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Lymphoma Diagnosis and Plasma Epstein‐Barr Virus Load during Vicriviroc Therapy: Results of the AIDS Clinical Trials Group A5211
Author(s) -
Athe Tsibris,
Roger Paredes,
Amy Chadburn,
Zhaohui Su,
Timothy J. Henrich,
Amy Krambrink,
Michael D. Hughes,
Judith A. Aberg,
Judith S. Currier,
Karen T. Tashima,
Catherine Godfrey,
Wayne Greaves,
Charles Flexner,
Paul R. Skolnik,
Timothy Wilkin,
Roy M. Gulick,
Daniel R. Kuritzkes
Publication year - 2009
Publication title -
clinical infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.44
H-Index - 336
eISSN - 1537-6591
pISSN - 1058-4838
DOI - 10.1086/597007
Subject(s) - medicine , lymphoma , epstein–barr virus , virus , immunology , viral load , lymph node , clinical trial , virology , pathology
Lack of functional CCR5 increases the severity of certain viral infections, including West Nile virus and tickborne encephalitis. In a phase II trial of the investigational CCR5 antagonist vicriviroc (AIDS Clinical Trials Group protocol A5211), 4 lymphomas occurred in study patients who received vicriviroc. Because of the known association between unregulated Epstein-Barr virus (EBV) replication and lymphoma in immunocompromised patients, we evaluated whether vicriviroc exposure was associated with lymphoma EBV antigen positivity and/or had an effect on plasma levels of EBV DNA.

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