TY - JOUR
T1 - International Society of Cell and Gene Therapy 2025 exosomes signature series
T2 - a thematic synthesis for advancing mesenchymal stromal cell-derived extracellular vesicle therapies
AU - Tertel, Tobias
AU - Giebel, Bernd
AU - Lee, Ryang Hwa
AU - Muraca, Maurizio
AU - Ortiz, Luis A.
AU - Parolini, Ornella
AU - Perruche, Sylvain
AU - Robbins, Paul D.
AU - Rohde, Eva
AU - Strader, Shannon R.
AU - Terai, Shuji
AU - Toh, Wei Seong
AU - Yarani, Reza
AU - Weiss, Daniel J.
AU - Wiest, Elani F.
AU - Lim, Sai Kiang
N1 - Rohde: MP Unit, Paracelsus Medical University, Salzburg, Austria Department of Transfusion Medicine, University Hospital Salzburg, Paracelsus Medical University, Salzburg, Austria; Ludwig Boltzmann Institute for Nanovesicular Precision Medicine at the Paris-Lodron University Salzburg, Salzburg, Austria
PY - 2025/11
Y1 - 2025/11
N2 - At the International Society of Cell and Gene Therapy (ISCT) 2025 Annual Meeting in New Orleans, mesenchymal stromal cell-derived extracellular vesicles (MSC-EVs) received unprecedented attention, reflecting their rapid shift from experimental concept to promising therapeutic candidates. Scientists, clinicians, industry leaders and regulators participated in focused sessions to examine the questions that will determine how, and when, these products can reach patients: What drives their therapeutic effects? How can manufacturing ensure consistent, clinically active preparations? What is required to gain regulatory confidence, and who will fund the journey? Four thematic threads emerged: (i) pinpointing the "active ingredient" in context-specific settings, (ii) aligning manufacturing with critical quality attributes and potency assays, (iii) engaging regulators as early as possible to align on mechanism-driven product definitions and (iv) ensuring sustainable funding, clear market positioning and trial designs that satisfy both regulatory and commercial requirements. This report summarizes these discussions into actionable priorities: define context-specific mechanisms, embed potency assays into early process development and manufacturing protocols, link analytics to clinical relevance and design development programs that unite scientific credibility with regulatory and market viability. The message from the
AB - At the International Society of Cell and Gene Therapy (ISCT) 2025 Annual Meeting in New Orleans, mesenchymal stromal cell-derived extracellular vesicles (MSC-EVs) received unprecedented attention, reflecting their rapid shift from experimental concept to promising therapeutic candidates. Scientists, clinicians, industry leaders and regulators participated in focused sessions to examine the questions that will determine how, and when, these products can reach patients: What drives their therapeutic effects? How can manufacturing ensure consistent, clinically active preparations? What is required to gain regulatory confidence, and who will fund the journey? Four thematic threads emerged: (i) pinpointing the "active ingredient" in context-specific settings, (ii) aligning manufacturing with critical quality attributes and potency assays, (iii) engaging regulators as early as possible to align on mechanism-driven product definitions and (iv) ensuring sustainable funding, clear market positioning and trial designs that satisfy both regulatory and commercial requirements. This report summarizes these discussions into actionable priorities: define context-specific mechanisms, embed potency assays into early process development and manufacturing protocols, link analytics to clinical relevance and design development programs that unite scientific credibility with regulatory and market viability. The message from the
KW - MSC secretome
KW - Clinical translation
KW - Extracellular vesicles
KW - Mesenchymal stromal cells
KW - Potency assays
KW - Regenerative medicine
KW - Single-vesicle analytics
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pmu_pure&SrcAuth=WosAPI&KeyUT=WOS:001669125400001&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.1016/j.jcyt.2025.102016
DO - 10.1016/j.jcyt.2025.102016
M3 - Original Article
C2 - 41520460
SN - 1465-3249
VL - 28
JO - CYTOTHERAPY
JF - CYTOTHERAPY
IS - 3
ER -