U.S. Department of Health and Human Services
NATIONAL INSTITUTES OF HEALTH NIH News
NIH Clinical Center (CC) <http://clinicalcenter.nih.gov/>
For Immediate Release: Wednesday, August 14, 2024
Contact: NIH Clinical Center Office of Communications, Yvonne Hylton, <e-mail:ccpressgroup@xxxxxxxxxx>, 240-731-4843
MEDIA AVAILABILITY
NEW IMAGING METHOD DETECTS FUNGAL INFECTIONS CAUSED BY ASPERGILLUS FUMIGATUS SOONER
WHAT:
Researchers at the National Institutes of Health's (NIH) Clinical Center and the National Heart, Lung and Blood Institute have developed and tested a new imaging method that will allow specific detection of Aspergillus fumigatus fungal infections in a timely manner in the future, without the need for invasive procedures. Delays in diagnosing fungal infections caused by Aspergillus and other fungi can put immunocompromised patients at risk for more serious illnesses or even death.
Due to their presence in the environment, many fungi evolved to use other sources of fuel besides glucose, such as by breaking down complex sugars into simple ones to produce energy. Aspergillus can break down a specific sugar, cellobiose, into two glucose molecules, while most other microbes and human cells cannot. The researchers developed a radioactive version of cellobiose which when injected in the blood, it can be visualized in the body using positron emission tomography (PET) scanners.
In this study, radioactive cellobiose ([18F]-Fluorocellobiose, [18F]-FCB) was injected in mice with fungal infections which were then imaged using a specialized PET scanner for small animals. The mice showed accumulation of radioactivity, while mice with bacterial infections or with noninfectious inflammation did not.
Researchers also found that the same radioactive tracer, [18F]-FCB, can determine if the mice with fungal infections are responding to treatment through PET images taken before and after starting treatment.
The study was funded by the Center for Infectious Disease Imaging (CIDI), a joint initiative between Radiology and Imaging Sciences (RIS) at the NIH Clinical Center and the National Institute of Allergy and Infectious Diseases (NIAID), in collaboration with the Chemistry and Synthesis Center (CSC) at the National Heart, Lung and Blood Institute (NHLBI).
WHO:
Dima A. Hammoud, M.D., Tenured Senior Investigator, NIH Clinical Center
ARTICLE:
Dima A. Hammoud, MD, et al. Development and preclinical validation of 2-Deoxy 2-[18F] Fluorocellobiose as an Aspergillus-specific PET tracer. Science Translational Medicine. August 14, 2024. DOI: 10.1126/scitranslmed.adl5934 <https://www.science.org/doi/10.1126/scitranslmed.adl5934>.
About the NIH Clinical Center (CC): The NIH Clinical Center is the world's largest hospital entirely devoted to clinical research. It is a national resource that makes it possible to rapidly translate scientific observations and laboratory discoveries into new approaches for diagnosing, treating, and preventing disease. Over 1,600 clinical research studies are conducted at the NIH Clinical Center, including those focused on cancer, infectious diseases, blood disorders, heart disease, lung disease, alcoholism and drug abuse. For more information about the Clinical Center, visit <www.cc.nih.gov>.
About the National Institutes of Health (NIH): NIH, the nation's medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit <www.nih.gov>.
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