Alessandra Mazzola , Clémentine Roger , Romain Lhotte , Maxime Mallet , Dominique Thabut , Jean-Luc Taupin , Filomena Conti
{"title":"HLA 进化分化对肝硬化肝移植候选者细菌感染风险的影响。","authors":"Alessandra Mazzola , Clémentine Roger , Romain Lhotte , Maxime Mallet , Dominique Thabut , Jean-Luc Taupin , Filomena Conti","doi":"10.1016/j.clim.2024.110399","DOIUrl":null,"url":null,"abstract":"<div><div>Bacterial infections are common in cirrhosis patients, increasing the risk of decompensation and death. The impact of HLA evolutionary divergence (HED) on infection risk hasn't been studied in humans before. We conducted a retrospective study on cirrhosis patients awaiting liver transplantation (LT) from January 2019 to February 2022, examining class I and II-HED effects on bacterial infections and cirrhosis decompensation.</div><div>We included 269 cirrhosis patients. Among them, 98 experienced 153 bacterial infections. Multivariable analysis after variable selection revealed that higher class II-HED was linked to fewer bacterial infections (<em>p</em> = 0.034), while class I-HED showed no effect (<em>p</em> = 0.074). Independent risk factors for bacterial infections included invasive procedures (<em>p</em> < 0.001), ICU hospitalization (p < 0.001), recent antibiotic treatment (<em>p</em> = 0.046), rifaximin use (<em>p</em> = 0.043), and cirrhosis decompensation (<em>p</em> = 0.002). Neither class I nor II-HED affected decompensation risk.</div><div>This pioneering study shows that high class II-HED levels may protect against bacterial infections in cirrhosis patients awaiting LT, suggesting an immunological mechanism at play.</div></div>","PeriodicalId":10392,"journal":{"name":"Clinical immunology","volume":"270 ","pages":"Article 110399"},"PeriodicalIF":4.5000,"publicationDate":"2024-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"HLA evolutionary divergence effect on bacterial infection risk in cirrhotic liver transplant candidates\",\"authors\":\"Alessandra Mazzola , Clémentine Roger , Romain Lhotte , Maxime Mallet , Dominique Thabut , Jean-Luc Taupin , Filomena Conti\",\"doi\":\"10.1016/j.clim.2024.110399\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Bacterial infections are common in cirrhosis patients, increasing the risk of decompensation and death. The impact of HLA evolutionary divergence (HED) on infection risk hasn't been studied in humans before. We conducted a retrospective study on cirrhosis patients awaiting liver transplantation (LT) from January 2019 to February 2022, examining class I and II-HED effects on bacterial infections and cirrhosis decompensation.</div><div>We included 269 cirrhosis patients. Among them, 98 experienced 153 bacterial infections. Multivariable analysis after variable selection revealed that higher class II-HED was linked to fewer bacterial infections (<em>p</em> = 0.034), while class I-HED showed no effect (<em>p</em> = 0.074). Independent risk factors for bacterial infections included invasive procedures (<em>p</em> < 0.001), ICU hospitalization (p < 0.001), recent antibiotic treatment (<em>p</em> = 0.046), rifaximin use (<em>p</em> = 0.043), and cirrhosis decompensation (<em>p</em> = 0.002). Neither class I nor II-HED affected decompensation risk.</div><div>This pioneering study shows that high class II-HED levels may protect against bacterial infections in cirrhosis patients awaiting LT, suggesting an immunological mechanism at play.</div></div>\",\"PeriodicalId\":10392,\"journal\":{\"name\":\"Clinical immunology\",\"volume\":\"270 \",\"pages\":\"Article 110399\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2024-11-17\",\"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/S1521661624005084\",\"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/S1521661624005084","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
HLA evolutionary divergence effect on bacterial infection risk in cirrhotic liver transplant candidates
Bacterial infections are common in cirrhosis patients, increasing the risk of decompensation and death. The impact of HLA evolutionary divergence (HED) on infection risk hasn't been studied in humans before. We conducted a retrospective study on cirrhosis patients awaiting liver transplantation (LT) from January 2019 to February 2022, examining class I and II-HED effects on bacterial infections and cirrhosis decompensation.
We included 269 cirrhosis patients. Among them, 98 experienced 153 bacterial infections. Multivariable analysis after variable selection revealed that higher class II-HED was linked to fewer bacterial infections (p = 0.034), while class I-HED showed no effect (p = 0.074). Independent risk factors for bacterial infections included invasive procedures (p < 0.001), ICU hospitalization (p < 0.001), recent antibiotic treatment (p = 0.046), rifaximin use (p = 0.043), and cirrhosis decompensation (p = 0.002). Neither class I nor II-HED affected decompensation risk.
This pioneering study shows that high class II-HED levels may protect against bacterial infections in cirrhosis patients awaiting LT, suggesting an immunological mechanism at play.
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.