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Role of Melatonin in the Regulation of Pain | JPR – Dove Medical Press

Shanshan Xie,1,2 Wenguo Fan,2,3 Hongwen He,2,4 Fang Huang1,2

1Department of Pediatric Dentistry, Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, Peoples Republic of China; 2Guangdong Provincial Key Laboratory of Stomatology, Guangzhou, Peoples Republic of China; 3Department of Anesthesiology, Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, Peoples Republic of China; 4Department of Oral Anatomy and Physiology, Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, Peoples Republic of China

Correspondence: Fang Huang; Hongwen HeGuanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, 74 Zhongshan Road 2, Guangzhou 510080, Peoples Republic of ChinaTel +86 20 87330570Fax +86 20 87330709Email hfang@mail.sysu.edu.cn; 497642565@qq.com

Abstract: Melatonin is a pleiotropic hormone synthesized and secreted mainly by the pineal gland in vertebrates. Melatonin is an endogenous regulator of circadian and seasonal rhythms. Melatonin is involved in many physiological and pathophysiological processes demonstrating antioxidant, antineoplastic, anti-inflammatory, and immunomodulatory properties. Accumulating evidence has revealed that melatonin plays an important role in pain modulation through multiple mechanisms. In this review, we examine recent evidence for melatonin on pain regulation in various animal models and patients with pain syndromes, and the potential cellular mechanisms.

Keywords: melatonin, pain, cellular mechanisms

This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License.By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.

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Role of Melatonin in the Regulation of Pain | JPR - Dove Medical Press

Drug to improve fetal growth may increase blood pressure and blood sugar levels in offspring – News-Medical.net

Research suggests that a drug recently assessed as a potential treatment for fetal growth restriction may cause high blood pressure and raise blood sugar levels in offspring. The study, which urges practitioners to consider both short- and long-term effects when treating people with this pregnancy complication, is published in the American Journal of Physiology-;Heart and Circulatory Physiology. It was chosen as an APSselect article for February.

Fetal (intrauterine) growth restriction is a condition in which an unborn baby is not growing to its full potential in the womb. Babies with fetal growth restriction have a lower-than-average birth weight and much higher risk of being stillborn. The condition is difficult to treat, in part because many medications carry the potential risk of damage to the fetus.

Sildenafil citrate-;a vasodilator most often used as a treatment for erectile dysfunction-;has recently been tested in international clinical trials in severe cases of fetal growth restriction. The results did not show the beneficial effect of fetal weight gain. "The focus of previous studies has been to assess [sildenafil citrate's] effects on the mother, fetus and in some cases, [newborn], but only one study has examined the effects of antenatal [sildenafil citrate] in the long term," researchers of the current study wrote.

To learn more about how sildenafil citrate affects offspring after birth, the researchers studied a mouse model of fetal growth restriction. One group of female mice received daily subcutaneous injections of the drug-;equivalent to a human dose-;during pregnancy ("treated"), while another group was left untreated ("control"). The research team then measured blood pressure, body weight and blood sugar levels of the pups born to both groups. Both males and females born to the treated group had higher blood pressure than those born to the control mice. Body weight did not change in male mice born to treated mothers, but female offspring from the treated group were significantly heavier than those born to the control group. In a test which helps look for evidence of diabetes, females born to treated dams also showed increased blood sugar levels following a sugar challenge, but males were unaffected.

"This study highlights the importance of assessing both the short- and long-term consequences of therapeutics administered during pregnancy," the researchers wrote. Results from animal models of fetal growth restriction may lead to "a more informed choice for the obstetrician and patient on the potential short- and long-term risk vs. benefits of treatments in utero."

Source:

Journal reference:

Renshall, L. J., et al. (2020) Antenatal sildenafil citrate treatment increases offspring blood pressure in the placental-specific Igf2 knockout mouse model of FGR. Translational Physiology. doi.org/10.1152/ajpheart.00568.2019.

Posted in: Child Health News | Medical Research News | Pharmaceutical News

Tags: Baby, Birth Weight, Blood, Blood Pressure, Blood Sugar, Diabetes, Erectile Dysfunction, Heart, High Blood Pressure, In Utero, Knockout, Knockout Mouse, Newborn, Physiology, Pregnancy, Research, therapeutics, Womb

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Drug to improve fetal growth may increase blood pressure and blood sugar levels in offspring - News-Medical.net

Moved by beauty – Point Reyes Light

I celebrated my birthday in January with a trip to Yosemite. The beauty was breathtaking: it had just snowed, and the trees were dusted fairytale-style in crystalline, glittering powder. Only a bobcats tracks were in the otherwise untouched snow before me. Wisps of mist, backlit by the morning sun, suffused the air with a sublime golden light. There was silence, stillness and staggering beauty.

On the return home I drove over Mount Tamalpais, coming out of the forest to see the late-afternoon sun begin its descent toward the horizon; the ocean was a deep blue, the light a soft golden, the grass a brilliant green. As I rounded the lagoon I saw our jaunty kingfisher neighbor on the wire, as usual. The clouds, the sky, the waterfowl bobbing around togetherthe beauty of it all moved me nearly to tears. I was awash with gratitude for the gift of returning home to such a place.

Beauty, like love, is as an essential balm for the soul. We may know this intuitively, but mounting science validates it. Several studies have demonstrated the human capacity to be moved by the beauty of the natural world, an emotional response that appears to be responsible for much of the wellbeing and happiness people experience through nature connection. People who were most moved by nature experienced the greatest benefit to their happiness and wellbeing, while those who were out in nature but not moved by its beauty did not experience the same benefits. Allowing natures beauty to move us emotionally makes us happier and healthier.

This is not to say that a person walking through a forest unmoved will not experience some benefit. By breathing in the beneficial phytochemicals that the plants release, we increase our cancer-fighting, immunity-boosting cells, and lower our levels of stress hormones and inflammatory cytokine. These changes decrease our likelihood of imbalance and disease and support physical, mental and emotional wellbeing.

In a large study of people participating in a nature-connecting public health intervention, those who scored highest on engagement with natural beauty also scored highest on wellbeing and happiness scales. These high-scoring people said they felt physiological sensations like a lump in the throat or expansiveness in the chest, or emotions like awe, admiration or upliftment when perceiving beauty in nature. They indicated having a spiritual experience, a sense of oneness, a connection with the universe, or a love for the entire world when perceiving natural beauty. They were moved, and they were happier and healthier, too.

Interestingly, those most moved by natural beauty also demonstrate more pro-social behaviors. In other words, the more we connect with beauty in nature, the more we feel drawn to connect with other humans in a caring way. We are social creatures, and deepening connections is nourishing to our minds and bodies. Being moved by natural beauty also makes us more likely to engage in caring, tending relationships with the natural world; the more people are moved by natural beauty, the more likely they are to engage in conservation work, plant a pollinator garden, or consider the welfare of the non-human living world.

Our physiology, thoughts and behaviors can also improve when we witness a beautiful act of care, generosity or kindnessmoral beauty. In studies, those who have the strongest emotional response to perceiving moral beauty or acts of uncommon goodness also scored the highest on scales rating a persons love of humanity and his or her desire to be of service. Witnessing moral beauty also triggers the release of oxytocin, the hormone that stimulates bonding and lowers stress hormones.

How can we cultivate our capacity to be elevated by beauty? While women tend to have a stronger emotional response to beauty, and so-called elevation virtuosos can be moved very readily, we can all strengthen this trait with attention and practice. Keeping a journal to record the beauty you see, including acts of moral beauty, hones our appreciation. So does focusing on natural beauty through observation, or through a creative practice like drawing. Walk outside and see what you noticethe fuzzy bud on the branch of the tree stirring from its slumber, the astonishing fragrance and design of the narcissus, the fascinating movements of the earthwormevery aspect of nature contains elegance and beauty that can delight and move you if you are open to it.

As we think about the social glue needed to hold our communities, our families and ourselves together during times of change and uncertainty, beautyparticularly in nature, in kind words and deeds, and in the emotions these elicitis indeed a therapeutic balm. Look for opportunities to be the agent of beauty. Be generous with your kindness, your extended hand, your smiling eyes. You will inspire people to be their best self and pass it on. Allow yourself to feel your feelings, even if it means being moved to tears in front of others. Some consider this sort of openness a superpowerand indeed it is.

Dr. Anna OMalley, an integrative family and community medicine physician with the Coastal Health Alliance, is the founding director of Natura Institute for Ecology and Medicine in the Commonweal Garden.

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IM Therapeutics Announces Appointment of Dr. Stephen Dilly to Board of Directors – Business Wire

WOBURN, Mass. & AURORA, Colo.--(BUSINESS WIRE)--ImmunoMolecular Therapeutics, Inc. (IM Therapeutics), a clinical stage company developing personalized therapies for autoimmune disease, announced today that Dr. Stephen Dilly has joined its Board of Directors.

Dr. Dilly brings three decades of executive management experience in the biopharmaceutical industry. Most recently, Dr. Dilly served as CEO and Board Member of Aimmune Therapeutics, where he currently serves as Special Advisor. Dr. Dilly has served in executive roles at Genentech, Chiron and SmithKline Beecham and has been associated with the development and launch of several marketed drugs. He holds an M.B.B.S. from the University of London and a Ph.D. in Cardiac Physiology from University of London.

Dr. Dilly also currently serves as Board Chairman of Cognoa, a pediatric behavioral health company, Board Chairman of DNAtrix, developing virus-driven immunotherapies, and is a Board member of Sangamo Therapeutics and Adjuvance Technologies.

IM Therapeutics was founded by world-class physician scientists based on seminal research showing that blocking action of certain human leukocyte antigen (HLA) gene variants can block the autoimmune response. The Company demonstrated this in a proof-of-concept Phase 1b human study in DQ8-positive type 1 diabetes.

We are excited to bring Stephen on board and gain from his experience in advancing new drugs through the clinic and steering corporate strategy at our stage of growth, said Nandan Padukone, Ph.D., CEO of IM Therapeutics. Stephen is a great addition to our team as we build our pipeline across autoimmune diseases.

I am truly intrigued by the underlying biology and the drug development approach against HLA targets at IM Therapeutics, said Dr. Dilly. It is exciting to see the teams achievements to-date and the promise to bring personalized therapies in type 1 diabetes, celiac disease and other autoimmune diseases, he added.

IM Therapeutics is developing personalized medicines for autoimmune diseases by building oral drug therapies against human leukocyte antigen (HLA) variants that confer high risk of disease. The Company platform screens millions of compounds for optimal docking within HLA proteins together with rational drug design and bioassays to develop targeted therapeutic candidates. Its lead drug, IMT-002, is directed at HLA DQ8 activity for treatment of type 1 diabetes. The Company is building a broad pipeline of drugs against HLA targets in autoimmune disorders including celiac disease. http://imtherapeutics.com/

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IM Therapeutics Announces Appointment of Dr. Stephen Dilly to Board of Directors - Business Wire

Immunology and Allergy Clinical Reference Group job with NHS England | 98674 – The BMJ

Clinical Reference Group (CRG) Chair Appointments

CRGs provide specialty-specific clinical advice and leadership to support NHS Englands responsibility for directly commissioned services. CRGs lead the development of clinical commissioning policies, service specifications and quality dashboards; advise on service reviews; horizon scan, provide advice on new technologies; identify opportunities to reduce clinical variation and improve value.

Immunology and AllergyClinical Reference Group

Following successful promotion of the CRG Chair to the Clinical Lead for the Blood & Infection Programme of Care, the position of Chair for the Specialised Immunology & Allergy Clinical Reference Group is now vacant. This CRG covers specialised treatment of certain immunological and allergic conditions.

All CRG Chair positions will be remunerated at 1PA per week. Please contact england.specialisedcommissioning@nhs.net for more information on how to apply and an opportunity to discuss these roles further with James Palmer, Medical Director. The closing date for these posts will be Midnight 23rd February 2020

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Immunology and Allergy Clinical Reference Group job with NHS England | 98674 - The BMJ

Kylie Jenner said her daughter Stormi is allergic to nuts, a year after the 2-year-old was hospitalized with an allergy – Business Insider

sourcePierre Suu/GC Images

A typical day of meals in the life of Kylie Jenner may include celery juice, bone broth, a tuna sandwich, or enchiladas.

But one food thats never on her households menu is nuts because her daughter, Stormi, is allergic to all of them, the 22-year-old Keeping Up With the Kardashians star and owner of Kylie Cosmetics said in a new video for Harpars Bazaar.

Stormi, who turned two last week, was hospitalized for a day last summer due to an allergy an ordeal that Jenner shared on Instagram at the time, without disclosing what exactly the allergy was.

God bless all the moms with sick babies, Jenner wrote on Instagram last summer after Stormi was treated and returned home safely. Im sending so much love and positive energy your way.

Allergies to tree nuts including almonds, Brazil nuts, cashews, hazelnuts, pecans, pistachios, and walnuts -are among the eight most common food allergies, affecting up to 1% of the US population, according to the American Academy of Allergy, Asthma, and Immunology.

An allergy to peanuts, which arent tree nuts, is especially and increasingly common among kids, with the number of affected children tripling between 1997 and 2008, Business Insider previously reported. Today, the US Food and Drug Administration reports about 1 million American children are allergic.

About 30% of people allergic to peanuts are also allergic to tree nuts. It sounds like Stormi is one of them.

Nut allergies of any type can can range from mild to severe, with the most mild cases causing symptoms like a runny nose and the most serious cases resulting in anaphylaxis, which can constrict breathing and be fatal.

Other symptoms can include stomach cramping, indigestion, hives, swelling, and fainting.

The only sure-fire way for a person with a nut allergy to prevent a reaction is to avoid the allergen entirely, but even with strict avoidance, inadvertent exposures can and do occur, Dr. Peter Marks, director of the FDAs Center for Biologics Evaluation and Research, said in a statement last week.

Thats why the administrations announcement Sunday, that it had approved the first drug, Palforzia, to help treat peanut allergies, was a relief for many parents and medical professionals.

When used in conjunction with peanut avoidance, Palforzia provides an FDA-approved treatment option to help reduce the risk of these allergic reactions in children with peanut allergy, Marks continued.

There have also been recent advances in peanut allergy prevention in the past several years, with guidelines from the National Institutes of Health updated in 2017 to advise parents on how to introduce at-risk babies to the nuts early on. Previously, parents were simply advised to avoid nuts altogether.

The update was based on strong research finding that the introduction of peanut early in life significantly lowered the risk of developing peanut allergy by age five, Dr. Daniel Rotrosen, director of NIAIDs division of allergy, immunology and transplantation, said in a statement.

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Kylie Jenner said her daughter Stormi is allergic to nuts, a year after the 2-year-old was hospitalized with an allergy - Business Insider

New success in treating allergies to peanuts and other foods – Science News for Students

Ten years ago at a kindergarten party, Isaac Judy took abite of a peanut-butter cookie. It tasted weird to him, so he spit it out. Hivessoon appeared on his face. His lips also began to swell. When his dad came topick him up, Isaac was coughing and wheezing. Riding in the car to the otherside of St. Louis, Mo., where they lived, Isaac fell asleep or so it seemed.

When Isaacs mother saw what was happening, she suspectedsomething more serious. He hadnt fallen asleep. He lost consciousness, JaelitheJudy explains. After a trip to the emergency room, her five-year-old recovered.But doctors confirmed her hunch: Isaac has a peanut allergy.

Just a few generations ago, hardly anyone talked about foodallergies. But over the past two decades, childhood food allergies in the UnitedStates have more than doubled. A little more than a year ago, a studyin Pediatrics reported that 7.6 percent of U.S. kids under age 18 havefood allergies. Thats almost 8 million youth about two students per classroom.And its much more than a childhood issue. Surprisingly, a studylast year in JAMA Network Open found that nearly 11 percent ofadults have food allergies, too. More than one in every four of them said they hadnot been allergic to foods as children.

These days nearly everyone has come across a family member orperson who has been touched by food allergies, or has one themselves,says Tamara Hubbard. She works in the suburbs of Chicago, Ill., as a licensedcounselor. Hubbard and a growing number of counselorsare helping families through the stress of managing food allergies.

For years, doctors have told families theres nothing they can do but avoid the trigger food or inject a fast-acting medication called epinephrine (Ep-ih-NEF-rinn) to stop a severe reaction. But researchers are learning more about why some people overreact to certain foods. And new treatments are emerging. Late last month, the first treatment for peanut allergy earned approval from the U.S. Food and Drug Administration. Another could do so within a year or so. Scientists also are continuing to develop and test other ways to treat food allergies.

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Allergic reactions occur when the immune system overreacts.Normally immune cells help fight bacteria, viruses and other pathogens. Yetsome peoples immune systems also react to harmless stuff like pollen or mold or peanuts, milk or other foods.

Such run-ins trigger a release of histamine (HIS-tuh-meen) and other chemicals. These molecules get the ball rolling for an allergic reaction, explains Tina Sindher. She works as an allergist at Stanford University School of Medicine in Palo Alto, Calif.

During an allergic reaction, someone may get itchy anddevelop hives. If the reaction worsens, the person might cough, wheeze andsuffer a whole-body reaction known as anaphylaxis(An-uh-fuh-LAX-iss). Thats what happened to Isaac and to Shea Tritts son,Gaines, in Abingdon, Va.

Gaines peanut allergy surfaced in the fall of 2012. At thetime, he was a baby and his diagnosis put the whole family on edge. For thenext few years he never trick-or-treated. He never went to a birthday party. Iwas scared to put him in preschool, says Tritt. My husband and I had a lot ofstress because he could tell I wasnt letting Gaines do normal things. So wewould argue.

Even Gaines older sister got nervous. If she went to aparty, she worried about bringing back traces of peanut-containing treats that mightsicken her brother, Tritt recalls. Living in such constant vigilance can be emotionallydraining for families with food allergies.

Anxious and desperate, Tritt wondered if her son would outgrow his allergies, and how she could ever find out. I became obsessed with information anything I could do to get us out of this situation, she says.

One day, Tritt saw a TV interview with David Stukus. Hes an allergist at Nationwide Childrens Hospital in Columbus, Ohio. Stukus saw that many patients with food allergy are fearful. They often are confused because theyre not getting the facts they need. So Stukus opened a Twitter account to spread evidence-based information. Tritt took note.

Looking at her sons blood-test results, year after year, Trittsuspected his immune response to peanuts was lessening. However, blood testscannot give a clear yes or no. These tests detect specialized immuneproteins. They are called IgE antibodies. These molecules trigger allergicreactions. But IgE levels only indicate that someone is sensitive to a certainfood. They cannot predict whether that person will react if they eat it. ProvingGaines had outgrown his peanut allergy would require an oral food challenge. And that would require that the patient eatincreasing amounts of the food while a doctor watches for allergicreactions.

Trouble is, Tritt could not find a local allergist toperform the food challenge. This procedure needs extra time and staff. It also runsa risk of triggering anaphylaxis. So, many clinics wont offer it unless apatients blood results are low low enough to suggest they would tolerate thefood. Gaines numbers had steadily dropped over the years but were still a tadtoo high.

For about half of people with peanut allergies, a bite or two of the wrong food typically contains enough peanut protein to trigger a reaction, notes Brian Vickery. He is a pediatric allergist at Emory University in Atlanta, Ga. For these people, he says, 100 milligrams (0.004 ounce) of peanut protein, or about one-third of a peanut kernel, can set off such a reaction.

Vickery used to work at Aimmune Therapeutics. ThisCalifornia company is developing a treatment for peanut allergy. It is calledoral immunotherapy, or OIT for short. The procedure involves each day eating awee bit of peanut protein pre-measured into capsules. The capsule dose goesup every few weeks over a period of months. If the treatment works, it canraise the immune systems threshold for the food. That means it would take moreof the food to trigger an allergic reaction. In other words, its possible for theperson to become bite-proof.

Aimmune tested its capsules or a dummy version called a placebo in 551 children and teens with peanut allergies. The starting dose was half a milligram (0.00002 ounce) of peanut protein. (One peanut contains 600 times that much.) Over a six-month period, the daily dose went up to 300 milligrams (0.01 ounce), or about one peanuts worth. And each day for six more months, participants had to continue eating that much.

During the study, many participants experienced allergicreactions to the peanut pills. Forty-five quit because of these unpleasantsymptoms. But among those who finished the study, two-thirds of the treatedgroup became bite-proof. After about a year, they could safely eat roughlytwo peanuts. Theyre still careful about avoiding peanuts, saysVickery. But it provides that additional margin of safety.

Those results appearedin the November 2018 New England Journal of Medicine.

Based on these and other findings, the FDA approved thosepeanut capsules on January 31.

Over the past decade and prior to the FDA approval, a small number of allergists had already started offering OIT using store-bought foods. Tritt found one such clinic several hours away. However, that clinic was not willing to give her son a peanut challenge to confirm whether he still was allergic.

Tritt didnt want to sign her son up for a long, costlytreatment if he might in fact be outgrowing his allergy.But they couldntknow for sure without the gold-standard test, that oral food challenge.

She discussed her dilemma with Stukus on Twitter. ReviewingGaines blood-test results, Stukus agreed to conduct the food challenge. Justbefore Gaines started kindergarten, his family travelled from Virginia to thedoctors clinic in Ohio. It was a nine-hour drive.

Gaines started the challenge with a small, laughableamount of peanut butter, Tritt recalls. Fifteen minutes later, he ate a bitmore. Then some more. Over several hours he chomped a dozen Reeses peanutbutter cups. And he never reacted.

The test proved Gaines had outgrown his allergy. That makeshim one of the lucky few. Many children outgrow some food allergies by the timethey enter school. But eight out of every 10 kids with allergies to peanuts or treenuts will remain allergic.

Gian Lagemann, a high school senior in Saratoga, Calif., isallergic to 11 kinds of nuts, including peanuts (which actually is not a nut; its a legume). When hestarted kindergarten, his mother brought no nuts allowed signs to theclassroom. She asked other parents to tell her whenever they brought in food so she could make sure it was safe for Gian. Every day Gian ate his lunch at adesignated peanut-free table.

Several years ago, Gians mom told her son about a peanutOIT trial. The study was starting nearby at Stanford University. For most ofmy life, I havent been able to eat things where the ingredient labels say maycontain peanuts or processed in a facility with peanuts, Gian says. Onceshe explained that [after the trial] Id be able to eat those foods, I waspretty happy. I was sold.

At the start of the trial, his family bought a bag of peanut flour. For about six months, Gian took his dose each day after dinner. He doesnt like the taste of peanuts. So he often mixed his dose into a spoonful of chocolate ice cream. The dose started at 1.3 milligrams of peanut protein (about 1/200th the amount in a peanut). Over the six-month trial it went up to 240 milligrams (0.008 ounce, or a little less than one peanuts worth).

More broadly, some 8,000 U.S. patients havetried such an oral therapy. Typically, about one in five will withdraw becauseof side effects or anxiety. Completing such a trial takes focusand discipline like playing sports. But, Gian recalls, They told us withevery dose we took, our body was just going to get stronger.

Participants also learned to expect some allergic reactions.If youre going to build your immune muscle against a food allergy, you knowyoure going to have a little ache during the process, says Kari Nadeau. ThisStanford allergist was a leader of the trial.

Gian felt a few such responses during the study. My throat would feel a little tight for 15 minutes, he says. But after that, it was fine. So he persevered. And it paid off. When the trial ended, he could eat a full peanut without having an allergic reaction. That means Gian now can safely eat candy with labels warning theyre made in facilities that process nuts. I was able to try Kit Kats for the first time, and Milky Ways, Gian says.

Two years ago, Isaac also tried this oral peanuttherapy. At the time, he was 13. But his experiences were quite different.During the treatment he suffered sinus and gastrointestinal troubles. He alsohad an anaphylactic reaction. Six months in, Isaac dropped out. He quit becausehe had developed an immune condition called eosinophilicesophagitis (Ee-oh-sin-oh-FILL-ick Ee-SOF-uh-JY-tis). The oral therapy triggersit in a small share of people.

And theres something else to keep in mind:People could lose their desensitization to peanut once they end the oraltherapy. That finding was confirmed in a 2019 study by Nadeaus team. Formany people, effective treatment might have to continue long-term.

Some people have taken part in research trialstesting a different treatment for peanut allergy a skin patch. Instead ofeating bits of peanut by mouth, patients every day stick a coin-sized disc ontotheir back or upper arm. Each disc contains a quarter-milligram of peanutprotein. Thats about a thousandth as much as whats in a peanut. (Bycomparison, Aimmunes capsules start with twice that much. Over months,patients then take doses that increase to 1, 10, 20, 100 and 300 milligrams.)From the patch, peanut proteins seep through the skin but do not enter theblood. Peanut patches are therefore less likely to cause anaphylaxis than is theoral therapy.

DBV Technologies in France makes the patch. This company conducted a year-long trial of its product in 356 children with peanut allergies. Nine in every 10 participants finished the trial. The most common side effect was a skin rash at the patch site. However, this trial didnt work as well as the company had hoped. By the end of the study, only a little more than one in every three patients treated could safely eat the exit dose of one to three peanuts. The study leaders reported their findings in the March 12, 2019 Journal of the American Medical Association.

Still, the patch has worked wonders forsome. In 2012, Sharon Wong was desperate. Her sons allergies to peanuts andtree nuts had intensified to an alarming degree. Once during a shopping trip,he went into a coughing fit while walking past a batch of freshly baked walnutcookies. At a restaurant buffet, he started vomiting after merely looking at asteamy tray of pesto pasta. (Pesto is made with pine nuts.)

It was really awful, recalls Wong. Wecannot control the air he breathes. But we didnt want to keep him confined athome. We wanted him to be able to go shopping, to go down the street, to go tofriends homes and not stress about his allergies.

That year she enrolled her son, then nine years old, in an earlier-stage peanut patch trial in the San Francisco Bay area of California. At first, it took just 1/240th of a peanut to trigger an allergic reaction. After two years on the patch, he could tolerate about six peanuts.

We feel more comfortable about travelinglonger distances and dining in restaurants with precautions in place, Wongwrote in a blog about the patch trial. Each mini-success gives usconfidence and improves our quality of life. My son is happier and healthier.

In August, the FDA plans to review data on the peanut patch and recommend if it should be approved. DBV Technologies is also researching and developing patches to treat milk and egg allergies. And as for oral therapies, Aimmune recently started a new trial for its egg-allergy treatment. The company is also developing an oral therapy for walnut allergy.

Scientists are studying other related approaches, too. One is an immune therapy that uses liquid droplets containing allergens. These are placed under the tongue rather than swallowed directly. Edwin Kim, an allergist at the University of North Carolina School of Medicine, in Chapel Hill, led one study of children treated for three to five years with this sublingual therapy. All had peanut allergies. Of the 37 kids who completed the study, two in every three could now consume 750 milligrams (0.03 ounce) or more of the peanut allergen. Kim, whose center has helped conduct studies for DBV and Aimmune (among other companies), reported the findings last November in the Journal of Allergy and Clinical Immunology.

Additional experimental treatments block other parts of theimmune response to allergens. Some act together with oral therapy, allowingfewer allergic reactions during therapy. Others supply helpful gut microbesthat seem to guard against food allergies. And one company is developing atoothpaste to treat peanut allergy.

In the end, each family must decide whether to seek anemerging treatment or stick with just avoiding exposure to the sensitizingfoods. Treatments require diligence. Theyre not yet widely available. And theydont always work. But if the allergy is unbearable, trying a new treatment mightprove worth the time and risk. Clearly, concludes Stukus, the Ohio doctor, food-allergymanagement is not one-size-fits-all.

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New success in treating allergies to peanuts and other foods - Science News for Students

Abu-Amer named J. Albert Key Professor – Washington University School of Medicine in St. Louis

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Professorship endows research into causes of inflammation and related skeletal problems

At the installation of Yousef Abu-Amer, PhD, as the J. Albert Key Professor are (from left) David H. Perlmutter, MD, executive vice chancellor for medical affairs, the George and Carol Bauer Dean of the School of Medicine and the Spencer T. and Ann W. Olin Distinguished Professor; Regis J. OKeefe, MD, PhD, the Fred C. Reynolds Professor and head of the Department of Orthopaedic Surgery; Abu-Amer; and Chancellor Andrew D. Martin.

Yousef Abu-Amer, PhD, a leading expert in inflammatory joint disease and bone loss, has been named the inaugural Dr. J. Albert Key Professor at Washington University School of Medicine in St. Louis.

The new professorship was created through the philanthropic legacy of J. Albert Key, MD, who chaired the Division of Orthopaedic Surgery at Washington University from 1930 until his death in 1955. Another Washington University professorship named for Key, the J. Albert Key Distinguished Professorship in Orthopaedic Surgery, is held by spine specialist Keith H. Bridwell, MD.

Abu-Amer was installed by Chancellor Andrew D. Martin and David H. Perlmutter, MD, executive vice chancellor for medical affairs, the George and Carol Bauer Dean of the School of Medicine and the Spencer T. and Ann W. Olin Distinguished Professor.

Through Dr. Keys philanthropic legacy and the support of the Department of Orthopaedic Surgery, this professorship allows us to continue to advance research and education in orthopedics while honoring and paying tribute to an esteemed surgeon and leader who also relished his role as a teacher and mentor, Martin said.

Said Perlmutter: Dr. Keys work as a physician-scientist investigating the roots of arthritis, disorders of the hip joint and deterioration of bone laid the groundwork for what has become an outstanding orthopedics department at the School of Medicine, making progress in both clinical injury management and research into the causes of bone and joint disorders. I believe he would have been proud to support the very important research Dr. Abu-Amer has advanced in their shared field.

Estimates indicate more than 60 million Americans suffer from inflammatory joint diseases and that arthritis is the leading cause of disability in the United States. Abu-Amer studies some of the most devastating complications of inflammatory arthritis: joint erosion and excessive bone loss associated with advanced and late stages of the disease. He is interested in deciphering the molecular mechanisms at the interface of inflammation and skeletal tissue to help doctors pinpoint therapeutic interventions.

Yousef is a leader in the investigation of inflammation and its molecular signatures in immune cells, bone cells and cartilage cells, said Regis J. OKeefe, MD, PhD, the Fred C. Reynolds Professor and head of the Department of Orthopaedic Surgery. He is working to improve our understanding of bone and joint degeneration and to develop better preventive and therapeutic responses. His work is significantly advancing our understanding of the relationship between inflammatory molecular pathways and major events, such as joint failure, that can require extensive surgical interventions.

Abu-Amer is a fellow of the American Society for Bone and Mineral Research and a former member of the organizations policy and publication committees. In 2002, he received the Kappa Delta Young Investigator Award from the American Academy of Orthopedic Surgeons. He is a standing member of the National Institutes of Healths (NIH) Skeletal Biology Structure and Regeneration Study Section and previously was a grant reviewer for NASA, the Department of Veterans Affairs, the Department of Defense and the Arthritis Foundation, and other funding agencies. He has had continuous funding from the NIH since 1999 and from Shriners Hospitals for Children since 2002.

Abu-Amer earned his bachelors and masters degrees and doctorate from the Hebrew University in Jerusalem. He completed his postdoctoral fellowship training in the Department of Pathology & Immunology at Washington University before joining the faculty in 1999. Abu-Amer also is a professor of cell biology & physiology, associate director of the Musculoskeletal Research Center and director of the Animal Models of Joint Injury and Disease Core at the School of Medicine.

Key graduated from the Johns Hopkins University School of Medicine in 1918 and trained in surgery and orthopedics at Boston Childrens Hospital and Massachusetts General Hospital in Boston. In 1926, Washington University recruited him to become director of research at what was previously known as St. Louis Shriners Hospital for Crippled Children. In 1930, he became head of orthopedic surgery, and in 1945, he established the School of Medicines orthopedic surgery residency.

Several awards bear his name, including the Mid-America Orthopaedic Associations J. Albert Key Award for Resident Research and the J. Albert Key Prize for Excellence in Medical Writing. At Washington University, the J. Albert Key Memorial Orthopaedic Library was established in his honor, and in 1989, Asa C. Jones, MD, and his wife, Dorothy, created the J. Albert Key Distinguished Professorship in Orthopaedic Surgery. Asa C. Jones, an orthopedic surgeon and 1942 graduate of the School of Medicine, was mentored by Key.

Key co-authored six editions of the book Management of Fractures, Dislocations and Sprains, at one time the definitive text on orthopedic trauma. He also was named president of the American Orthopaedic Association in 1946 and of the Orthopaedic Research Society in 1955.

Washington University School of Medicines 1,500 faculty physicians also are the medical staff of Barnes-Jewish and St. Louis Childrens hospitals. The School of Medicine is a leader in medical research, teaching and patient care, ranking among the top 10 medical schools in the nation by U.S. News & World Report. Through its affiliations with Barnes-Jewish and St. Louis Childrens hospitals, the School of Medicine is linked to BJC HealthCare.

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Abu-Amer named J. Albert Key Professor - Washington University School of Medicine in St. Louis

Dr. Chen Liu appointed the Brady Professor of Pathology – Yale News

Dr. Chen Liu

Dr. Chen Liu, recently named as the Anthony N. Brady Professor of Pathology, is an expert in viral hepatitis, liver cancer immunotherapy, graft-versus-host disease, and cancer epigenetics. His appointment will be effective March 1.

In November, Liu was named chair of the Department of Pathology at Yale School of Medicine and chief of pathology at Yale New Haven Hospital, also effective March 1. He is currently professor and chair of pathology, immunology, and laboratory medicine at New Jersey Medical School and at Robert Wood Johnson (RWJ) Medical School at Rutgers University, where he chairs the Center for Dermatology. He also is chief of service at University Hospital in Newark and RWJ University Hospital in New Brunswick and chief of the Division of Oncological Pathology at the Rutgers Cancer Institute of New Jersey.

Lius research team has made significant contributions to the understanding of virus or alcohol-induced carcinogenesis, cancer biomarker discovery and novel therapies using small molecules and immunotherapy. His research work has been continuously funded by the National Institutes of Health and other agencies. He has published more than 240 peer-reviewed articles and book chapters, and holds five patents and pending applications. As a gastrointestinal and liver pathologist, he provides expert consultations for both adult and pediatric patients.

After obtaining his medical degree at Tong Liao Medical College at Inner Mongolia University of Nationality and completing his postgraduate training at Peking Union Medical College in China, Liu received his Ph.D. in pathology from the University of Pennsylvania School of Medicine. He completed his residency in anatomical and clinical pathology at Medical College of Pennsylvania, held an oncological pathology fellowship at M.D. Anderson Cancer Hospital, and had postdoctoral training at Scripps Clinic. Before his appointments at Rutgers in 2015, he was professor and vice chair of pathology, immunology, and laboratory medicine at the University of Florida, where he also held an endowed chair in gastrointestinal and liver research.

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Dr. Chen Liu appointed the Brady Professor of Pathology - Yale News

Health Promotion and Wellness now accepting applications for peer educators – Penn State News

UNIVERSITY PARK, Pa. Health Promotion and Wellness(HPW), a unit of Penn State Student Affairs, is currently accepting applications for HealthWorks, a peer outreach and education program designed to promote healthy behaviors among students at University Park. Applications for the 2020-21 academic year are currently being accepted through Feb. 28.

HealthWorks offers two unique opportunities for students with an interest in health and wellness to get involved on campus. These opportunities include facilitating one-on-one wellness services with peers and conducting educational workshops and outreach events. During the application process, interested students will have the option to prioritize which opportunity they are most interested in.

Participation in the program involves a three-semester commitment (one semester of training and two semesters of service). For this reason, students who wish to apply must plan to graduate in fall 2021 or later.

Training for the program requires completion of a three-credit course in biobehavioral health, which is offered during the fall semester. Topics covered in the course include alcohol and other drugs, sexual health, nutrition, physical activity, sleep, stress, and other health topics that are relevant to the college population. There are no prerequisites to register for the course.

Upon successful completion of the training course, students complete 45 hours of service each semester. Students participate in one of two sets of service activities: 1) providing free wellness services about stress and time management, physical activity, nutrition, sleep, sexual health, and healthy relationships; or 2) conducting educational workshops and other health promotion initiatives (e.g., Love Your Body Week), staffing outreach tables, assisting with healthy cooking demonstrations, writing content for Healthy Penn State social media, and providing HIV test counseling.

Being a part of HealthWorks has been one of the most rewarding experiences Ive had while here at Penn State," said Christine Woods, a junior majoring in immunology and infectious disease. This unique opportunity allows me to connect with my fellow peers and delve into the world of health and wellness. Beyond that, HealthWorks has taught me marketable skills in leadership, communication and holistic wellness that I am grateful and excited to apply not only during my remaining time at Penn State, but later in my professional career."

For more information about HealthWorks, including an application to apply, visit HPW's HealthWorks webpage.

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Health Promotion and Wellness now accepting applications for peer educators - Penn State News