Virological and immunological efficacy of metabolically favorable antiretroviral therapy regimens in HIV patients who had no previous treatment
https://doi.org/10.21292/2075-1230-2020-98-5-24-31
Abstract
The objective: to study efficacy and safety of metabolically favorable antiretroviral therapy regimens (ART), their effect on HIV RNA levels, levels of CD4, CD8 T lymphocytes, and the ratio of CD4/CD8 in HIV patients who had no previous treatment.
Subjects and methods. The study included 80 patients with HIV infection who no received ART previously, 67 of them – without clinical manifestations of HIV infection, 13 – with HIV associated diseases. The virological and immunological efficacy of three ART regimens was evaluated: rilpivirine + emtricitabine + tenofovir (RPV + FTC + TDF); dolutegravir, emtricitabine, tenofovir (DTG, FTC, TDF); raltegravir, etravirine, lamivudine (RAL, ETR, 3TC) during the first 6 months of treatment.
Results. By the end of the 6th month of ART, the rate of decrease of viral load compared to the initial level increased in the series RPV + FTS + TDF < RAL, ETR, 3TC < DTG, FTC, TDF. The number of CD4 T-lymphocytes and the ratio of CD4/CD8 increased in all three ART regimens; the number of CD8 T-lymphocytes varied depending on the treatment regimen, the presence or absence of clinical manifestations. The assessment of ART efficacy should be based on the clinical signs of HIV infection. To assess treatment efficacy, it is necessary to control the viral load and three immunological parameters: the number of CD4, CD8 T-lymphocytes, and the ratio of CD4/CD8.
About the Authors
E. I. VeselovaRussian Federation
Elena I. Veselova Researcher of Infectious Pathology Department
K. A. Kocharyan
Russian Federation
Karina A. Kocharyan Candidate of Medical Sciences, Infectious Disease Physician
O. V. Lovacheva
Russian Federation
Olga V. Lovacheva Doctor of Medical Sciences, Professor, Head Researcher
G. D. Kaminskiy
Russian Federation
Grigoriy D. Kaminskiy Doctor of Medical Sciences, Head of Infectious Pathology Department
A. G. Samoylova
Russian Federation
Anastasiya G. Samoylova Doctor of Medical Sciences, First Deputy Director
I. A. Vasilyeva
Russian Federation
Irina A. Vasilyeva Doctor of Medical Sciences, Professor, Director
References
1. Veselova E.I., Kaminskiy G.D., Samoylova А.G., Vasilyeva I.А. HIV reservoir in HIV patients. Tuberculosis and Lung Diseases, 2019, vol. 97, no. 5, pp. 50-57. (In Russ.)
2. Voronin E.E., Аfonina L.Yu., Rozenberg V.Ya., Latysheva I.B., Kaminskiy G.D., Bulankov Yu.I., Melnikova T.N., Radzikhovskaya M.V., Fomin Yu.А. VICH-infektsiya u vzroslykh: klinicheskie rekomendatsii. [HIV infection in adults: clinical guidelines]. 2017, 64 p.
3. Rukovodstvo o vremeni naznacheniya antiretrovirusnoy terapii i po dokontaktnoy profilaktike VICH-infektsii. [Guideline on when to start antiretroviral therapy and on pre-exposure prophylaxis for HIV]. WHO, 2015, 78 p.
4. Casado J.L., Monsalvo M., Rojo A.M., Fontecha M., Rodriguez-Sagrado M.A. Dolutegravir and rilpivirine for the maintenance treatment of virologically suppressed HIV-1 infection. Expert. Rev. Clin. Pharmacol., 2018, vol. 11, no. 6, pp. 561-570.
5. Cunha J., Maselli L.M.F., Bassi Stern A.C., Spada C., Bydlowski S.P. Impact of antiretroviral therapy on lipid metabolism of human immunodeficiency virus-infected patients: Old and new drugs. World J. Virol., 2015, vol. 4, no. 2, pp. 56-77.
6. Gianotti N., Poli A., Nozza S., Spagnuolo V., Tambussi G., Bossolasco S., Cinque P., Maillard M., Cernuschi M., Galli L., Lazzarin A., Castagna A. Efficacy and safety in clinical practice of a rilpivirine, tenofovir and emtricitabine single-tablet regimen in virologically suppressed HIV-positive patients on stable antiretroviral therapy. J. Int. AIDS Soc., 2015, vol. 18, no. 1, pp. 20037. doi: 10.7448/IAS.18.1.20037.
7. Goebel F., Yakovlev A., Pozniak A.L., Vinogradova E., Boogaerts G., Hoetelmans R., de Béthune M.P., Peeters M., Woodfall B. Short-term antiviral activity of TMC278 ‒ a novel NNRTI ‒ in treatment-naive HIV-1-infected subjects. AIDS, 2006, vol. 20, no. 13, pp. 1721-1726.
8. Gruzdev B., Rakhmanova A., Doubovskaya E., Yakovlev A. et al. A randomized, double-blind, placebo-controlled trial of TMC125 as 7-day monotherapy in antiretroviral naive, HIV-1 infected subjects. AIDS, 2003, vol. 17, no. 17, pp. 2487-2494.doi: 10.1097/00002030-200311210-00011.
9. Gupta S.K., Slaven J.E., Kamendulis L.M., Liu Z. A randomized, controlled trial of the effect of rilpivirine versus efavirenz on cardiovascular risk in healthy volunteers. J. Antimicrob. Chemother., 2015, vol. 70, no. 10, pp. 2889-2893.
10. Han W.M., Apornpong T., Kerr S.J., Hiransuthikul A., Gatechompol S., Do T., Ruxrungtham K., Avihingsanon A. CD4/CD8 ratio normalization rates and low ratio as prognostic marker for non-AIDS defining events among long-term virologically suppressed people living with HIV. AIDS Res. Ther., 2018, vol. 15, no. 1, pp. 13. doi: 10.1186/s12981-018-0200-4.
11. Johnson M.A., Moore K.H., Yuen G.J., Bye A., Pakes G.E. Clinical pharmacokinetics of lamivudine. Clin. Pharmacokinet., 1999, vol. 36, no. 1, pp. 41-66.
12. Louie M., Hogan C., Hurley A., Simon V. et al. Determining the antiviral activity of tenofovir disoproxil fumarate in treatment-naive chronically HIV-1-infected individuals. AIDS, 2003, vol. 17, no. 8, pp. 1151-1156. doi: 10.1097/00002030-200305230-00006.
13. Markowitz M., Morales-Ramirez J.O., Nguyen B.Y., Kovacs C.M., Steigbigel R.T., Cooper D.A., Liporace R., Schwartz R., Isaacs R., Gilde L.R., Wenning L., Zhao J., Teppler H. Antiretroviral activity, pharmacokinetics, and tolerability of MK-0518, a novel inhibitor of HIV-1 integrase, dosed as monotherapy for 10 days in treatment-naive HIV-1-infected individuals. J. Acquir. Immune Defic. Syndr., 2006, vol. 43, no. 5, pp. 509-515.
14. Min S., Sloan L., DeJesus E., Hawkins T. et al. Antiviral activity, safety, and pharmacokinetics/pharmacodynamics of dolutegravir as 10-day monotherapy in HIV-1-infected adults. AIDS, 2011, vol. 25, no. 14, pp. 1737-1745.
15. Mondi A., Cozzi-Lepri A., Tavelli A., Rusconi S., Vichi F., Ceccherini-Silberstein F., Calcagno A., De Luca A., Maggiolo F., Marchetti G., Antinori A., d'Arminio Monforte A. Icona Foundation Study Group. Effectiveness of dolutegravir-based regimens as either first-line or switch antiretroviral therapy: data from the Icona cohort. J. Int. AIDS Soc., 2019, vol. 22, no. 1, pp. e25227. doi: 10.1002/jia2.25227.
16. Rousseau F.S., Wakeford C., Mommeja-Marin H., Sanne I. et al. Prospective randomized trial of emtricitabine versus lamivudine short-term monotherapy in human immunodeficiency virus-infected patients. J. Infect. Dis., 2003, vol. 188, no. 11, pp. 1652-1658. doi: 10.1086/379667.
17. Trickey A., May M.T., Schommers P., Tate J., Ingle S.M., Guest J.L., Gill M.J., Zangerle R., Saag M., Reiss P., Monforte A.D., Johnson M., Lima V.D., Sterling T.R., Cavassini M., Wittkop L., Costagliola D., Sterne J.A.C. CD4:CD8 ratio and CD8 count as prognostic markers for mortality in human immunodeficiency virus-infected patients on antiretroviral therapy: The Antiretroviral Therapy Cohort Collaboration (ART-CC). Clin. Infect. Dis., 2017, vol. 65, no. 6, pp. 959-966.
Review
For citations:
Veselova E.I., Kocharyan K.A., Lovacheva O.V., Kaminskiy G.D., Samoylova A.G., Vasilyeva I.A. Virological and immunological efficacy of metabolically favorable antiretroviral therapy regimens in HIV patients who had no previous treatment. Tuberculosis and Lung Diseases. 2020;98(5):24-31. (In Russ.) https://doi.org/10.21292/2075-1230-2020-98-5-24-31



































