Impact of age and telomere length on circulating T cells and rejection risk after lung transplantation for idiopathic pulmonary fibrosis

被引:3
作者
Snyder, Mark E. [1 ,2 ,3 ,8 ]
Anderson, Michaela R. [4 ]
Benvenuto, Luke J. [5 ]
Sutton, Rachel M. [1 ]
Bondonese, Anna [1 ]
Koshy, Ritchie [1 ]
Burke, Robin [1 ]
Clifford, Sarah [1 ]
Craig, Andrew [1 ]
Iasella, Carlo J. [1 ,6 ]
Hannan, Stefanie J. [1 ]
Popescu, Iulia [1 ]
Zhang, Yingze [1 ]
Sanchez, Pablo G. [7 ]
Alder, Jonathan K. [1 ]
Mcdyer, John F. [1 ,3 ]
机构
[1] Univ Pittsburgh, Dept Med, Pittsburgh, PA USA
[2] Univ Pittsburgh, Dept Immunol, Pittsburgh, PA USA
[3] Univ Pittsburgh, Starzl Transplantat Inst, Pittsburgh, PA USA
[4] Univ Penn, Dept Med, Philadelphia, PA USA
[5] Columbia Univ, Irving Med Ctr, Dept Med, New York, NY USA
[6] Univ Pittsburgh, Dept Pharmacol, Pittsburgh, PA USA
[7] Univ Pittsburgh, Dept Cardiothorac Surg, Pittsburgh, PA USA
[8] UPMC Montifiore Hosp, NW6283459 Fifth Ave, Pittsburgh, PA 15213 USA
关键词
lung transplantation; telomere length; aging; rejection; T cells; BRONCHIOLITIS OBLITERANS; NAIVE; HEART;
D O I
10.1016/j.healun.2023.08.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Most idiopathic pulmonary fibrosis (IPF) lung transplant recipients (IPF-LTRs) have short telomere (ST) length. Inherited mutations in telomere-related genes are associated with the development of T cell immunodeficiency. Despite this, IPF-LTRs with telomere-related rare variants are not protected from acute cellular rejection (ACR). We set out to determine the impact of both age and telomere length on the circulating T cell compartment and ACR burden of IPF-LTRs.METHODS: We identified 106 IPF-LTRs who had telomere length testing using flowFISH (57 with short telomeres and 49 with long telomeres) as well as a subset from both cohorts who had cryo-preserved PBMC at least 1 time point, 6 months posttransplantation. Circulating T cells from before transplantation and at 6 and 12 months posttransplantation were analyzed using multiparameter flow cytometry to study phenotype and functional capacity, and bulk T cell receptor sequencing was per-formed to study repertoire diversity. Linear regression was used to study the relationship of age and telomere length on early (within 1 year) and late (between 1 and 2 years) ACR.RESULTS: IPF-LTRs with ST were found to have premature "aging" of their circulating T cell compartment, with age-agnostic elevations in posttransplant terminal differentiation of CD8+ T cells, in-creased granzyme B positivity of both CD8+ and CD4+ T cells, upregulation of the exhaustion marker, CD57, and chemotactic protein CCR5, and enhanced T cell receptor clonal expansion. Additionally, we found a significant decline in early ACR burden with increasing age, but only in the ST cohort.CONCLUSIONS: IPF-LTRs with ST have premature "aging" of their circulating T cell compartment posttransplantation and a clear age-related decline in ACR burden. J Heart Lung Transplant 2023;42:1666-1677 (c) 2023 The Authors. Published by Elsevier Inc. on behalf of International Society for Heart and Lung Transplantation. This is an open access article under the CC BY-NC-ND license (http://creative-commons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:1666 / 1677
页数:12
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