- Addi and Cassi’s FDA Cyclodextrin Submission
- Meet Addi and Cassi
- What is Niemann Pick Type C disease?
- Cyclodextrin and Drug Delivery
- Cyclodextrin and Odor Prevention
- Cyclodextrin on Wikipedia
- Cyclodextrin Overview - List of Uses and Drugs
- Cyclodextrin Scientific Papers
- Procter & Gamble Cyclodextrin Overview
- Society Of Cyclodextrins
- Sporanox: Approved Drug Containing Cyclodextrin
- CoQ10 and Cyclodextrin
- Cyclodextrin Releases Trapped Cholesterol
- KTVU Story On The Power of Cyclodextrin
- Take Drug Additive, Not Drug?
- Washington DC HIV/AIDs Epidemic
- Dr. James E. K. Hildreth, HIV/AIDS
- Dr. John Dietschy, Niemann Pick Type C
- Dr. Lajos Szente
- Dr. Len Kritharides, Vascular & Cholesterol Research
- Dr. Steven Walkley, Niemann Pick Type C
New non-drug fix for HIV?
June 30th, 2009
The Scientist Magazine
By Alison McCook
30th June 2009
Researchers are slowly establishing a connection between an extremely rare genetic disease and HIV — and homing in on a safe, non-prescription compound that could treat both.
Recently, James Hildreth at the Meharry Medical College School of Medicine in Nashville, Tenn., and his colleagues found that cells affected by Niemann-Pick Type C (NPC), which disrupts cholesterol trafficking, were unable to release HIV, suggesting these cells would not spread the virus.
These findings, published May 27 in the Journal of Virology, are rooted in a hypothesis Hildreth has explored for a long time: that “cholesterol is somehow essential” to HIV, he said. For instance, HIV-1 relies on specialized structures known as lipid rafts, which are rich in cholesterol, to infect new cells.
That line of thinking has led him to investigate whether a compound widely employed by the food and chemical industries (and used as a drug solubilizer) which depletes cells of cholesterol could serve as a preventative agent — or even a treatment — for HIV. And his growing body of evidence is suggesting the compound, known as cyclodextrin, might do just that.
“There are very few [compounds] that rival the safety profile” of cyclodextrin, said Hildreth. If further research confirms it has an effect on a disease that affects millions of people worldwide, that would be a major advance, he noted. “It’s been exciting for me from the beginning.”
Cyclodextrin appears to also show some benefit in NPC, pointing further to a connection between HIV and the rare genetic disease. Indeed, a family with identical 5-year-old twins with NPC recently received permission from the US Food and Drug Administration to give the girls regular infusions of cyclodextrin. NPC leads to marked abnormalities in the liver and brain and is invariably fatal.
“You have no idea what a relief it is to have something to try,” said Chris Hempel, mother to Addi and Cassi. The girls have so far received several infusions, starting with one continuous 4-day infusion, and are now getting a series of 8-hour weekly infusions of increasing doses. Hempel said the girls improved remarkably after the first 4-day infusion, showing better control of their head and neck and better balance, and were more affectionate and responsive to people. These improvements waned a bit once the girls switched to weekly doses, but seem to be returning as the doses increase.
In a previous experiment, Hildreth and his colleagues found that adding cyclodextrin to uninfected cells to deplete cellular cholesterol warded off HIV infection. Restoring normal cholesterol levels removed that protection. In a mouse model of HIV, cyclodextrin prevented vaginal transmission of the virus by infected cells.
In a primate model, the data were somewhat less promising. When macaques received topical cyclodextrin before being exposed to the virus, the treatment appeared to prevent infection initially, but offered little protection upon re-exposure to SIV, again following cyclodextrin prophylaxis.
Hildreth said that may be because the animals received a massive dose of the virus — “way more than you?d ever see in seminal fluid in a natural setting” — and the batches of cyclodextrin used for the repeated doses were not of the same quality. He said he is now repeating the study using a “physiologically relevant” amount of the virus. “We’re pretty confident.”
Hildreth explained that NPC is likely disrupting HIV transmission by affecting the trafficking of the viral protein Gag. “The very dramatic thing in NPC cells is the Gag protein seems to never make it to the plasma membrane.”
Currently, Hildreth is developing cyclodextrin as a microbicide against HIV. He has filed an investigational new drug application with the FDA, and is investigating whether the compound could serve as a therapeutic.
Steven Walkley, who studies lysosomal storage disorders such as NPC at Albert Einstein College of Medicine in New York, said his own data show cyclodextrin has a “remarkable” effect on mice with NPC. “They’re living literally twice as long as they would otherwise, ” he said. “We were very surprised, to say the least.” (He and his colleagues have submitted their findings for publication.)
Walkley noted that his mice receive 4000 milligrams per kilogram of cyclodextrin — 10 times a recent dose the Hempel girls received — and he hasn?t noticed any side effects. However, it’s still unclear how exactly cyclodextrin is warding off NPC, which means there could be some side effects scientists have not yet discovered, he added. “Maybe there’s something going on and we just haven’t found it yet.”
Peter Pentchev, a retired scientist who worked with NPC for decades at the National Institutes of Health, echoed Walkley’s opinion about the promise of cyclodextrin in NPC, dubbing it the “perfect drug” for the disease. He cautioned, though, that “we know what [cyclodextrin] does, but we don’t know why or how.” But scientists are working on those questions, he added. “In the next year, I’d be really surprised if we don’t get some answers.”
Hempel, too, has failed to notice a single side effect since her girls began cyclodextrin infusions. “We’re proving the safety of this compound,” she said. “I definitely feel like Addi and Cassi are leading the way here, not only for NPC kids, but potentially for AIDS patients.”
Filed under News | Comment (0)Cyclodextrin As A Therapeutic “Drug” For HIV AIDS, Niemann Pick Type C and other Viruses
April 16th, 2009
Addi and Cassi’s first round of cyclodextrin infusions have been going smoothly at Renown Regional Medical Center in Reno, Nevada. We’re now into our third day of continuous infusions of hydroxy propel beta cyclodextrin (HPBCD) into the girls’ bloodstreams and they don’t seem to be experiencing any negative side effects. I feel as if it’s having a positive and immediate effect. Addi was talking yesterday afternoon and stringing together more than one word — “I like my toys, I’m brave enough, I need your help, “Bye” to Dr. Hastings, and “Ad” for her name Addison. Even Cassi came out with a few words - “Mommy, No.” This is quite encouraging to us but we’re not yet sure if it’s a result of the cyclodextrin treatment.
Addi and Cassi’s blood work-ups have come back “normal” following the cyclodextrin infusions. There was a slight elevation in both girls’ eosinophils after 24 hours but it was minor. We also had to change Addi’s port access needle as it was not working properly and we were unable to draw blood. Unfortunately, we had to re-install the needle on her chest without any numbing cream. Ouch!
I found out this morning that researchers were looking at the same cyclodextrin (HPBCD) and Niemann Pick Type C disease back in 1996 — 13 years ago! I received this information from a scientist in Europe and I almost had a heart attack when I read the scientific abstract.
Somehow cyclodextrin research as it relates to Niemann Pick Type C was not thoroughly pursued with all angles exhausted by scientists. This simply can not happen again — not only for Niemann Pick Type C disease but for HIV/AIDS and potentially other viruses like Herpes that are inactivated and killed by cyclodextrin.
I worry about the future of cyclodextrin research. We can’t count on pharmaceutical companies to research cyclodextrin or bring therapeutic products with cyclodextrin to people as they are focused on profits and patents on new drugs that take millions of dollars and years to make. Cyclodextrin is an inexpensive and non-toxic compound that can be deployed tomorrow — far too EASY! But the HIV/AIDS pharma companies should be watching cyclodextrin very closely. I believe the smart ones will start investing into research and try and create new patents around cyclodextrin since the Niemann Pick Type C cholesterol gene/protein on Chromosome 18 is the culprit in HIVs ability to assemble itself in the human body.
It’s time that the National Institutes of Health (NIH) Office of AIDS Research or the Centers For Disease Control and Prevention or some other government agency steps in and redirects money into cyclodextrin research to study this potentially life-saving compound that has very broad applications.
I am also asking for help from private citizens and global foundations such as The Gates Foundation, The Clinton Foundation, Elton John AIDS Foundation, amfAR and One.org to step in and help by taking a closer look at cyclodextrin and it’s relationship to cholesterol metabolism and killer viruses like HIV/AIDS. We must make sure cyclodextrin is properly tested as a therapeutic agent whether money can be made from it or not (which is can be!)
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