Meng Lu , Jia-yan Leng , Chen-yun Xu , Chao-ran Lv , Zhen Qian , Yan Zhou , Di Yu , Jun Qian
{"title":"双不相关脐带血移植成功治疗1例供体特异性抗原阳性成人患者的极严重再生障碍性贫血:1例报告和复习。","authors":"Meng Lu , Jia-yan Leng , Chen-yun Xu , Chao-ran Lv , Zhen Qian , Yan Zhou , Di Yu , Jun Qian","doi":"10.1016/j.trim.2025.102241","DOIUrl":null,"url":null,"abstract":"<div><div>To overcome the cell-dose barrier of cord blood, double unrelated umbilical cord blood transplantation (UCBT) has become increasingly common in adults with severe aplastic anemia (SAA). Pre-existing donor-specific anti-HLA antibodies (DSAs) represent a risk factor for graft failure (GF). Desensitization therapy should be conducted to reduce circulating DSA levels, thereby decreasing the risk of GF. This report details a case of a female patient with acquired SAA and pre-transplantation anti-HLA antibodies. Desensitization with rituximab, intravenous immunoglobulin (IVIG), and plasma exchange (PE) was performed before transplantation with a conditioning regimen of fludarabine (30 mg/m<sup>2</sup> for six days) and cyclophosphamide (50 mg/kg/d for four days). DSA titers were significantly reduced; the patient was successfully treated with double unrelated UCBT. Currently, complete remission (CR) status has been maintained for over a year after UCBT, with no signs of graft-vs-host disease. Our findings support the use of double-unit unrelated UCBT in adult patients with SAA when cell doses of single-unit UCB are inadequate. Monitoring and reducing DSA levels before and after UCBT is an efficient way to reduce the risk of GF.</div></div>","PeriodicalId":23304,"journal":{"name":"Transplant immunology","volume":"91 ","pages":"Article 102241"},"PeriodicalIF":1.6000,"publicationDate":"2025-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Successful treatment of very severe aplastic anemia with double unrelated umbilical cord blood transplantation in a donor-specific antigen positive adult patient: A case report and review\",\"authors\":\"Meng Lu , Jia-yan Leng , Chen-yun Xu , Chao-ran Lv , Zhen Qian , Yan Zhou , Di Yu , Jun Qian\",\"doi\":\"10.1016/j.trim.2025.102241\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>To overcome the cell-dose barrier of cord blood, double unrelated umbilical cord blood transplantation (UCBT) has become increasingly common in adults with severe aplastic anemia (SAA). Pre-existing donor-specific anti-HLA antibodies (DSAs) represent a risk factor for graft failure (GF). Desensitization therapy should be conducted to reduce circulating DSA levels, thereby decreasing the risk of GF. This report details a case of a female patient with acquired SAA and pre-transplantation anti-HLA antibodies. Desensitization with rituximab, intravenous immunoglobulin (IVIG), and plasma exchange (PE) was performed before transplantation with a conditioning regimen of fludarabine (30 mg/m<sup>2</sup> for six days) and cyclophosphamide (50 mg/kg/d for four days). DSA titers were significantly reduced; the patient was successfully treated with double unrelated UCBT. Currently, complete remission (CR) status has been maintained for over a year after UCBT, with no signs of graft-vs-host disease. Our findings support the use of double-unit unrelated UCBT in adult patients with SAA when cell doses of single-unit UCB are inadequate. Monitoring and reducing DSA levels before and after UCBT is an efficient way to reduce the risk of GF.</div></div>\",\"PeriodicalId\":23304,\"journal\":{\"name\":\"Transplant immunology\",\"volume\":\"91 \",\"pages\":\"Article 102241\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-05-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Transplant immunology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0966327425000693\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Transplant immunology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0966327425000693","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
Successful treatment of very severe aplastic anemia with double unrelated umbilical cord blood transplantation in a donor-specific antigen positive adult patient: A case report and review
To overcome the cell-dose barrier of cord blood, double unrelated umbilical cord blood transplantation (UCBT) has become increasingly common in adults with severe aplastic anemia (SAA). Pre-existing donor-specific anti-HLA antibodies (DSAs) represent a risk factor for graft failure (GF). Desensitization therapy should be conducted to reduce circulating DSA levels, thereby decreasing the risk of GF. This report details a case of a female patient with acquired SAA and pre-transplantation anti-HLA antibodies. Desensitization with rituximab, intravenous immunoglobulin (IVIG), and plasma exchange (PE) was performed before transplantation with a conditioning regimen of fludarabine (30 mg/m2 for six days) and cyclophosphamide (50 mg/kg/d for four days). DSA titers were significantly reduced; the patient was successfully treated with double unrelated UCBT. Currently, complete remission (CR) status has been maintained for over a year after UCBT, with no signs of graft-vs-host disease. Our findings support the use of double-unit unrelated UCBT in adult patients with SAA when cell doses of single-unit UCB are inadequate. Monitoring and reducing DSA levels before and after UCBT is an efficient way to reduce the risk of GF.
期刊介绍:
Transplant Immunology will publish up-to-date information on all aspects of the broad field it encompasses. The journal will be directed at (basic) scientists, tissue typers, transplant physicians and surgeons, and research and data on all immunological aspects of organ-, tissue- and (haematopoietic) stem cell transplantation are of potential interest to the readers of Transplant Immunology. Original papers, Review articles and Hypotheses will be considered for publication and submitted manuscripts will be rapidly peer-reviewed and published. They will be judged on the basis of scientific merit, originality, timeliness and quality.