Prospectives of developing therapeutic HPV vaccines
- 作者: Raevskaya N.M.1, Nikitina T.N.1, Simbirtsev A.S.2, Solovyeva I.L.3, Volgin A.R.1, Korovkin A.S.1
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隶属关系:
- Scientific Centre for Expert Evaluation of Medicinal Products of the Ministry of Health of the Russian Federation
- State Research Institute of Highly Pure Biopreparations FMBA
- Ulyanovsk State University
- 期: 卷 14, 编号 4 (2024)
- 页面: 655-671
- 栏目: REVIEWS
- URL: https://ogarev-online.ru/2220-7619/article/view/268699
- DOI: https://doi.org/10.15789/2220-7619-POD-17636
- ID: 268699
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Human papillomavirus (HPV) represents one of the most serious global public health problems. Malignant female and male diseases mainly result from persistent HPV infection. Cancer belongs to a high mortality rate disease. It has been established that HPV infection causes about 70% vaginal cancer, 50% male genital cancer, 90% anal cancer and 60% head-and-neck cancer. Annually, a large number of people develop various HPV-caused cancer types, dominated by cervical cancer, one of the most common and aggressive types of cancer that threatens health holding the fourth place among most female common cancer worldwide. According to the World Health Organization (WHO), in 2020, about 600 cases of cervical cancer are recorded daily in different countries. Emergence of cervical cancer is closely related to factors such as long-term (persistent) HPV infection and somatic mutations of the host genome. Although HPV infection can be detected and cured early with highly effective screening methods and surgical procedures, the carcinogenic risk of HPV related diseases constantly increases, which elimination faces certain difficulties, especially in low- and mid-developed countries. The most acceptable solution to this is development and implementation of therapeutic vaccines for prevention and treatment of HPV related diseases. Three licensed HPV vaccines based on L1 type virus-like particles (L1-VLPs) technology are available globally: bivalent (HPV-2), quadrivalent (HPV-4) and nonavalent (HPV-9) vaccines. These vaccines demonstrated effectiveness in reducing HPV-related cervical cancer rate by up to 90% worldwide. However, the therapeutic effect of these vaccines on persistent HPV infection and lesions has not been observed. Therapeutic HPV vaccines candidates targeted Ye6/Ye7 cancer proteins activate cellular immunity that eliminates existing HPV infection. Here we review types, mechanisms of action and clinical effects of therapeutic HPV vaccines, as well as current and future developments in the field for prevention and treatment of HPV related diseases.
作者简介
Natalja Raevskaya
Scientific Centre for Expert Evaluation of Medicinal Products of the Ministry of Health of the Russian Federation
编辑信件的主要联系方式.
Email: raevskayanm@expmed.ru
PhD (Biology), Expert of the Allergens, Cytokines and Other Immunomodulators Department, Centre for Biological Medicinal Products Evaluation and Control
俄罗斯联邦, MoscowT. Nikitina
Scientific Centre for Expert Evaluation of Medicinal Products of the Ministry of Health of the Russian Federation
Email: raevskayanm@expmed.ru
PhD (Medicine), Head Expert of the Allergens, Cytokines and Other Immunomodulators Department, Centre for Biological Medicinal Products Evaluation and Control
俄罗斯联邦, MoscowA. Simbirtsev
State Research Institute of Highly Pure Biopreparations FMBA
Email: raevskayanm@expmed.ru
RAS Corresponding Member, DSc (Medicine), Professor, Head Researcher
俄罗斯联邦, St. PetersburgI. Solovyeva
Ulyanovsk State University
Email: raevskayanm@expmed.ru
DSc (Medicine), Professor, Head of the Department of Pediatrics, Faculty of Medicine named after T.Z. Biktimirov, Institute of Medicine, Ecology and Physical Education
俄罗斯联邦, UlyanovskA. Volgin
Scientific Centre for Expert Evaluation of Medicinal Products of the Ministry of Health of the Russian Federation
Email: raevskayanm@expmed.ru
PhD (Medicine), Deputy Director, Centre for Biological Medicinal Products Evaluation and Control
俄罗斯联邦, MoscowA. Korovkin
Scientific Centre for Expert Evaluation of Medicinal Products of the Ministry of Health of the Russian Federation
Email: raevskayanm@expmed.ru
PhD (Medicine), Director of the Centre for Biological Medicinal Products Evaluation and Control
俄罗斯联邦, Moscow参考
- Аляутдина О.С., Прилуцкая В.Ю. Текущие проблемы и будущие направления вакцинации против вируса папилломы человека (ВПЧ) // Безопасность и риск фармакотерапии. 2020. Т. 8, № 3. С. 141–150. [Alyautdina О.S., Prilutskaya V.Yu. Ongoing challenges and future directions in Human papillomavirus vaccination. Bezopasnost’ i risk farmakoterapii = Safety and Risk of Pharmacotherapy, 2020, vol. 8, no. 3, pp. 141–150. (In Russ. )] doi: 10.30895/2312-7821-2020-8-3-141-150
- Винокурова С.В. Вирусы папилломы человека 6 и 11 типов: распространенность, патогенность и онкогенность // Вопросы практической кольпоскопии. Генитальные инфекции. 2022. T. 4. С. 6–16. [Vinokurova S.V. Human papillomavirus types 6 and 11: prevalence, pathogenicity and oncogenicity. Voprosy prakticheskoi kolposkopii. Genitalnye infekcii = Issues of Practical Colposcopy. Genital Infections, 2022, vol. 4, pp. 6–16. (In Russ.)] doi: 10.46393/27826392_2022_4_6
- Зароченцева Н.В., Краснопольский В.И., Белая Ю.М. Успехи вакцинопрофилактики ВПЧ-ассоциированных заболеваний и рака шейки матки в мире и в России. Обзор литературы // Вопросы практической кольпоскопии. Генитальные инфекции. 2022. Т. 1. C. 8–16. [Zarochentseva N.V., Krasnopolsky V.I., Belaya Yu.M. Progress in vaccination of HPV-associated diseases and cervical cancer in the world and in Russia. Literature review. Voprosy prakticheskoi kolposkopii. Genitalnye infekcii = Colposcopy Issues. Genital Infections, 2020, vol. 1, pp. 8–16. (In Russ.)]
- Каира А.Н., Свитич О.А., Политова Н.Г. Папилломавирусная инфекция — эпидемиология и профилактика: учебное пособие. М., 2022. [Kaira A.N., Svitich O.A., Politova N.G. Papillomavirus infection — epidemiology and prevention. Mosсow, 2022. (In Russ.)]
- Каптильный В.А., Ефимова В.А., Лазаренко А.Н. Возможности и перспективы таргетной терапии персистирующей папилломавирусной инфекции // Архив акушерства и гинекологии им. В.Ф. Снегирева. 2023. Т. 10, № 1. С. 13–24. [Kaptilnyy V.A., Efimova V.A., Lazarenko A.N. Possibilities and prospects of targeted therapy for persistent human papillomavirus infection. Arkhiv akusherstva i ginekologii im. V.F. Snegireva = V.F. Snegirev Archives of Obstetrics and Gynecology, 2023, vol. 10, no. 1, pp. 13–24. (In Russ.)] doi: 10.17816/2313-8726-2023-10-1-13-24
- Куценко И.И., Боровиков И.О., Томина О.В., Горринг Х.И., Булгакова В.П., Боровикова О.И. Вакцинация против вируса папилломы человека после адъювантной терапии цервикальных интраэпителиальных неоплазий // Кубанский научный медицинский вестник. 2022. T. 29, № 3. С. 103–120. [Kutsenko I.I., Borovikov I.O., Tomina O.V., Gorring Kh.I., Bulgakova V.P., Borovikova O.I. Vaccination against human papillomavirus after adjuvant therapy of cervical in-traepithelial neoplasia. Kubanskii naychnyi medicinskij vestnik = Kuban Scientific Medical Bulletin, 2022, vol. 29, no. 3, pp. 103–120. (In Russ.)] doi: 10.25207/1608-6228-2022-29-3-103-120
- Михалев Д.Е., Байдик О.Д., Мухамедов М.Р., Александров Г.О. Роль вируса папилломы человека в развитии потенциально злокачественных заболеваний и плоскоклеточных карцином слизистой оболочки полости рта // Российский стоматологический журнал. 2022. Т. 26, № 3. С. 267–276. [Mikhalev D.E., Baydik O.D., Mukhamedov M.R., Aleksandrov G.O. The role of the human papilloma virus in the development of potentially malignant diseases and squamous cell carcinomas of the oral mucosa. Rossiiskii stomatologicheskii zhurnal = Russian Journal of Dentistry, 2022, vol. 26, no. 3, pp. 267–276. (In Russ)] doi: 10.17816/1728-2802-2022-26-3-267-276
- Пестрикова Т.Ю., Исмайлова А.Ф., Юрасова Е.А., Юрасов И.В. Папилломавирусная инфекция как междисциплинарная проблема современного здравоохранения // Дальневосточный медицинский журнал. 2022. № 1. С. 99–103. [Pestrikova T.Y., Ismaylova I.F., Yurasova E.A., Yurasov I.V. Papilloma virus infection as an interdisciplinary problem of current healthcare. Dal’nevostochnyi meditsinskii zhurnal = Far Eastern Medical Journal, 2022, no. 1, pp. 99–103. (In Russ.)] doi: 10.35177/1994-5191-2022-1-17
- Полатова Д.Ш., Мадаминов А.Ю. Основные молекулярные механизмы канцерогенеза, индуцированного вирусом папилломы человека // Злокачественные опухоли. 2021. Т. 11, № 4. С. 39–47. [Polatova D. Sh., Madaminov A.Yu. Main molecular mechanisms of carcinogenesis induced by human papillomavirus. Zlokachestvennye opykholi = Malignant Tumors, 2021, vol. 11, no. 4, pp. 39–47. (In Russ.)] doi: 10.1765/2313-805X-2021-11-2-31-40
- Рябова Е.И., Деркаев А.А., Есмагамбетов И.Б., Щебляков Д.В., Довгий М.А., Бырихина Д.В., Прокофьев В.В., Чемоданова И.П. Сравнение различных технологий получения рекомбинантного аденоассоциированного вируса в лабораторном масштабе // БИОпрепараты. Профилактика, диагностика, лечение. 2021. Т. 21, № 4. С. 266–278. [Ryabova E.I., Derkaev A.A., Esmagambetov I.B., Shcheblyakov D.V., Dovgiy M.A., Byrikhina D.V., Prokofiev V.V., Chemodanova I.P. Comparison of different technologies for producing recombinant adeno-associated virus on a laboratory scale. Biopreparaty. Profilaktika, diagnostika, lečenie = Biological Products. Prevention, Diagnosis, Treatment, 2021, vol. 21, no. 4, pp. 266–278. (In Russ.)] doi: 10.30895/2221-996X-2021-21-4-266-278
- Седова Е.С., Первойкина К.А., Щербинин Д.Н., Шмаров М.М. Генетические конструкции, выполняющие функции адъювантов, в составе вакцин на основе аденовирусных векторов // Иммунология. 2022. Т. 43, № 1. С. 5–17. [Sedova E.S., Pervoykina K.A., Shcherbinin D.N., Shmarov M.M. Genetic constructs as adjuvants in vaccines based on adenoviral vectors. Immunologiya = Immynologiya, 2022, vol. 43, no. 1, pp. 5–17. (In Russ.)] doi: 10.33029/0206-4952- 2021-42-6-5-17
- Шамшева О.В. Эволюция национального календаря профилактических прививок. Результаты и перспективы // Детские инфекции. 2022. Т. 21, № 1. С. 5–15. [Shamsheva O.V. Evolution of the national vaccination calendar. Results and prospects. Detskie infektsii = Children Infections, 2022, vol. 21, no. 1, pp. 5–15. (In Russ.)] doi: 10.22627/2072-8107-2022-21-1-5-15
- Afrough B., Dowall S., Hewson R. Emerging viruses and current strategies for vaccine intervention. Clin. Exp. Immunol., 2019, vol. 196, no. 2, pp. 157–166. doi: 10.1111/cei.13295
- Alvarez R.D., Huh W.K., Bae S., Lamb L.S., Jr., Conner M.G., Boyer J., Wang C., Hung Ch-Fu, Sauter E., Paradis M., Adams E., Hester Sh., Jackson B., Wu T., Trimble C. A Pilot Study of Pngvl4a-CRT/E7(detox) for the Treatment of Patients With HPV16+ Cervical Intraepithelial Neoplasia 2/3 (CIN2/3). Gynecol. Oncol., 2007, vol. 140, no. 2, pp. 245–252. doi: 10.1016/j.ygyno.2015.11.026
- Angelo M.G., Zima J., Tavares Da Silva F., Baril L., Arellano F. Post-licensure safety surveillance for Human papillomavirus-16/18-AS04-adjuvanted vaccine: more than 4 years of experience. Pharmacoepidemiol. Drug Saf., 2014, vol. 23, no. 5, pp. 456–465. doi: 10.1002/pds.3593
- Arribillaga L., Echeverria I., Belsue V., Gomez T., Lozano T., Casares N., Villanueva L., Domingos-Pereira S. , Romero P., Nardelli-Haefliger D., Hervás-Stubbs S. , Sarobe P., Rodriguez M. , Carrascosa J., Zürcher Th., Lasarte J. Bivalent therapeutic vaccine against HPV16/18 genotypes consisting of a fusion protein between the extra domain a from human fibronectin and HPV16/18 E7 viral antigens. J. Immunother., 2020, vol. 8, no. 1: e000704. doi: 10.1136/jitc-2020-000704
- Barouch D.H., Kik S.V., Weverling G.J., Dilan R., King S.L., Maxfield L.F., Clark S., Ng’ang’a D., Brandariz K.L., Abbink P., Sinangil F., Bruyn G., Gray G. E, Roux S., Bekker L-G., Dilraj A., Kibuuka H., Robb M.L., Michael N.L., Anzala O., Amornkul P.N., Gilmour J., Hural J., Buchbinder S.P., Seaman M.S., Dolin R., Baden L.R., Carville A., Mansfield K.G., Pau M.G., Goudsmit J. International Seroepidemiology of Adenovirus Serotypes 5, 26, 35, and 48 in Pediatric and Adult Populations. Vaccine, 2011, vol. 29, no. 32, pp. 5203–5209 doi: 10.1016/j.vaccine.2011.05.025
- Basu P., Mehta A., Jain M., Gupta S., Nagarkar R.V., John S., Petit R. A Randomized Phase 2 Study of ADXS11-001 Listeria Monocytogenes-Listeriolysin O Immunotherapy With or Without Cisplatin in Treatment of Advanced Cervical Cancer. Int. J. Gynecol. Cancer, 2018, vol. 28, no. 4, pp. 764–772. doi: 10.1097/igc.0000000000001235
- Becker K.A., Florin L., Sapp C., Sapp M. Dissection of Human Papillomavirus Type 33 L2 Domains Involved in Nuclear Domains (ND) 10 Homing and Reorganization. Virology, 2003, vol. 314, no. 1, pp. 161–167. doi: 10.1016/s0042-6822(03)00447-1
- Boilesen D.R., Nielsen K.N., Holst P.J. Novel Antigenic Targets of HPV Therapeutic Vaccines. Vaccines, 2021, vol. 9, no. 11: 1262. doi: 10.3390/vaccines9111262
- Bossler F., Hoppe-Seyler K., Hoppe-Seyler F. PI3K/AKT/mTOR Signaling Regulates the Virus/Host Cell Crosstalk in HPV-Positive Cervical Cancer Cells. Int. J. Mol. Sci., 2019, vol. 20, no. 9: 2188. doi: 10.3390/ijms20092188
- Brun J.L., Dalstein V., Leveque J., Mathevet P., Raulic P., Baldauf J.J., Scholl S., Huynh B., Douvier S., Riethmuller D., Clavel C., Birembaut Ph., Calenda V., Baudin M., Bory J.P. Regression of High-Grade Cervical Intraepithelial Neoplasia With TG4001 Targeted Immunotherapy. Am. J. Obstetr. Gynecol., 2011, vol. 204, no. 2, pp. 169.e1–169.e8. doi: 10.1016/j.ajog.2010.09.020
- Buck C.B., Day P.M., Trus B.L. The Papillomavirus Major Capsid Protein L1. Virology, 2013, vol. 445, no. 1–2, pp. 169–174. doi: 10.1016/j.virol.2013.05.038
- Burd E.M. Human Papillomavirus and Cervical Cancer. Clin. Microbiol. Rev., 2003, vol. 16, no. 1, pp. 1–17. doi: 10.1128/cmr.16.1.1-17.2003
- Cabo Beltran O.R., Rosales Ledezma R. MVA E2 Therapeutic Vaccine for Marked Reduction in Likelihood of Recurrence of Respiratory Papillomatosis. Head Neck, 2019, vol. 41, no. 3, pp. 657–665. doi: 10.1002/hed.25477
- Chandra J., Woo W.P., Finlayson N., Liu H.Y., McGrath M., Ladwa R., Brauer M., Xu Y., Hanson S., Panizza B., Frazer I.H., Porceddu S.V. A Phase 1, Single Centre, Open Label, Escalating Dose Study to Assess the Safety, Tolerability and Immunogenicity of a Therapeutic Human Papillomavirus (HPV) DNA Vaccine (AMV002) for HPV-Associated Head and Neck Cancer (HNC). Cancer Immunol. Immunother., 2021, vol. 70, no. 3, pp. 743–753. doi: 10.1007/s00262-020-02720-7
- Chen M., Huang L., Wang J. Deficiency of Bim in Dendritic Cells Contributes to Overactivation of Lymphocytes and Autoimmunity. Blood, 2007, vol. 109, no. 10, pp. 4360–4367. doi: 10.1182/blood-2006-11-056424
- Chen C.H., Wu T.C. Experimental Vaccine Strategies for Cancer Immunotherapy. J. Biomed. Sci., 1998, vol. 5, no. 4, pp. 231–252. doi: 10.1007/bf02255855
- Cheng L., Wang Y., Du J. Human Papillomavirus Vaccines: An Updated Review. Vaccines, 2020, vol. 8, no. 3: 3915. doi: 10.3390/vaccines8030391
- Cheng W.F., Hung C.F., Chai C.Y., Hsu K.F., He L., Ling M., Wu T.-C.T.-C. Tumor-Specific Immunity and Antiangiogenesis Generated by a DNA Vaccine Encoding Calreticulin Linked to a Tumor Antigen. J. Clin. Invest., 2001, vol. 108, no. 5, pp. 669–678. doi: 10.1172/jci12346
- Cory L., Chu C. ADXS-HPV: A Therapeutic Listeria Vaccination Targeting Cervical Cancers Expressing the HPV E7 Antigen. Hum. Vaccines Immunotherapeut., 2014, vol. 10, no. 11, pp. 3190–3195. doi: 10.4161/hv.34378
- Çuburu N., Khan S., Thompson C.D., Kim R., Vellinga J., Zahn R., Lowy D.R., Scheper G., Schiller J.T. Adenovirus Vector-Based Prime-Boost Vaccination via Heterologous Routes Induces Cervicovaginal CD8(+) T Cell Responses Against HPV16 Oncoproteins. Int. J. Cancer, 2018, vol. 142, no. 7, pp. 1467–1479. doi: 10.1002/ijc.31166
- Diebold S.S., Kaisho T., Hemmi H., Akira S., Reis e Sousa C. Innate Antiviral Responses by Means of TLR7-Mediated Recognition of Single-Stranded RNA. Science, 2004, vol. 303, no. 5663, pp. 1529–1531. doi: 10.1126/science.1093616
- Dilley S., Miller K.M., Huh W.K. Human Papillomavirus Vaccination: Ongoing Challenges and Future Directions. Gynecol. Oncol., 2020, vol. 156, no. 2, pp. 498–502. doi: 10.1016/j.ygyno.2019.10.018
- Dyson N., Howley P.M., Münger K., Harlow E. The Human Papilloma Virus-16 E7 Oncoprotein is Able to Bind to the Retinoblastoma Gene Product. Science, 1989, vol. 243, no. 4893, pp. 934–937. doi: 10.1126/science.2537532
- Eberhardt C.S., Kissick H.T., Patel M.R., Cardenas M.A., Prokhnevska N., Obeng R.C., Nasti T.H., Griffith C.C., Im S.J., Wang X., Shin D.M., Carrington M., Chen Z.G., Sidney J., Sette A., Saba N.F., Wieland A., Ahmed R. Functional HPV-Specific PD-1(+) Stem-Like CD8 T Cells in Head and Neck Cancer. Nature, 2021, vol. 597, no. 7875, pp. 279–284. doi: 10.1038/s41586-021-03862-z
- Egawa K. Do Human Papillomaviruses Target Epidermal Stem Cells. Dermatology, 2003, vol. 207, no. 3, pp. 251–254. doi: 10.1159/000073085
- Ewer K.J., Lambe T., Rollier C.S., Spencer A.J., Hill A.V., Dorrell L. Viral Vectors as Vaccine Platforms: From Immunogenicity to Impact. Curr. Opin. Immunol., 2016, vol. 41, pp. 47–54. doi: 10.1016/j.coi.2016.05.014
- Flogging Gardasil. Nat. Biotechnol., 2007, vol. 25, no. 3: 261. doi: 10.1038/nbt0307-261
- Ford K., Hanley C.J., Mellone M., Szyndralewiez C., Heitz F., Wiesel P., Wood O., Machado M., Lopez M-A., Ganesan A.-P., Wang C., Chakravarthy A., Fenton T.R., King E.V., Vijayanand P., Ottensmeier C.H., Al-Shamkhani A., Savelyeva N., Thomas G.J. NOX4 Inhibition Potentiates Immunotherapy by Overcoming Cancer-Associated Fibroblast-Mediated CD8 T-Cell Exclusion From Tumors. Cancer Res., 2020, vol. 80, no. 9, pp. 1846–1860. doi: 10.1158/0008-5472.Can-19-3158
- Gao Q., Dong X., Xu Q., Zhu L., Wang F., Hou Y., Chao C.-C. Therapeutic Potential of CRISPR/Cas9 Gene Editing in Engineered T-Cell Therapy. Cancer, 2019, vol. 8, no. 9, pp. 4254–4264. doi: 10.1002/cam4.2257
- Garland S.M., Kjaer S.K., Muñoz N., Block S.L., Brown D.R., DiNubile M.J., Lindsay B.R., Kuter B.J., Perez G., Dominiak-Felden G., Saah A.J., Drury R., Das R., Velicer C. Impact and Effectiveness of the Quadrivalent Human Papillomavirus Vaccine: A Systematic Review of 10 Years of Real-World Experience. Clin. Infect. Dis., 2016, vol. 63, no. 4, pp. 519–527. doi: 10.1093/cid/ciw354
- Gomez-Gutierrez J.G., Elpek K.G., Montes de Oca-Luna R., Shirwan H., Sam Zhou H., McMasters K.M. Vaccination With an Adenoviral Vector Expressing Calreticulin-Human Papillomavirus 16 E7 Fusion Protein Eradicates E7 Expressing Established Tumors in Mice. Cancer Immunol. Immunother., 2007, vol. 56, no. 7, pp. 997–1007. doi: 10.1007/s00262-006-0247-2
- Graham S.V. The Human Papillomavirus Replication Cycle, and its Links to Cancer Progression: A Comprehensive Review. Clin. Sci., 2017, vol. 131, no. 17, pp. 2201–2221. doi: 10.1042/cs20160786
- Grunwitz C., Salomon N., Vascotto F., Selmi A., Bukur T., Diken M., Kreitera S., Türecia Ö., Sahin U. HPV16 RNA-LPX Vaccine Mediates Complete Regression of Aggressively Growing HPV-Positive Mouse Tumors and Establishes Protective T Cell Memory. Oncoimmunology, 2019, vol. 8, no. 9: e1629259. doi: 10.1080/2162402x.2019.1629259
- Guirnalda P., Wood L., Paterson Y. Listeria Monocytogenes and its Products as Agents for Cancer Immunotherapy. Adv. Immunol., 2012, vol. 113, pp. 81–118. doi: 10.1016/b978-0-12-394590-7.00004-x
- Hancock G., Hellner K., Dorrell L. Therapeutic HPV Vaccines. Best Pract. Res. Clin. Obstetr. Gynaecol., 2018, vol. 47, pp. 59–72. doi: 10.1016/j.bpobgyn.2017.09.008
- Hanna E., Bachmann G. HPV Vaccination With Gardasil: A Breakthrough in Women’s Health. Expert Opin. Biol. Ther., 2006, vol. 6, no. 11, pp. 1223–1227. doi: 10.1517/14712598.6.11.1223
- Herrero R., González P., Markowitz L.E. Present Status of Human Papillomavirus Vaccine Development and Implementation. Lancet Oncol., 2015, vol. 16, no. 5, pp. e206–e216. doi: 10.1016/s1470-2045(14)70481-4
- Hu Z., Ma D. The Precision Prevention and Therapy of HPV-Related Cervical Cancer: New Concepts and Clinical Implications. Cancer Med., 2018, vol. 7, no. 10, pp. 5217–5236. doi: 10.1002/cam4.1501
- Huber B., Wang J.W., Roden R.B. S., Kirnbauer R. RG1-VLP and Other L2-Based, Broad-Spectrum HPV Vaccine Candidates. J. Clin., 2021, vol. 10, no. 5: 1044. doi: 10.3390/jcm10051044
- Ikeda Y., Adachi K., Tomio K., Eguchi-Kojima S., Tsuruga T., Uchino-Mori M., Taguchi A., Komatsu A., Nagamatsu T., Oda K., Kawana-Tachikawa A., Uemura Y., Igimi S., Osuga Y., Fujii T., Kawana K. A Placebo-Controlled, Double-Blind Randomized (Phase IIB) Trial of Oral Administration With HPV16 E7-Expressing Lactobacillus, GLBL101c, for the Treatment of Cervical Intraepithelial Neoplasia Grade 2 (Cin2). Vaccines, 2021, vol. 9, no. 4: 329. doi: 10.3390/vaccines9040329
- Joura E.A., Giuliano A.R., Iversen O.E., Bouchard C., Mao C., Mehlsen J., Moreira E.D., Ngan Y., Petersen L.K., Lazcano-Ponce E., Pitisuttithum P., Restrepo J.A., Stuart G., Woelber L., Yang Y.C., Cuzick J., Garland S.M., Huh W., Kjaer S.K., Bautista O.M., Chan I.S.F., Chen J., Gesser R., Moeller E., Ritter M., Vuocolo S., Luxembourg A. A 9-Valent HPV Vaccine Against Infection and Intraepithelial Neoplasia in Women. New Engl. J. Med., 2015, vol. 372, no. 8, pp. 711–723. doi: 10.1056/NEJMoa1405044
- Kalnin K., Chivukula S., Tibbitts T., Yan Y., Stegalkina S., Shen L., Cieszynski J., Costa V., Sabharwal R., Anderson S.F., Christensen N., Jagu S., Roden R.B.S., Kleanthous H. Incorporation of RG1 Epitope Concatemers Into a Self-Adjuvanting Flagellin-L2 Vaccine Broaden Durable Protection Against Cutaneous Challenge With Diverse Human Papillomavirus Genotypes. Vaccine, 2017, vol. 35, no. 37, pp. 4942–4951. doi: 10.1016/j.vaccine.2017.07.086
- Kawana K., Adachi K., Kojima S., Taguchi A., Tomio K., Yamashita A., Nishida H., Nagasaka K., Arimoto T., Yokoyama T., Wada-Hiraike O., Oda K., Sewaki T., Osuga Y., Fujii T. Oral Vaccination Against HPV E7 for Treatment of Cervical Intraepithelial Neoplasia Grade 3 (CIN3) Elicits E7-Specific Mucosal Immunity in the Cervix of CIN3 Patients. Vaccine, 2014, vol. 32, no. 47, pp. 6233–6239. doi: 10.1016/j.vaccine.2014.09.020
- Kawasaki T., Kawai T., Akira S. Recognition of Nucleic Acids by Pattern-Recognition Receptors and its Relevance in Autoimmunity. Immunol. Rev., 2011, vol. 243, no. 1, pp. 61–73. doi: 10.1111/j.1600-065X.2011.01048.x
- Khan S., Oosterhuis K., Wunderlich K., Bunnik E.M., Bhaggoe M., Boedhoe S., Karia S., Steenbergen R.D.M., Bosch L., Serroyen J., Janssen S., Schuitemaker H., Vellinga J., Scheper G., Zahn R., Custers J. Development of a Replication-Deficient Adenoviral Vector-Based Vaccine Candidate for the Interception of HPV16- and HPV18-Induced Infections and Disease. Int. J. Cancer, 2017, vol. 141, no. 2, pp. 393–404. doi: 10.1002/ijc.30679
- Kim T.J., Jin H.T., Hur S.Y., Yang H.G., Seo Y.B., Hong S.R., Lee C.-W., Kim S., Woo J.-W., Park K.S., Hwang Y.-Y., Park J., Lee I.-H., Lim K.-T., Lee K.-H., Jeong M.S., Surh C.D., Suh Y.S., Park J.S., Sung Y.C. Clearance of Persistent HPV Infection and Cervical Lesion by Therapeutic DNA Vaccine in CIN3 Patients. Nat. Commun., 2014, vol. 5: 5317. doi: 10.1038/ncomms6317
- Komdeur F.L., Singh A., van de Wall S., Meulenberg J.J.M., Boerma A., Hoogeboom B.N., Paijens S.T., Oyarce C., de Bruyn M., Schuuring E., Regts J., Marra R., Werner N., Sluis J., van der Zee A.G.J., Wilschut J.C., Allersma D.P., van Zanten C.J., Kosterink J.G.W., Jorritsma-Smit A., Yigit R., Nijman H.W., Daemen T. First-In-Human Phase I Clinical Trial of an SFV-Based RNA Replicon Cancer Vaccine Against HPV-Induced Cancers. Mol. Ther., 2021, vol. 29, no. 2, pp. 611–625. doi: 10.1016/j.ymthe.2020.11.002
- Kreimer A.R., González P., Katki H.A., Porras C., Schiffman M., Rodriguez A.C., Solomon D., Jiménez S., Schiller J.T., Lowy D.R., van Doorn L.-J., Struijk L., Quint W., Chen S., Wacholder S., Hildesheim A., Herrero R. Efficacy of a Bivalent HPV 16/18 Vaccine Against Anal HPV 16/18 Infection Among Young Women: A Nested Analysis Within the Costa Rica Vaccine Trial. Lancet Oncol., 2011, vol. 12, no. 9, pp. 862–870. doi: 10.1016/s1470-2045(11)70213-3
- Lang Kuhs K.A., Gonzalez P., Rodriguez A.C., van Doorn L.J., Schiffman M., Struijk L., Chen S., Quint W., Lowy D.R., Porras C., DelVecchio C., Jimenez S., Safaeian M., Schiller J.T., Wacholder S., Herrero R., Hildesheim A., Kreimer A.R. Reduced Prevalence of Vulvar HPV16/18 Infection Among Women Who Received the HPV16/18 Bivalent Vaccine: A Nested Analysis Within the Costa Rica Vaccine Trial. J. Infect. Dis., 2014, vol. 210, no. 12, pp. 1890–1899. doi: 10.1093/infdis/jiu357
- Lazcano-Ponce E., Stanley M., Muñoz N., Torres L., Cruz-Valdez A., Salmerón J., Rojas R., Herrero R., Hernández-Ávila M. Overcoming Barriers to HPV Vaccination: non-Inferiority of Antibody Response to Human Papillomavirus 16/18 Vaccine in Adolescents Vaccinated With a Two-Dose vs. A Three-Dose Schedule at 21 Months. Vaccine, 2014, vol. 32, no. 6, pp. 725–732. doi: 10.1016/j.vaccine.2013.11.059
- Lee S.Y., Kang T.H., Knoff J., Huang Z., Soong R.S., Alvarez R.D., Hung C.-F., Wu T.-C. Intratumoral Injection of Therapeutic HPV Vaccinia Vaccine Following Cisplatin Enhances HPV-Specific Antitumor Effects. Cancer Immunol. Immunother., 2013, vol. 62, no. 7, pp. 1175–1185. doi: 10.1007/s00262-013-1421-y
- Lei J., Osen W., Gardyan A., Hotz-Wagenblatt A., Wei G., Gissmann L., Eichmüller S., Löchelt M. Replication-Competent Foamy Virus Vaccine Vectors as Novel Epitope Scaffolds for Immunotherapy. PLoS One, 2015, vol. 10, no. 9: e0138458. doi: 10.1371/journal.pone.0138458
- Li X., Jiang S., Tapping R.I. Toll-Like Receptor Signaling in Cell Proliferation and Survival. Cytokine, 2010, vol. 49, no. 1, pp. 1–9. doi: 10.1016/j.cyto.2009.08.010
- Liu D.W., Tsao Y.P., Kung J.T., Ding Y.A., Sytwu H.K., Xiao X., Shen S.-L. Recombinant Adeno-Associated Virus Expressing Human Papillomavirus Type 16 E7 Peptide DNA Fused With Heat Shock Protein DNA as a Potential Vaccine for Cervical Cancer. J. Virol., 2000, vol. 74, no. 6, pp. 2888–2894. doi: 10.1128/jvi.74.6.2888-2894.2000
- Lungwitz U., Breunig M., Blunk T., Göpferich A. Polyethylenimine-Based non-Viral Gene Delivery Systems. Eur. J. Pharmaceut. Biopharmaceut., 2005, vol. 60, no. 2, pp. 247–266. doi: 10.1016/j.ejpb.2004.11.011
- Macartney K.K., Chiu C., Georgousakis M., Brotherton J.M. Safety of Human Papillomavirus Vaccines: A Review. Drug Saf., 2013, vol. 36, no. 6, pp. 393–412. doi: 10.1007/s40264-013-0039-5
- Maciag P.C., Radulovic S., Rothman J. The First Clinical Use of a Live-Attenuated Listeria Monocytogenes Vaccine: A Phase I Safety Study of Lm-LLO-E7 in Patients With Advanced Carcinoma of the Cervix. Vaccine, 2009, vol. 27, no. 30, pp. 3975–3983. doi: 10.1016/j.vaccine.2009.04.041
- Malone R.W., Felgner P.L., Verma I.M. Cationic Liposome-Mediated RNA Transfection. Proc. Natl Acad. Sci. USA, 1989, vol. 86, no. 16, pp. 6077–6081. doi: 10.1073/pnas.86.16.6077
- Mansilla C., Berraondo P., Durantez M., Martínez M., Casares N., Arribillaga L., Rudilla F., Fioravanti J., Lozano T., Villanueva L., Sarobe P., Borras F., Leclerc C., Prieto J, Lasarte J.J. Eradication of Large Tumors Expressing Human Papillomavirus E7 Protein by Therapeutic Vaccination With E7 Fused to the Extra Domain a From Fibronectin. Int. J. Cancer, 2012, vol. 131, no. 3, pp. 641–651. doi: 10.1002/ijc.26412
- Markowitz L.E., Liu G., Hariri S., Steinau M., Dunne E.F., Unger E.R. Prevalence of HPV After Introduction of the Vaccination Program in the United States. Pediatrics, 2016, vol. 137, no. 3: e20151968. doi: 10.1542/peds.2015-1968
- Maruggi G., Zhang C., Li J., Ulmer J.B., Yu D. mRNA as a Transformative Technology for Vaccine Development to Control Infectious Diseases. Mol. Ther., 2019, vol. 27, no. 4, pp. 757–772. doi: 10.1016/j.ymthe.2019.01.020
- McIntyre M.C., Ruesch M.N., Laimins L.A. Human Papillomavirus E7 Oncoproteins Bind a Single Form of Cyclin E in a Complex With Cdk2 and P107. Virology, 1996, vol. 215, no. 1, pp. 73–82. doi: 10.1006/viro.1996.0008
- Melamed A., Margul D.J., Chen L., Keating N.L., Del Carmen M.G., Yang J., Seagle B.-L.L., Alexander A., Seagle B.-L.L., Alexander A., Shahabi S., Rauh-Hain J.A. Survival After Minimally Invasive Radical Hysterectomy for Early-Stage Cervical Cancer. New Engl. J. Med., 2018, vol. 379, no. 20, pp. 1905–1914. doi: 10.1056/NEJMoa1804923
- Mohsen M.O., Zha L., Cabral-Miranda G., Bachmann M.F. Major Findings and Recent Advances in Virus-Like Particle (VLP)-Based Vaccines. Semin. Immunol., 2017, vol. 34, pp. 123–132. doi: 10.1016/j.smim.2017.08.014
- Moody C.A., Laimins L.A. Human Papillomavirus Oncoproteins: Pathways to Transformation. Nat. Rev. Cancer, 2010, vol. 10, no. 8, pp. 550–560. doi: 10.1038/nrc2886
- Nagarsheth N.B., Norberg S.M., Sinkoe A.L., Adhikary S., Meyer T.J., Lack J.B., Warner A.C., Schweitzer C., Doran S.L., Korrapati S., Stevanović S., Trimble C.L., Kanakry J.A., Bagheri M.H., Ferraro E., Astrow S.H., Bot A., Faquin William C., Stroncek D., Gkitsas N., Highfill S., Hinrichs C.S. TCR-Engineered T Cells Targeting E7 for Patients With Metastatic HPV-Associated Epithelial Cancers. Nat. Med., 2021, vol. 27, no. 3, pp. 419–425. doi: 10.1038/s41591-020-01225-1
- Nardelli-Haefliger D., Wirthner D., Schiller J.T., Lowy D.R., Hildesheim A., Ponci F., Grandi P. Specific Antibody Levels at the Cervix During the Menstrual Cycle of Women Vaccinated With Human Papillomavirus 16 Virus-Like Particles. J. Natl Cancer Inst., 2003, vol. 95, no. 15, pp. 1128–1137. doi: 10.1093/jnci/djg018
- Pardi N., Hogan M.J., Porter F.W., Weissman D. mRNA Vaccines — a New Era in Vaccinology. Nat. Rev. Drug Discovery, 2018, vol. 17, no. 4, pp. 261–279. doi: 10.1038/nrd.2017.243
- Paris R., Bejrachandra S., Thongcharoen P., Nitayaphan S., Pitisuttithum P., Sambor A., Gurunathan S., Francis D., Ratto-Kim S., Karnasuta C., Souza M.S. de, Polonis V.R., Brown A.E., Kim J.H., Stephens H.A. HLA Class II Restriction of HIV-1 Clade-Specific Neutralizing Antibody Responses in Ethnic Thai Recipients of the RV144 Prime-Boost Vaccine Combination of ALVAC-HIV and AIDSVAX(®) B/E. Vaccine, 2012, vol. 30, no. 5, pp. 832–836. doi: 10.1016/j.vaccine.2011.11.002
- Peng S., Kim T.W., Lee J.H., Yang M., He L., Hung C.F., Wu T.-C. Vaccination With Dendritic Cells Transfected With BAK and BAX siRNA Enhances Antigen-Specific Immune Responses by Prolonging Dendritic Cell Life. Hum. Gene Ther., 2005, vol. 16, no. 5, pp. 584–593. doi: 10.1089/hum.2005.16.584
- Porras C., Tsang S.H., Herrero R., Guillén D., Darragh T.M., Stoler M.H., Hildesheim A., Wagner S., Boland J., Lowy D.R, Schiller J.T., Schiffman M., Schussler J., Gail M.H., Quint W., Ocampo R., Morales J., Rodríguez A.C., Hu S., Sampson J.N., Kreimer A.R. Efficacy of the Bivalent HPV Vaccine Against HPV 16/18-Associated Precancer: Long-Term Follow-Up Results From the Costa Rica Vaccine Trial. Lancet Oncol., 2020, vol. 21, no. 12, pp. 1643–1652. doi: 10.1016/s1470-2045(20)30524-6
- Rajcáni J., Mosko T., Rezuchová I. Current Developments in Viral DNA Vaccines: Shall They Solve the Unsolved. Rev. Med. Virol., 2005, vol. 15, no. 5, pp. 303–325. doi: 10.1002/rmv.467
- Ren F., Xu Y., Mao L., Ou R., Ding Z., Zhang X., Tang J., Li B., Jia Z., Tian Z., Ni B., Wu Y. Heat Shock Protein 110 Improves the Antitumor Effects of the Cytotoxic T Lymphocyte Epitope E7(49-57) in Mice. Cancer Biol. Ther., 2010, vol. 9, no. 2, pp. 134–141. doi: 10.4161/cbt.9.2.10391
- Rosales C., Graham V.V., Rosas G.A., Merchant H., Rosales R. A Recombinant Vaccinia Virus Containing the Papilloma E2 Protein Promotes Tumor Regression by Stimulating Macrophage Antibody-Dependent Cytotoxicity. Cancer Immunol. Immunother., 2000, vol. 49, no. 7, pp. 347–360. doi: 10.1007/s002620000125
- Rosales R., López-Contreras M., Rosales C., Magallanes-Molina J.R., Gonzalez-Vergara R., Arroyo-Cazarez J.M., Ricardez-Arenas A., Follo-Valencia A. del, Padilla-Arriaga S., Guerrero M.V., Pirez M.A., Arellano-Fiore C., Villarreal F. Regression of Human Papillomavirus Intraepithelial Lesions is Induced by MVA E2 Therapeutic Vaccine. Hum. Gene Ther., 2014, vol. 25, no. 12, pp. 1035–1049. doi: 10.1089/hum.2014.024
- Santesso N., Mustafa R.A., Wiercioch W., Kehar R., Gandhi S., Chen Y., Cheung A., Hopkins J., Khatib R., Ma B., Mustafa A.A., Lloyd N., Wu D., Broutet N., Schünemann H.J. Systematic Reviews and Meta-Analyses of Benefits and Harms of Cryotherapy, LEEP, and Cold Knife Conization to Treat Cervical Intraepithelial Neoplasia. Int. J. Gynaecol. Obstetr., 2016, vol. 132, no. 3, pp. 266–271. doi: 10.1016/j.ijgo.2015.07.026
- Santin A.D., Bellone S., Palmieri M., Ravaggi A., Romani C., Tassi R., Roman J.J., Burnett A., Pecorelli S., Cannon M.J. HPV16/18 E7-Pulsed Dendritic Cell Vaccination in Cervical Cancer Patients With Recurrent Disease Refractory to Standard Treatment Modalities. Gynecol. Oncol., 2016, vol. 100, no. 3, pp. 469–478. doi: 10.1016/j.ygyno.2005.09.040
- Santin A.D., Hermonat P.L., Ravaggi A., Chiriva-Internati M., Zhan D., Pecorelli S., Parham G.P., Cannon M.J. Induction of Human Papillomavirus- Specific CD4(+) and CD8(+) Lymphocytes by E7-Pulsed Autologous Dendritic Cells in Patients With Human Papillomavirus Type 16- and 18-Positive Cervical Cancer. J. Virol., 1999, vol. 73, no. 7, pp. 5402–5410. doi: 10.1128/jvi.73.7.5402-5410.1999
- Schellenbacher C., Roden R., Kirnbauer R. Chimeric L1-L2 Virus-Like Particles as Potential Broad-Spectrum Human Papillomavirus Vaccines. J. Virol., 2009, vol. 83, no. 19, pp. 10085–10095. doi: 10.1128/jvi.01088-09
- Schiffman M., Solomon D. Clinical Practice. Cervical-Cancer Screening With Human Papillomavirus and Cytologic Cotesting. New Engl. J. Med., 2013, vol. 369, no. 24, pp. 2324–2331. doi: 10.1056/NEJMcp1210379
- Schwarz T.F., Spaczynski M., Schneider A., Wysocki J., Galaj A., Schulze K., Poncelet S.M., Catteau G., Thomas F., Descamps D. Persistence of Immune Response to HPV-16/18 AS04-Adjuvanted Cervical Cancer Vaccine in Women Aged 15-55 Years. Hum. Vaccines, 2011, vol. 7, no. 9, pp. 958–965. doi: 10.4161/hv.7.9.15999
- Siegel R.L., Miller K.D., Jemal A. Cancer Statistics. CA Cancer J. Clin., 2016, vol. 66, no. 1, pp. 7–30. doi: 10.3322/caac.21332
- Smith J.A., Haberstroh F.S., White E.A., Livingston D.M., DeCaprio J.A., Howley P.M. SMCX and Components of the TIP60 Complex Contribute to E2 Regulation of the HPV E6/E7 Promoter. Virology, 2018, vol. 470, рр. 311–321. doi: 10.1016/j.virol.2014.08.022
- Stanley M., Joura E., Yen G.P., Kothari S., Luxembourg A., Saah A., Walia A., Perez G., Khoury H., Badgley D., Brown D.R. Systematic Literature Review of Neutralizing Antibody Immune Responses to non-Vaccine Targeted High-Risk HPV Types Induced by the Bivalent and the Quadrivalent Vaccines. Vaccine, 2021, vol. 39, no. 16, pp. 2214–2223. doi: 10.1016/j.vaccine.2021.01.060
- Tagliamonte M., Petrizzo A., Tornesello M.L., Buonaguro F.M., Buonaguro L. Antigen-Specific Vaccines for Cancer Treatment. Hum. Vaccines Immunotherapeut., 2014, vol. 10, no. 11, pp. 3332–3346. doi: 10.4161/21645515.2014.973317
- Takeuchi O., Akira S. Pattern Recognition Receptors and Inflammation. Cell, 2010, vol. 140, no. 6, pp. 805–820. doi: 10.1016/j.cell.2010.01.022
- Tewari K.S., Sill M.W., Long III H.J., Penson R.T., Huang H., Ramondetta L.M., Landrum L.M., Oaknin A., Reid T.J., Leitao M.M., Michael H.E., Monk B.J. Improved Survival With Bevacizumab in Advanced Cervical Cancer. New Engl. J. Med., 2014, vol. 370, no. 8, pp. 734–743. doi: 10.1056/NEJMoa1309748
- Tumban E., Peabody J., Peabody D.S., Chackerian B. A Universal Virus-Like Particle-Based Vaccine for Human Papillomavirus: Longevity of Protection and Role of Endogenous and Exogenous Adjuvants. Vaccine, 2013, vol. 31, no. 41, pp. 4647–4654. doi: 10.1016/j.vaccine.2013.07.052
- Tyler M., Tumban E., Chackerian B. Second-Generation Prophylactic HPV Vaccines: Successes and Challenges. Expert Rev. Vaccines, 2014, vol. 13, no. 2, pp. 247–255. doi: 10.1586/14760584.2014.865523
- Valdez Graham V., Sutter G., José M.V., García-Carranca A., Erfle V., Moreno Mendoza N., Merchant H., Rosales R. Human Tumor Growth is Inhibited by a Vaccinia Virus Carrying the E2 Gene of Bovine Papillomavirus. Cancer, 2000, vol. 88, no. 7, pp. 1650–1662. doi: 10.1002/(sici)1097-0142(20000401)88:7<1650::aid-cncr20>3.0.co;2-l
- Wang B., Li X., Liu L., Wang M. β-Catenin: Oncogenic Role and Therapeutic Target in Cervical Cancer. Biol. Res., 2020, vol. 53, no. 1: 33. doi: 10.1186/s40659-020-00301-7
- Wang J.W., Roden R.B. L2, the Minor Capsid Protein of Papillomavirus. Virology, 2013, vol. 445, no. 1–2, pp. 175–186. doi: 10.1016/j.virol.2013.04.017
- Wang R., Pan W., Jin L., Huang W., Li Y., Wu D., Gao C., Ma D., Liao S. Human Papillomavirus Vaccine Against Cervical Cancer: Opportunity and Challenge. Cancer Lett., 2020, vol. 471, pp. 88–102. doi: 10.1016/j.canlet.2019.11.039
- Wang T.L., Ling M., Shih I.M., Pham T., Pai S.I., Lu Z., Kurman R.J., Pardoll D.M., Wu T.-C. Intramuscular Administration of E7-Transfected Dendritic Cells Generates the Most Potent E7-Specific Anti-Tumor Immunity. Gene Ther., 2000, vol. 7, no. 9, pp. 726–733. doi: 10.1038/sj.gt.3301160
- Wendel Naumann R., Leath C.A., 3rd. Advances in Immunotherapy for Cervical Cancer. Curr. Opin. Oncol., 2020, vol. 32, no. 5, pp. 481–487. doi: 10.1097/cco.0000000000000663
- Woodham A.W., Cheloha R.W., Ling J., Rashidian M., Kolifrath S.C., Mesyngier M., Duarte J.N., Bader J.M., Skeate J.G., Da Silva D.M., Kast W.M., Ploegh H.L. Nanobody-Antigen Conjugates Elicit HPV-Specific Antitumor Immune Responses. Cancer Immunol. Res., 2018, vol. 6, no. 7, pp. 870–880. doi: 10.1158/2326-6066.Cir-17-0661
- Yang A., Farmer E., Wu T.C., Hung C.F. Perspectives for Therapeutic HPV Vaccine Development. J. Biomed. Sci., 2016, vol. 23, no. 1: 75. doi: 10.1186/s12929-016-0293-9
- Zhai L., Tumban E. Gardasil-9: A Global Survey of Projected Efficacy. Antiviral Res., 2016, vol. 130, pp. 101–109. doi: 10.1016/j.antiviral.2016.03.016
- Zur Hausen H. Papillomaviruses and Cancer: From Basic Studies to Clinical Application. Nat. Rev. Cancer, 2002, vol. 2, no. 5, pp. 342–350. doi: 10.1038/nrc798
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