<p>Late presentation of HIV-1 infection is linked to gut dysbiosis, impaired immune reconstitution, excess inflammation, immune activation, and increased morbidity and mortality. It is unclear if antiretroviral therapy initiation can reverse HIV-associated gut dysbiosis at all, or if specific antiretroviral regimens are more effective in restoring the gut microbiota than others. This has important implications for the long-term health of individuals with HIV. In this multicenter, open-label, randomized clinical trial (NCT02337322), 88 antiretroviral-naïve individuals with advanced HIV-1 infection (median CD4+ T cells of 34 cells/mm<sup>3</sup>) were randomized (1:1) to initiate lamivudine/abacavir plus either dolutegravir or ritonavir-boosted darunavir, and were followed for 2 years. Both groups had similar HIV-1 suppression rates and recovery of CD4+ T cells. However, treatment with dolutegravir led to increased gut microbial richness and diversity and enrichment of specific microbial taxa and metabolic pathways. These changes were associated with reduced inflammation and lower immune activation, outcomes that did not occur with darunavir/ritonavir. After two years, participants on dolutegravir-based therapy had gut microbiota profiles more closely resembling those of people without HIV, compared to individuals taking darunavir/ritonavir. In summary, dolutegravir-based therapy restores the gut microbiota more effectively than darunavir/ritonavir in patients who present late with HIV.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

Dolutegravir restores gut microbiota in late-stage HIV-1 unlike darunavir: an open-label, randomized clinical trial

  • Francesc Català-Moll,
  • Carlos Blázquez-Bondia,
  • Judit Farré-Badia,
  • Ferran Torres,
  • Christian Manzardo,
  • Eva Bonfill,
  • Adrià Curran,
  • Pere Domingo,
  • Daniel Podzamczer,
  • Lluís Force,
  • Vicenç Falcó,
  • Mariona Parera,
  • Maria Casadellà,
  • José Maria Miró,
  • Marc Noguera-Julian,
  • Roger Paredes,
  • Alessandra Borgognone,
  • Nel Marín,
  • Oriol Careta,
  • Valentina Triviño,
  • Anna Cruceta,
  • Nuria Climent,
  • Francisco Lozano,
  • Montserrat Plana,
  • Juan Ambrosioni,
  • Cristina Rovira,
  • Carmen Hurtado,
  • Maria José Maleno,
  • Alexy Inciarte,
  • Anna Castelli,
  • Emma Fernández,
  • Carmen Ligero,
  • Sandra Serrano,
  • Maria Ángeles Marcos,
  • Elisa Rubio,
  • Jordi Vila,
  • Elisa de Lazzari,
  • Jose M. Gatell,
  • Daniela Malano-Barletta,
  • Paula Suanzes,
  • Esteve Ribera,
  • Ariadna Torrella,
  • Bibiana Planas,
  • Mar Gutierrez,
  • Gracia Mateo,
  • Jèssica Muñoz,
  • Ana García,
  • Kanura Lamarca,
  • Lucía Millan,
  • Judit Fernández,
  • Isabel Mur,
  • Noemí Corbacho,
  • M. Ema Molas,
  • Maria Saumoy,
  • Laura Acerete,
  • Nerea Rozas,
  • Elena Ferrer,
  • Benito Garcia,
  • Maria Silvana Diyacovo,
  • Josefa Torres,
  • Ana Silva,
  • Juan Manuel Tiraboschi,
  • Arkaitz Imaz,
  • Cristina Padilla,
  • Pilar Barrufet,
  • Xavier Boquet,
  • Gloria Sempere

摘要

Late presentation of HIV-1 infection is linked to gut dysbiosis, impaired immune reconstitution, excess inflammation, immune activation, and increased morbidity and mortality. It is unclear if antiretroviral therapy initiation can reverse HIV-associated gut dysbiosis at all, or if specific antiretroviral regimens are more effective in restoring the gut microbiota than others. This has important implications for the long-term health of individuals with HIV. In this multicenter, open-label, randomized clinical trial (NCT02337322), 88 antiretroviral-naïve individuals with advanced HIV-1 infection (median CD4+ T cells of 34 cells/mm3) were randomized (1:1) to initiate lamivudine/abacavir plus either dolutegravir or ritonavir-boosted darunavir, and were followed for 2 years. Both groups had similar HIV-1 suppression rates and recovery of CD4+ T cells. However, treatment with dolutegravir led to increased gut microbial richness and diversity and enrichment of specific microbial taxa and metabolic pathways. These changes were associated with reduced inflammation and lower immune activation, outcomes that did not occur with darunavir/ritonavir. After two years, participants on dolutegravir-based therapy had gut microbiota profiles more closely resembling those of people without HIV, compared to individuals taking darunavir/ritonavir. In summary, dolutegravir-based therapy restores the gut microbiota more effectively than darunavir/ritonavir in patients who present late with HIV.