IMPROvE-CED Trial: Intracoronary Autologous CD34+ Cell Therapy for Treatment of Coronary Endothelial Dysfunction in Patients With Angina and Nonobstructive Coronary Arteries

Author:

Corban Michel T.12,Toya Takumi1ORCID,Albers Diana1,Sebaali Faten1,Lewis Bradley R.3ORCID,Bois John1,Gulati Rajiv1ORCID,Prasad Abhiram1,Best Patricia J.M.1,Bell Malcolm R.1,Rihal Charanjit S.1ORCID,Prasad Megha1,Ahmad Ali1ORCID,Lerman Lilach O.14ORCID,Solseth Mary L.5,Winters Jeffrey L.5ORCID,Dietz Allan B.5ORCID,Lerman Amir1ORCID

Affiliation:

1. Department of Cardiovascular Medicine (M.T.C., T.T., D.A., F.S., J.B., R.G., A.P., P.J.M.B., M.R.B., C.S.R., M.P., A.A., L.O.L., A.L.), Mayo Clinic, Rochester, MN.

2. Division of Cardiology, Department of Medicine, University of Arizona College of Medicine-Tucson (M.T.C.).

3. Department of Biomedical Statistics and Informatics (B.R.L.), Mayo Clinic, Rochester, MN.

4. Division of Nephrology and Hypertension, Department of Medicine (L.O.L.), Mayo Clinic, Rochester, MN.

5. Division of Transfusion Medicine, Department of Laboratory Medicine and Pathology (M.L.S., J.L.W., A.B.D.), Mayo Clinic, Rochester, MN.

Abstract

Background: Coronary endothelial dysfunction (CED) causes angina/ischemia in patients with nonobstructive coronary artery disease (NOCAD). Patients with CED have decreased number and function of CD34+ cells involved in normal vascular repair with microcirculatory regenerative potential and paracrine anti-inflammatory effects. We evaluated safety and potential efficacy of intracoronary autologous CD34+ cell therapy for CED. Methods: Twenty NOCAD patients with invasively diagnosed CED and persistent angina despite maximally tolerated medical therapy underwent baseline exercise stress test, GCSF (granulocyte colony stimulating factor)-mediated CD34+ cell mobilization, leukapheresis, and selective 1×10 5 CD34+ cells/kg infusion into left anterior descending. Invasive CED evaluation and exercise stress test were repeated 6 months after cell infusion. Primary end points were safety and effect of intracoronary autologous CD34+ cell therapy on CED at 6 months of follow-up. Secondary end points were change in Canadian Cardiovascular Society angina class, as-needed sublingual nitroglycerin use/day, Seattle Angina Questionnaire scores, and exercise time at 6 months. Change in CED was compared with that of 51 historic control NOCAD patients treated with maximally tolerated medical therapy alone. Results: Mean age was 52±13 years; 75% were women. No death, myocardial infarction, or stroke occurred. Intracoronary CD34+ cell infusion improved microvascular CED (%acetylcholine-mediated coronary blood flow increased from 7.2 [−18.0 to 32.4] to 57.6 [16.3–98.3]%; P =0.014), decreased Canadian Cardiovascular Society angina class (3.7±0.5 to 1.7±0.9, Wilcoxon signed-rank test, P =0.00018), and sublingual nitroglycerin use/day (1 [0.4–3.5] to 0 [0–1], Wilcoxon signed-rank test, P =0.00047), and improved all Seattle Angina Questionnaire scores with no significant change in exercise time at 6 months of follow-up. Historic control patients had no significant change in CED. Conclusions: A single intracoronary autologous CD34+ cell infusion was safe and may potentially be an effective disease-modifying therapy for microvascular CED in humans. Registration: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT03471611.

Funder

Mayo Clinic Transform the Practice Award

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Physiology

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