Human leukocyte antigens antibodies after lung transplantation: Primary results of the HALT study
Adult
Graft Rejection
Male
Immunology
610
Clinical sciences
clinical research/practice
Medical and Health Sciences
03 medical and health sciences
Postoperative Complications
0302 clinical medicine
lung transplantation/pulmonology
Clinical Research
HLA Antigens
Isoantibodies
Risk Factors
616
lung transplantation
rejection: T cell mediated
Humans
histocompatibility
Prospective Studies
monitoring: immune
Lung
pulmonology
Aged
Transplantation
Biomedical and Clinical Sciences
Prevention
Histocompatibility Testing
Graft Survival
Organ Transplantation
Middle Aged
Prognosis
practice
major histocompatibility complex
Tissue Donors
3. Good health
Survival Rate
clinical research
rejection: antibody-mediated
Surgery
Female
Follow-Up Studies
Lung Transplantation
DOI:
10.1111/ajt.14893
Publication Date:
2018-04-24T10:32:51Z
AUTHORS (17)
ABSTRACT
Donor-specific antibodies (DSA) to mismatched human leukocyte antigens (HLA) are associated with worse outcomes after lung transplantation. To determine the incidence and characteristics of DSA early after lung transplantation, we conducted a prospective multicenter observational study that used standardized treatment and testing protocols. Among 119 transplant recipients, 43 (36%) developed DSA: 6 (14%) developed DSA only to class I HLA, 23 (53%) developed DSA only to class II HLA, and 14 (33%) developed DSA to both class I and class II HLA. The median DSA mean fluorescence intensity (MFI) was 3197. We identified a significant association between the Lung Allocation Score and the development of DSA (HR = 1.02, 95% CI: 1.001-1.03, P = .047) and a significant association between DSA with an MFI ≥ 3000 and acute cellular rejection (ACR) grade ≥ A2 (HR = 2.11, 95% CI: 1.04-4.27, P = .039). However, we did not detect an association between DSA and survival. We conclude that DSA occur frequently early after lung transplantation, and most target class II HLA. DSA with an MFI ≥ 3000 have a significant association with ACR. Extended follow-up is necessary to determine the impact of DSA on other important outcomes.
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CITATIONS (53)
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