- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT02648516
Safety and Efficacy of Allogenic Adoptive Immune Therapy for Immune Reconstitution in Chronic HIV-1 Infected Patients
Safety and Efficacy of Allogenic Adoptive Immune Therapy for Immune Reconstitution Failure in Chronic HIV-1 Infected Patients
Panoramica dello studio
Stato
Intervento / Trattamento
Descrizione dettagliata
There is not a consensus definition of immunologic nonresponder individuals. In this study, we described patients whose cluster of differentiation 4(CD4)+ T-cell count remained below 200 cells/ul after 2 years of effective antiviral as immunologic nonresponders, in which viroimmunological dissociation implies a greater risk of AIDS related and non-AIDS-related illnesses. Immune-based therapy such as interleukin (IL)-2 and IL-7 have been shown to increase CD4 T-cell counts but yielded no clinical benefit in a large randomized study. We have reported that umbilical cord Tissue Mesenchymal Stem Cells (UC-MSC) treatment is safe and can significantly decrease systemic immune overactivation and improve immune reconstitution in INR patients. Meanwhile, we did not find that there was a significantly transitory increase in peripheral CD4 T-cell counts within 1-2 weeks since the onset of each MSC infusion. More important, umbilical cord-MSCs were found to be with a potential to produce IL-7 and T-cell growth factor transforming growth factor (TGF)-β in vitro and in vivo and preferentially expand CD4 T-cell response in the recipients. Therefore, development of novel interventions to reduce immune overactivation/inflammation and enhance immune reconstitution in INRs is a high priority.
Granulocyte colony-stimulating factor (G-CSF)-mobilized donor peripheral blood mononuclear cells (MNCs) are a heterogeneous population of immune cells that have a potential role in immunomodulation and hemopoiesis. Here, we hypothesized that human leukocyte antigen (HLA)-mismatched MNCs transfusion can be used to comprehensively restore or boost the host holistic immune system for INR patients, to the degree similar as immune responders.
The purpose of this study is to investigate the safety and initial efficacy of allogeneic adoptive immune therapy (AAIT) for INR patients. 20 INR patients received i.v. transfusion one round (3 times) of 2.0-3.0*10E8 cells/kg of MNCs as the treated group. All of them received the conventional treatment for AIDS. The CD4 T cell numbers, HIV reservoir, side effects, symptom improvement, control of opportunistic infections and will be evaluated during the 96-week follow up.
Tipo di studio
Iscrizione (Anticipato)
Fase
- Fase 2
- Fase 1
Contatti e Sedi
Luoghi di studio
-
-
Beijing
-
Beijing, Beijing, Cina, 100069
- Reclutamento
- Beijing 302 Hospital
-
Contatto:
- Ji-yuan Zhang, PhD
-
Contatto:
- Yan-mei Jiao, PhD
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
Inclusion Criteria:
- Immune non-responders with chronic HIV-1 infection
- Antiretroviral therapy (ART) for at least 24 months prior to study entry and continue within the 24 months after study entry
- CD4 count less than or equal to 200 cells/mm3 continuously and more than 50 cells/mm3 before entry and at screening, obtained within 30 days prior to study entry
- Viral load less than or equal to 50 copies/mL obtained within 12 months prior to study entry
- Certain specified laboratory values obtained within 30 days prior to study entry. More information on this criterion can be found in the study protocol
- Documentation that pre-entry specimen for the primary immune activation endpoint responses has been obtained
- No history of Centers for Disease Control and Prevention (CDC) category C AIDS-related opportunistic infections
- Karnofsky performance score greater than or equal to 70 within 30 days prior to study entry
- Ability and willingness to provide informed consent
Exclusion Criteria:
- Coinfection with other virus, including serum hepatitis C virus RNA positive, or one of followings are positive in anti-hepatitis A virus/anti-HDV/anti-hepatitis delta virus plus alanine aminotransferase (ALT) more than 80 IU/L
- History of combination with other severe diseases including renal, circulatory, respiratory, digestive, endocrine, neural and immunological diseases and tumors
- White blood cell (WBC) <2.5*10E9/L, platlet counts <50*10E9/L, Hb <80g/L, lactate >2 mmol/L
- Allergic constitution
- Pregnancy or lactation
- Accepting other immunomodulatory drugs within 6 months prior screening
- Drug addiction
- Other conditions possibly influencing the trial
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Sperimentale: Conventional plus AAIT
Participants will receive ART plus a dose of allogenic adoptive immune transfusion (3 times of MNCs transfusions) from day 0 through the week 2 study visit.
|
Participants will receive ART and taken i.v., at a dose of 2-3*10E8 MNCs/kg body at baseline, week 1 and 2.
Altri nomi:
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
The changes of CD4 T cell counts
Lasso di tempo: At Baseline and week 1, 2, 4, 8, 12, 24, 36, 48, 60, 72, 84, 96
|
marker for host immunity
|
At Baseline and week 1, 2, 4, 8, 12, 24, 36, 48, 60, 72, 84, 96
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
The changes of HIV-1 DNA
Lasso di tempo: At Baseline and up to week 96
|
marker for HIV-1 reservoir
|
At Baseline and up to week 96
|
|
The ratio of CD4 and CD8 T cells
Lasso di tempo: At Baseline and week 1, 2, 4, 8, 12, 24, 36, 48, 60, 72, 84, 96
|
marker for host immunity
|
At Baseline and week 1, 2, 4, 8, 12, 24, 36, 48, 60, 72, 84, 96
|
|
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Lasso di tempo: At Baseline and up to week 96
|
marker for safety
|
At Baseline and up to week 96
|
Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: Wang Fu-Sheng, Beijing 302 Hospital
Pubblicazioni e link utili
Pubblicazioni generali
- Hutter G. Stem cell transplantation in strategies for curing HIV/AIDS. AIDS Res Ther. 2016 Sep 13;13(1):31. doi: 10.1186/s12981-016-0114-y. eCollection 2016.
- Zhang Z, Fu J, Xu X, Wang S, Xu R, Zhao M, Nie W, Wang X, Zhang J, Li T, Su L, Wang FS. Safety and immunological responses to human mesenchymal stem cell therapy in difficult-to-treat HIV-1-infected patients. AIDS. 2013 May 15;27(8):1283-93. doi: 10.1097/QAD.0b013e32835fab77.
- Corbeau P, Reynes J. Immune reconstitution under antiretroviral therapy: the new challenge in HIV-1 infection. Blood. 2011 May 26;117(21):5582-90. doi: 10.1182/blood-2010-12-322453. Epub 2011 Mar 14.
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Anticipato)
Completamento dello studio (Anticipato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Infezioni da virus a RNA
- Malattie virali
- Infezioni
- Infezioni a trasmissione ematica
- Malattie trasmissibili
- Malattie sessualmente trasmissibili, virali
- Malattie trasmesse sessualmente
- Infezioni da lentivirus
- Infezioni da retroviridae
- Sindromi da deficit immunologico
- Malattie del sistema immunitario
- Malattie da virus lenti
- Infezioni da HIV
- Sindrome da immunodeficienza acquisita
Altri numeri di identificazione dello studio
- Beijing302-010
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su Virus dell'immunodeficienza umana
-
University General Hospital of PatrasReclutamentoIschemia cerebrale | Ketamina | Solfato di magnesio | Remifentanil | Anestesia con sevoflurano | Propofol/Remifentanil | S 100beta | S100 Beta Protein, Human | Enolasi specifica per neuroniGrecia
-
ModernaTX, Inc.Reclutamento
-
Nicola IrwinCompletatoRicoveri per virus respiratorio sinciziale | Prevenzione del virus respiratorio sinciziale | Infezione da virus respiratorio sinciziale (RSV).Australia
-
Nicola IrwinThe University of New South Wales; Kirby InstituteCompletatoRicoveri per virus respiratorio sinciziale | Infezione da virus respiratorio sinciziale (RSV). | Immunizzazione contro il virus respiratorio sincizialeAustralia
-
Sanofi Pasteur, a Sanofi CompanyAttivo, non reclutanteVolontari sani | Virus di Epstein-Barr (EBV)Australia
-
Menzies School of Health ResearchUniversity of Sydney; Murdoch Childrens Research InstituteNon ancora reclutamentoVirus respiratorio sinciziale (RSV) | Virus delle infezioni respiratorieAustralia
-
University of OxfordReclutamentoVirus respiratorio sinciziale | Virus respiratorio sinciziale, umanoTailandia, Repubblica democratica popolare del Laos
-
National Institute of Allergy and Infectious Diseases...CompletatoSano | Infezione da virus di Epstein BarrStati Uniti
-
Sanofi Pasteur, a Sanofi CompanyCompletatoInfezione da virus respiratorio sinciziale | Infezione da metapneumovirus | Infezione da virus parainfluenzaleAustralia
-
Suzhou Abogen Biosciences Co., Ltd.Abogen Biosciences (Shanghai) Co., LtdAttivo, non reclutante
Prove cliniche su Conventional plus AAIT
-
Assiut UniversityCompletatoTecnica EPO nell'Estrazione della Testa FetaleEgitto
-
Rigshospitalet, DenmarkNon ancora reclutamentoArresto cardiaco | Stimolazione del sistema di conduzione | Terapia di risincronizzazione cardiaca (CRT)Svezia, Danimarca, Finlandia, Norvegia
-
Beijing 302 HospitalCompletatoVirus dell'immunodeficienza umana | Immunodeficienza
-
Qure Healthcare, LLCLineagenCompletatoDisabilità intellettuale | Ritardo dello sviluppoStati Uniti
-
Farmaceutici Damor SpaReclutamentoFerite e lesioni | Infezione della ferita | Guarire la feritaItalia
-
ResMedCompletatoApnea notturna, ostruttiva | Apnea notturna, centraleGermania
-
Ethicon, Inc.Completato
-
University of South CarolinaNational Cancer Institute (NCI); American Cancer Society, Inc.CompletatoCancro al senoStati Uniti
-
Johns Hopkins UniversityCenters for Medicare and Medicaid Services; Jewish Community Services; Johns Hopkins...CompletatoDemenza | Onere del caregiverStati Uniti
-
University of Maryland, BaltimoreNational Institute on Aging (NIA)Completato