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...
Main Authors: | , , , , , , , , , , , , |
---|---|
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 |
id |
doaj-66dc7f04811d4ae3a96b61ad9464d957 |
---|---|
record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
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 |
work_keys_str_mv |
AT mariatrujillorodriguez mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial AT pompeyoviciana mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial AT inmaculadarivasjeremias mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial AT anaialvarezrios mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial AT antonioruizgarcia mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial AT olgaespinosaibanez mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial AT salvadorariassantiago mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial AT julianamartinezatienza mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial AT rosariomata mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial AT olgafernandezlopez mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial AT ezequielruizmateos mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial AT aliciagutierrezvalencia mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial AT luisflopezcortes mesenchymalstromalcellsinhumanimmunodeficiencyvirusinfectedpatientswithdiscordantimmuneresponseearlyresultsofaphaseiiiclinicaltrial |
_version_ |
1724211436737003520 |
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 |