over the forecast period. The emergence of gene therapy coupled with the developments in stem cell and tissue engineering are expected to fuel the market growth. In addition, increasing regulatory approvals for advanced therapy medicinal products have propelled the market growth. The ongoing COVID-19 pandemic created lucrative opportunities for the operating players owing to the urgent need for the development of new therapies against SARS-COV-2. Several initiatives are being implemented in the cell and gene therapy manufacturing industry, including the T-cell therapy space.
For instance, based on the previous research insights, Singapore-based Duke-NUS medical schools emerging infectious diseases research program demonstrated the utility of these immunotherapies in treating patients with COVID-19 infection. The presence of several programs and continuous investments by government and private agencies to support R&D also accelerate the industrys progress. Like National Institutes of Health (NIH) supports the scientific research community through NIH Regenerative Medicine Program, NIH Stem Cell Libraries & Projects, NIH Stem Cell Unit, and others. Similarly, initiatives adopted by market players to raise finance for the R&D of regenerative medicine support the market progression.
Gather more insights about the market drivers, restrains and growth of the Global Regenerative Medicine market
In addition, companies are collaborating to strengthen their R&D capabilities to develop and commercialize innovative therapies to ensure their availability to their customers locally or worldwide. For instance, in July 2021, Pharming Group N.V. and Orchard Therapeutics collaborated for the development and commercialization of OTL-105, an investigational ex vivo autologous Hematopoietic Stem Cell (HSC) gene therapy for the treatment of Hereditary Angioedema (HAE).
Moreover, technological advancements in stem cell-based therapies have revolutionized the perspective of researchers toward regenerative medicine. Advances in stem cell therapy have accelerated the developments in regenerative medicine. For instance, haematogenic stem cells currently are being used to treat leukemia and blood disorders. Also, nanotechnology is a powerful tool for engineering stem cells and regenerative medicine. With the introduction of new technology, nanofabrication techniques can now allow researchers to develop nanofiber scaffolds.
Regenerative Medicine Market Segmentation
Based on the Product Insights, the market is segmented into Therapeutics, Tools, Banks, and Services.
Based on the Therapeutic Category Insights, the market is segmented into Dermatology, Musculoskeletal, Immunology & Inflammation, Oncology, Cardiovascular, Ophthalmology, and Others.
Based on the Regenerative Medicine Regional Insights, the market is segmented into North America, Europe, Asia Pacific, Latin America, and Middle East & Africa.
Market Share Insights:
Key Companies Profile:
Key companies invest heavily in the development of regenerative therapies to meet the demand for unmet clinical needs. The market is highly competitive as the companies are focusing on the introduction of therapies for oncology & age-related degenerative disorders.
Some of the prominent companies in the global regenerative medicine market are:
Order a free sample PDF of the Regenerative Medicine Market Intelligence Study, published by Grand View Research.
About Grand View Research
Grand View Research is a full-time market research and consulting company registered in San Francisco, California. The company fully offers market reports, both customized and syndicates, based on intense data analysis. It also offers consulting services to business communities and academic institutions and helps them understand the global and business scenario to a significant extent. The company operates across multitude of domains such as Chemicals, Materials, Food and Beverages, Consumer Goods, Healthcare, and Information Technology to offer consulting services.
Web: https://www.grandviewresearch.com
Media ContactCompany Name: Grand View Research, Inc.Contact Person: Sherry James, Corporate Sales Specialist U.S.A.Email: Send EmailPhone: 1888202951Address:Grand View Research, Inc. 201 Spear Street 1100 San Francisco, CA 94105, United StatesCity: San FranciscoState: CaliforniaCountry: United StatesWebsite: https://www.grandviewresearch.com/industry-analysis/regenerative-medicine-market
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Top Beverly Hills Plastic Surgeon, Dr. John Anastasatos, Explores Cell-Assisted Lipotransfer (CAL) with Breast Augmentation in New Publication -…
Posted: June 4, 2022 at 2:39 am
The article titled "Cell-Assisted Lipotransfer in Breast Augmentation Surgery: Clinical Outcomes and Considerations for Future Research" was recently published on the Cureus medical site.
LOS ANGELES, June 3, 2022 /PRNewswire-PRWeb/ -- Dr. John Anastasatos is a well-respected, board-certified plastic surgeon in Beverly Hills, CA, who recently co-authored the peer-reviewed article titled, "Cell-Assisted Lipotransfer in Breast Augmentation Surgery: Clinical Outcomes and Considerations for Future Research," which was published on March 2, 2022. Autologous fat transfer is a widely used surgical technique for breast augmentation surgery, but it has been associated with various complications, including post-surgical fat resorption. In the article, Dr. Anastasatos contributes his knowledge on state-of-the-art methods used to harvest, process, optimize and utilize fat for breast augmentation and reconstruction purposes and techniques to optimize fat grafting longevity and increase survival of the fat where it is placed. Dr. Anastasatos' study explores a novel technique, referred to as cell-assisted lipotransfer, or CAL, and how it has shown promising results in terms of reducing fat resorption. The informative article explores the ways in which cell-assisted lipotransfer is different from the autologous fat transfer, as well as how and why adipose-derived stem cells may contribute towards limiting fat resorption.
Link to Article: Cureus | Cell-Assisted Lipotransfer in Breast Augmentation Surgery: Clinical Outcomes and Considerations for Future Research
"Our study determined that CAL may still be a new technique, but its promising results, through the prism of multiple isolation systems, highlight the great potential for use in clinical practice," says Dr. John Anastasatos.
More about Dr. John Anastasatos:
At Los Angeles Plastic Surgery, Dr. John Anastasatos is highly regarded for his extraordinary skill in cosmetic, reconstructive, and revision procedures, including gold-standard facelifts, breast augmentations, body lift procedures, liposuction and non-surgical treatments. Raised in the United States but with family roots in Athens, Greece, Dr. Anastasatos attended Brown University and was accepted to their medical school. He then completed general surgical training at Columbia-Presbyterian Hospital, an affiliate of Columbia University. After finishing his cosmetic and reconstructive residency at the University of Alabama, Birmingham, he completed a fellowship in hand surgery, upper extremity, and microsurgery. During this time, Dr. Anastasatos served as an attending surgeon at UAB Hospitals, The Children's Hospital, and VA Hospital. He established his own practice in Southern California in 2007 and opened a second location in Athens, Greece. To schedule a consultation with Dr. John Anastasatos or for more information about his practice locations in Beverly Hills, CA, or Athens, Greece, please call (310) 888-4048, or visit his website http://www.LosAngelesPlasticSurgery.com.
Media Contact
Dr. John Anastasatos, Los Angeles Plastic Surgery, (310) 888-4048, drjohnanastasatos@gmail.com
SOURCE Los Angeles Plastic Surgery
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Top Beverly Hills Plastic Surgeon, Dr. John Anastasatos, Explores Cell-Assisted Lipotransfer (CAL) with Breast Augmentation in New Publication -...
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Graduate Theses and Dissertations – University of Arkansas
Posted: June 4, 2022 at 2:35 am
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Graduate Theses and Dissertations - University of Arkansas
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First Clinical Trial of Transplanted 3D Ear Using Human Cells Proves Successful via 3DBio Therapeutics – Tech Times
Posted: June 4, 2022 at 2:33 am
Leading experts among 3D printing manufacturers and regenerative medicine company 3DBio Therapeutics have successfully performed a clinical trial of transplanting a 20-year-old female's ear utilizing a 3D-printed iteration made from the same female's cells.
The doctors involved relayed key details surrounding the trial amid a press release, yet had to refrain from fully unearthing all of the secrets behind their efforts with the so-called AuriNovo ear due to proprietary concerns.
The woman treated with the 3D-printed ear implant suffered from a rare genetic birth deformity, called microtia, which either causes one or both ears to not grow at all or grow in an underdeveloped manner.
Nearly 1,500 US children are born with the condition, thus spurring 3DBio Therapeutics to enact a clinical trial involving so far a total of 11 participants with their AuriNovo ear implant.
The 3D printed ear implant relies on the client's own tissue to replace their deformed or missing ear. Usually, such patients suffering from microtia accept grafts taken from their ribs or alternative synthetic materials, but 3DBio Therapeutics does it vastly differently, as the tissue engineering and regenerative medicine company instead opts to leverage the patient's cartilage cells from the existing ear following a biopsy.
Related Article:Pig Heart Transplant Patient Dies, Cause of Death Unknown-Xenotransplantation Not Yet Effective?
From there, the team takes the cells and grows them via 3D printing technology, shaping the newly-formed product into the patient's ear.
Utilizing the patient's own cells ensures that the AuriNovo ear will be less likely to be rejected from the client. Plus, over time, the new appendage will continue regenerating throughout that particular patient's life.
"This is truly a historic moment for patients with microtia, and more broadly, for the regenerative medicine field as we are beginning to demonstrate the real-world application of next-generation tissue engineering technology," says Chief Executive Officer and co-founder of 3DBio Therapeutics, Daniel Cohen, within the press release. "It is the culmination of more than seven years of our company's focused efforts to develop a uniquely differentiated technology platform meeting the FDA's requirements for therapeutic manufacturing of reconstructive implants."
Similar advancements in the fields of tissue engineering and regenerative medicine have proven to witness astounding growth, evidenced best via a heart transplant initiated in early January of this year, wherein the patient was given a pig heart as substitute for their muscular organ.
Unfortunately, the patient would later die due to a viral pig infection, but does lend credence to the potential of 3D printed heart transplants, and continued tissue engineering efforts in line with stem cell research.
The groundbreaking achievement provided via 3DBio Therapeutics was documented in a New York Times feature, wherein both doctors voiced even more information surrounding their 3D printed ear transplant.
Of those involved in the procedure, San Antonia's pediatric ear reconstructive surgeon Dr. Arturo Bonilla offered the most heartwarming of all considerations on the future of the AuriNovo project:
"This is so exciting, sometimes I have to temper myself a little bit. If everything goes as planned, this will revolutionize the way this is done."
Read Also:Scientists Successfully 3D Print Human Corneas; This Breakthrough Can Be the Solution for Transplant Shortage
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How Protein Nanoparticle Vaccines Have The Potential To Be Developed Into ‘Safer’ Covid-19 Vaccines: Study – ABP Live
Posted: June 4, 2022 at 2:30 am
New Delhi: A nanoparticle vaccine which combines two proteins that induce immune responses against SARS-CoV-2 has the potential to be developed into 'broader' and 'safe' Covid-19 vaccines, according to a new study.
The Covid-19 pandemic, or the SARS-CoV-2 pandemic, has claimed more than six million deaths since 2019, and is a public health burden worldwide. The rapid evolution of SARS-CoV-2 is characterised by the emergence of several significant variants, including Delta and Omicron.
The study, led by researchers in the Institute for Biomedical Sciences at Georgia State University, was recently published in the journal Small.
A nanoparticle-based vaccine is one in which the receptor-binding domain (RBD), which is a part of the spike protein of SARS-CoV-2, is attached to a protein designed to form nanometre-sized protein particles, or nanoparticles, according to a study by the US National Institutes of Health (NIH), which was published in the journal, Nature. SARS-CoV-2 attaches itself to cells using the spike protein.
These nanoparticles could be composed of lipids, metal and non-metal inorganics, several polymers, and virus-like particles which have been tested for research, according to a study published by the National Center for Biotechnology Information (NCBI), NIH. Virus-like-particles (VLP) are self-assembling nanoparticles lacking infectious nucleic acid.
Hyderabad-based Serum Institute of India's Covovax is a nanoparticle-based vaccine, manufactured by technology transfer from Novavax.
The spike protein (S) on SARS-CoV-2 is the preferred target antigen for vaccine development, based on its essential function and neutralising epitopes to combat the virus. An epitope is the part of an antigen molecule to which an antibody attaches itself.
The new study was conducted in mice, with the researchers investigating the immune response induced by two proteins, the spike protein and the relatively conserved stem subunit (S2) of the spike protein. The researchers found that the assembly of the two proteins into double-layered protein nanoparticles improves the immunogenicity of the proteins. Immunogenicity is defined as the ability of a molecule or substance to provoke an immune response.
In a statement released by Georgia State University, Dr Baozhong Wang, senior author of the study, said the entire S protein has been used as the major antigen in vaccines against the ongoing pandemic, adding that as the number of infections continues to rise, more and more variants have appeared and supplanted the ancestral virus.
Since the variants have superseded and replaced the ancestral virus, the efficacy and protection of current vaccines are under constant threat and need continuous improvement, Wang explained.
He further said that in contrast, the stem subunit of the spike protein is more conserved and has fewer mutations across lineages. He added that the stem could induce effective antibody neutralisation and vigorous antibody-dependent cellular cytotoxicity (ADCC) activity against multiple variants of S protein. ADCC, also known as antibody-dependent cell-mediated cytotoxicity, is a type of immune reaction in which a target cell or microbe is coated with antibodies and killed by certain types of white blood cells.
Wang explained that the work shows that the stabilised stem subunit could be a potential antigen for a SARS-CoV-2 universal vaccine against unpredictable variants.
According to the study, immunisation with the stem-induced balanced Immunoglobulin G (IgG) antibodies occurred through potent and broad ADCC activity, which is a type of immune reaction on which infected cells are coated with antibodies that recruit certain types of white blood cells to kill the infected cells. The study also found that the double-layered protein nanoparticles constructed from the stem and the full-length spike protein induced more robust ADCC and neutralising antibodies than the stem and spike protein, respectively.
The nanoparticles were observed to produce more potent and balanced serum IgG antibodies than the corresponding soluble protein mixture. The researchers also found that the immune responses are sustained for at least four months after the immunisation.
The stem induces a more balanced IgG isotype antibody. In immunology, antibodies or immunoglobulins are classified into several types called isotopes or classes. The double-layered nanoparticles not only have a more balanced IgG isotype antibody induced by the stem, but also long-lasting immune responses, and excellent safety profiles. As a result, the nanoparticles have the potential to be developed into broader SARS-CoV-2 vaccines, the authors noted in the study.
Dr Yao Ma, the first author of the study, said the stabilised, conserved S2 stem subunit demonstrated its potential as a universal SARS-CoV-2 vaccine candidate against unpredictable variants. The double-layered protein nanoparticles incorporating the full-length spike protein and the S2 stem induced robust and long-term immune responses, and exhibited a safety profile in the primary studies, Ma added. This provides an option for current SARS-CoV-2 vaccine development.
Ma further said that the pandemic is far from over, and new variants continue to emerge and pose a massive threat to human health. In order to avoid another pandemic with an unpredictable new variant, the updating of vaccines needs to keep pace with the times.
Nanoparticles help improve vaccine efficacy, by targeting desired antigen-presenting cells to improve immunisation strategies. They protect the antigen (foreign particle) from early proteolytic degradation (degradation of protein by hydrolytic enzymes), control antigen release, and facilitate antigen uptake.
Current vaccines cause cells in the body to make a version of the spike protein to elicit an immune response. Putting multiple copies of the RBD on nanoparticles enhances immune response, recent studies have found. The NIH researchers tested nanoparticle-based vaccines in monkeys and found that most of the monkeys had no virus in their lower respiratory tracts two days after exposure.
Nanoparticle-based vaccines contain a strand of genetic code that provides instructions for building a version of the spike protein, according to an article by the University of Pittsburgh Medical Center, US. Host cells build the protein when they see the genetic code.
The immune system begins building antibodies against the protein, which help the immune system fight the coronavirus. The body builds up an army of antibodies, which can fight off a Covid-19 infection before it causes disease.
Since mRNA is very fragile on its own, it would degrade in the body if it is injected simply as a strand. Hence, the genetic material is protected with a nanoparticle, which preserves the mRNA long enough to carry it into the bodys cells so that they can begin making the proteins.
The use of nanoparticles in vaccine formulations allows not only improved antigen stability and immunogenicity, but also targeted delivery and slow release, according to a article published in the journal, Elsevier.
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Pancreatic Cancer Therapy Experiment Saves Woman; Is It A Breakthrough? – Kaiser Health News
Posted: June 4, 2022 at 2:28 am
Researchers point out that another pancreatic cancer patient who received the same therapy did not respond to the treatment and died. But the highly personalized immunotherapy is being called "an important step along the way to devising treatments that might help lung, colon, and other cancers.
The New York Times:Reprogrammed Cells Attack And Tame Pancreatic Cancer In One WomanResearchers have managed to tame pancreatic cancer in a woman whose cancer was far advanced and after other forms of treatment had failed. The experiment that helped her is complex and highly personalized and is not immediately applicable to most cancer patients. Another pancreatic cancer patient, who received the same treatment, did not respond and died of her disease. Nonetheless, a leading journal The New England Journal of Medicine published a report of the study on Wednesday. (Kolata, 6/1)
AP:Novel Genetic Experiment Shrinks Tough-To-Treat CancerIn a novel experiment, a woman with advanced pancreatic cancer saw her tumors dramatically shrink after researchers in Oregon turbocharged her own immune cells, highlighting a possible new way to someday treat a variety of cancers. Kathy Wilkes isnt cured but said whats left of her cancer has shown no sign of growth since the one-time treatment last June. I knew that regular chemotherapy would not save my life and I was going for the save, said Wilkes, of Ormond Beach, Florida, who tracked down a scientist thousands of miles away and asked that he attempt the experiment. (Neergaard, 6/1)
KGW8:Portland Doctors 'First In World' To Apply New Cancer TherapyDoctors at the Providence Cancer Institute (PCI) in Portland are celebrating the successful application of a new immunotherapy to drastically reduce a patient's tumor size. ... With this single-patient success story, Dr. Eric Tran, with Earle A. Chiles Research Institute, and Providence oncologist Dr. Rom Leidner plan to expand trials to treat 24 more patients over the next two to three years. They noted similar efforts have not always been successful. (Ettlin, 6/1)
Also
Stat:How Companies Are Responding To Cancer Immunotherapy ShortageThe shortage of manufacturing slots for CAR-T cells, which has left myeloma patients dying on a wait list, came as a surprise to drugmakers and clinicians alike. When the Food and Drug Administration approved the first myeloma CAR-T product from Bristol Myers Squibb in spring of 2021, there were already four other lymphoma and leukemia CAR-T therapies on the market. Those werent facing severe supply constraints so people hadnt expected there to be issues supplying ide-cel, Bristols myeloma CAR-T, said Yi Lin, the director of the cell therapy program at the Mayo Clinic. But after the approval, the demand quickly overwhelmed Bristols ability to create CAR-T for myeloma and supply chain issues during the pandemic made it more difficult to ramp up production. (Chen, 6/2)
Stat:'How Do You Decide?' Cancer Patients Die Waiting For CAR-T TherapyWithin two years of being diagnosed with multiple myeloma, Shawn Goltzene had blasted through nearly all his options. An initial stem cell transplant couldnt hold off the cancer for more than half a year. With each new therapy his doctors tried, the cancer would surge out of remission within weeks striking the bones in his back and legs. We hit him with everything, the whole kitchen sink, said Krina Patel, the director of the myeloma cell therapy program at MD Anderson Cancer Center and Goltzenes clinician. She tried putting him on a clinical trial for an immunotherapy drug. It blew right through him. He quickly got to fourth-line therapy. (Chen, 6/2)
Austin American-Statesman:Dell Medical School Trying To End Desert In Austin Bladder Cancer CareDorothy De La Garza had frequent urinary tract infections. Then she was told she had "an overactive bladder." "Everyone assumes a woman is leaking because she's old," the 78-year-old from Austin said. After years of being on antibiotics on and off, and going to both a urologist and her primary care doctor for the same symptoms, De La Garza was diagnosed with bladder cancer in 2016."Bladder cancer is sneaky," she said.(Villalpando, 5/31)
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Global Human Embryonic Stem Cell Market To Be Driven By The Rapid Technological Advancements In The Forecast Period Of 2022-2027 The Greater…
Posted: June 4, 2022 at 2:28 am
The new report by Expert Market Research titled, GlobalHuman Embryonic Stem Cell MarketReport and Forecast 2022-2027, gives an in-depth analysis of the global human embryonic stem cell market, assessing the market based on its segments like applications and major regions. The report tracks the latest trends in the industry and studies their impact on the overall market. It also assesses the market dynamics, covering the key demand and price indicators, along with analysing the market based on the SWOT and Porters Five Forces models.
Get a Free Sample Report with Table of Contents: https://bit.ly/3M9nlum
The key highlights of the report include:
Market Overview (2017-2027)
Historical Market Size (2020): USD 0.7 billion Forecast CAGR (2022-2027): 10%
The human embryonic stem cell market is being driven by the thriving medical sector. The rising demand for embryonic stem cells can be attributed to the increasing prevalence of chronic diseases around the world owing to the rising adoption of unhealthy and sedentary lifestyle among the youth and middle-class population. The increased risk of premature death as a result of chronic diseases is a growing concern. Therefore, human embryonic stem cells are gaining popularity in the medical sector. Furthermore, the increase in research grants and private as well as public funding for the development of effective and safe stem cell therapy products is further aiding the market growth. The rising investments from key players towards enhancing human embryonic cell therapy is expected to aid the market growth in the forecast period. In post-COVID days, as the various sectors recover from the negative impacts of the pandemic, human embryonic stem cells are likely to witness a rise in demand.
Industry Definition and Major Segments
Human embryonic stem cells, also known as human embryonic stem cells are self-replicating cells derived from human fetal tissue or human embryos that develop into tissues and cells of 3 primary layers. Furthermore, human embryonic stem cells are pluripotent and are roughly 3-5 days old. It is highly versatile, as it may split into new stem cells and even transform into any type of cell in the human body, allowing it to regenerate or repair any diseased organ or tissue.
Read Full Report with Table of Contents: https://bit.ly/3x9uczx
The human embryonic stem cell market, on the basis of application, can be segmented into:
Regenerative Medicine Stem Cell Biology Research Tissue Engineering Toxicology Testing
The regional markets for human embryonic stem cell include:
North America Europe Asia Pacific Latin America Middle East and Africa
Among these, North America represents a significant share of the human embryonic stem cell market.
Market Trends
The rising population along with the rapidly evolving medical infrastructure of emerging economies like India and China is expected to provide an impetus to the human embryonic stem cell market. Furthermore, technological advancements and increasing research and development investments and initiatives are expected to generate opportunities in the market. Researchers and scientists are increasingly leaning toward the transformation of human embryonic stem cells into a number of mature cell types that represent various tissues and organs in the body, as embryonic cells provide unequalled data relating to a variety of disorders. The increasing efforts by the governments of various nations towards enhancing human embryonic stem cell therapy is likely to be another key trend bolstering the market growth in the forecast period.
Key Market Players
The major players in the market Astellas Pharma Inc, Stemcell Technologies Inc., Biotime INC, Thermo Fisher Scientific, Inc., among others. The report covers the market shares, capacities, plant turnarounds, expansions, investments and mergers and acquisitions, among other latest developments of these market players.
About Us:
Expert Market Research (EMR) is a leading market research and business intelligence company, ensuring its clients remain at the vanguard of their industries by providing them with exhaustive and actionable market data through its syndicated and custom market reports, covering over 15 major industry domains. The companys expansive and ever-growing database of reports, which are constantly updated, includes reports from industry verticals like chemicals and materials, food and beverages, energy and mining, technology and media, consumer goods, pharmaceuticals, agriculture, and packaging.
EMR leverages its state-of-the-art technological and analytical tools, along with the expertise of its highly skilled team of over 100 analysts and more than 3000 consultants, to help its clients, ranging from Fortune 1,000 companies to small and medium-sized enterprises, easily grasp the expansive industry data and help them in formulating market and business strategies, which ensure that they remain ahead of the curve.
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Global Human Embryonic Stem Cell Market To Be Driven By The Rapid Technological Advancements In The Forecast Period Of 2022-2027 The Greater...
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Dedication, Achievement and Grace in Cancer Care – Curetoday.com
Posted: June 4, 2022 at 2:28 am
In a field populated by highly skilled and deeply compassionate nursing oncology professionals, Kathryn Buttner, B.S.N., RN, BMTCN, director of stem cell transplant and cellular therapy at the John Theurer Cancer Center, stands out by fulfilling her role with unique dedication, significant achievement and abundant grace.
Beginning as a staff nurse in stem cell transplant at Hackensack University Medical Center in 1999, Kate identified oncology and bone marrow transplant as areas of focus very early in her career while working with a 94-year-old patient during an oncology rotation and then with a 22-year-old patient. Though they were in opposite stages of life, she was inspired by each patients hope and determination and was motivated to meet their needs with cutting-edge technology and innate empathy.
As she sees it, Oncology patients give back more than you can ever give to them. It makes you want to move mountains to help them in any way you can.
A natural team builder focused on collaboration, Kate is passionate about facilitating excellent patient care and is adept at designing and implementing policies and procedures to ensure this. She is quick to credit her team. In leadership, in everything I do, its about the staff around me. Theyre with me every moment of the day to achieve what we achieve, she says.
Kate has been instrumental in operationalizing key initiatives, including helping start an onsite cellular therapy lab to provide CAR-T cell therapy to patients and pivoting during the COVID-19 pandemic to ensure the rapid creation of a high-titer convalescent plasma program while simultaneously sustaining the existing program. To this end, she is involved in updating a 12-chapter handbook for patients on bone marrow transplant.
Kate treats others as she would want to be treated, including team members and patients. Her work is centered on making sure they have the best experience possible, working with staff members every day to make sure theyre on the same page and doing the most they can do for their patients by giving them the respect they deserve and the dignity they need.
I have always had great admiration for Kates ability to lead so many people in different disciplines with such professionalism. I recently transitioned into a new role and have had the great pleasure of closely witnessing how much responsibility actually falls directly onto her plate.
Kate has the unique gift of being able to develop true relationships with her team. Her door is always open, and she is available to everyone on an individual basis and personal level. It has been one of the great honors of my nursing career to work with and learn from Kate.
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Efficacy and Safety of MSC Cell Therapies for Hospitalized Patients with COVID-19: A Systematic Review and Meta-Analysis – DocWire News
Posted: June 4, 2022 at 2:28 am
This article was originally published here
Stem Cells Transl Med. 2022 May 28:szac032. doi: 10.1093/stcltm/szac032. Online ahead of print.
ABSTRACT
MSC (a.k.a. mesenchymal stem cell or medicinal signaling cell) cell therapies show promise in decreasing mortality in acute respiratory distress syndrome (ARDS) and suggest benefits in treatment of COVID-19-related ARDS. We performed a meta-analysis of published trials assessing the efficacy and adverse events (AE) rates of MSC cell therapy in individuals hospitalized for COVID-19. Systematic searches were performed in multiple databases through November 3, 2021. Reports in all languages, including randomized clinical trials (RCTs), non-randomized interventional trials, and uncontrolled trials, were included. Random effects model was used to pool outcomes from RCTs and non-randomized interventional trials. Outcome measures included all-cause mortality, serious adverse events (SAEs), AEs, pulmonary function, laboratory, and imaging findings. A total of 736 patients were identified from 34 studies, which included 5 RCTs (n = 235), 7 non-randomized interventional trials (n = 370), and 22 uncontrolled comparative trials (n = 131). Patients aged on average 59.4 years and 32.2% were women. When compared with the control group, MSC cell therapy was associated with a reduction in all-cause mortality (RR = 0.54, 95% CI: 0.35-0.85, I 2 = 0.0%), reduction in SAEs (IRR = 0.36, 95% CI: 0.14-0.90, I 2 = 0.0%) and no significant difference in AE rate. A sub-group with pulmonary function studies suggested improvement in patients receiving MSC. These findings support the potential for MSC cell therapy to decrease all-cause mortality, reduce SAEs, and improve pulmonary function compared with conventional care. Large-scale double-blinded, well-powered RCTs should be conducted to further explore these results.
PMID:35640138 | DOI:10.1093/stcltm/szac032
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Efficacy and Safety of MSC Cell Therapies for Hospitalized Patients with COVID-19: A Systematic Review and Meta-Analysis - DocWire News
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