Affiliations 

  • 1 University Clinic for HPV-related gynecological disease, Department of Obstetrics and Gynecology, Gødstrup Hospital, Herning, Denmark; NIDO - Center for research and education, Gødstrup Hospital, Herning, Denmark; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark
  • 2 School of Public Health, Université de Montréal, Montreal, QC, Canada
  • 3 Reproductive & Neonatal Infectious Diseases, Department of Obstetrics and Gynaecology, University of Melbourne, Melbourne, Australia; Centre for Women's Infectious Diseases Research, Royal Women's Hospital, Infection and Immunity, Murdoch Children's Research, Melbourne, Australia
  • 4 Department of Obstetrics and Gynaecology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia
  • 5 Aberdeen Centre for Women's Health Research, University of Aberdeen, Aberdeen UK
  • 6 Boston Medical Center/Boston University Chobanian and Avedesian School of Medicine, Boston, MA, USA
  • 7 All India Institute of Medical Sciences, New Delhi, India
  • 8 Department of Population Health Sciences, Duke University School of Medicine, Durham, NC, USA; Department of Mathematics, Duke University, Durham, NC, USA
  • 9 Division of Global Health, National Cancer Institute, Bethesda, USA
  • 10 University Clinic for HPV-related gynecological disease, Department of Obstetrics and Gynecology, Gødstrup Hospital, Herning, Denmark; NIDO - Center for research and education, Gødstrup Hospital, Herning, Denmark; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark. Electronic address: ahlauridsen@clin.au.dk
Am J Obstet Gynecol, 2025 Feb 19.
PMID: 39983886 DOI: 10.1016/j.ajog.2025.02.029

Abstract

Recently, the International Papillomavirus Society (IPVS) convened a working group on cervical HPV latency, which resulted in an updated understanding of the HPV natural history. While the previous HPV natural history model considered HPV detection a result of HPV acquisition or possibly re-infection, and loss of HPV detection a result of viral clearance, the updated understanding of the HPV natural history is more nuanced. Thus, HPV detection may occur as a result of autoinoculation, deposition from a recent sex act, or as a redetection of a previously acquired infection. Similarly, loss of HPV detection likely reflects immune control rather than complete viral clearance. As it is practically impossible to identify the "true" source of a new HPV detection or determine why HPV is no longer detectable, we propose that health care providers and researchers use the terminology HPV detected vs HPV not detected. Moreover, we describe the updated understanding in a clinical context. Specifically, we discuss the potential implications of the updated understanding on clinical counseling in screening, and recommendations on cervical screening and HPV vaccination. We also suggest key phrases health care providers may use when counseling women attending routine HPV-based cervical screening.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.