Cybele Lara R. Abad, Alex Zimmet, Aruna K. Subramanian
{"title":"肺结核患者的实体器官移植","authors":"Cybele Lara R. Abad, Alex Zimmet, Aruna K. Subramanian","doi":"10.1111/ctr.70528","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Deferral of solid organ transplantation (SOT) in recipients with tuberculosis (TB) disease (active TB) is recommended until anti-tuberculosis treatment (ATT) is completed. However, SOT is often urgent, and there are instances where SOT cannot be safely delayed.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>We report two cases with TB disease who were transplanted before completion of ATT in our institution and searched PubMed, EMBASE, and MEDLINE databases from inception to August 2025, to retrieve all other published cases of <i>Mycobacterium tuberculosis</i> among SOT candidates with active TB disease at time of transplantation.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Sixty-four detailed cases were identified while two cohort studies had aggregated data on 101 cases of TB disease among kidney transplant (KT) candidates. The majority of cases were liver transplant (LT) candidates (60/64, 93.7%); the rest were heart (2/64), kidney (1/64), or lung (1/64) candidates. About half of LT candidates were urgently transplanted because of ATT induced hepatic failure (35/60, 58.3%). Among LT candidates, pulmonary tuberculosis was most common (39/60, 65%) followed by extrapulmonary (EPTB) (17/60, 28.3%), and disseminated TB (4/60, 6.7%). ATT was started prior to transplantation in 44/60 (73.3%) candidates, while 16/60 (26.7%) were started after SOT. The majority (40/44, 90.9%) were on first line therapy, with transplantation occurring a median of 54.5 (range 2–180) days after starting ATT. Many ATT regimens were modified in the post-transplant phase (31/44, 70.4%). Of nine mortalities among LT recipients, only one was directly attributable to TB disease. For both cohort studies on KT candidates, EPTB was the most common form of TB disease (44/71 and 26/30). ATT was taken a median of 3.8 and 3 months, respectively, prior to SOT. All continuation phase posttransplant ATT were rifampicin-sparing with median duration of 12.27 and 14 months, respectively. There were no deaths attributable to TB disease.</p>\n </section>\n \n <section>\n \n <h3> Conclusions</h3>\n \n <p>Favorable outcomes after SOT are feasible despite TB disease and incomplete pre-transplant anti-TB treatment. The urgent need for a life-saving transplant procedure should be weighed against the risks of transplantation in a patient with active tuberculosis. Completion of at least 2-month intensive first-line TB treatment (e.g., isoniazid, rifampicin, pyrazinamide, ethambutol, [HRZE]) is recommended with use of a rifamycin-based regimen to optimize sterilization. Although rifamycins are preferred for treatment, a rifampicin-sparing regimen may be more manageable post-transplantation to avoid drug–drug interactions, especially if longer courses of treatment are used.</p>\n </section>\n </div>","PeriodicalId":10467,"journal":{"name":"Clinical Transplantation","volume":"40 4","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2026-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Solid Organ Transplantation Among Transplant Candidates With TB Disease\",\"authors\":\"Cybele Lara R. Abad, Alex Zimmet, Aruna K. Subramanian\",\"doi\":\"10.1111/ctr.70528\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Deferral of solid organ transplantation (SOT) in recipients with tuberculosis (TB) disease (active TB) is recommended until anti-tuberculosis treatment (ATT) is completed. However, SOT is often urgent, and there are instances where SOT cannot be safely delayed.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>We report two cases with TB disease who were transplanted before completion of ATT in our institution and searched PubMed, EMBASE, and MEDLINE databases from inception to August 2025, to retrieve all other published cases of <i>Mycobacterium tuberculosis</i> among SOT candidates with active TB disease at time of transplantation.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Sixty-four detailed cases were identified while two cohort studies had aggregated data on 101 cases of TB disease among kidney transplant (KT) candidates. The majority of cases were liver transplant (LT) candidates (60/64, 93.7%); the rest were heart (2/64), kidney (1/64), or lung (1/64) candidates. About half of LT candidates were urgently transplanted because of ATT induced hepatic failure (35/60, 58.3%). Among LT candidates, pulmonary tuberculosis was most common (39/60, 65%) followed by extrapulmonary (EPTB) (17/60, 28.3%), and disseminated TB (4/60, 6.7%). ATT was started prior to transplantation in 44/60 (73.3%) candidates, while 16/60 (26.7%) were started after SOT. The majority (40/44, 90.9%) were on first line therapy, with transplantation occurring a median of 54.5 (range 2–180) days after starting ATT. Many ATT regimens were modified in the post-transplant phase (31/44, 70.4%). Of nine mortalities among LT recipients, only one was directly attributable to TB disease. For both cohort studies on KT candidates, EPTB was the most common form of TB disease (44/71 and 26/30). ATT was taken a median of 3.8 and 3 months, respectively, prior to SOT. All continuation phase posttransplant ATT were rifampicin-sparing with median duration of 12.27 and 14 months, respectively. There were no deaths attributable to TB disease.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusions</h3>\\n \\n <p>Favorable outcomes after SOT are feasible despite TB disease and incomplete pre-transplant anti-TB treatment. The urgent need for a life-saving transplant procedure should be weighed against the risks of transplantation in a patient with active tuberculosis. Completion of at least 2-month intensive first-line TB treatment (e.g., isoniazid, rifampicin, pyrazinamide, ethambutol, [HRZE]) is recommended with use of a rifamycin-based regimen to optimize sterilization. Although rifamycins are preferred for treatment, a rifampicin-sparing regimen may be more manageable post-transplantation to avoid drug–drug interactions, especially if longer courses of treatment are used.</p>\\n </section>\\n </div>\",\"PeriodicalId\":10467,\"journal\":{\"name\":\"Clinical Transplantation\",\"volume\":\"40 4\",\"pages\":\"\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2026-04-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Transplantation\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/ctr.70528\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"SURGERY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Transplantation","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/ctr.70528","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"SURGERY","Score":null,"Total":0}
Solid Organ Transplantation Among Transplant Candidates With TB Disease
Background
Deferral of solid organ transplantation (SOT) in recipients with tuberculosis (TB) disease (active TB) is recommended until anti-tuberculosis treatment (ATT) is completed. However, SOT is often urgent, and there are instances where SOT cannot be safely delayed.
Methods
We report two cases with TB disease who were transplanted before completion of ATT in our institution and searched PubMed, EMBASE, and MEDLINE databases from inception to August 2025, to retrieve all other published cases of Mycobacterium tuberculosis among SOT candidates with active TB disease at time of transplantation.
Results
Sixty-four detailed cases were identified while two cohort studies had aggregated data on 101 cases of TB disease among kidney transplant (KT) candidates. The majority of cases were liver transplant (LT) candidates (60/64, 93.7%); the rest were heart (2/64), kidney (1/64), or lung (1/64) candidates. About half of LT candidates were urgently transplanted because of ATT induced hepatic failure (35/60, 58.3%). Among LT candidates, pulmonary tuberculosis was most common (39/60, 65%) followed by extrapulmonary (EPTB) (17/60, 28.3%), and disseminated TB (4/60, 6.7%). ATT was started prior to transplantation in 44/60 (73.3%) candidates, while 16/60 (26.7%) were started after SOT. The majority (40/44, 90.9%) were on first line therapy, with transplantation occurring a median of 54.5 (range 2–180) days after starting ATT. Many ATT regimens were modified in the post-transplant phase (31/44, 70.4%). Of nine mortalities among LT recipients, only one was directly attributable to TB disease. For both cohort studies on KT candidates, EPTB was the most common form of TB disease (44/71 and 26/30). ATT was taken a median of 3.8 and 3 months, respectively, prior to SOT. All continuation phase posttransplant ATT were rifampicin-sparing with median duration of 12.27 and 14 months, respectively. There were no deaths attributable to TB disease.
Conclusions
Favorable outcomes after SOT are feasible despite TB disease and incomplete pre-transplant anti-TB treatment. The urgent need for a life-saving transplant procedure should be weighed against the risks of transplantation in a patient with active tuberculosis. Completion of at least 2-month intensive first-line TB treatment (e.g., isoniazid, rifampicin, pyrazinamide, ethambutol, [HRZE]) is recommended with use of a rifamycin-based regimen to optimize sterilization. Although rifamycins are preferred for treatment, a rifampicin-sparing regimen may be more manageable post-transplantation to avoid drug–drug interactions, especially if longer courses of treatment are used.
期刊介绍:
Clinical Transplantation: The Journal of Clinical and Translational Research aims to serve as a channel of rapid communication for all those involved in the care of patients who require, or have had, organ or tissue transplants, including: kidney, intestine, liver, pancreas, islets, heart, heart valves, lung, bone marrow, cornea, skin, bone, and cartilage, viable or stored.
Published monthly, Clinical Transplantation’s scope is focused on the complete spectrum of present transplant therapies, as well as also those that are experimental or may become possible in future. Topics include:
Immunology and immunosuppression;
Patient preparation;
Social, ethical, and psychological issues;
Complications, short- and long-term results;
Artificial organs;
Donation and preservation of organ and tissue;
Translational studies;
Advances in tissue typing;
Updates on transplant pathology;.
Clinical and translational studies are particularly welcome, as well as focused reviews. Full-length papers and short communications are invited. Clinical reviews are encouraged, as well as seminal papers in basic science which might lead to immediate clinical application. Prominence is regularly given to the results of cooperative surveys conducted by the organ and tissue transplant registries.
Clinical Transplantation: The Journal of Clinical and Translational Research is essential reading for clinicians and researchers in the diverse field of transplantation: surgeons; clinical immunologists; cryobiologists; hematologists; gastroenterologists; hepatologists; pulmonologists; nephrologists; cardiologists; and endocrinologists. It will also be of interest to sociologists, psychologists, research workers, and to all health professionals whose combined efforts will improve the prognosis of transplant recipients.