Saturday, March 16, 2013

Making bread safe for celiacs

By Alix Stuart, Boston Globe Correspondent  
March 11, 2013
(Reprinted without permission)

When Leslie Williams, a former pharmaceutical executive, agreed to meet a visiting professor from Australia in Boston for a lecture, she thought it would be a routine lunch in her role as a business mentor.  But the meeting, three years ago at the Boston Cambridge Marriott, turned into an intense five-hour discussion as Dr. Robert Anderson explained how his research into celiac disease promised to render the destructive disorder obsolete.

An autoimmune disease triggered by gluten proteins in wheat, barley, and rye, celiac disease affects­ some 3 million Americans. Untreated, it can destroy digestive tract tissue and can lead to anemia, osteoporosis, infertility, neurological dysfunction, or even cancer.

Currently, the only solution is to avoid gluten altogether. That means not eating standard versions of bread, pasta, and pizza, or anything else that contains even traces of wheat, including soy sauce and some candy, such as Twizzlers.  Dr. Robert Anderson’s research is zeroing in on a potential vaccine against celiac disease.

But as Anderson explained that afternoon to Williams, his research was zeroing in on a vaccine to cure celiac disease.  
The science “struck me as quite special and possibly­ game-changing,” Williams recalled.

She agreed to work with Anderson, and in short order Williams lined up seed capital from an angel investor and then went to Australia to unravel legal­ agreements around Anderson’s research and his company. Within the year, ImmusanT was formed, with Williams as chief executive and Anderson­ as chief scientific officer. By its first ­anniversary, the firm had $20 million in venture funding.

ImmusanT is headquartered in the biotech boomtown of Kendall Square in Cambridge and is conducting clinical trials for its vaccine, NexVax2, under “fast-track” designation from the Food and Drug Administration for diseases for which no comparable therapies exist.

“If it works, you’ll see the entire paradigm of treatment for celiac changed,” said Sundar Kodiyalam, managing director for the venture investor Vatera Healthcare and an ImmusanT board member. His firm was so enamored of the science that it invested before the company had persuasive clinical data.

Beyond ImmusanT, Boston has become a locus for research into celiac disease. Massachusetts General Hospital scored a coup when it recently convinced a leading researcher, Dr. Alessio Fasano, to head its new celiac treatment and research center. “Our mission is to make life normal for people with celiac disease,” Fasano said at a ceremony marking the opening of the Mass. General center in February.

With similar research units at Beth Israel Deaconess Medical Center and Children’s Hospital Boston, the city now has “a critical mass of expertise” in celiac disease, said Dr. Ronald Kleinman, physician in chief of Mass. General’s pediatric unit.

“I’m not sure that I see miracles happening” with the research underway now, said Lee Graham, chairwoman of Healthy Villi, a 900-member support group for celiac sufferers in New England. “But the gathering that’s happening in Boston is terrific, and tremendously encouraging to us.”  Formerly at the University of Maryland, Fasano in 2003 published a landmark analysis in which he determined that celiac disease affects many more people than previously thought: about 1 out of 100 people. Up to that point, the scientific wisdom was that celiac was relatively rare, and that a gluten-free diet worked as a sufficient “cure.”


But Fasano and others have since shown that some patients who avoid gluten continue to suffer gastric distress, leading to the conclusion that diet alone is not enough.  Not surprisingly, with the market for gluten-free foods at $4.2 billion, ImmunsanT has some company in the race for a solution.   One rival is Alba Therapeutics, a Maryland company that Fasano helped start in 2005. (He is no longer involved in the company, though he owns some stock.) The other is Alvine Pharmaceuticals, of San Carlos, Calif., spawned from research at Stanford University.

Both companies are working on pill-based therapies to counteract the unintentional consumption of small amounts of gluten; complements to the gluten-free diet rather than replacements. And both are preparing for Phase 2b clinical trials to determine if their medicines work, and at what doses.  Alba’s compound targets zonulin, a protein that is believed to contribute to “leaks” in the gut that allow gluten to infiltrate the digestive system. Cephalon Inc., now owned by Teva Pharmaceuticals, has a $7 million option to buy Alba if its drug proves effective.

Alvine’s therapy involves an enzyme that decomposes gluten into harmless particles before it reaches the gut. Patients in its most recent trials who consumed gluten for six weeks while taking the Alvine compound showed little or no damage to their intestines, with some even showing improved conditions.  
ImmusanT’s drug is at a much earlier stage of development. At the time he lunched with Williams, Anderson was a professor at the Walter and Eliza Hall Institute in Melbourne, Australia. He had a start-up, Nexpep Pty Ltd., and was in need of funding to continue developing a celiac vaccine.

Anderson said he was struck by how many patients struggled with a gluten-free diet, which can be less healthy than typical diets.   “Having a treatment that would allow full recovery and return to normal diet would be life-changing for patients, and may motivate more patients to be checked for celiac disease,” he said.

Williams, meanwhile, had worked at Merck, GlaxoSmithKline, and other drug makers and was chief executive of Ventaira Pharmaceuticals when it was sold to Battelle in 2007.

In his research, Anderson had latched on to a key catalyst: the three gluten peptides that are believed to be at root of the reaction patients suffer from gluten. NexVax2 essentially tries to reeducate the immune system to tolerate those peptides. Initial study results indicate that ImmunsanT has identified the correct peptides, and that Nexvax2 is safe to take — two important steps.

Still, there are many questions. For one thing, ImmunsanT’s early volunteers maintained gluten-free diets during the study, so its not clear how well the vaccine works in the presence of gluten. And it will work only for an as-yet undefined subset of celiac sufferers.  Even so, Fasano, who has no connection to the company, calls the concept behind the ImmunsanT’s vaccine “the holy grail” that would allow patients to eat regular bread, pasta, and other gluten-rich foods.


Though ImmusanT and the other firms are small, Williams and others in the field said the pharmaceutical industry has a keen interest in their research.   Moreover, because celiac disease is currently the most well understood autoimmune disorder, many scientists believe the research could serve as a springboard to drugs for larger markets.  “It’s not just about curing celiac,” Fasano said. “It’s about treating MS and diabetes, and all these other autoimmune conditions, and that is where industry really takes an interest.”

Sunday, February 24, 2013

Starting your own Celiac or Gluten Intolerance Support Group - Part I

Find your passion
So you think you want to start a Support Group. Well you’ll need to find your passion for the task first. If you can’t do something like this with love and determination then you might as well give up now and allow someone else to take over. Better still hunt around a bit and drive the distance to join another group or locate one online. Starting a Support Group is no easy task…it will take hours of effort on your part just to get things started. Once you’ve got it started it will take on a life of its own and you can sit back and relax a bit. But you’ve got to be passionate about what you want to accomplish - then just jump in with both feet and get things moving.
Find a location
Location, location, location…yes, it is that important. More important is it has to be free. So you want a spot that’s easy to get to, has plenty of parking, and allows for handicapped access…and it has to be free. It’s my understanding that in the US at least most Community Facilities are obligated to give back to the Communities that support them; which often translates into free space…and sometimes into free coffee/tea too. Don’t be ashamed to ask for more…you might just be surprised at what you receive. Our Support Group has been getting free space, free coffee/tea/juice AND free GF lunch for over 3 years now.
Be consistent
Before you start making all those phone calls, or sending out all those emails…think about when you want your meetings. Since it’s only you right now, just go ahead and be selfish and pick a few days and times that work best for you. But you must be consistent. People tend to look for the patterns in their life…they like things they can count on to be there when they expect them. So choose a date and time that works for you this month, every month, ad infinitum. Now once you start making those phone calls and sending those emails you may need to be a bit flexible…but you get the idea and you at least have a starting point. First Tuesday of every month at 7:pm or the second Saturday of every month at 10:am pick a few that work for you and keep those in mind when negotiating for your space. And don’t forget that most meetings run about an hour and a half to two hours long.
Getting started
So now it’s time to get started and find that location. Don’t go racing around like a spider in the rain...use the phone…use the computer. Set up a Gmail account specifically for your Support Group. Start contacting Hospitals, Community Centers, Libraries, you name it. Any Facility that might have meeting rooms and is supported by the Community is eligible. Even large Attorney’s offices, Doctors’ offices, Medical buildings, Senior Housing complexes or Hotels are places to call. Ask right up front if they have any free space available for your monthly Support Group Meeting. Don’t be disappointed by the No’s…respond politely and move on to the next one. Ask the No’s if they can recommend a place that would have some free meeting space. When they ask tell them you need free space for a Support Group for people living and coping with Celiac Disease and Gluten Intolerance. Don’t be shy…get the word started…you never know who you’re talking to and who might be looking for your Support Group in the future.
The space
What you’ll want is a meeting room that can handle at least 25 people…perhaps more. Our group is very small…about 12-24 people…but there’s a group just north of us that has 40-50 people every month, and one further south that can number in the hundreds. You’ll want a room that provides chairs…tables are nice…but chairs are important! Some may want you to setup and cleanup yourself for each meeting. That means you’re on your own for the first few meetings. Don’t be afraid to put people to work when they start showing up for your meetings. People love to be needed…and you’ll be needing them to help setup and cleanup or you’ll be stuck doing it all by yourself and it won’t be long before you resent that. Ask if the facility can provide coffee/tea or if they have vending machines that your members have access to. Ask about bathrooms. If they keep their bathrooms under lock and key it may not be the ideal place for your meeting. Ask if it’s ok to bring food in…you may want to do the occasional pot luck or bring in samples for people to try out. If you can do it…go and visit the space before you commit to it. It’s not going to do you any good if it’s in the middle of a construction zone, or near an area that’s loud and busy, or even hidden deep down in the bowels of an ancient building. Once you’ve found what you want…give them your dates for at least 6 months – preferably 12 months – and ask them to make certain your group is placed on their calendar.
Tell the world
So now you’ve got your free space and you’re on the calendar…it’s time to get the word out. Hopefully, while you’ve been getting all the work done…you’ve been telling anyone who would listen what you’re planning to do. And I mean everyone! Anyone who would stand still for five minutes and listen…your Doctor, your friends, your family, the mailman, the taxi driver…you never know who will need you in the future. Remember that Gmail address you set up…that’s going to be your main form of contact for a while. Be cautious about passing out your personal phone number. Use the email address as often as possible. I actually have two emails…the first is my spam filter…it gets used on EVERYTHING…even my business cards (I’ll get into that later). I check that email daily and anything that comes through that I want to read or answer I forward it over to my second address and then handle it from there. Set up a Facebook account with your Gmail address. Post your meeting location and dates everywhere. Do a search for others in your area that might be looking for Support Groups. Poke around on Google for any online groups or calendars that might be willing to carry your meeting information. There are tons of ways to advertise your Support Group for free…hunt them down and use them well.
 
Now that you have the first building blocks in place it's time for the most important step...show up for your first meeting!!  Be there at least 30 minutes early...bring a friend along just in case no-one else shows up...and stay for the meeting.  First month, every month for at least three months.  If you're getting the word out...they will begin showing up.  If you build it...they will come.  Don't get discouraged.  Keep trying.  If after three months you're still sitting in the meeting room alone...well, then you may want to consider it wasn't the right time to do it.  You can consider trying a bit harder to get the word out...or release your reservation on the hall and go home.  But I really don't think you'll be doing that.  I honestly think that in three months you'll be needing to read Starting your own Celiac or Gluten Intolerance Support Group part II...good luck!!
 
Website: http://glutenfreeforlifeexpo1.blogspot.com
Email:
GlutenFreeforLifeExpo@Gmail.com
FaceBook: http://www.facebook.com/glutenfree.inflorida
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Meeting: 4th Saturday of every month except December
The Plaza, 385 Alternate Keene Road, Largo, FL 33771

Friday, January 18, 2013

Celiac & Gluten-Intolerance to be considered Disabilities??

Food Service Vulnerable to Food Allergy Lawsuits
By: MARY CLARE JALONICK
 
People with severe food allergies have a new tool in their attempt to find menus that fit their diet: federal disabilities law. And that could leave schools, restaurants and anyplace else that serves food more vulnerable to legal challenges over food sensitivities. A settlement stemming from a lack of gluten-free foods available to students at a Massachusetts university could serve as a precedent for people with other allergies or conditions, including peanut sensitivities or diabetes. Institutions and businesses subject to the Americans With Disabilities Act could be open to lawsuits if they fail to honor requests for accommodations by people with food allergies. Colleges and universities are especially vulnerable because they know their students and often require them to eat on campus, Eve Hill of the Justice Department's civil rights division says. But a restaurant also could be liable if it blatantly ignored a customer's request for certain foods and caused that person to become ill, though that case might be harder to argue if the customer had just walked in off the street, Hill says. The settlement with Lesley University, reached last month but drawing little attention will require the Cambridge, Mass., institution to serve gluten-free foods and make other accommodations for students who have celiac disease. At least one student complained to the federal government after the school would not exempt the student from a meal plan even though the student couldn't eat the food. "All colleges should heed this settlement and take steps to make accommodations," says Alice Bast, president and founder of the National Foundation for Celiac Awareness. "To our community this is definitely a precedent."
People who suffer from celiac disease don't absorb nutrients well and can get sick from the gluten found in wheat, rye and barley. The illness, which affects around 2 million Americans, causes abdominal pain, bloating and diarrhea, and people who have it can suffer weight loss, fatigue, rashes and other problems. Celiac is a diagnosed illness that is more severe than gluten sensitivity, which some people self-diagnose. Ten years ago, most people had never heard of celiac disease. But awareness has exploded in recent years, for reasons that aren't entirely clear. Some researchers say it was under-diagnosed, others say it's because people eat more processed wheat products like pastas and baked goods than in past decades, and those items use types of wheat that have a higher gluten content. Gluten-free diets have expanded beyond those with celiac disease. Millions of people are buying gluten-free foods because they say they make them feel better, even if they don't have a wheat allergy. Americans were expected to spend $7 billion on gluten-free foods last year. With so many people suddenly concerned with gluten content, colleges and universities have had to make accommodations. Some will allow students to be exempted from meal plans, while others will work with students individually. They may need to do even more now as the federal government is watching. "These kids don't want to be isolated," Bast says. "Part of the college experience is being social. If you can't even eat in the school cafeteria then you are missing out on a big part of college life." Under the Justice Department agreement, Lesley University says it will not only provide gluten-free options in its dining hall but also allow students to pre-order, provide a dedicated space for storage and preparation to avoid cross-contamination, train staff about food allergies and pay a $50,000 cash settlement to the affected students. "We are not saying what the general meal plan has to serve or not," Hill says. "We are saying that when a college has a mandatory meal plan they have to be prepared to make reasonable modifications to that meal plan to accommodate students with disabilities."
The agreement says that food allergies may constitute a disability under the Americans With Disabilities Act, if they are severe enough. The definition was made possible under 2009 amendments to the disability law that allowed for episodic impairments that substantially limit activity. "By preventing people from eating, they are really preventing them from accessing their educational program," Hill says of the school and its students. Mary Pat Lohse, the chief of staff and senior adviser to Lesley University's president, says the school has been working with the Justice Department for more than three years to address students' complaints. She says the school has already implemented most parts of the settlement and will continue to update policies to serve students who need gluten-free foods. "The settlement agreement provides a positive road map for other colleges and universities to follow," Lohse says. Joan Rector McGlockton of the National Restaurant Association says that restaurants have taken notice of an increasing demand for gluten free options, "drawing attention to the importance of providing these options as well as the preparation methods involved in serving these options." The group has a training program for restaurants so they will know what to do when food allergy issues arise. Some say the Justice Department decision goes too far. Hans von Spakovsky, a fellow at the conservative Heritage Foundation who worked in the civil rights division of the Justice Department under President George W. Bush, says food allergies shouldn't apply under the disability act. He adds that the costs could be substantial when schools are already battling backlash from high tuition costs. "I certainly encourage colleges and universities to work with students on this issue, but the fact that this is a federal case and the Justice Department is going to be deciding what kind of meals could be served in a dining hall is just absurd," he says.

Whether the government is involved or not, schools and other food service establishments are likely to hear from those who want more gluten-free foods. Dhanu Thiyagarajan, a sophomore at the University of Pittsburgh, says she decided to speak up when she arrived at school and lost weight because there were too few gluten-free options available. Like Lesley University, the University of Pittsburgh requires that on-campus students participate in a meal plan. Thiyagarajan eventually moved off campus so she could cook her own food, but not before starting an organization of students who suffer from wheat allergies like hers. She says she is now working with food service at the school and they have made a lot of progress, though not enough for her to move back on campus. L. Scott Lissner, the disability coordinator at Ohio State University, says he has seen similar situations at his school, though people with food allergies have not traditionally thought of themselves as disabled. He says schools will eventually have to do more than just exempt students from a meal plan. "This is an early decision on a growing wave of needs that universities are going to have to address," he says of the Lesley University agreement.
 
Carolanne LeBlanc
Meeting:  4th Saturday of every month except December
The
Plaza, 385 Alternate Keene Road, Largo, FL 33771

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