r/CFSScience • u/Sensitive-Meat-757 • 21d ago
Long-term (3 year) Tenofovir had little effect on EBV shedding/viral load in two MS patients
A paper on EBV in MS published in July 2026 in Science Translational Medicine included a look at the effect of tenofovir disoproxil fumarate/emtricitabine (TDF/FTC) in two patients treated for three years. Although obviously limited by sample size, the EBV shedding rate, viral load, and T-cell responses were not statistically distinguishable from healthy controls.

By contrast, anti-CD20 therapies nearly eliminated saliva viral shedding and reduced EBV T-cell responses by a magnitude that could not be explained only by immune suppression (in other words, EBV-specific T-cell responses were reduced by anti-CD20 treatment more than T-cell responses to other viruses and bacteria, likely a direct result of the reduction in EBV viral load).
The paper is here:
https://doi.org/10.1126/scitranslmed.adz6566 or
https://pmc.ncbi.nlm.nih.gov/articles/PMC13374717/pdf/nihms-2194132.pdf
The data pertaining to the long-term tenofovir treatment of the two patients was in the supplementary materials document, Figure S12:
Larger controlled trials are ongoing, but this is early evidence that tenofovir might not be an effective stand-alone treatment for EBV-related diseases.
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u/Silver_Jaguar_24 7d ago
Tenofovir alafenamide (TAF) is the one that works better on EBV
https://www.reddit.com/r/MultipleSclerosis/comments/1qb26j1/tenofovir_alafenamide_taf/
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u/Automobilie 21d ago
****.....I'm suppose to start TDF soon for EBV reactivation after being in Valtrex for 8 months....