Treatment of Refractory cGVHD by Donor-derived Treg Cell Injection Combined With Recombinant Human Interleukin-2

Launched by SHANGHAI GENERAL HOSPITAL, SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE · Apr 2, 2025

Keywords

ClinConnect Summary

This clinical trial is investigating a new treatment for patients with refractory chronic graft-versus-host disease (cGVHD), a condition that can occur after a stem cell transplant. The study will look at the safety and effectiveness of injecting specialized immune cells called Treg cells, which come from a donor, along with a medication called interleukin-2. The goal is to see if this combination can help patients who have not responded well to standard treatments.

To be eligible for this trial, participants need to be between 18 and 70 years old and must have moderate to severe cGVHD that has not improved with previous steroid treatments. They should have had a stem cell transplant and must be stable on their medications before starting the trial. Participants can expect to receive the Treg cell injections and will be monitored closely for any side effects and how well the treatment works. It’s important to note that this study is not yet recruiting participants, so there will be further announcements on when it will start.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Subjects aged 18-70 years old, male or female;
• • The subjects had received allo-HSCT, including cord blood transplantation;
• * TSubjects with moderate/severe cGVHD that meets the NIH diagnostic criteria (031) for steroid dependence or resistance, meeting one of the following:
• • 1. There was no improvement in cGVHD in initial treatment patients treated with \> 0.5mg/kg/ day or 1 mg/kg/ day every other day for at least 4 weeks;
• • 2. Steroid dependence: predtisone dose \> 0.25 mg/kg/d or \> 0.5 mg/kg/qod cGVHD relapse or progression; cGVHD recurred after two attempts to gradually reduce prednisone dose at an interval of at least 8 weeks, with prednisone dose \> 0.25 mg/kg/day to be maintained.
• • Prednisone dose \> 0.25 mg/kg/d for more than 4 weeks; Subjects must maintain a stable prednisone dose for 4 weeks prior to the first Treg cell infusion and not increase or discontinue other immunosuppressants (including cyclosporine, tacrolimus, and sirolimus);
• • The ECOG score of the subjects was 0-2;
• • the expected survival of the subject is more than 3 months;
• * Liver, kidney, heart and lung function meet the following requirements (except liver and kidney dysfunction caused by cGVHD) :
• • 1. Creatinine clearance (calculated by Cockcroft Gault formula) ≥60 mL/min;
• • 2. Cardiac ejection fraction greater than 50%, no clinically significant electrocardiogram changes;
• • 3. Forced expiratory volume (FEV1) in the first second of baseline lung function ≥50%, and FEV1 decline caused by cGVHD could be included;
• • 4. Total bilirubin ≤2.0ULN; ALT and AST≤3ULN, ALT and AST increases caused by cGVHD could be included in the group.
• • Hematopoietic function: neutrophils \>1×10\^9/L, platelets \>25×10\^9/L; Supportive treatments such as platelet transfusion and other cytokines are excluded.
• • The subject or the subject's guardian can understand this experiment and has signed the informed consent.
• • Donor age 14-70 years old, male or female;
• • The ECOG score of the donor is 0-1;
• • The donor must be a hematopoietic stem cell donor who underwent allo-HSCT prior to the subject;
• • Female donors must test negative for serum or urine beta-human chorionic gonadotropin (HCG) within 3 weeks of blood collection;
• • The donor can establish the necessary venous access for collection, without the contraindication of white blood cell collection; If peripheral venous leukocyte collection is insufficient, be willing to insert a central catheter; (15) The donor agrees to donate and signs a consent form.
• Exclusion Criteria:
• • Subjects had a recurrence of primary malignant disease before receiving Treg treatment;
• • The subjects had persistent, recurrent or delayed aGVHD;
• • Continuous use of prednisone \>1 mg/kg/day is required;
• • The severity of the subject's cGVHD cannot be assessed by physical examination or laboratory examination;
• • overlap syndrome；
• • The subjects had major organ (cardio-cerebrovascular, pulmonary) dysfunction not caused by cGVHD, and had previous (within 3 months) gastrointestinal active bleeding; History of uncontrolled hypertension or hypertensive crisis or hypertensive encephalopathy, history or evidence of significant cardiovascular and cerebrovascular risk, including any of the following conditions: congestive heart failure, unstable angina pectoris, clinically significant arrhythmias (e.g., ventricular fibrillation, ventricular tachycardia, etc.); History of arterial thrombosis (such as stroke, transient ischemic attack) within the last 3 months; A history of symptomatic deep vein thrombosis, pulmonary embolism, or coronary angiogenesis, defibrillation, or any clinically relevant complication or disease within the last 6 months that could pose a risk to subject safety or interfere with study evaluation, procedure, or completion;
• • The subjects are hemodialysis patients;
• • The subject or donor has an active, uncontrolled bacterial, viral, or fungal infection that requires treatment；
• • The subjects are pregnant or lactating women; Subjects who plan to become pregnant during the post-transfusion study, or within 1 year of completion or withdrawal from the study;
• • Participants who had received IL-2 therapy or drug therapy targeting IL-2 within 4 weeks prior to enrollment；
• • Received DLI treatment within 100 days before enrollment;
• • Received CAR-T or similar engineered cell therapy within 100 days prior to enrollment;
• • Had received new cGVHD therapies (including imatinib, BTK inhibitors, rituximab and other immunosuppressants) within 4 weeks before enrollment after transplantation;
• • Have a history of microvascular diseases such as TMA, hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, etc；
• • Subjects with poor IL-2 treatment compliance;
• • Participants who participated in other CGVHD-related clinical studies within 4 weeks prior to enrollment;
• • Subjects who are known to be allergic to any component of Treg cell injection;
• • Any situation that the investigator believes would compromise the safety of the subject or interfere with the study purpose, or that the investigator considers it inappropriate to participate in the study;
• • Having a medical condition that affects the signing of written informed consent or the inability to follow study procedures; Unwilling or unable to comply with research requirements;
• • The donor was a pregnant woman.