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Human leukocyte antigen mismatch on lung transplantation outcomes.
Firoz, Ahad; Kashem, Mohammed; Zhao, Huaqing; Geier, Steven; Toyoda, Yoshiya.
Afiliación
  • Firoz A; Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.
  • Kashem M; Department of Cardiovascular Surgery, Temple University Hospital, Philadelphia, PA, USA.
  • Zhao H; Department of Biomedical Education and Data Science, Lewis Katz School of Medicine, Philadelphia, PA, USA.
  • Geier S; Department of Pathology and Laboratory Medicine, Temple University Hospital, Philadelphia, PA, USA.
  • Toyoda Y; Department of Cardiovascular Surgery, Temple University Hospital, Philadelphia, PA, USA.
Eur J Cardiothorac Surg ; 62(2)2022 07 11.
Article en En | MEDLINE | ID: mdl-35224623
OBJECTIVES: Human leucocyte antigen (HLA) mismatch is a known risk factor for renal transplantation; however, there are conflicting and limited data on its ramifications within lung transplantation (LTx). Therefore, our study evaluated the effects of total HLA, HLA-A, -B and -DR mismatches on LTx outcomes. METHODS: We retrospectively examined the United Network for Organ Sharing database for adult patients who had undergone LTx for the first time between January 2005 and July 2021. Total HLA mismatch (0-3, 4, 5 and 6) and HLA locus mismatch (0-1 and 2) were analysed, with the end points of interest being mortality and bronchiolitis obliterans syndrome (BOS) development. RESULTS: Kaplan-Meier curve analysis found a significant difference in both overall survival (n = 27 651; 11 830 events) and BOS development (n = 25 444; 8901 events) for the total number of HLA (P < 0.001, P < 0.001), HLA-A (P < 0.001, P = 0.006) and HLA-DR (P < 0.001, P < 0.001) mismatches. With reference to 0-3 total HLA mismatches, multivariable Cox regression model found that 6 mismatches had an increased risk of mortality (P = 0.002) while 4 (P = 0.010), 5 (P = 0.007) and 6 (P < 0.001) mismatches had an increased risk of BOS. HLA-B mismatch was not associated with an increased mortality (P = 0.975) or BOS risk (P = 0.512). CONCLUSIONS: This study demonstrates a significant relationship between increased HLA mismatches and BOS development, with decreased overall survival only apparent with 6 mismatches. HLA-A and -DR mismatches were associated with an increased risk of mortality and BOS development compared to groups with at least 1 locus match.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bronquiolitis Obliterante / Trasplante de Pulmón Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Eur J Cardiothorac Surg Asunto de la revista: CARDIOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bronquiolitis Obliterante / Trasplante de Pulmón Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: Eur J Cardiothorac Surg Asunto de la revista: CARDIOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos