Literature DB >> 25246338

Co-infusion of donor adipose tissue-derived mesenchymal and hematopoietic stem cells helps safe minimization of immunosuppression in renal transplantation - single center experience.

Aruna V Vanikar1, Hargovind L Trivedi, Ashutosh Kumar, Saroj Chooramani Gopal, Himanshu V Patel, Manoj R Gumber, Vivek B Kute, Pankaj R Shah, Shruti D Dave.   

Abstract

BACKGROUND: Stem cell therapy (SCT) is used for immunosuppression minimization in renal transplantation (RT). We carried out a prospective study to evaluate the benefits of co-infusion of donor adipose-derived mesenchymal stem cells (AD-MSC) + hematopoietic stem cells (HSC) in living donor RT (LDRT) under non-myeloablative conditioning.
METHODS: In a demographically balanced three-armed LDRT trial with 95 patients in each arm, group-1 received portal co-infusion of AD-MSC + HSC, group-2 received HSC and group-3 received no SCT. Lymphoid irradiation and anti-thyroglobulin were used for conditioning.
RESULTS: SCT was safe. At 1 and 5 years post-transplant, patient survival was 100% and 94.7% in group-1, 100% and 95.7% in group-2, and 94.7% and 84% in group-3, death-censored graft survival was 100% and 94.6% in group-1, 100% and 91.3% in group-2, and 98.9% and 94.4% in group-3 with mean serum creatinine (mg/dL) of 1.38 and 1.39 in group-1, 1.48 and 1.51 in group-2, and 1.29 and 1.42 and in group-3. Rejection episodes and immunosuppression requirement were lesser in SCT groups versus controls with best results noted in group-1.
CONCLUSION: Coinfusion of donor AD-MSC +HSC in portal circulation pre-transplant under non-myeloablative conditioning is safe and effective for immunosuppression minimization in LDRT.

Entities:  

Keywords:  Adipose tissue-derived mesenchymal stem cells; hematopoietic stem cells; minimization of immunosuppression; rejection; renal transplantation

Mesh:

Substances:

Year:  2014        PMID: 25246338     DOI: 10.3109/0886022X.2014.950931

Source DB:  PubMed          Journal:  Ren Fail        ISSN: 0886-022X            Impact factor:   2.606


  11 in total

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Journal:  Front Immunol       Date:  2018-07-24       Impact factor: 7.561

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