Clinical Study of BRL-101 in the Treatment of Sickle Cell Disease

Inclusion Criteria: 1. Fully understood this study and voluntarily signed the written informed consent form. 2. Aged between 3 and 35 years. 3. Be diagnosed with Sickle Cell Disease (SCD), with a genotype of βS/βS, βS/β+ or βS/β0. 4. A Lansky/Karnofsky Performance Status (LPS) score of ≥80. 5. Suitable for autologous hematopoietic stem cell transplantation. 6. Have good compliance and are willing to adhere to visit schedules, trial protocols, laboratory tests, and other trial procedures. 7. Agree to participating in long-term follow-up studies. 8. Subjects of childbearing potential must use effective contraception for at least 6 months following cell reinfusion during the study. Exclusion Criteria: \- Subjects meeting any of the following criteria are not eligible for enrolment in the study: 1. Known contraindications, intolerance, or hypersensitivity to hematopoietic stem cell mobilizers, busulfan injection, or dimethyl sulfoxide (DMSO) or study drug-related components. 2. Eligible for allogeneic hematopoietic stem cell transplantation and have found HLA-identical donors. 3. Prior allo-HSCT, gene therapy or gene editing therapy. 4. Clinically significant and active bacterial, viral, fungal, or parasitic infection as determined by the investigator. 5. HbF level \>15.0%, irrespective of concomitant treatment with HbF inducing treatments such as HU. 6. Treatment with regular RBC transfusions that, in the opinion of the investigator, cannot be interrupted after engraftment. 7. More than 10 unplanned hospitalizations or emergency department visits related to SCD in the 1 year before screening and the investigator considered this to be a significant chronic pain rather than an acute pain crisis. 8. A history of clinically significant transcranial Doppler (TCD) test abnormalities or test abnormalities in the opinion of the investigator. 9. History of untreated Moyamoya disease or presence of Moyamoya disease at screening that in the opinion of the investigator puts the subjects at the risk of bleeding. 10. The subject has participated in other clinical studies and used drugs within 3 months before screening. 11. White blood cell count \< 3 × 109/L and/or platelet count \< 100 × 109/L not due to hypersplenism as judged by the investigator. 12. INR \> 1.5×ULN, APTT \> 1.5×ULN. 13. Creatinine \> 1.5 × ULN or endogenous creatinine clearance \< 60 ml/min (calculated according to the Cockcroft-Gault formula, see Appendix 3). 14. ALT or AST\> 3×ULN, or direct bilirubin value \> 2.5×ULN. 15. Severe iron overload with serum ferritin ≥ 5000 ng/ml, liver iron \> 15 mg Fe/g dry weight (or liver MRIT2\* \< 1.4 ms or \> 588 Hz), or heart MRI-T2\* \< 10 ms. 16. LVEF \< 50%. 17. DLco \< 50% predicted (corrected haemoglobin or/and alveolar volume) or forced vital capacity (FVC) (measured/predicted) \< 60% (For children for whom DLco could not be determined), or abnormal blood gas analysis (for younger children with undetectable ventilatory function only). 18. Hepatitis B virus surface antigen (HBsAg) positive or HBV-DNA positive; hepatitis C virus (HCV) antibody positive; human immunodeficiency virus (HIV) antibody positive; syphilis (TP) -specific antibody positive; Epstein-Barr virus EBV-DNA positive; cytomegalovirus CMV-DNA positive. 19. History of a significant bleeding disorder. 20. History or family history of malignancy or myeloproliferative disorder. 21. Any prior or current cardiovascular system diseases, such as congestive heart failure, arrhythmia, myocardial disease, valvular heart disease or pulmonary hypertension; cirrhosis, liver fibrosis or active hepatitis; central nervous system diseases or mental illness. 22. Presence of immune dysfunction or endocrine disorders, such as insulin-dependent diabetes mellitus, hyperthyroidism, or insufficiency. 23. Pregnant or breastfeeding females. 24. Any condition that, in the opinion of the investigator, would make participation in this clinical study inappropriate.