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BCL6 BTB-specific inhibition via FX1 treatment reduces Tfh cells and reverses lymphoid follicle hyperplasia in Indian rhesus macaque (Macaca mulatta).

Yanhui Cai | Meagan A Watkins | Fengtian Xue | Yong Ai | Huiming Cheng | Cecily C Midkiff | Xiaolei Wang | Xavier Alvarez | Adi Narayana Reddy Poli | Joseph M Salvino | Ronald S Veazey | Luis J Montaner
Journal of medical primatology | 2020

The BTB domain of B-cell lymphoma 6 (BCL6) protein was identified as a therapeutic target for B-cell lymphoma. This study compared the pharmacokinetics (PK) of the BCL6 BTB inhibitor (FX1) between mice and macaques, as well as evaluating its lymphoid suppressive effect in uninfected macaques with lymphoid hyperplasia.

Pubmed ID: 31571234

Research resources used in this publication

None found

Additional research tools detected in this publication

Antibodies used in this publication

None found

Associated grants

  • Agency: NIAID NIH HHS, United States
    Id: UM1 AI126620
  • Agency: NCI NIH HHS, United States
    Id: P30 CA010815
  • Agency: NIH HHS, United States
    Id: P51 OD011104
  • Agency: NIAID NIH HHS, United States
    Id: P30 AI045008
  • Agency: NIH HHS, United States
    Id: S10 OD019964

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Tulane National Primate Research Center (tool)

RRID:SCR_008167

Center focused on understanding human health problems, including infectious diseases that require the use of nonhuman primates to develop diagnostics, therapeutics and preventive strategies. Primary research interests include developing vaccines, treatments and diagnostic tools for infectious diseases such as AIDS, tuberculosis, CMV, COVID-19, Lyme disease, and malaria. TNPRC has both biosafety level 2 and biosafety level 3 laboratories facilities to accommodate various research needs, and is the only National Primate Research Center with Regional Biosafety Laboratory.

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