Format

Send to

Choose Destination
J Clin Invest. 2019 Nov 1;129(11):5020-5032. doi: 10.1172/JCI128323.

T cell repertoire remodeling following post-transplant T cell therapy coincides with clinical response.

Author information

1
QIMR Centre for Immunotherapy and Vaccine Development, QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
2
School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane, Queensland, Australia.
3
Department of Nephrology, Princess Alexandra Hospital, Brisbane, Queensland, Australia.
4
School of Clinical Medicine, The University of Queensland, Brisbane, Queensland, Australia.
5
Queensland Lung Transplant Service, The Prince Charles Hospital, Brisbane, Queensland, Australia.

Abstract

BACKGROUNDImpaired T cell immunity in transplant recipients is associated with infection-related morbidity and mortality. We recently reported the successful use of adoptive T cell therapy (ACT) against drug-resistant/recurrent cytomegalovirus in solid-organ transplant recipients.METHODSIn the present study, we used high-throughput T cell receptor Vβ sequencing and T cell functional profiling to delineate the impact of ACT on T cell repertoire remodeling in the context of pretherapy immunity and ACT products.RESULTSThese analyses indicated that a clinical response was coincident with significant changes in the T cell receptor Vβ landscape after therapy. This restructuring was associated with the emergence of effector memory T cells in responding patients, while nonresponders displayed dramatic pretherapy T cell expansions with minimal change following ACT. Furthermore, immune reconstitution included both adoptively transferred clonotypes and endogenous clonotypes not detected in the ACT products.CONCLUSIONThese observations demonstrate that immune control following ACT requires significant repertoire remodeling, which may be impaired in nonresponders because of the preexisting immune environment. Immunological interventions that can modulate this environment may improve clinical outcomes.TRIAL REGISTRATIONAustralian New Zealand Clinical Trial Registry, ACTRN12613000981729.FUNDINGThis study was supported by funding from the National Health and Medical Research Council, Australia (APP1132519 and APP1062074).

KEYWORDS:

Immunology; Immunotherapy; T cells; T-cell receptor; Transplantation

PMID:
31415240
PMCID:
PMC6819118
[Available on 2020-02-01]
DOI:
10.1172/JCI128323
Free full text

Supplemental Content

Full text links

Icon for American Society for Clinical Investigation
Loading ...
Support Center