Pseudomonas aeruginosa and acute rejection independently increase the risk of donor-specific antibodies after lung transplantation

被引:41
作者
Kulkarni, Hrishikesh S. [1 ]
Tsui, Kevin [2 ]
Sunder, Suraj [1 ]
Ganninger, Alex [1 ]
Tague, Laneshia K. [1 ]
Witt, Chad A. [1 ]
Byers, Derek E. [1 ]
Trulock, Elbert P. [1 ]
Nava, Ruben [3 ]
Puri, Varun [3 ]
Kreisel, Daniel [3 ]
Mohanakumar, Thalachallour [4 ]
Gelman, Andrew E. [3 ,5 ]
Hachem, Ramsey R. [1 ]
机构
[1] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[2] Advocate Christ Med Ctr, Chicago, IL USA
[3] Washington Univ, Sch Med, Dept Surg, St Louis, MO 63110 USA
[4] St Josephs Hosp, Norton Thorac Inst, Phoenix, AZ USA
[5] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
基金
美国国家卫生研究院;
关键词
alloantibody; antibody biology; clinical research; practice; graft survival; immunobiology; infection and infectious agents - bacterial; lung (allograft) function; dysfunction; lung transplantation; pulmonology; BRONCHIOLITIS OBLITERANS SYNDROME; PRIMARY GRAFT DYSFUNCTION; ALLOGRAFT DYSFUNCTION; MEDIATED REJECTION; CYSTIC-FIBROSIS; CLASS-II; IMPACT; COLONIZATION; PATHOGENESIS; EXPRESSION;
D O I
10.1111/ajt.15687
中图分类号
R61 [外科手术学];
学科分类号
摘要
Factors contributing to donor-specific HLA antibody (DSA) development after lung transplantation have not been systematically evaluated. We hypothesized that the isolation of Pseudomonas aeruginosa in respiratory specimens would increase the risk of DSA development. Our objective was to determine the risk of DSA development associated with the isolation of Pseudomonas aeruginosa after lung transplantation. We conducted a single-center retrospective cohort study of primary lung transplant recipients and examined risk factors for DSA development using Cox regression models. Of 460 recipients, 205 (45%) developed DSA; the majority developed Class II DSA (n = 175, 85%), and 145 of 205 (71%) developed DSA to HLA-DQ alleles. Univariate time-dependent analyses revealed that isolation of Pseudomonas from respiratory specimens, acute cellular rejection, and lymphocytic bronchiolitis are associated with an increased risk of DSA development. In multivariable analyses, Pseudomonas isolation, acute cellular rejection, and lymphocytic bronchiolitis remained independent risk factors for DSA development. Additionally, there was a direct association between the number of positive Pseudomonas cultures and the risk of DSA development. Our findings suggest that pro-inflammatory events including acute cellular rejection, lymphocytic bronchiolitis, and Pseudomonas isolation after transplantation are associated with an increased risk of DSA development.
引用
收藏
页码:1028 / 1038
页数:11
相关论文
共 54 条
[1]   Microbes and Allogeneic Transplantation [J].
Alegre, Maria-Luisa ;
Bartman, Caroline ;
Chong, Anita S. .
TRANSPLANTATION, 2014, 97 (01) :5-11
[2]   Introduction to the Analysis of Survival Data in the Presence of Competing Risks [J].
Austin, Peter C. ;
Lee, Douglas S. ;
Fine, Jason P. .
CIRCULATION, 2016, 133 (06) :601-609
[3]   Host-Pathogen Interactions and Chronic Lung Allograft Dysfunction [J].
Belperio, John ;
Palmer, Scott M. ;
Weigt, S. Sam .
ANNALS OF THE AMERICAN THORACIC SOCIETY, 2017, 14 :S242-S246
[4]   Immunological link between primary graft dysfunction and chronic lung allograft rejection [J].
Bharat, Ankit ;
Kuo, Elbert ;
Steward, Nancy ;
Aloush, Aviva ;
Hachem, Ramsey ;
Trulock, Elbert P. ;
Patterson, G. Alexander ;
Meyers, Bryan F. ;
Mohanakumar, T. .
ANNALS OF THORACIC SURGERY, 2008, 86 (01) :189-197
[5]   Lung-Restricted Antibodies Mediate Primary Graft Dysfunction and Prevent Allotolerance after Murine Lung Transplantation [J].
Bharat, Ankit ;
Chiu, Stephen ;
Zheng, Zhikun ;
Sun, Haiying ;
Yeldandi, Anjana ;
DeCamp, Malcolm M. ;
Perlman, Harris ;
Budinger, G. R. Scott ;
Mohanakumar, Thalachallour .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2016, 55 (04) :532-541
[6]   Pseudomonas aeruginosa Induced Airway Epithelial Injury Drives Fibroblast Activation: A Mechanism in Chronic Lung Allograft Dysfunction [J].
Borthwick, L. A. ;
Suwara, M. I. ;
Carnell, S. C. ;
Green, N. J. ;
Mahida, R. ;
Dixon, D. ;
Gillespie, C. S. ;
Cartwright, T. N. ;
Horabin, J. ;
Walker, A. ;
Olin, E. ;
Rangar, M. ;
Gardner, A. ;
Mann, J. ;
Corris, P. A. ;
Mann, D. A. ;
Fisher, A. J. .
AMERICAN JOURNAL OF TRANSPLANTATION, 2016, 16 (06) :1751-1765
[7]   Pseudomonas aeruginosa colonization of the allograft after lung transplantation and the risk of bronchiolitis obliterans syndrome [J].
Botha, Phil ;
Archer, Lynda ;
Anderson, Rachel L. ;
Lordan, Jim ;
Dark, John H. ;
Corris, Paul A. ;
Gould, Kate ;
Fisher, Andrew J. .
TRANSPLANTATION, 2008, 85 (05) :771-774
[8]   Lung transplant infection [J].
Burguete, Sergio R. ;
Maselli, Diego J. ;
Fernandez, Juan F. ;
Levine, Stephanie M. .
RESPIROLOGY, 2013, 18 (01) :22-38
[9]   Detection and clinical impact of human leukocyte antigen antibodies in lung transplantation: A systematic review and meta-analysis [J].
Courtwright, A. ;
Diamond, J. M. ;
Wood, I. ;
Guleria, I. ;
Milford, E. ;
El-Chemaly, S. ;
Goldberg, H. J. .
HLA, 2018, 91 (02) :102-111
[10]   Microbiome in the pathogenesis of cystic fibrosis and lung transplant-related disease [J].
Cribbs, Sushma K. ;
Beck, James M. .
TRANSLATIONAL RESEARCH, 2017, 179 :84-96