| Literature DB >> 31064750 |
Jeffrey I Cohen1, Irini Manoli2, Kennichi Dowdell1, Tammy A Krogmann1, Deborah Tamura3, Pierce Radecki1, Wei Bu1, Siu-Ping Turk4, Kelly Liepshutz1, Ronald L Hornung5, Hiva Fassihi6, Robert P Sarkany6, Lori L Bonnycastle2, Peter S Chines2, Amy J Swift2, Timothy G Myers7, Melissa A Levoska3, John J DiGiovanna3, Francis S Collins2,8, Kenneth H Kraemer3, Stefania Pittaluga9, Elaine S Jaffe9.
Abstract
Patients with classic hydroa vacciniforme-like lymphoproliferative disorder (HVLPD) typically have high levels of Epstein-Barr virus (EBV) DNA in T cells and/or natural killer (NK) cells in blood and skin lesions induced by sun exposure that are infiltrated with EBV-infected lymphocytes. HVLPD is very rare in the United States and Europe but more common in Asia and South America. The disease can progress to a systemic form that may result in fatal lymphoma. We report our 11-year experience with 16 HVLPD patients from the United States and England and found that whites were less likely to develop systemic EBV disease (1/10) than nonwhites (5/6). All (10/10) of the white patients were generally in good health at last follow-up, while two-thirds (4/6) of the nonwhite patients required hematopoietic stem cell transplantation. Nonwhite patients had later age of onset of HVLPD than white patients (median age, 8 vs 5 years) and higher levels of EBV DNA (median, 1 515 000 vs 250 000 copies/ml) and more often had low numbers of NK cells (83% vs 50% of patients) and T-cell clones in the blood (83% vs 30% of patients). RNA-sequencing analysis of an HVLPD skin lesion in a white patient compared with his normal skin showed increased expression of interferon-γ and chemokines that attract T cells and NK cells. Thus, white patients with HVLPD were less likely to have systemic disease with EBV and had a much better prognosis than nonwhite patients. This trial was registered at www.clinicaltrials.gov as #NCT00369421 and #NCT00032513.Entities:
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Year: 2019 PMID: 31064750 PMCID: PMC6598378 DOI: 10.1182/blood.2018893750
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 25.476