Saliva Polymerase Chain Reaction Assay for Detection and Follow-up of Herpesvirus Reactivation in Patients With Drug Reaction With Eosinophilia and Systemic Symptoms (DRESS)

被引:20
作者
Descamps, Vincent [1 ]
Avenel-Audran, Martine [2 ]
Valeyrie-Allanore, Laurence [3 ]
Bensaid, Benoit [4 ]
Barbaud, Annick [5 ]
Al Jawhari, Mustafa [6 ]
Ranger-Rogez, Sylvie [6 ]
机构
[1] Bichat Claude Bernard Hosp, AP HP, Dept Dermatol, F-75018 Paris, France
[2] CHU Angers, Dept Dermatol, Angers, France
[3] Henri Mondor Hosp, AP HP, Dept Dermatol, Creteil, France
[4] Pierre Benite Hosp, Dept Dermatol, Lyon, France
[5] Dept Dermatol, Nancy, France
[6] Dupuytren Hosp, Dept Virol, Limoges, France
关键词
HYPERSENSITIVITY SYNDROME; HEALTHY-ADULTS; 6; INFECTION; ASSOCIATION; LOAD;
D O I
10.1001/jamadermatol.2013.2018
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Importance: Reactivations of human herpesviruses (HHVs) contribute to the development of drug reaction with eosinophilia and systemic symptoms (DRESS). Diagnosis of HHV reactivation is conventionally based on quantitative real-time polymerase chain reaction (PCR) analysis of blood samples, but these viruses are present in the oropharynx and are shed in saliva. Objective: To evaluate the use of a saliva PCR assay for demonstrating HHV shedding in patients with DRESS. Design: Shedding of HHV in saliva was prospectively studied in patients with DRESS. Reactivations of HHV, including HHV-6, HHV-7, cytomegalovirus (CMV), and Epstein-Barr virus (EBV), were studied by performing quantitative real-time PCR analysis of blood samples obtained at admission) and serial samples of saliva obtained within the first 2 weeks of DRESS; saliva samples from controls were compared. Participants: The study included 5 patients who met definite criteria for DRESS and 15 controls (5 immunosuppressed patients and 10 healthy adults). Main Outcome Measures: DNA viral loads of HHV, including HHV-6, HHV-7, CMV, and EBV as measured with real-time PCR in blood and saliva samples from patients with DRESS and saliva samples from immunosuppressed and healthy controls. Results: The PCR assay demonstrated shedding of HHV-7, EBV, HHV-6, and CMV, listed by order of magnitude. The DNA viral loads in blood and saliva samples, also measured with real-time PCR, were found to be close. In 1 patient, reactivations in saliva preceded clinical manifestations of CMV disease. Significant production of HHV-7 and EBV was demonstrated in saliva samples from the controls, but neither HHV-6 nor CMV were detected. Conclusions and Relevance: The saliva PCR assay is a useful tool for demonstration and follow-up of HHV reactivation. The interpretation of HHV viral loads in saliva differs according to HHV type.
引用
收藏
页码:565 / 569
页数:5
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