Association Between Antibodies That Bind Epstein-Barr Virus (EBV) gp350 and gH/gL and Shedding of EBV in Saliva From Nasopharyngeal Carcinoma Multiplex Family Members in Taiwan

Author:

Liu Kai-Lin12,Hsu Wan-Lun34ORCID,Bu Wei5,Yu Kelly J2,Wang Cheng-Ping6,Chien Yin-Chu7,Chen Tseng-Cheng6,Chen Chien-Jen7,Hildesheim Allan28,Middeldorp Jaap M9,Waterboer Tim10,Cohen Jeffrey I5,Coghill Anna E11,Liu Zhiwei2

Affiliation:

1. Department of Biology, Department of Healthcare Management & Policy, University of Pennsylvania , Philadelphia, Pennsylvania , USA

2. Division of Cancer Epidemiology and Genetics, National Cancer Institute , Bethesda, Maryland , USA

3. Master Program of Big Data in Medical Healthcare Industry, College of Medicine, Fu Jen Catholic University , New Taipei City , Taiwan

4. Data Science Center, College of Medicine, Fu Jen Catholic University , New Taipei City , Taiwan

5. Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Bethesda, Maryland , USA

6. Department of Otolaryngology, National Taiwan University Hospital and National Taiwan University, College of Medicine , Taipei , Taiwan

7. Genomics Research Center, Academia Sinica , Taipei , Taiwan

8. Agencia Costarriciense de Investigaciones Biologicas , San Jose , Costa Rica

9. Department of Pathology, Vrije Universiteit Medical Center , Amsterdam , The Netherlands

10. Division of Infections and Cancer Epidemiology, German Cancer Research Center , Heidelberg , Germany

11. Cancer Epidemiology Program, Division of Population Science, H. Lee Moffitt Cancer Center and Research Institute , Tampa, Florida , USA

Abstract

Abstract Elevated levels of Epstein-Barr virus (EBV) gp350 and gH/gL antibodies have been associated with a lower risk of developing nasopharyngeal carcinoma (NPC), although the evidence remains inconclusive and unexplained. We conducted a longitudinal study within a high-risk Taiwanese cohort, analyzing total immunoglobulin against EBV-gp350 and -gH/gL in blood and EBV DNA shedding in saliva. Contrary to our hypothesis—that elevated levels of antibodies previously shown to be associated with a lower NPC risk should result in a decrease in EBV shedding in saliva—higher anti-gp350 antibodies at baseline were significantly associated with detectable EBV DNA in saliva at follow-up (odds ratio [OR], 1.99 [95% confidence interval {CI}, 1.03–3.97]; P = .04). Higher anti-EBV-gH/gL antibodies at baseline were not significantly associated with risk of detectable EBV DNA at follow-up (OR, 0.69 [95% CI, .35–1.32]; P = .26). These findings underscore the complexity of virus–host interactions and emphasize the need for further investigations into their role in EBV-associated diseases.

Funder

National Cancer Institute

Division of Intramural Research, National Institute of Allergy and Infectious Diseases

National Science Council of Taiwan

Publisher

Oxford University Press (OUP)

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