Mesenchymal stromal cells in human immunodeficiency virus‐infected patients with discordant immune response: Early results of a phase I/II clinical trial

Abstract Between 15% and 30% of HIV‐infected subjects fail to increase their CD4+ T‐cell counts despite continuous viral suppression (immunological nonresponders [INRs]). These subjects have a higher morbidity and mortality rate, but there are no effective treatments to reverse this situation so far...

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Main Authors: María Trujillo‐Rodríguez, Pompeyo Viciana, Inmaculada Rivas‐Jeremías, Ana I. Álvarez‐Ríos, Antonio Ruiz‐García, Olga Espinosa‐Ibáñez, Salvador Arias‐Santiago, Juliana Martínez‐Atienza, Rosario Mata, Olga Fernández‐López, Ezequiel Ruiz‐Mateos, Alicia Gutiérrez‐Valencia, Luis F. López‐Cortés
Format: Article
Language:English
Published: Wiley 2021-04-01
Series:Stem Cells Translational Medicine
Subjects:
Online Access:https://doi.org/10.1002/sctm.20-0213
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author María Trujillo‐Rodríguez
Pompeyo Viciana
Inmaculada Rivas‐Jeremías
Ana I. Álvarez‐Ríos
Antonio Ruiz‐García
Olga Espinosa‐Ibáñez
Salvador Arias‐Santiago
Juliana Martínez‐Atienza
Rosario Mata
Olga Fernández‐López
Ezequiel Ruiz‐Mateos
Alicia Gutiérrez‐Valencia
Luis F. López‐Cortés
spellingShingle María Trujillo‐Rodríguez
Pompeyo Viciana
Inmaculada Rivas‐Jeremías
Ana I. Álvarez‐Ríos
Antonio Ruiz‐García
Olga Espinosa‐Ibáñez
Salvador Arias‐Santiago
Juliana Martínez‐Atienza
Rosario Mata
Olga Fernández‐López
Ezequiel Ruiz‐Mateos
Alicia Gutiérrez‐Valencia
Luis F. López‐Cortés
Mesenchymal stromal cells in human immunodeficiency virus‐infected patients with discordant immune response: Early results of a phase I/II clinical trial
Stem Cells Translational Medicine
clinical trial
HIV infection
immunological nonresponders
mesenchymal stromal cells
author_facet María Trujillo‐Rodríguez
Pompeyo Viciana
Inmaculada Rivas‐Jeremías
Ana I. Álvarez‐Ríos
Antonio Ruiz‐García
Olga Espinosa‐Ibáñez
Salvador Arias‐Santiago
Juliana Martínez‐Atienza
Rosario Mata
Olga Fernández‐López
Ezequiel Ruiz‐Mateos
Alicia Gutiérrez‐Valencia
Luis F. López‐Cortés
author_sort María Trujillo‐Rodríguez
title Mesenchymal stromal cells in human immunodeficiency virus‐infected patients with discordant immune response: Early results of a phase I/II clinical trial
title_short Mesenchymal stromal cells in human immunodeficiency virus‐infected patients with discordant immune response: Early results of a phase I/II clinical trial
title_full Mesenchymal stromal cells in human immunodeficiency virus‐infected patients with discordant immune response: Early results of a phase I/II clinical trial
title_fullStr Mesenchymal stromal cells in human immunodeficiency virus‐infected patients with discordant immune response: Early results of a phase I/II clinical trial
title_full_unstemmed Mesenchymal stromal cells in human immunodeficiency virus‐infected patients with discordant immune response: Early results of a phase I/II clinical trial
title_sort mesenchymal stromal cells in human immunodeficiency virus‐infected patients with discordant immune response: early results of a phase i/ii clinical trial
publisher Wiley
series Stem Cells Translational Medicine
issn 2157-6564
2157-6580
publishDate 2021-04-01
description Abstract Between 15% and 30% of HIV‐infected subjects fail to increase their CD4+ T‐cell counts despite continuous viral suppression (immunological nonresponders [INRs]). These subjects have a higher morbidity and mortality rate, but there are no effective treatments to reverse this situation so far. This study used data from an interrupted phase I/II clinical trial to evaluate safety and immune recovery after INRs were given four infusions, at baseline and at weeks 4, 8, and 20, with human allogeneic mesenchymal stromal cells from adipose tissue (Ad‐MSCs). Based on the study design, the first 5 out of 15 INRs recruited received unblinded Ad‐MSC infusions. They had a median CD4+ nadir count of 16/μL (range, 2‐180) and CD4+ count of 253 cells per microliter (171‐412) at baseline after 109 (54‐237) months on antiretroviral treatment and 69 (52‐91) months of continuous undetectable plasma HIV‐RNA. After a year of follow‐up, an independent committee recommended the suspension of the study because no increase of CD4+ T‐cell counts or CD4+/CD8+ ratios was observed. There were also no significant changes in the phenotype of different immunological lymphocyte subsets, percentages of natural killer cells, regulatory T cells, and dendritic cells, the inflammatory parameters analyzed, and cellular associated HIV‐DNA in peripheral blood mononuclear cells. Furthermore, three subjects suffered venous thrombosis events directly related to the Ad‐MSC infusions in the arms where the infusions were performed. Although the current study is based on a small sample of participants, the findings suggest that allogeneic Ad‐MSC infusions are not effective to improve immune recovery in INR patients or to reduce immune activation or inflammation. ClinicalTrials.gov identifier: NCT0229004. EudraCT number: 2014‐000307‐26.
topic clinical trial
HIV infection
immunological nonresponders
mesenchymal stromal cells
url https://doi.org/10.1002/sctm.20-0213
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spelling doaj-66dc7f04811d4ae3a96b61ad9464d9572021-03-20T09:13:37ZengWileyStem Cells Translational Medicine2157-65642157-65802021-04-0110453454110.1002/sctm.20-0213Mesenchymal stromal cells in human immunodeficiency virus‐infected patients with discordant immune response: Early results of a phase I/II clinical trialMaría Trujillo‐Rodríguez0Pompeyo Viciana1Inmaculada Rivas‐Jeremías2Ana I. Álvarez‐Ríos3Antonio Ruiz‐García4Olga Espinosa‐Ibáñez5Salvador Arias‐Santiago6Juliana Martínez‐Atienza7Rosario Mata8Olga Fernández‐López9Ezequiel Ruiz‐Mateos10Alicia Gutiérrez‐Valencia11Luis F. López‐Cortés12Unidad Clínica Enfermedades Infecciosas, Microbiología y Medicina Preventiva, Hospital Universitario Virgen del Rocío/Instituto Biomedicina de Sevilla/CSIC/Universidad de Sevilla Avd. Manuel Siurto s/n SEVILLA España SpainUnidad Clínica Enfermedades Infecciosas, Microbiología y Medicina Preventiva, Hospital Universitario Virgen del Rocío/Instituto Biomedicina de Sevilla/CSIC/Universidad de Sevilla Avd. Manuel Siurto s/n SEVILLA España SpainUnidad Clínica Enfermedades Infecciosas, Microbiología y Medicina Preventiva, Hospital Universitario Virgen del Rocío/Instituto Biomedicina de Sevilla/CSIC/Universidad de Sevilla Avd. Manuel Siurto s/n SEVILLA España SpainDepartamento de Bioquímica Clínica Hospital Universitario Virgen del Rocío/Consejo Superior de Investigaciones Científicas (CSIC)/Servicio Andaluz de Salud (SAS)/Universidad de Sevilla Seville SpainUnidad de Producción Celular e Ingeniería Tisular Complejo Hospitalario Universitario de Granada Granada SpainUnidad de Producción Celular e Ingeniería Tisular Complejo Hospitalario Universitario de Granada Granada SpainUnidad de Producción Celular e Ingeniería Tisular Complejo Hospitalario Universitario de Granada Granada SpainRed Andaluza en Diseño y Traslación de Terapias Avanzadas Fundación Pública Andaluza Progreso y Salud Seville SpainRed Andaluza en Diseño y Traslación de Terapias Avanzadas Fundación Pública Andaluza Progreso y Salud Seville SpainRed Andaluza en Diseño y Traslación de Terapias Avanzadas Fundación Pública Andaluza Progreso y Salud Seville SpainUnidad Clínica Enfermedades Infecciosas, Microbiología y Medicina Preventiva, Hospital Universitario Virgen del Rocío/Instituto Biomedicina de Sevilla/CSIC/Universidad de Sevilla Avd. Manuel Siurto s/n SEVILLA España SpainUnidad Clínica Enfermedades Infecciosas, Microbiología y Medicina Preventiva, Hospital Universitario Virgen del Rocío/Instituto Biomedicina de Sevilla/CSIC/Universidad de Sevilla Avd. Manuel Siurto s/n SEVILLA España SpainUnidad Clínica Enfermedades Infecciosas, Microbiología y Medicina Preventiva, Hospital Universitario Virgen del Rocío/Instituto Biomedicina de Sevilla/CSIC/Universidad de Sevilla Avd. Manuel Siurto s/n SEVILLA España SpainAbstract Between 15% and 30% of HIV‐infected subjects fail to increase their CD4+ T‐cell counts despite continuous viral suppression (immunological nonresponders [INRs]). These subjects have a higher morbidity and mortality rate, but there are no effective treatments to reverse this situation so far. This study used data from an interrupted phase I/II clinical trial to evaluate safety and immune recovery after INRs were given four infusions, at baseline and at weeks 4, 8, and 20, with human allogeneic mesenchymal stromal cells from adipose tissue (Ad‐MSCs). Based on the study design, the first 5 out of 15 INRs recruited received unblinded Ad‐MSC infusions. They had a median CD4+ nadir count of 16/μL (range, 2‐180) and CD4+ count of 253 cells per microliter (171‐412) at baseline after 109 (54‐237) months on antiretroviral treatment and 69 (52‐91) months of continuous undetectable plasma HIV‐RNA. After a year of follow‐up, an independent committee recommended the suspension of the study because no increase of CD4+ T‐cell counts or CD4+/CD8+ ratios was observed. There were also no significant changes in the phenotype of different immunological lymphocyte subsets, percentages of natural killer cells, regulatory T cells, and dendritic cells, the inflammatory parameters analyzed, and cellular associated HIV‐DNA in peripheral blood mononuclear cells. Furthermore, three subjects suffered venous thrombosis events directly related to the Ad‐MSC infusions in the arms where the infusions were performed. Although the current study is based on a small sample of participants, the findings suggest that allogeneic Ad‐MSC infusions are not effective to improve immune recovery in INR patients or to reduce immune activation or inflammation. ClinicalTrials.gov identifier: NCT0229004. EudraCT number: 2014‐000307‐26.https://doi.org/10.1002/sctm.20-0213clinical trialHIV infectionimmunological nonrespondersmesenchymal stromal cells