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First-in-man use of a cardiovascular cell-derived secretome in heart failure. Case report.
Menasché, Philippe; Renault, Nisa K; Hagège, Albert; Puscas, Tania; Bellamy, Valérie; Humbert, Camille; Le, Laetitia; Blons, Hélène; Granier, Clémence; Benhamouda, Nadine; Bacher, Anne; Churlaud, Guillaume; Sabatier, Brigitte; Larghero, Jérôme.
Affiliation
  • Menasché P; AP-HP, Department of Cardiovascular Surgery, Hôpital Européen Georges Pompidou, Paris, France; Université Paris Cité, Inserm, PARCC, Paris, France. Electronic address: philippe.menasche@aphp.fr.
  • Renault NK; FUJIFILM Cellular Dynamics, Inc (FCDI), Madison, WI, USA.
  • Hagège A; Université Paris Cité, Inserm, PARCC, Paris, France; AP-HP, Department of Cardiology, Hôpital Européen Georges Pompidou, Paris, France.
  • Puscas T; AP-HP, Department of Cardiology, Hôpital Européen Georges Pompidou, Paris, France.
  • Bellamy V; Université Paris Cité, Inserm, PARCC, Paris, France.
  • Humbert C; AP-HP, Hôpital Saint-Louis, MEARY Centre for Cell and Gene Therapy, Paris, France.
  • Le L; AP-HP, Department of Pharmacy, Hôpital Européen Georges Pompidou, Paris, France; UFR Pharmacie, Université Paris-Saclay, Lip(Sys)(2) Lipides, Systèmes Analytiques et Biologiques, Orsay, France.
  • Blons H; AP-HP, Department of Biochemistry, Pharmacogenetics and Molecular Oncology, Paris Cancer Institute CARPEM, Hôpital Européen Georges Pompidou, Paris, France.
  • Granier C; Université Paris Cité, Inserm, PARCC, Paris, France; Department of Immunology, APHP, Hôpital Européen Georges Pompidou, Paris, France.
  • Benhamouda N; Université Paris Cité, Inserm, PARCC, Paris, France; Department of Immunology, APHP, Hôpital Européen Georges Pompidou, Paris, France.
  • Bacher A; AP-HP, Department of Cardiology, Hôpital Européen Georges Pompidou, Paris, France.
  • Churlaud G; AP-HP, Hôpital Saint-Louis, MEARY Centre for Cell and Gene Therapy, Paris, France.
  • Sabatier B; AP-HP, Pharmacy, Hôpital Européen Georges-Pompidou, Pharmacie, Paris, France; Université Paris-Saclay, Faculté de Pharmacie, Pharmacie Clinique, Orsay, France; HeKA Team, INRIA/INSERM U 1138, CRC/PSC, Paris, France.
  • Larghero J; AP-HP, Hôpital Saint-Louis, MEARY Centre for Cell and Gene Therapy, Paris, France; Université Paris Cité, AP-HP, Hôpital Saint-Louis, Clinical Investigation Center in Biotherapies CIC-BT, INSERM, Paris, France.
EBioMedicine ; 103: 105145, 2024 May.
Article in En | MEDLINE | ID: mdl-38713924
ABSTRACT

BACKGROUND:

There is increased evidence that the effects of stem cells can mostly be duplicated by administration of their secretome which might streamline the translation towards the clinics.

METHODS:

The 12-patient SECRET-HF phase 1 trial has thus been designed to determine the feasibility and safety of repeated intravenous injections of the extracellular vesicle (EV)-enriched secretome of cardiovascular progenitor cells differentiated from pluripotent stem cells in severely symptomatic patients with drug-refractory left ventricular (LV) dysfunction secondary to non-ischemic dilated cardiomyopathy. Here we report the case of the first treated patient (baseline NYHA class III; LV Ejection Fraction25%) in whom a dose of 20 × 109 particles/kg was intravenously infused three times three weeks apart.

FINDINGS:

In addition to demonstrating the feasibility of producing a cardiac cell secretome compliant with Good Manufacturing Practice standards, this case documents the excellent tolerance of its repeated delivery, without any adverse events during or after infusions. Six months after the procedure, the patient is in NYHA Class II with improved echo parameters, a reduced daily need for diuretics (from 240 mg to 160 mg), no firing from the previously implanted automatic internal defibrillator and no alloimmunization against the drug product, thereby supporting its lack of immunogenicity.

INTERPRETATION:

The rationale underlying the intravenous route is that the infused EV-enriched secretome may act by rewiring endogenous immune cells, both circulating and in peripheral organs, to take on a reparative phenotype. These EV-modified immune cells could then traffic to the heart to effect tissue repair, including mitigation of inflammation which is a hallmark of cardiac failure.

FUNDING:

This trial is funded by the French Ministry of Health (Programme Hospitalier de Recherche CliniqueAOM19330) and the "France 2030" National Strategy Program (ANR-20-F2II-0003). It is sponsored by Assistance Publique-Hôpitaux de Paris.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Secretome / Heart Failure Limits: Humans / Male / Middle aged Language: En Journal: EBioMedicine Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Secretome / Heart Failure Limits: Humans / Male / Middle aged Language: En Journal: EBioMedicine Year: 2024 Type: Article