https://news.tulane.edu/news/tulane-scientist-awarded-grant-develop-novel-lyme-therapy

Tulane scientist awarded grant to develop novel Lyme therapy

May 21, 2019 1:00 PM
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Leslie Tate ltate1@tulane.edu
Research in Real Time
Geetha Parthasarathy

Geetha Parthasarathy, PhD (third from left), a research scientist at Tulane National Primate Research Center, received the 2019 Laure Woods Emerging Leader Award from the Bay Area Lyme Foundation. She was awarded a $100,000 grant, designed to be a catalyst for future research, particularly in the areas of Lyme diagnostics and novel therapies. She is pictured with another Emerging Leader Award recipient and Bay Area Lyme Foundation representatives. (Photo provided by Bay Area Lyme Foundation)

Geetha Parthasarathy, PhD, a research scientist at Tulane National Primate Research Center, was one of two researchers awarded a $100,000 grant last weekend at the Bay Area Lyme Foundation’s seventh annual LymeAid event. Parthasarathy received the 2019 Laure Woods Emerging Leader Award, a grant designed by Bay Area Lyme Foundation to be a catalyst for future research, particularly in the areas of Lyme diagnostics and novel therapies.

Lyme disease is a potentially disabling tick-borne infectious disease that is essentially inflammatory in nature, affecting various organs of the body. Parthasarathy’s grant project will investigate the use of novel supplemental therapeutics for the treatment of acute Lyme neuroborreliosis, a nervous system disorder affecting the central and peripheral nervous systems. Parthasarathy discovered that a certain growth factor receptor is activated in brain cells in response to the Lyme disease bacterium Borrelia burgodorferi, and that the activation of this receptor seems to induce inflammation. This grant project aims to determine if growth factor inhibitors, such as those traditionally used in cancer treatment, could reduce that inflammation.

This is of particular importance given that for some individuals certain neurological symptoms can persist even after they are treated for Lyme disease using the typical recommended antibiotic regimen. Currently, there are no additional treatments to offer these patients, who are often in need of additional therapies to combat what is known as post-treatment Lyme disease syndrome. Parthasarathy’s grant project is pre-clinical, meaning that the therapy will be tested on tissue samples as opposed to live subjects. If successful, she hopes that this therapy will move on to animal model pre-clinical trials.

There is not a lot of funding for new therapies to combat Lyme, so it’s wonderful to get support for this project and to be able to try new approaches that can help people return to health,” Parthasarathy said.

Lyme disease is the fastest-growing infectious disease in the nation, newly infecting approximately 300,000 individuals yearly — more than hepatitis, HIV, tuberculosis, West Nile and Zika virus combined. Lyme is acquired after a bite from an infected tick, and often causes severe and complicated health issues that are difficult to treat. Lyme is also difficult to diagnose, and many people with the infection suffer for years without knowing that Lyme is the cause of the deterioration in the health status. Approximately $1 million was raised at the LymeAid event this year, 100 percent of which will go directly to fund scientific research, education and prevention programs for Lyme disease.

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**Comment**

Great news.

Question: Why is there a lack of funding for Lyme, the fastest growing infectious disease in the nation that affects more people than hepatitis, HIV, tuberculosis, West Nile, and Zika COMBINED?  HELLOOOOOO?

As to the black legged tick being the sole perp – that’s highly doubtful:  https://madisonarealymesupportgroup.com/2019/05/24/microbiology-professor-im-convinced-lyme-disease-is-transmittable-from-person-to-person/

https://madisonarealymesupportgroup.com/2018/06/19/33-years-of-documentation-of-maternal-child-transmission-of-lyme-disease-and-congenital-lyme-borreliosis-a-review/

https://madisonarealymesupportgroup.com/2017/02/24/pcos-lyme-my-story/

There’s a lot of myths needing to be busted.