Background. The management of patients with asymptomatic papillomavirus infection is still a controversial issue. Previous studies have demonstrated the potential of using immunomodulatory therapy in patients with latent form of HPV-infection.
OBJECTIVE
To optimize therapy in subjects with latent form of papillomavirus infection.
MATERIAL AND METHODS
Prospective randomized controlled trial included 66 patients infected by HPV. Patients of study group received 3 courses of recombinant IFN alpha-2b with antioxidants by 1 suppository per rectum in a dose of 3 000 000 IU at the bedtime for 10 days. Patients of comparative group remained under medical observation without pharmacological intervention. A qualitative change of HPV content was identified and a quantitative load of HPV was monitored after 4 weeks in patients of both groups.
RESULTS
Complete elimination of identified HPV genotypes has been found in 64.5% of patients in the study group, while in the comparison group only in 5.7% (p<0.001). The lack of qualitative changes in HPV content has been revealed in 68.6% of patients in the comparison group and in 12.9% of patients in the study group. The analysis of total viral load after treatment showed a reliable advantage of recombinant IFN alpha-2b: viral load reduced by 3.5 times in the study group, viral load did not change in the comparison group.
CONCLUSION
The study demonstrated a pronounced positive effect of examined drug in the treatment of papillomavirus infection latent forms. Course therapy with recombinant IFN alpha-2b combined with antioxidants allowed to achieve positive dynamics in 80% of patients, including complete HPV elimination in 64.5% and reduction of viral load by 3.5 times.
Contribution of Authors:
Authors’ contributions:
The concept and design of the study — I.V. Polesko, A.A. Khaldin
Collecting and interpreting the data — D.A. Abukhaltam Akhmad, D.G. Kim
Statistical analysis — D.A. Abukhaltam Akhmad
Drafting the manuscript — D.A. Abukhaltam Akhmad
Revising the manuscript — I.V. Polesko, A.A. Khaldin
1* — lg копий ДНК/105 клеток.