Zainab M. Golwala , Helena Spiridou Goncalves , Ranjita Devi Moirangthem , Grace Evans , Sabrina Lizot , Coco de Koning , Alexandrine Garrigue , Marta Martin Corredera , Juan Moises Ocampo-Godinez , Evey Howley , Susanne Kricke , Arnold Awuah , Irene Obiri-Yeboa , Rajeev Rai , Neil Sebire , Fanette Bernard , Victoria Bordon Cueto De Braem , Kaan Boztug , Theresa Cole , Andrew R. Gennery , Alexandra Y. Kreins
{"title":"体外t淋巴细胞生成分析有助于基因不明的t淋巴细胞减少症的纠正治疗选择。","authors":"Zainab M. Golwala , Helena Spiridou Goncalves , Ranjita Devi Moirangthem , Grace Evans , Sabrina Lizot , Coco de Koning , Alexandrine Garrigue , Marta Martin Corredera , Juan Moises Ocampo-Godinez , Evey Howley , Susanne Kricke , Arnold Awuah , Irene Obiri-Yeboa , Rajeev Rai , Neil Sebire , Fanette Bernard , Victoria Bordon Cueto De Braem , Kaan Boztug , Theresa Cole , Andrew R. Gennery , Alexandra Y. Kreins","doi":"10.1016/j.clim.2025.110453","DOIUrl":null,"url":null,"abstract":"<div><div>Persistent selective T-lymphocytopenia is found both in SCID and congenital athymia. Without molecular diagnosis, it is challenging to determine whether HCT or thymus transplantation ought to be performed. <em>Ex vivo</em> T-lymphopoiesis assays have been proposed to assist clinical decision-making for genetically undefined patients. We investigated 20 T-lymphocytopenic patients, including 13 patients awaiting first-line treatment and 7 patients with failed immune reconstitution after previous HCT or thymus transplantation. Whilst developmental blocks in <em>ex vivo</em> T-lymphopoiesis indicated hematopoietic cell-intrinsic defects, successful T-lymphocyte differentiation required careful interpretation, in conjunction with clinical status, immunophenotyping, and genetic investigations. Of the 20 patients, 13 proceeded to treatment, with successful immune reconstitution observed in 4 of the 6 patients post-HCT and 4 of the 7 patients after thymus transplantation, the latter including two patients who had previously undergone HCT. Whilst further validation and standardization are required, we conclude that assessing <em>ex vivo</em> T-lymphopoiesis during the diagnostic pathway for genetically undefined T-lymphocytopenia improves patient outcomes by facilitating corrective treatment choice.</div></div>","PeriodicalId":10392,"journal":{"name":"Clinical immunology","volume":"274 ","pages":"Article 110453"},"PeriodicalIF":4.5000,"publicationDate":"2025-02-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ex vivo T-lymphopoiesis assays assisting corrective treatment choice for genetically undefined T-lymphocytopenia\",\"authors\":\"Zainab M. Golwala , Helena Spiridou Goncalves , Ranjita Devi Moirangthem , Grace Evans , Sabrina Lizot , Coco de Koning , Alexandrine Garrigue , Marta Martin Corredera , Juan Moises Ocampo-Godinez , Evey Howley , Susanne Kricke , Arnold Awuah , Irene Obiri-Yeboa , Rajeev Rai , Neil Sebire , Fanette Bernard , Victoria Bordon Cueto De Braem , Kaan Boztug , Theresa Cole , Andrew R. Gennery , Alexandra Y. Kreins\",\"doi\":\"10.1016/j.clim.2025.110453\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Persistent selective T-lymphocytopenia is found both in SCID and congenital athymia. Without molecular diagnosis, it is challenging to determine whether HCT or thymus transplantation ought to be performed. <em>Ex vivo</em> T-lymphopoiesis assays have been proposed to assist clinical decision-making for genetically undefined patients. We investigated 20 T-lymphocytopenic patients, including 13 patients awaiting first-line treatment and 7 patients with failed immune reconstitution after previous HCT or thymus transplantation. Whilst developmental blocks in <em>ex vivo</em> T-lymphopoiesis indicated hematopoietic cell-intrinsic defects, successful T-lymphocyte differentiation required careful interpretation, in conjunction with clinical status, immunophenotyping, and genetic investigations. Of the 20 patients, 13 proceeded to treatment, with successful immune reconstitution observed in 4 of the 6 patients post-HCT and 4 of the 7 patients after thymus transplantation, the latter including two patients who had previously undergone HCT. Whilst further validation and standardization are required, we conclude that assessing <em>ex vivo</em> T-lymphopoiesis during the diagnostic pathway for genetically undefined T-lymphocytopenia improves patient outcomes by facilitating corrective treatment choice.</div></div>\",\"PeriodicalId\":10392,\"journal\":{\"name\":\"Clinical immunology\",\"volume\":\"274 \",\"pages\":\"Article 110453\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2025-02-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical immunology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1521661625000282\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical immunology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1521661625000282","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
Ex vivo T-lymphopoiesis assays assisting corrective treatment choice for genetically undefined T-lymphocytopenia
Persistent selective T-lymphocytopenia is found both in SCID and congenital athymia. Without molecular diagnosis, it is challenging to determine whether HCT or thymus transplantation ought to be performed. Ex vivo T-lymphopoiesis assays have been proposed to assist clinical decision-making for genetically undefined patients. We investigated 20 T-lymphocytopenic patients, including 13 patients awaiting first-line treatment and 7 patients with failed immune reconstitution after previous HCT or thymus transplantation. Whilst developmental blocks in ex vivo T-lymphopoiesis indicated hematopoietic cell-intrinsic defects, successful T-lymphocyte differentiation required careful interpretation, in conjunction with clinical status, immunophenotyping, and genetic investigations. Of the 20 patients, 13 proceeded to treatment, with successful immune reconstitution observed in 4 of the 6 patients post-HCT and 4 of the 7 patients after thymus transplantation, the latter including two patients who had previously undergone HCT. Whilst further validation and standardization are required, we conclude that assessing ex vivo T-lymphopoiesis during the diagnostic pathway for genetically undefined T-lymphocytopenia improves patient outcomes by facilitating corrective treatment choice.
期刊介绍:
Clinical Immunology publishes original research delving into the molecular and cellular foundations of immunological diseases. Additionally, the journal includes reviews covering timely subjects in basic immunology, along with case reports and letters to the editor.