Anna Dukat-Mazurek , Wojtek Karolak , Hanna Zielińska , Patrycja Specjał , Grażyna Moszkowska , Jacek Wojarski , Karolina Lipka , Justyna Fercho , Marta Gallas , Dariusz Rystwiej , Fanny Sunesson , Lin Akily , William Karlsen , Marcin Sawczuk , Piotr Trzonkowski , Sławomir Żegleń
{"title":"肺移植后抗hla - DQ抗体的可能意义-单中心研究","authors":"Anna Dukat-Mazurek , Wojtek Karolak , Hanna Zielińska , Patrycja Specjał , Grażyna Moszkowska , Jacek Wojarski , Karolina Lipka , Justyna Fercho , Marta Gallas , Dariusz Rystwiej , Fanny Sunesson , Lin Akily , William Karlsen , Marcin Sawczuk , Piotr Trzonkowski , Sławomir Żegleń","doi":"10.1016/j.humimm.2025.111597","DOIUrl":null,"url":null,"abstract":"<div><div>The role of anti-HLA antibodies in solid organ transplantation has long been recognized, particularly with respect to graft rejection and patient survival. This study aimed to evaluate the impact of <em>de novo</em> donor-specific antibodies (DSA) on graft failure and mortality in Polish lung transplant recipients. The study included 112 patients who had a well-defined immune status prior to transplantation. The presence and specificity of anti-HLA antibodies were assessed using the Luminex platform. We identified 26 patients (23%) as having increased immunological risk. Pre-transplant DSAs were detected in 13 recipients. Post-transplantation, the development of <em>de novo</em> DSAs was evaluated, with a cumulative incidence of 11%. Our findings confirmed that lung transplant recipients with donor-specific immunization frequently develop antibodies targeting antigens at the HLA-DQ locus. Notably, 90% (9 out of 10) of immunized patients exhibited high mean fluorescence intensity (MFI) levels of anti-DQ antibodies. These antibodies were shown to be harmful, with mortality significantly higher in immunized patients: 50% of patients with anti-DQ antibodies died, compared to only 15% in those without DSAs. This is the first study of its kind in the Polish population, confirming that strategies to prevent and treat DQ DSAs may improve outcomes for lung transplant recipients.</div></div>","PeriodicalId":55047,"journal":{"name":"Human Immunology","volume":"86 6","pages":"Article 111597"},"PeriodicalIF":2.2000,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Possible significance of anti-HLA DQ antibodies after lung transplantation – Single centre study\",\"authors\":\"Anna Dukat-Mazurek , Wojtek Karolak , Hanna Zielińska , Patrycja Specjał , Grażyna Moszkowska , Jacek Wojarski , Karolina Lipka , Justyna Fercho , Marta Gallas , Dariusz Rystwiej , Fanny Sunesson , Lin Akily , William Karlsen , Marcin Sawczuk , Piotr Trzonkowski , Sławomir Żegleń\",\"doi\":\"10.1016/j.humimm.2025.111597\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The role of anti-HLA antibodies in solid organ transplantation has long been recognized, particularly with respect to graft rejection and patient survival. This study aimed to evaluate the impact of <em>de novo</em> donor-specific antibodies (DSA) on graft failure and mortality in Polish lung transplant recipients. The study included 112 patients who had a well-defined immune status prior to transplantation. The presence and specificity of anti-HLA antibodies were assessed using the Luminex platform. We identified 26 patients (23%) as having increased immunological risk. Pre-transplant DSAs were detected in 13 recipients. Post-transplantation, the development of <em>de novo</em> DSAs was evaluated, with a cumulative incidence of 11%. Our findings confirmed that lung transplant recipients with donor-specific immunization frequently develop antibodies targeting antigens at the HLA-DQ locus. Notably, 90% (9 out of 10) of immunized patients exhibited high mean fluorescence intensity (MFI) levels of anti-DQ antibodies. These antibodies were shown to be harmful, with mortality significantly higher in immunized patients: 50% of patients with anti-DQ antibodies died, compared to only 15% in those without DSAs. This is the first study of its kind in the Polish population, confirming that strategies to prevent and treat DQ DSAs may improve outcomes for lung transplant recipients.</div></div>\",\"PeriodicalId\":55047,\"journal\":{\"name\":\"Human Immunology\",\"volume\":\"86 6\",\"pages\":\"Article 111597\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-10-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Human Immunology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0198885925003684\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Immunology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0198885925003684","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}
Possible significance of anti-HLA DQ antibodies after lung transplantation – Single centre study
The role of anti-HLA antibodies in solid organ transplantation has long been recognized, particularly with respect to graft rejection and patient survival. This study aimed to evaluate the impact of de novo donor-specific antibodies (DSA) on graft failure and mortality in Polish lung transplant recipients. The study included 112 patients who had a well-defined immune status prior to transplantation. The presence and specificity of anti-HLA antibodies were assessed using the Luminex platform. We identified 26 patients (23%) as having increased immunological risk. Pre-transplant DSAs were detected in 13 recipients. Post-transplantation, the development of de novo DSAs was evaluated, with a cumulative incidence of 11%. Our findings confirmed that lung transplant recipients with donor-specific immunization frequently develop antibodies targeting antigens at the HLA-DQ locus. Notably, 90% (9 out of 10) of immunized patients exhibited high mean fluorescence intensity (MFI) levels of anti-DQ antibodies. These antibodies were shown to be harmful, with mortality significantly higher in immunized patients: 50% of patients with anti-DQ antibodies died, compared to only 15% in those without DSAs. This is the first study of its kind in the Polish population, confirming that strategies to prevent and treat DQ DSAs may improve outcomes for lung transplant recipients.
期刊介绍:
The journal''s scope includes understanding the genetic and functional mechanisms that distinguish human individuals in their immune responses to allografts, pregnancy, infections or vaccines as well as the immune responses that lead to autoimmunity, allergy or drug hypersensitivity. It also includes examining the distribution of the genes controlling these responses in populations.
Research areas include:
Studies of the genetics, genomics, polymorphism, evolution, and population distribution of immune-related genes
Studies of the expression, structure and function of the products of immune-related genes
Immunogenetics of susceptibility to infectious and autoimmune disease, and allergy
The role of the immune-related genes in hematopoietic stem cell, solid organ, and vascularized composite allograft transplant
Histocompatibility studies including alloantibodies, epitope definition, and T cell alloreactivity
Studies of immunologic tolerance and pregnancy
T cell, B cell, NK and regulatory cell functions, particularly related to subjects within the journal''s scope
Pharmacogenomics and vaccine development in the context of immune-related genes
Human Immunology considers immune-related genes to include those encoding classical and non-classical HLA, KIR, MIC, minor histocompatibility antigens (mHAg), immunoglobulins, TCR, BCR, proteins involved in antigen processing and presentation, complement, Fc receptors, chemokines and cytokines. Other immune-related genes may be considered.
Human Immunology is also interested in bioinformatics of immune-related genes and organizational topics impacting laboratory processes, organ allocation, clinical strategies, and registries related to autoimmunity and transplantation.