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RESULTS OF A PILOT CLINICAL TRIAL OF DENDRITICCELL BASED VACCINES FOR TREATMENT OF RECURRENT HERPESVIRUS INFECTION

https://doi.org/10.15789/1563-0625-2016-5-425-436

Abstract

Chronic recurrent infections caused by herpes simplex virus (HSV) types 1 and 2 represent a serious medical and social challenge. Given an important role of immune system in surveillance of viral infections, an induced enhancement of antigen-specific immune response seems to be a promising approach to treatment of recurrent HSV infections, in particular, using dendritic cell (DCs) vaccines. The present paper contains results of an open pilot study evaluating efficacy and safety of dendritic-cell vaccines in the patients with recurrent HSV infections. Twenty-nine patients including 14 persons with labial herpes, and 15, with genital herpes have been enrolled in this study. DCs were generated in presence of GM-CSF and IFNα and then loaded with recombinant viral proteins (HSV1gD or HSV2gD). These cells were applied in 2 rounds of vaccination performed within 9 months. Immunotherapy with DCs did not induce sufficient side effects, and was accompanied by more than two-fold decrease in relapse rate and increased length of remissions during the 9-month period of treatment. Later on, we revealed a reduced frequency of relapses, and a 3-fold increase in remission duration over the subsequent 6-month follow up. The clinical effect during the treatment and at later terms (a half-year observation) was noted with both labial and genital herpes, as registered in the majority of patients, being associated with induction of antigen-specific proliferative response and normalization of reduced mitogenic responsiveness of mononuclear cells towards ConA. The patients’ survey at longer terms (more than 24 months) has shown that the beneficial effect of immunotherapy, in terms of reduced relapse rates, was maintained in 77.8% of the respondents by 48 months (a median follow-up term). At this time, the antigen specific proliferative response was maintained in 66.7% of patients. The data obtained suggest that the dendritic-cell vaccines may be a promising approach to the treatment of recurrent labial and genital herpes.

About the Authors

O. Yu. Leplina
Research Institute of Fundamental and Clinical Immunology
Russian Federation

PhD, MD (Medicine), Leading Research Associate, Laboratory of Cellular Immunotherapy,

630099, Novosibirsk, Yadrintsevskaya str., 14



N. M. Starostina
Research Institute of Fundamental and Clinical Immunology
Russian Federation

PhD (Medicine), Honored Doctor of the Russian Federation, Head, Department of Immunology, Clinics of Immunopathology,

Novosibirsk



D. D. Blinova
Research Institute of Fundamental and Clinical Immunology
Russian Federation

Doctor (Immunology), Department of Immunology, Clinics of Immunopathology,

Novosibirsk



O. I. Zheltova
Research Institute of Fundamental and Clinical Immunology
Russian Federation

PhD (Medicine), Doctor (Immunology), Department of Immunology, Clinics of Immunopathology,

Novosibirsk



E. A. Oleinik
Research Institute of Fundamental and Clinical Immunology
Russian Federation

Postdoc Fellow, Laboratory of Cellular Immunotherapy,

Novosibirsk



T. V. Tyrinova
Research Institute of Fundamental and Clinical Immunology
Russian Federation

PhD (Medicine), Research Associate, Laboratory of Cellular Immunotherapy,

Novosibirsk



A. A. Ostanin
Research Institute of Fundamental and Clinical Immunology
Russian Federation

PhD, MD (Medicine), Professor, Main Research Associate, Laboratory of Cellular Immunotherapy,

Novosibirsk



E. R. Chernykh
Research Institute of Fundamental and Clinical Immunology
Russian Federation

PhD, MD (Medicine), Professor, Corresponding Member, Russian Academy of Sciences, Head, Laboratory of Cellular Immunotherapy,

Novosibirsk



References

1. Веретенникова М. Современная фармакотерапия герпеса с использованием различных лекарственных форм // Фундаментальные исследования, 2014. № 8. С. 1630-1634. [Veretennikova M.A. Current treatment of herpes with using different pharmaceutical forms. Fundamental`nye issledovaniya = Fundamental Research, 2014, no. 8, pp. 1630-1634. (In Russ.)]

2. Желтова О.И., Старостина Н.М., Тихонова М.А., Леплина О.Ю., Черных Е.Р., Останин А.А. Особенности иммунитета больных с хроническими рецидивирующими инфекциями // Иммунология, 2011. № 4. С. 205-209. [Zheltova O.I., Starostina N.M., Tikhonova M.A., Leplina O.Yu., Chernykh E.R., Ostanin A.A. Immunity features of patients with chronic recurrent infections. Immunologiya = Immunology, 2011, no. 4, pp. 205-209. (In Russ.)]

3. Леплина О.Ю, Желтова О.И., Борисова А.Е.. Старостина Н.М, Останин А.А., Черных Е.Р. Вакцины на основе дендритных клеток в лечении герпетической инфекции // Вестник Уральской медицинской академической науки, 2011. №2/2 (35). С. 38-39. [Leplina O.Yu., Zheltova O.I., Borisova A.E., Starostina N.M., Ostanin A.A., Chernykh E.R. Dendritic cells vaccines in the treatment of herpetic infection. Vestnik Ural`skoy meditsinskoy akademicheskoy nauki = Bulletin of the Ural Medical Academic Science, 2011, no. 2/2 (35), pp. 38-39. (In Russ.)]

4. Черных Е.Р., Леплина О.Ю., Тихонова М.А., Курганова Е.В., Стрельцова Е.И., Останин А.А., Козлов В.А. Феномен Т-клеточной анергии при хирургическом сепсисе // Медицинская иммунология, 2003. Т. 5, № 5/6. С. 529-538. [Chernykh E.R., Leplina O.Yu., Tikhonova M.A., Kurganova E.V., Streltsova E.I., Ostanin A.A., Kozlov V.A. T cell anergy in surgical sepsis. Meditsinskaya immunologiya = Medical Immunology (Russia), 2003, Vol. 5, no. 5-6, pp. 529-538. (In Russ.)]

5. Шульженко А.Е., Зуйкова И.Н. Подходы к иммунотерапии рецидивирующего простого герпеса // Эффективная фармакотерапия в акушерстве и гинекологии, 2010. №3. C. 44-49. [Shulzhenko A.E., Zuikova I.N. Approaches to the immunotherapy of recurrent herpes simplex. Effektivnaya farmakoterapiya v akusherstve i ginekologii = Effective Pharmacotherapy, 2010, no. 3, pp. 44-49. (In Russ.)]

6. Aurelian L. Herpes simplex virus type 2 vaccines: new ground for optimism? Clin. Diagn. Lab. Immunol., 2004, Vol. 11, no. 3, pp. 437-445.

7. Bedoui S., Gebhardt T. Interaction between dendritic cells and T cells during peripheral virus infections: a role for antigen presentation beyond lymphoid organs. Curr. Opin. Immunol., 2011, Vol. 23, no. 1, pp. 124-130.

8. Bedoui S., Greyer M. The role of dendritic cells in immunity against primary herpes simplex virus infections. Front Microbiol., 2014, no. 5, p. 533.

9. BenMohamed L., Bertrand G., McNamara C.D., Gras-Masse H., Hammer J., Wechsler S.L., Nesburn A.B. Identification of novel immunodominant CD4+ Th1-type T-cell peptide epitopes from herpes simplex virus glycoprotein D that confer protective immunity. J. Virol., 2003, Vol. 77, no. 17, pp. 9463-9473.

10. Bettahi I., Zhang X., Afifi R.E., BenMohamed L. Protective immunity to genital herpes simplex virus type 1 and type 2 provided by self-adjuvanting lipopeptides that drive dendritic cell maturation and elicit a polarized Th1 immune response. Viral. Immunol., 2006, Vol. 19, no. 2, pp. 220-236.

11. Bitan M., Weiss L., Reibstein I., Zeira M., Fellig Y., Slavin S., Zcharia E., Nagler A., Vlodavsky I. Heparanase upregulates Th2 cytokines, ameliorating experimental autoimmune encephalitis. Mol. Immunol., 2010, Vol. 47, no. 10, pp. 1890-1898.

12. Bourne N., Bravo F.J., Francotte M., Bernstein D.I., Myers M.G., Slaoui M., Stanberry L.R. Herpes simplex virus (HSV) type 2 glycoprotein D subunit vaccines and protection against genital HSV-1 or HSV-2 disease in guinea pigs. J Infect Dis., 2003, Vol. 187, no. 4, pp. 542-549.

13. Chi C.C., Wang S.H., Delamere F.M., Wojnarowska F., Peters M.C., Kanjirath P.P. Interventions for prevention of herpes simplex labialis (cold sores on the lips). Cochrane Database Syst Rev., 2015, no. 8, CD010095.

14. Cunninghama A., Griffithsb P., Leonec P., Mindeld A., Patele R., Stanberryf L., Whitleyg R. Current management and recommendations for access to antiviral therapy of herpes labialis. J. Clin. Virol., 2012, Vol. 53, no. 1, pp. 6-11.

15. Della Bella S., Nicola S., Riva A., Biasin M., Clerici M., Villa M.L. Functional repertoire of dendritic cells generated in granulocyte macrophage-colony stimulating factor and interferon-α. J. Leukoc. Biol., 2004, Vol. 75, no. 1, pp. 106-116.

16. Dhodapkar M.V., Steinman R.M., Sapp M., Desai H., Fossella C., Krasovsky J., Donahoe S.M., Dunbar P.R., Cerundolo V., Nixon D.F., Bhardwaj N. Rapid generation of broad T-cell immunity in humans after a single injection of mature dendritic cells. J. Clin. Invest., 1999, Vol. 104, no. 2, pp. 173-180.

17. Dyakonova V.A., Dambaeva S.V., Pinegin B.V., Khaitov R.M. Study of interaction between the polyoxidonium immunomodulator and the human immune system cells. Int. Immunopharmacol., 2004, Vol. 4, no. 13, pp. 1615-1623.

18. García F., Plana M., Climent N., Leon A., Gatell J.M., Gallart T. Dendritic cell based vaccines for HIV infection: the way ahead. Hum. Vaccin. Immunother., 2013, Vol. 9, no. 11, pp. 2445-2452.

19. Ghasemi M., Erturk M., Buruk K., Sonmez M. Induction of potent protection against acute and latent herpes simplex virus infection in mice vaccinated with dendritic cells. Cytotherapy, 2013, Vol. 15, no. 3, pp. 352-361.

20. Kabanov V.A. From synthetic polyelectrolytes to polymer-subunit vaccines. Pure Appl. Chem., 2004, Vol. 76, no. 9, pp. 1659-1677.

21. Kobelt D., Lechmann M., Steinkasserer A. The interaction between dendritic cells and herpes simplex virus-1. Curr. Top. Microbiol. Immunol., 2003, Vol. 276, pp. 145-161.

22. Korthals M., Safaian N., Kronenwett R., Maihofer D., Schott M., Papewalis C., Diaz Blanco E., Winter M., Czibere A., Haas R., Kobbe G., Fenk R. Monocyte derived dendritic cells generated by IFN-alpha acquire mature dendritic and natural killer cell properties as shown by gene expression analysis. J. Transl. Med., 2007, Vol. 5, pp. 46-57.

23. Le Cleach L., Trinquart L., Do G., Maruani A., Lebrun-Vignes B., Ravaud P., Chosidow O. Oral antiviral therapy for prevention of genital herpes outbreaks in immunocompetent and nonpregnant patients. Cochrane Database Syst Rev., 2014, no. 8, CD009036.

24. Lebrun-Vignes B., Bouzamondo A., Dupuy A., Guillaume J.C., Lechat P., Chosidow O. A meta-analysis to assess the efficacy of oral antiviral treatment to prevent genital herpes outbreaks. J. Am. Acad. Dermatol., 2007, Vol. 57, no. 2, pp. 238-246.

25. Lee H.K., Zamora M., Linehan M.M., Iijima N., Gonzalez D., Haberman A., Iwasaki A. Differential roles of migratory and resident DCs in T cell priming after mucosal or skin HSV-1 infection. J. Exp. Med., 2009, Vol. 206, no. 2, pp. 359-370.

26. Luo J., Li J., Chen R.L., Nie L., Huang J., Liu Z.W., Luo L., Yan X.J. Autologus dendritic cell vaccine for chronic hepatitis B carriers: A pilot, open label, clinical trial in human volunteers. Vaccine, 2010, Vol. 28, no. 13, pp. 2497-2504.

27. McKenna D.B., Neill W.A., Norval M. Herpes simplex virus specific immune responses in subjects with frequent and infrequent orofacial recrudescences. Br. J. Dermatol., 2001, Vol. 144, no. 3, pp. 459-464.

28. Mysliwska J., Trzonkowski P., Bryl E., Lukaszuk K., Myśliwski A. Lower interleukin-2 and higher serum tumor necrosis factor levels are associated with perimenstrual, recurrent, facial herpes simplex infection in young women. Eur. Cytokine Netw., 2000, Vol. 11, no. 3, pp. 397-406.

29. Pollara G., Speidel K., Samady L., Rajpopat M., McGrath Y., Ledermann J., Coffin R.S., Katz D.R., Chain B. Herpes simplex virus infection of dendritic cells: balance among activation, inhibition, and immunity. J. Infect. Dis., 2003, Vol. 187, no. 2, pp. 165-178.

30. Powell B.S., Andrianov A.K., Fusco P.C. Polyionic vaccine adjuvants: another look at aluminum salts and polyelectrolytes. Clin. Exp. Vaccine Res., 2015, Vol. 4, no. 1, pp. 23-45.

31. Rooney J.F., Straus S.E., Mannix M.L., Wohlenberg C.R., Alling D.W., Dumois J.A. Notkins A.L. Oral acyclovir to suppress frequently recurring herpes labialis. A double-blind, placebo-controlled trial. Ann. Intern. Med., 1993, Vol. 118, no. 4, pp. 268-272.

32. Sancho-Shimizu V., Perez De Diego R., Jouanguy E., Zhang S.Y., and Casanova, J. L. Inborn errors of anti-viral interferon immunity in humans. Curr. Opin. Virol., 2011, Vol. 1, no. 6, pp. 487-496.

33. Santini S., Pucchini T., Lapenta C., Parlato S., Logozzi M., Belardelli F. A new type 1 IFN-mediated pathway for the rapid differentiation of monocytes into highly active dendritic cells. Stem. Сells, 2003, Vol. 21, no. 3, pp. 357-362.

34. Schon E., Harandi A.M., Nordstrom I., Holmgren J., Eriksson K. Dendritic cell vaccination protects mice against lethality caused by genital herpes simplex virus type-2 infection. J. Reprod. Immunol., 2001, Vol. 50, no. 2, pp. 87-104.

35. Shin H., Iwasaki A. Generating protective immunity against genital herpes. Trends Immunol., 2013, Vol. 34, no. 10, pp. 487-494.

36. Singh R., Kumar A., Creery W.D., Ruben M., Giulivi A., Diaz-Mitoma F. Dysregulated expression of IFN-gamma and IL-10 and impaired IFN-gamma-mediated responses at different disease stages in patients with genital herpes simplex virus-2 infection. Clin. Exp. Immunol., 2003, Vol. 133, no. 1, pp. 97-107.

37. Stanberry L.R., Cunningham A.L., Mindel A., Scott L.L., Spruance S.L., Aoki F.Y., Lacey C.J. Prospects for control of herpes simplex virus disease through immunization. Clin. Infect. Dis., 2000, Vol. 30, no. 3, pp. 549-566.

38. Stanberry L.R., Spruance S.L., Cunningham A.L., Bernstein D.I., Mindel A., Sacks S., Tyring S., Aoki F.Y., Slaoui M., Denis M., Vandepapeliere P., Dubin G. GlaxoSmithKline Herpes Vaccine Efficacy Study Group. Glycoprotein-D-adjuvant vaccine to prevent genital herpes. N. Engl. J. Med., 2002, Vol. 347, no. 21, pp. 1652-1661.

39. Straus S.E., Takiff H.E., Seidlin M., Bachrach S., Lininger L., Di Giovanna J.J., Western K.A., Smith H.A., Lehrman S.N., Creagh-Kirk T. Suppression of frequently recurring genital herpes. A placebo-controlled double-blind trial of oral acyclovir. N. Engl. J. Med., 1984, Vol. 310, no. 24, pp. 1545-1550.

40. Thurner B., Roder C., Dieckmann D., Heuer M., Kruse M., Glaser A., Keikavoussi P., Kampgen E., Bender A., Schuler G. Generation of large numbers of fully mature and stable dendritic cells from leukapheresis products for clinical applications. J. Immunol. Meth., 1999, Vol. 223, no. 1, pp. 1-15.

41. Van Lint A., Ayers M., Brooks A.G., Coles R.M., Heath W.R., Carbone F.R. Herpes simplex virus-specific CD8+ T cells can clear established lytic infections from skin and nerves and can partially limit the early spread of virus after cutaneous inoculation. J. Immunol., 2004, Vol. 172, no. 1, pp. 392-397.

42. Zabaleta A., D’Avola D., Echeverria I., Llopiz D., Silva L., Villanueva L., Riezu-Boj J., Larrea E., Pereboev A., Lasarte J., Rodriguez-Lago I., Inarrairaegui M., Sangro B., Prieto J., Sarobe P. Clinical testing of a dendritic cell targeted therapeutic vaccine in patients with chronic hepatitis C virus infection. Mol. Ther. Methods Clin. Dev., 2015, Vol. 2, p. 15006.

43. Zhu J., Peng T., Johnston C., Phasouk K., Kask A.S., Klock A. Immune surveillance by CD8-α + skin-resident T cells in human herpes virus infection. Nature, 2013, Vol. 497, pp. 494-497.


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For citations:


Leplina O.Yu., Starostina N.M., Blinova D.D., Zheltova O.I., Oleinik E.A., Tyrinova T.V., Ostanin A.A., Chernykh E.R. RESULTS OF A PILOT CLINICAL TRIAL OF DENDRITICCELL BASED VACCINES FOR TREATMENT OF RECURRENT HERPESVIRUS INFECTION. Medical Immunology (Russia). 2016;18(5):425-436. (In Russ.) https://doi.org/10.15789/1563-0625-2016-5-425-436

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