Вопросы вирусологии. 2022; 67: 193-205
Лекарственная устойчивость ВИЧ: прежние и современные тенденции
https://doi.org/10.36233/0507-4088-113Аннотация
ВИЧ-инфекция является неизлечимым заболеванием, однако эффективная антиретровирусная терапия (АРТ) позволяет добиться установления неопределяемой вирусной нагрузки, сохранения функции иммунной системы и здоровья пациента. В связи с постоянным ростом применения АРТ и высокой изменчивостью ВИЧ, особенно у пациентов, получающих по разным причинам так называемую субоптимальную терапию, растёт частота возникновения лекарственной устойчивости (ЛУ). В свою очередь, наличие ЛУ у ВИЧ-инфицированного пациента влияет на эффективность терапии, что влечёт за собой ограничение выбора и удорожание схем лечения, прогрессирование заболевания и, следовательно, повышенный риск летального исхода, а также передачи инфекции партнёрам. Рассмотрены основные проблемы ЛУ, её виды и причины развития, а также факторы, связанные с её развитием. Описаны основные мутации ЛУ по каждому из классов препаратов.
Список литературы
1. Федеральный научно-методический Центр по профи- лактике и борьбе со СПИДом. Справка ВИЧ в России на 31.12.2021 г. Available at: http://www.hivrussia.info/wp-content/uploads/2022/03/Spravka-VICH-v-Rossii-na-31.12.2021-g..pdf
2. WHO. The HIV drug resistance report – 2012. Available at: https://apps.who.int/iris/handle/10665/75183
3. Perera M.R., Wills M.R., Sinclair J.H. HCMV antivirals and strategies to target the latent reservoir. Viruses. 2021; 13(5): 817. https://doi.org/10.3390/v13050817
4. Frange P., Leruez-Ville M. Maribavir, brincidofovir and letermovir: Efficacy and safety of new antiviral drugs for treating cytomegalovirus infections. Med. Mal. Infect. 2018; 48(8): 495–502. https://doi.org/10.1016/j.medmal.2018.03.006
5. Wittkop L., Gunthard H.F., de Wolf F., Dunn D., Cozzi-Lepri A., de Luca A., et al. Effect of transmitted drug resistance on virological and immunological response to initial combination antiretroviral therapy for HIV (EuroCoord-CHAIN joint project): a European multicohort study. Lancet Infect. Dis. 2011; 11(5): 363–71. https://doi.org/10.1016/S1473-3099(11)70032-9
6. Macdonald V., Mbuagbaw L., Jordan M.R., Mathers B., Jay S., Baggaley R., et al. Prevalence of pretreatment HIV drug resistance in key populations: a systematic review and meta-analysis. J. Int. AIDS Soc. 2020; 23(12): e25656. https://doi.org/10.1002/jia2.25656
7. Gupta-Wright A., Fielding K., van Oosterhout J.J., Alufandika M., Grint D.J., Chimbayo E., et al. Virological failure, HIV-1 drug resistance, and early mortality in adults admitted to hospital in Malawi: an observational cohort study. Lancet HIV. 2020; 7(9): e620–8. https://doi.org/10.1016/s2352-3018(20)30172-7
8. Moraka N.O., Garcia-Broncano P., Hu Z., Ajibola G., Bareng O.T., Pretorius-Holme M., et al. Patterns of pretreatment drug resistance mutations of very early diagnosed and treated infants in Botswana. AIDS. 2021; 35(15): 2413–21. https://doi.org/10.1097/qad.0000000000003041
9. Willim R., Shadabi E., Sampathkumar R., Li L., Balshaw R., Kimani J., et al. High level of pre-treatment HIV-1 drug resistance and its association with HLA class I-mediated restriction in the Pumwani Sex Worker cohort. Viruses. 2022; 14(2): 273. https://doi.org/10.3390/v14020273
10. Weidle P.J., Mastro T.D., Grant A.D., Nkengasong J., Macharia D. HIV/AIDS treatment and HIV vaccines for Africa. Lancet. 2002; 359(9325): 2261–7. https://doi.org/10.1016/s0140-6736(02)09297-8
11. Little S.J., Holte S., Routy J.P., Daar E.S., Markowitz M., Collier A.C., et al. Antiretroviral-drug resistance among patients recently infected with HIV. N. Engl. J. Med. 2002; 347(6): 385–94. https://doi.org/10.1056/NEJMoa013552
12. Blower S., Volberding P. What can modeling tell us about the threat of antiviral drug resistance? Curr. Opin. Infect. Dis. 2002; 15(6): 609–14. https://doi.org/10.1097/00001432-200212000-00009
13. Hecht F.M., Grant R.M., Petropoulos C.J., Dillon B., Chesney M.A., Tian H., et al. Sexual transmission of an HIV-1 variant resistant to multiple reverse-transcriptase and protease inhibitors. N. Engl. J. Med. 1998; 339(5): 307–11. https://doi.org/10.1056/nejm199807303390504
14. Ammaranond P., Cunningham P., Oelrichs R., Suzuki K., Harris C., Leas L., et al. Rates of transmission of antiretroviral drug resistant strains of HIV-1. J. Clin. Virol. 2003; 26(2): 153–61. https://doi.org/10.1016/s1386-6532(02)00114-2
15. Bertagnolio S., Beanland R.L., Jordan M.R., Doherty M., Hirnschall G. The World Health Organization’s response to emerging human immunodeficiency virus drug resistance and a call for global action. J. Infect. Dis. 2017; 216(Suppl. 9): S801–4. https://doi.org/10.1093/infdis/jix402
16. Лага В.Ю., Немыкин А.В., Бегма Е.Н., Страхова А.М., Васильева Н.А., Ожмегова Е.Н. и др. Молекулярно-генетический анализ вариантов ВИЧ-1, циркулирующих в Республике Крым. ВИЧ-инфекция и иммуносупрессии. 2019; 11(4): 91–7. https://doi.org/10.22328/2077-9828-2019-11-4-91-97
17. Van Cleef G.F., Fisher E.J., Polk R.E. Drug interaction potential with inhibitors of HIV protease. Pharmacotherapy. 1997; 17(4): 774–8.
18. King J.R., Wynn H., Brundage R., Acosta E.P. Pharmacokinetic enhancement of protease inhibitor therapy. Clin. Pharmacokinet. 2004; 43(5): 291–310. https://doi.org/10.2165/00003088-200443050-00003
19. Larder B. Mechanisms of HIV-1 drug resistance. AIDS. 2001; 15(Suppl. 5): S27–34. https://doi.org/10.1097/00002030-200100005-00005
20. Deeks S.G., Wrin T., Liegler T., Hoh R., Hayden M., Barbour J.D., et al. Virologic and immunologic consequences of discontinuing combination antiretroviral-drug therapy in HIV-infected patients with detectable viremia. N. Engl. J. Med. 2001; 344(7): 472–80. https://doi.org/10.1056/nejm200102153440702
21. Bangsberg D.R., Deeks S.G. Is average adherence to HIV antiretroviral therapy enough? J. Gen. Intern. Med. 2002; 17(10): 812–3. https://doi.org/10.1046/j.1525-1497.2002.20812.x
22. Viswanathan S., Detels R., Mehta S.H., Macatangay B.J., Kirk G.D., Jacobson L.P. Level of adherence and HIV RNA suppression in the current era of highly active antiretroviral therapy (HAART). AIDS Behav. 2015; 19(4): 601–11. https://doi.org/10.1007/s10461-014-0927-4
23. Parienti J.J., Bangsberg D.R., Verdon R., Gardner E.M. Better adherence with once-daily antiretroviral regimens: a meta-analysis. Clin. Infect. Dis. 2009; 48(4): 484–8. https://doi.org/10.1086/596482
24. Bangsberg D.R., Ragland K., Monk A., Deeks S.G. A single tablet regimen is associated with higher adherence and viral suppression than multiple tablet regimens in HIV+ homeless and marginally housed people. AIDS. 2010; 24(18): 2835–40. https://doi.org/10.1097/QAD.0b013e328340a209
25. AIDSinfo. Side Effects of Anti-HIV Medications. Available at: https://doh.dc.gov/sites/default/files/dc/sites/doh/publication/attachments/sideeffectanithivmeds.pdf
26. Caramelli B. Cardiovascular risk and metabolic effects in HIV patients. In: Proceedings of 29th World Congress of Internal Medicine. Buenos Aires; 2008: 16–20.
27. Richman D.D. HIV chemotherapy. Nature. 2001; 410(6831): 995–1001. https://doi.org/10.1038/35073673
28. Bangsberg D.R., Moss A.R., Deeks S.G. Paradoxes of adherence and drug resistance to HIV antiretroviral therapy. J. Antimicrob. Chemother. 2004; 53(5): 696–9. https://doi.org/10.1093/jac/dkh162
29. Bennett D.E., Jordan M.R., Bertagnolio S., Hong S.Y., Ravasi G., McMahon J.H., et al. HIV drug resistance early warning indicators in cohorts of individuals starting antiretroviral therapy between 2004 and 2009: World Health Organization global report from 50 countries. Clin. Infect. Dis. 2012; 54(Suppl. 4): S280–9. https://doi.org/10.1093/cid/cis207
30. WHO. Global report on early warning indicators of HIV drug resistance – 2016. Available at: http://apps.who.int/iris/bitstream/handle/10665/246219/9789241511179-eng.pdf?sequence=1
31. Rojas Sánchez P., Domínguez S., Jiménez De Ory S., Prieto L., Rojo P., Mellado P., et al. Trends in drug resistance prevalence, HIV-1 variants and clinical status in HIV-1-infected pediatric population in Madrid: 1993 to 2015 analysis. Pediatr. Infect. Dis. J. 2018; 37(3): e48–57. https://doi.org/10.1097/inf.0000000000001760
32. Schmidt D., Kollan C., Fätkenheuer G., Schülter E., Stellbrink H.J., Noah C., et al. Estimating trends in the proportion of transmitted and acquired HIV drug resistance in a long term observational cohort in Germany. PLoS One. 2014; 9(8): e104474. https://doi.org/10.1371/journal.pone.0104474
33. Кириченко А.А., Киреев Д.Е., Шлыкова А.В., Лопатухин А.Э., Лаповок И.А., Салеева Д.В. и др. Лекарственная устойчивость ВИЧ-1 у пациентов с вирусологической неэффективностью АРТ в России (2013-2021 гг.). Эпидемиология и инфекционные болезни. Актуальные вопросы. 2021; 11(3): 53–62. https://doi.org/10.18565/epidem.2021.11.3.53-62
34. Rhee S.Y., Jordan M.R., Raizes E., Chua A., Parkin N., Kantor R., et al. HIV-1 drug resistance mutations: potential applications for point-of-care genotypic resistance testing. PLoS One. 2015; 10(12): e0145772. https://doi.org/10.1371/journal.pone.0145772
35. Pimentel V., Pingarilho M., Alves D., Diogo I., Fernandes S., Miranda M., et al. Molecular epidemiology of HIV-1 infected migrants followed up in Portugal: Trends between 2001-2017. Viruses. 2020; 12(3): 268. https://doi.org/10.3390/v12030268
36. Campbell T.B., Shulman N.S., Johnson S.C., Zolopa A.R., Young R.K., Bushman L., et al. Antiviral activity of lamivudine in salvage therapy for multidrug-resistant HIV-1 infection. Clin. Infect. Dis. 2005; 41(2): 236–42. https://doi.org/10.1086/430709
37. Kuritzkes D.R. Clinical significance of drug resistance in HIV-1 infection. AIDS. 1996; 10(Suppl. 5): S27–31. https://doi.org/10.1097/00002030-199612005-00005
38. Turner D., Brenner B., Wainberg M.A. Multiple effects of the M184V resistance mutation in the reverse transcriptase of human immunodeficiency virus type 1. Clin. Diagn. Lab. Immunol. 2003; 10(6): 979–81. https://doi.org/10.1128/cdli.10.6.979-981.2003
39. Petrella M., Wainberg M.A. Might the M184V substitution in HIV-1 RT confer clinical benefit? AIDS Rev. 2002; 4(4): 224–32.
40. Melikian G.L., Rhee S.Y., Varghese V., Porter D., White K., Taylor J., et al. Non-nucleoside reverse transcriptase inhibitor (NNRTI) cross-resistance: implications for preclinical evaluation of novel NNRTIs and clinical genotypic resistance testing. J. Antimicrob. Chemother. 2014; 69(1): 12–20. https://doi.org/10.1093/jac/dkt316
41. Kuritzkes D.R., Lalama C.M., Ribaudo H.J., Marcial M., Meyer W.A. 3rd, Shikuma C., et al. Preexisting resistance to nonnucleoside reverse-transcriptase inhibitors predicts virologic failure of an efavirenz-based regimen in treatment-naive HIV-1-infected subjects. J. Infect. Dis. 2008; 197(6): 867–70. https://doi.org/10.1086/528802
42. Gallant J.E., DeJesus E., Arribas J.R., Pozniak A.L., Gazzard B., Campo R.E., et al. Tenofovir DF, emtricitabine, and efavirenz vs. zidovudine, lamivudine, and efavirenz for HIV. N. Engl. J. Med. 2006; 354(3): 251–60. https://doi.org/10.1056/NEJMoa051871
43. Hofstra L.M., Sauvageot N., Albert J., Alexiev I., Garcia F., Struck D., et al. Transmission of HIV drug resistance and the predicted effect on current first-line regimens in Europe. Clin. Infect. Dis. 2016; 62(5): 655–63. https://doi.org/10.1093/cid/civ963
44. Wensing A.M., Calvez V., Ceccherini-Silberstein F., Charpentier C., Günthard H.F., Paredes R., et al. 2019 update of the drug resistance mutations in HIV-1. Top. Antivir. Med. 2019; 27(3): 111–21.
45. Fun A., Wensing A.M., Verheyen J., Nijhuis M. Human immunodeficiency virus gag and protease: partners in resistance. Retrovirology. 2012; 9: 63. https://doi.org/10.1186/1742-4690-9-63
46. Rabi S.A., Laird G.M., Durand C.M., Laskey S., Shan L., Bailey J.R., et al. Multi-step inhibition explains HIV-1 protease inhibitor pharmacodynamics and resistance. J. Clin. Invest. 2013; 123(9): 3848–60. https://doi.org/10.1172/jci67399
47. Gupta U., Jain N.K. Non-polymeric nano-carriers in HIV/AIDS drug delivery and targeting. Adv. Drug Deliv. Rev. 2010; 62(4-5): 478–90. https://doi.org/10.1016/j.addr.2009.11.018
48. Orta-Resendiz A., Rodriguez-Diaz R.A., Angulo-Medina L.A., Hernandez-Flores M., Soto-Ramirez L.E. HIV-1 acquired drug resistance to integrase inhibitors in a cohort of antiretroviral therapy multi-experienced Mexican patients failing to raltegravir: a cross-sectional study. AIDS Res. Ther. 2020; 17(1): 6. https://doi.org/10.1186/s12981-020-0262-y
49. Castagna A., Maggiolo F., Penco G., Wright D., Mills A., Grossberg R., et al. Dolutegravir in antiretroviral-experienced patients with raltegravir- and/or elvitegravir-resistant HIV-1: 24-week results of the phase III VIKING-3 study. J. Infect. Dis. 2014; 210(3): 354–62. https://doi.org/10.1093/infdis/jiu051
50. Smith S.J., Zhao X.Z., Burke T.R. Jr., Hughes S.H. Efficacies of Cabotegravir and Bictegravir against drug-resistant HIV-1 integrase mutants. Retrovirology. 2018; 15(1): 37. https://doi.org/10.1186/s12977-018-0420-7
51. Eron J.J., Clotet B., Durant J., Katlama C., Kumar P., Lazzarin A., et al. Safety and efficacy of dolutegravir in treatment-experienced subjects with raltegravir-resistant HIV type 1 infection: 24-week results of the VIKING Study. J. Infect. Dis. 2013; 207(5): 740–8. https://doi.org/10.1093/infdis/jis750
52. Mesplède T., Wainberg M.A. Resistance against integrase strand transfer inhibitors and relevance to HIV persistence. Viruses. 2015; 7(7): 3703–18. https://doi.org/10.3390/v7072790
53. Hassounah S.A., Alikhani A., Oliveira M., Bharaj S., Ibanescu R.I., Osman N., et al. Antiviral activity of bictegravir and cabotegravir against integrase inhibitor-resistant SIVmac239 and HIV-1. Antimicrob. Agents Chemother. 2017; 61(12): e01695-17. https://doi.org/10.1128/aac.01695-17
54. Rizzardini G., Overton E.T., Orkin C., Swindells S., Arasteh K., Górgolas Hernández-Mora M., et al. Long-acting injectable cabotegravir + rilpivirine for HIV maintenance therapy: week 48 pooled analysis of phase 3 ATLAS and FLAIR trials. J. Acquir. Immune Defic. Syndr. 2020; 85(4): 498–506. https://doi.org/10.1097/qai.0000000000002466
55. Anstett K., Brenner B., Mesplede T., Wainberg M.A. HIV drug resistance against strand transfer integrase inhibitors. Retrovirology. 2017; 14(1): 36. https://doi.org/10.1186/s12977-017-0360-7
56. Viani R.M., Alvero C., Fenton T., Acosta E.P., Hazra R., Townley E., et al. Safety, pharmacokinetics and efficacy of dolutegravir in treatment-experienced HIV-1 infected adolescents: Forty-eightweek Results from IMPAACT P1093. Pediatr. Infect. Dis. J. 2015; 34(11): 1207–13. https://doi.org/10.1097/inf.0000000000000848
57. Cahn P., Pozniak A.L., Mingrone H., Shuldyakov A., Brites C., Andrade-Villanueva J.F., et al. Dolutegravir versus raltegravir in antiretroviral-experienced, integrase-inhibitor-naive adults with HIV: week 48 results from the randomised, double-blind, non-inferiority SAILING study. Lancet. 2013; 382(9893): 700–8. https://doi.org/10.1016/s0140-6736(13)61221-0
58. Lepik K.J., Harrigan P.R., Yip B., Wang L., Robbins M.A., Zhang W.W., et al. Emergent drug resistance with integrase strand transfer inhibitor-based regimens. AIDS. 2017; 31(10): 1425–34. https://doi.org/10.1097/qad.0000000000001494
59. Claborn K.R., Meier E., Miller M.B., Leffingwell T.R. A systematic review of treatment fatigue among HIV-infected patients prescribed antiretroviral therapy. Psychol. Health Med. 2015; 20(3): 255–65. https://doi.org/10.1080/13548506.2014.945601
60. Overton E.T., Richmond G., Rizzardini G., Jaeger H., Orrell C., Nagimova F., et al. Long-acting cabotegravir and rilpivirine dosed every 2 months in adults with HIV-1 infection (ATLAS-2M), 48-week results: a randomised, multicentre, open-label, phase 3b, non-inferiority study. Lancet. 2021; 396(10267): 1994–2005. https://doi.org/10.1016/s0140-6736(20)32666-0
61. Kirichenko A., Lapovok I., Baryshev P., van de Vijver D., van Kampen J.J.A., Boucher C.A.B., et al. Genetic features of HIV-1 integrase sub-subtype A6 predominant in Russia and predicted susceptibility to INSTIs. Viruses. 2020; 12(8): 838. https://doi.org/10.3390/v12080838
62. Marcelin A.G., Charpentier C., Jary A., Perrier M., Margot N., Callebaut C., et al. Frequency of capsid substitutions associated with GS-6207 in vitro resistance in HIV-1 from antiretroviral-naive and -experienced patients. J. Antimicrob. Chemother. 2020; 75(6): 1588–90. https://doi.org/10.1093/jac/dkaa060
63. Grobler J.A., Huang Q., Hazuda D., Lai M. Efficacy of MK-8591м against diverse HIV-1 subtypes and NRTI-resistant clinical isolates. In: International Congress of Drug Therapy in HIV Infection (HIV Glasgow). Glasgow; 2018.
64. Celum C., Baeten J.M. Tenofovir-based pre-exposure prophylaxis for HIV prevention: evolving evidence. Curr. Opin. Infect. Dis. 2012; 25(1): 51–7. https://doi.org/10.1097/QCO.0b013e32834ef5ef
65. Grant R.M., Lama J.R., Anderson P.L., McMahan V., Liu A.Y., Vargas L., et al. Preexposure chemoprophylaxis for HIV prevention in men who have sex with men. N. Engl. J. Med. 2010; 363(27): 2587–99. https://doi.org/10.1056/NEJMoa1011205
66. Andrei G., Lisco A., Vanpouille C., Introini A., Balestra E., van den Oord J., et al. Topical tenofovir, a microbicide effective against HIV, inhibits herpes simplex virus-2 replication. Cell Host Microbe. 2011; 10(4): 379–89. https://doi.org/10.1016/j.chom.2011.08.015
67. Gibas K.M., van den Berg P., Powell V.E., Krakower D.S. Drug resistance during HIV pre-exposure prophylaxis. Drugs. 2019; 79(6): 609–19. https://doi.org/10.1007/s40265-019-01108-x
Problems of Virology. 2022; 67: 193-205
HIV drug resistance: past and current trends
Ozhmegova E. N., Bobkova M. R.
https://doi.org/10.36233/0507-4088-113Abstract
HIV infection is incurable, but effective antiretroviral therapy (ART) makes it possible to achieve an undetectable viral load (VL), to preserve the function of the immune system and to prevent the patient’s health. Due to the constant increase in the use of ART and the high variability of HIV, especially in patients receiving so-called suboptimal therapy for various reasons, the incidence of drug resistance (DR) is increasing. In turn, the presence of DR in an HIV-infected patient affects the effectiveness of therapy, which leads to a limited choice and an increase in the cost of treatment regimens, disease progression and, consequently, an increased risk of death, as well as transmission of infection to partners. The main problems of drug resistance, its types and causes, as well as factors associated with its development are considered. The main drug resistance mutations for each of the drug classes are described.
References
1. Federal'nyi nauchno-metodicheskii Tsentr po profi- laktike i bor'be so SPIDom. Spravka VICh v Rossii na 31.12.2021 g. Available at: http://www.hivrussia.info/wp-content/uploads/2022/03/Spravka-VICH-v-Rossii-na-31.12.2021-g..pdf
2. WHO. The HIV drug resistance report – 2012. Available at: https://apps.who.int/iris/handle/10665/75183
3. Perera M.R., Wills M.R., Sinclair J.H. HCMV antivirals and strategies to target the latent reservoir. Viruses. 2021; 13(5): 817. https://doi.org/10.3390/v13050817
4. Frange P., Leruez-Ville M. Maribavir, brincidofovir and letermovir: Efficacy and safety of new antiviral drugs for treating cytomegalovirus infections. Med. Mal. Infect. 2018; 48(8): 495–502. https://doi.org/10.1016/j.medmal.2018.03.006
5. Wittkop L., Gunthard H.F., de Wolf F., Dunn D., Cozzi-Lepri A., de Luca A., et al. Effect of transmitted drug resistance on virological and immunological response to initial combination antiretroviral therapy for HIV (EuroCoord-CHAIN joint project): a European multicohort study. Lancet Infect. Dis. 2011; 11(5): 363–71. https://doi.org/10.1016/S1473-3099(11)70032-9
6. Macdonald V., Mbuagbaw L., Jordan M.R., Mathers B., Jay S., Baggaley R., et al. Prevalence of pretreatment HIV drug resistance in key populations: a systematic review and meta-analysis. J. Int. AIDS Soc. 2020; 23(12): e25656. https://doi.org/10.1002/jia2.25656
7. Gupta-Wright A., Fielding K., van Oosterhout J.J., Alufandika M., Grint D.J., Chimbayo E., et al. Virological failure, HIV-1 drug resistance, and early mortality in adults admitted to hospital in Malawi: an observational cohort study. Lancet HIV. 2020; 7(9): e620–8. https://doi.org/10.1016/s2352-3018(20)30172-7
8. Moraka N.O., Garcia-Broncano P., Hu Z., Ajibola G., Bareng O.T., Pretorius-Holme M., et al. Patterns of pretreatment drug resistance mutations of very early diagnosed and treated infants in Botswana. AIDS. 2021; 35(15): 2413–21. https://doi.org/10.1097/qad.0000000000003041
9. Willim R., Shadabi E., Sampathkumar R., Li L., Balshaw R., Kimani J., et al. High level of pre-treatment HIV-1 drug resistance and its association with HLA class I-mediated restriction in the Pumwani Sex Worker cohort. Viruses. 2022; 14(2): 273. https://doi.org/10.3390/v14020273
10. Weidle P.J., Mastro T.D., Grant A.D., Nkengasong J., Macharia D. HIV/AIDS treatment and HIV vaccines for Africa. Lancet. 2002; 359(9325): 2261–7. https://doi.org/10.1016/s0140-6736(02)09297-8
11. Little S.J., Holte S., Routy J.P., Daar E.S., Markowitz M., Collier A.C., et al. Antiretroviral-drug resistance among patients recently infected with HIV. N. Engl. J. Med. 2002; 347(6): 385–94. https://doi.org/10.1056/NEJMoa013552
12. Blower S., Volberding P. What can modeling tell us about the threat of antiviral drug resistance? Curr. Opin. Infect. Dis. 2002; 15(6): 609–14. https://doi.org/10.1097/00001432-200212000-00009
13. Hecht F.M., Grant R.M., Petropoulos C.J., Dillon B., Chesney M.A., Tian H., et al. Sexual transmission of an HIV-1 variant resistant to multiple reverse-transcriptase and protease inhibitors. N. Engl. J. Med. 1998; 339(5): 307–11. https://doi.org/10.1056/nejm199807303390504
14. Ammaranond P., Cunningham P., Oelrichs R., Suzuki K., Harris C., Leas L., et al. Rates of transmission of antiretroviral drug resistant strains of HIV-1. J. Clin. Virol. 2003; 26(2): 153–61. https://doi.org/10.1016/s1386-6532(02)00114-2
15. Bertagnolio S., Beanland R.L., Jordan M.R., Doherty M., Hirnschall G. The World Health Organization’s response to emerging human immunodeficiency virus drug resistance and a call for global action. J. Infect. Dis. 2017; 216(Suppl. 9): S801–4. https://doi.org/10.1093/infdis/jix402
16. Laga V.Yu., Nemykin A.V., Begma E.N., Strakhova A.M., Vasil'eva N.A., Ozhmegova E.N. i dr. Molekulyarno-geneticheskii analiz variantov VICh-1, tsirkuliruyushchikh v Respublike Krym. VICh-infektsiya i immunosupressii. 2019; 11(4): 91–7. https://doi.org/10.22328/2077-9828-2019-11-4-91-97
17. Van Cleef G.F., Fisher E.J., Polk R.E. Drug interaction potential with inhibitors of HIV protease. Pharmacotherapy. 1997; 17(4): 774–8.
18. King J.R., Wynn H., Brundage R., Acosta E.P. Pharmacokinetic enhancement of protease inhibitor therapy. Clin. Pharmacokinet. 2004; 43(5): 291–310. https://doi.org/10.2165/00003088-200443050-00003
19. Larder B. Mechanisms of HIV-1 drug resistance. AIDS. 2001; 15(Suppl. 5): S27–34. https://doi.org/10.1097/00002030-200100005-00005
20. Deeks S.G., Wrin T., Liegler T., Hoh R., Hayden M., Barbour J.D., et al. Virologic and immunologic consequences of discontinuing combination antiretroviral-drug therapy in HIV-infected patients with detectable viremia. N. Engl. J. Med. 2001; 344(7): 472–80. https://doi.org/10.1056/nejm200102153440702
21. Bangsberg D.R., Deeks S.G. Is average adherence to HIV antiretroviral therapy enough? J. Gen. Intern. Med. 2002; 17(10): 812–3. https://doi.org/10.1046/j.1525-1497.2002.20812.x
22. Viswanathan S., Detels R., Mehta S.H., Macatangay B.J., Kirk G.D., Jacobson L.P. Level of adherence and HIV RNA suppression in the current era of highly active antiretroviral therapy (HAART). AIDS Behav. 2015; 19(4): 601–11. https://doi.org/10.1007/s10461-014-0927-4
23. Parienti J.J., Bangsberg D.R., Verdon R., Gardner E.M. Better adherence with once-daily antiretroviral regimens: a meta-analysis. Clin. Infect. Dis. 2009; 48(4): 484–8. https://doi.org/10.1086/596482
24. Bangsberg D.R., Ragland K., Monk A., Deeks S.G. A single tablet regimen is associated with higher adherence and viral suppression than multiple tablet regimens in HIV+ homeless and marginally housed people. AIDS. 2010; 24(18): 2835–40. https://doi.org/10.1097/QAD.0b013e328340a209
25. AIDSinfo. Side Effects of Anti-HIV Medications. Available at: https://doh.dc.gov/sites/default/files/dc/sites/doh/publication/attachments/sideeffectanithivmeds.pdf
26. Caramelli B. Cardiovascular risk and metabolic effects in HIV patients. In: Proceedings of 29th World Congress of Internal Medicine. Buenos Aires; 2008: 16–20.
27. Richman D.D. HIV chemotherapy. Nature. 2001; 410(6831): 995–1001. https://doi.org/10.1038/35073673
28. Bangsberg D.R., Moss A.R., Deeks S.G. Paradoxes of adherence and drug resistance to HIV antiretroviral therapy. J. Antimicrob. Chemother. 2004; 53(5): 696–9. https://doi.org/10.1093/jac/dkh162
29. Bennett D.E., Jordan M.R., Bertagnolio S., Hong S.Y., Ravasi G., McMahon J.H., et al. HIV drug resistance early warning indicators in cohorts of individuals starting antiretroviral therapy between 2004 and 2009: World Health Organization global report from 50 countries. Clin. Infect. Dis. 2012; 54(Suppl. 4): S280–9. https://doi.org/10.1093/cid/cis207
30. WHO. Global report on early warning indicators of HIV drug resistance – 2016. Available at: http://apps.who.int/iris/bitstream/handle/10665/246219/9789241511179-eng.pdf?sequence=1
31. Rojas Sánchez P., Domínguez S., Jiménez De Ory S., Prieto L., Rojo P., Mellado P., et al. Trends in drug resistance prevalence, HIV-1 variants and clinical status in HIV-1-infected pediatric population in Madrid: 1993 to 2015 analysis. Pediatr. Infect. Dis. J. 2018; 37(3): e48–57. https://doi.org/10.1097/inf.0000000000001760
32. Schmidt D., Kollan C., Fätkenheuer G., Schülter E., Stellbrink H.J., Noah C., et al. Estimating trends in the proportion of transmitted and acquired HIV drug resistance in a long term observational cohort in Germany. PLoS One. 2014; 9(8): e104474. https://doi.org/10.1371/journal.pone.0104474
33. Kirichenko A.A., Kireev D.E., Shlykova A.V., Lopatukhin A.E., Lapovok I.A., Saleeva D.V. i dr. Lekarstvennaya ustoichivost' VICh-1 u patsientov s virusologicheskoi neeffektivnost'yu ART v Rossii (2013-2021 gg.). Epidemiologiya i infektsionnye bolezni. Aktual'nye voprosy. 2021; 11(3): 53–62. https://doi.org/10.18565/epidem.2021.11.3.53-62
34. Rhee S.Y., Jordan M.R., Raizes E., Chua A., Parkin N., Kantor R., et al. HIV-1 drug resistance mutations: potential applications for point-of-care genotypic resistance testing. PLoS One. 2015; 10(12): e0145772. https://doi.org/10.1371/journal.pone.0145772
35. Pimentel V., Pingarilho M., Alves D., Diogo I., Fernandes S., Miranda M., et al. Molecular epidemiology of HIV-1 infected migrants followed up in Portugal: Trends between 2001-2017. Viruses. 2020; 12(3): 268. https://doi.org/10.3390/v12030268
36. Campbell T.B., Shulman N.S., Johnson S.C., Zolopa A.R., Young R.K., Bushman L., et al. Antiviral activity of lamivudine in salvage therapy for multidrug-resistant HIV-1 infection. Clin. Infect. Dis. 2005; 41(2): 236–42. https://doi.org/10.1086/430709
37. Kuritzkes D.R. Clinical significance of drug resistance in HIV-1 infection. AIDS. 1996; 10(Suppl. 5): S27–31. https://doi.org/10.1097/00002030-199612005-00005
38. Turner D., Brenner B., Wainberg M.A. Multiple effects of the M184V resistance mutation in the reverse transcriptase of human immunodeficiency virus type 1. Clin. Diagn. Lab. Immunol. 2003; 10(6): 979–81. https://doi.org/10.1128/cdli.10.6.979-981.2003
39. Petrella M., Wainberg M.A. Might the M184V substitution in HIV-1 RT confer clinical benefit? AIDS Rev. 2002; 4(4): 224–32.
40. Melikian G.L., Rhee S.Y., Varghese V., Porter D., White K., Taylor J., et al. Non-nucleoside reverse transcriptase inhibitor (NNRTI) cross-resistance: implications for preclinical evaluation of novel NNRTIs and clinical genotypic resistance testing. J. Antimicrob. Chemother. 2014; 69(1): 12–20. https://doi.org/10.1093/jac/dkt316
41. Kuritzkes D.R., Lalama C.M., Ribaudo H.J., Marcial M., Meyer W.A. 3rd, Shikuma C., et al. Preexisting resistance to nonnucleoside reverse-transcriptase inhibitors predicts virologic failure of an efavirenz-based regimen in treatment-naive HIV-1-infected subjects. J. Infect. Dis. 2008; 197(6): 867–70. https://doi.org/10.1086/528802
42. Gallant J.E., DeJesus E., Arribas J.R., Pozniak A.L., Gazzard B., Campo R.E., et al. Tenofovir DF, emtricitabine, and efavirenz vs. zidovudine, lamivudine, and efavirenz for HIV. N. Engl. J. Med. 2006; 354(3): 251–60. https://doi.org/10.1056/NEJMoa051871
43. Hofstra L.M., Sauvageot N., Albert J., Alexiev I., Garcia F., Struck D., et al. Transmission of HIV drug resistance and the predicted effect on current first-line regimens in Europe. Clin. Infect. Dis. 2016; 62(5): 655–63. https://doi.org/10.1093/cid/civ963
44. Wensing A.M., Calvez V., Ceccherini-Silberstein F., Charpentier C., Günthard H.F., Paredes R., et al. 2019 update of the drug resistance mutations in HIV-1. Top. Antivir. Med. 2019; 27(3): 111–21.
45. Fun A., Wensing A.M., Verheyen J., Nijhuis M. Human immunodeficiency virus gag and protease: partners in resistance. Retrovirology. 2012; 9: 63. https://doi.org/10.1186/1742-4690-9-63
46. Rabi S.A., Laird G.M., Durand C.M., Laskey S., Shan L., Bailey J.R., et al. Multi-step inhibition explains HIV-1 protease inhibitor pharmacodynamics and resistance. J. Clin. Invest. 2013; 123(9): 3848–60. https://doi.org/10.1172/jci67399
47. Gupta U., Jain N.K. Non-polymeric nano-carriers in HIV/AIDS drug delivery and targeting. Adv. Drug Deliv. Rev. 2010; 62(4-5): 478–90. https://doi.org/10.1016/j.addr.2009.11.018
48. Orta-Resendiz A., Rodriguez-Diaz R.A., Angulo-Medina L.A., Hernandez-Flores M., Soto-Ramirez L.E. HIV-1 acquired drug resistance to integrase inhibitors in a cohort of antiretroviral therapy multi-experienced Mexican patients failing to raltegravir: a cross-sectional study. AIDS Res. Ther. 2020; 17(1): 6. https://doi.org/10.1186/s12981-020-0262-y
49. Castagna A., Maggiolo F., Penco G., Wright D., Mills A., Grossberg R., et al. Dolutegravir in antiretroviral-experienced patients with raltegravir- and/or elvitegravir-resistant HIV-1: 24-week results of the phase III VIKING-3 study. J. Infect. Dis. 2014; 210(3): 354–62. https://doi.org/10.1093/infdis/jiu051
50. Smith S.J., Zhao X.Z., Burke T.R. Jr., Hughes S.H. Efficacies of Cabotegravir and Bictegravir against drug-resistant HIV-1 integrase mutants. Retrovirology. 2018; 15(1): 37. https://doi.org/10.1186/s12977-018-0420-7
51. Eron J.J., Clotet B., Durant J., Katlama C., Kumar P., Lazzarin A., et al. Safety and efficacy of dolutegravir in treatment-experienced subjects with raltegravir-resistant HIV type 1 infection: 24-week results of the VIKING Study. J. Infect. Dis. 2013; 207(5): 740–8. https://doi.org/10.1093/infdis/jis750
52. Mesplède T., Wainberg M.A. Resistance against integrase strand transfer inhibitors and relevance to HIV persistence. Viruses. 2015; 7(7): 3703–18. https://doi.org/10.3390/v7072790
53. Hassounah S.A., Alikhani A., Oliveira M., Bharaj S., Ibanescu R.I., Osman N., et al. Antiviral activity of bictegravir and cabotegravir against integrase inhibitor-resistant SIVmac239 and HIV-1. Antimicrob. Agents Chemother. 2017; 61(12): e01695-17. https://doi.org/10.1128/aac.01695-17
54. Rizzardini G., Overton E.T., Orkin C., Swindells S., Arasteh K., Górgolas Hernández-Mora M., et al. Long-acting injectable cabotegravir + rilpivirine for HIV maintenance therapy: week 48 pooled analysis of phase 3 ATLAS and FLAIR trials. J. Acquir. Immune Defic. Syndr. 2020; 85(4): 498–506. https://doi.org/10.1097/qai.0000000000002466
55. Anstett K., Brenner B., Mesplede T., Wainberg M.A. HIV drug resistance against strand transfer integrase inhibitors. Retrovirology. 2017; 14(1): 36. https://doi.org/10.1186/s12977-017-0360-7
56. Viani R.M., Alvero C., Fenton T., Acosta E.P., Hazra R., Townley E., et al. Safety, pharmacokinetics and efficacy of dolutegravir in treatment-experienced HIV-1 infected adolescents: Forty-eightweek Results from IMPAACT P1093. Pediatr. Infect. Dis. J. 2015; 34(11): 1207–13. https://doi.org/10.1097/inf.0000000000000848
57. Cahn P., Pozniak A.L., Mingrone H., Shuldyakov A., Brites C., Andrade-Villanueva J.F., et al. Dolutegravir versus raltegravir in antiretroviral-experienced, integrase-inhibitor-naive adults with HIV: week 48 results from the randomised, double-blind, non-inferiority SAILING study. Lancet. 2013; 382(9893): 700–8. https://doi.org/10.1016/s0140-6736(13)61221-0
58. Lepik K.J., Harrigan P.R., Yip B., Wang L., Robbins M.A., Zhang W.W., et al. Emergent drug resistance with integrase strand transfer inhibitor-based regimens. AIDS. 2017; 31(10): 1425–34. https://doi.org/10.1097/qad.0000000000001494
59. Claborn K.R., Meier E., Miller M.B., Leffingwell T.R. A systematic review of treatment fatigue among HIV-infected patients prescribed antiretroviral therapy. Psychol. Health Med. 2015; 20(3): 255–65. https://doi.org/10.1080/13548506.2014.945601
60. Overton E.T., Richmond G., Rizzardini G., Jaeger H., Orrell C., Nagimova F., et al. Long-acting cabotegravir and rilpivirine dosed every 2 months in adults with HIV-1 infection (ATLAS-2M), 48-week results: a randomised, multicentre, open-label, phase 3b, non-inferiority study. Lancet. 2021; 396(10267): 1994–2005. https://doi.org/10.1016/s0140-6736(20)32666-0
61. Kirichenko A., Lapovok I., Baryshev P., van de Vijver D., van Kampen J.J.A., Boucher C.A.B., et al. Genetic features of HIV-1 integrase sub-subtype A6 predominant in Russia and predicted susceptibility to INSTIs. Viruses. 2020; 12(8): 838. https://doi.org/10.3390/v12080838
62. Marcelin A.G., Charpentier C., Jary A., Perrier M., Margot N., Callebaut C., et al. Frequency of capsid substitutions associated with GS-6207 in vitro resistance in HIV-1 from antiretroviral-naive and -experienced patients. J. Antimicrob. Chemother. 2020; 75(6): 1588–90. https://doi.org/10.1093/jac/dkaa060
63. Grobler J.A., Huang Q., Hazuda D., Lai M. Efficacy of MK-8591m against diverse HIV-1 subtypes and NRTI-resistant clinical isolates. In: International Congress of Drug Therapy in HIV Infection (HIV Glasgow). Glasgow; 2018.
64. Celum C., Baeten J.M. Tenofovir-based pre-exposure prophylaxis for HIV prevention: evolving evidence. Curr. Opin. Infect. Dis. 2012; 25(1): 51–7. https://doi.org/10.1097/QCO.0b013e32834ef5ef
65. Grant R.M., Lama J.R., Anderson P.L., McMahan V., Liu A.Y., Vargas L., et al. Preexposure chemoprophylaxis for HIV prevention in men who have sex with men. N. Engl. J. Med. 2010; 363(27): 2587–99. https://doi.org/10.1056/NEJMoa1011205
66. Andrei G., Lisco A., Vanpouille C., Introini A., Balestra E., van den Oord J., et al. Topical tenofovir, a microbicide effective against HIV, inhibits herpes simplex virus-2 replication. Cell Host Microbe. 2011; 10(4): 379–89. https://doi.org/10.1016/j.chom.2011.08.015
67. Gibas K.M., van den Berg P., Powell V.E., Krakower D.S. Drug resistance during HIV pre-exposure prophylaxis. Drugs. 2019; 79(6): 609–19. https://doi.org/10.1007/s40265-019-01108-x
События
-
Журнал «Концепт: Философия, религия, культура» принят в Scopus >>>
9 июл 2025 | 13:25 -
К платформе Elpub присоединился журнал «The BRICS Health Journal» >>>
10 июн 2025 | 12:52 -
Журнал «Неотложная кардиология и кардиоваскулярные риски» присоединился к Elpub >>>
6 июн 2025 | 09:45 -
К платформе Elpub присоединился «Медицинский журнал» >>>
5 июн 2025 | 09:41 -
НЭИКОН принял участие в конференции НИИ Организации здравоохранения и медицинского менеджмента >>>
30 мая 2025 | 10:32