Pharmacological Effects of Ex Vivo Mesenchymal Stem Cell Immunotherapy in Patients with Acute Kidney Injury and Underlying Systemic Inflammation

Author:

Swaminathan Madhav1ORCID,Kopyt Nelson2,Atta Mohamed G.3ORCID,Radhakrishnan Jai4ORCID,Umanath Kausik56ORCID,Nguyen Sunny7,O'Rourke Brian7,Allen Ashley7,Vaninov Natalie7,Tilles Arno7,LaPointe Elizabeth7,Blair Andrew7,Gemmiti Chris7,Miller Brian7,Parekkadan Biju78ORCID,Barcia Rita N.7

Affiliation:

1. Department of Anesthesiology  Duke University School of Medicine, Duke University, Durham, North Carolina, USA

2. Nephrology Section, Department of Medicine  Lehigh Valley Health Network, Allentown, Pennsylvania, USA

3. Department of Medicine, Division of Nephrology  Johns Hopkins School of Medicine, Baltimore, Maryland, USA

4. Columbia University Medical Center, Division of Nephrology  NY Presbyterian Hospital/Columbia, New York, New York, USA

5. Division of Nephrology and Hypertension  Henry Ford Hospital, Detroit, Michigan, USA

6. Division of Nephrology and Hypertension  Wayne State University, Detroit, Michigan, USA

7. Sentien Biotechnologies, Lexington, Massachusetts, USA

8. Department of Surgery, Center for Surgery, Innovation, and Bioengineering, Massachusetts General Hospital  Harvard Medical School and Shriners Hospitals for Children, Boston, Massachusetts, USA

Abstract

Abstract Mesenchymal stem cells (MSCs) have natural immunoregulatory functions that have been explored for medicinal use as a cell therapy with limited success. A phase Ib study was conducted to evaluate the safety and immunoregulatory mechanism of action of MSCs using a novel ex vivo product (SBI-101) to preserve cell activity in patients with severe acute kidney injury. Pharmacological data demonstrated MSC-secreted factor activity that was associated with anti-inflammatory signatures in the molecular and cellular profiling of patient blood. Systems biology analysis captured multicompartment effects consistent with immune reprogramming and kidney tissue repair. Although the study was not powered for clinical efficacy, these results are supportive of the therapeutic hypothesis, namely, that treatment with SBI-101 elicits an immunotherapeutic response that triggers an accelerated phenotypic switch from tissue injury to tissue repair. Ex vivo administration of MSCs, with increased power of testing, is a potential new biological delivery paradigm that assures sustained MSC activity and immunomodulation.

Funder

National Institutes of Health National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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