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A phase 1 study of donor regulatory T-cell infusion plus low-dose interleukin-2 for steroid-refractory chronic graft-vs-host disease

Chronic graft-versus-host disease (cGVHD) remains a frequent cause of nonrelapse morbidity and mortality after allogeneic hematopoietic stem cell transplantation. Despite recent advances, options for steroid-refractory (SR) cGVHD are limited. In previous trials of low-dose interleukin-2 (LD IL-2), t...

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Autores principales: Whangbo, Jennifer S., Nikiforow, Sarah, Kim, Haesook T., Wahl, Jonathan, Reynolds, Carol G., Rai, Sharmila C., Kim, Soomin, Burden, Andrew, Alho, Ana C., Lacerda, João F., Alyea, Edwin P., Cutler, Corey S., Ho, Vincent T., Antin, Joseph H., Soiffer, Robert J., Ritz, Jerome, Koreth, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society of Hematology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647832/
https://www.ncbi.nlm.nih.gov/pubmed/35475885
http://dx.doi.org/10.1182/bloodadvances.2021006625
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author Whangbo, Jennifer S.
Nikiforow, Sarah
Kim, Haesook T.
Wahl, Jonathan
Reynolds, Carol G.
Rai, Sharmila C.
Kim, Soomin
Burden, Andrew
Alho, Ana C.
Lacerda, João F.
Alyea, Edwin P.
Cutler, Corey S.
Ho, Vincent T.
Antin, Joseph H.
Soiffer, Robert J.
Ritz, Jerome
Koreth, John
author_facet Whangbo, Jennifer S.
Nikiforow, Sarah
Kim, Haesook T.
Wahl, Jonathan
Reynolds, Carol G.
Rai, Sharmila C.
Kim, Soomin
Burden, Andrew
Alho, Ana C.
Lacerda, João F.
Alyea, Edwin P.
Cutler, Corey S.
Ho, Vincent T.
Antin, Joseph H.
Soiffer, Robert J.
Ritz, Jerome
Koreth, John
author_sort Whangbo, Jennifer S.
collection PubMed
description Chronic graft-versus-host disease (cGVHD) remains a frequent cause of nonrelapse morbidity and mortality after allogeneic hematopoietic stem cell transplantation. Despite recent advances, options for steroid-refractory (SR) cGVHD are limited. In previous trials of low-dose interleukin-2 (LD IL-2), the immunomodulatory properties of regulatory T cells (Tregs) have been harnessed to treat SR-cGVHD safely and effectively. In the present study, we combined a single infusion of Treg-enriched lymphocytes (Treg DLI) from the original stem cell donor with in vivo Treg expansion using LD IL-2 (1 × 10(6) IU/m(2) per day for 8 weeks) in 25 adult patients with SR-cGVHD. Treg were not expanded ex vivo. Treg DLI was initiated at 0.1 × 10(6) cells per kg patient and escalated to a maximum dose of 1 × 10(6) cells per kg. Treg DLI plus LD IL-2 was well tolerated and led to partial responses (PR) in 5 of 25 patients (20%) after 8 weeks of therapy. Ten additional patients (40%) had stable disease with minor responses not meeting PR criteria. Patients at all dose levels had similar Treg expansion without significant changes in CD4(+) conventional T cells or CD8(+) T cells. High-throughput sequencing of the T-cell receptor β locus showed selective improvement of Treg diversity. A subset of DLI-derived Treg clones showed preferential expansion at week 8 and long-term persistence 1-year postinfusion. We demonstrate for the first time that infusion of polyclonal healthy donor Tregs followed by expansion with LD IL-2 is safe in patients with SR-cGVHD, thus establishing a foundation for future adoptive Treg therapies in the posttransplant setting. This trial was registered at www.clinicaltrials.gov as #NCT01937468.
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spelling pubmed-96478322022-11-14 A phase 1 study of donor regulatory T-cell infusion plus low-dose interleukin-2 for steroid-refractory chronic graft-vs-host disease Whangbo, Jennifer S. Nikiforow, Sarah Kim, Haesook T. Wahl, Jonathan Reynolds, Carol G. Rai, Sharmila C. Kim, Soomin Burden, Andrew Alho, Ana C. Lacerda, João F. Alyea, Edwin P. Cutler, Corey S. Ho, Vincent T. Antin, Joseph H. Soiffer, Robert J. Ritz, Jerome Koreth, John Blood Adv Regular Article Chronic graft-versus-host disease (cGVHD) remains a frequent cause of nonrelapse morbidity and mortality after allogeneic hematopoietic stem cell transplantation. Despite recent advances, options for steroid-refractory (SR) cGVHD are limited. In previous trials of low-dose interleukin-2 (LD IL-2), the immunomodulatory properties of regulatory T cells (Tregs) have been harnessed to treat SR-cGVHD safely and effectively. In the present study, we combined a single infusion of Treg-enriched lymphocytes (Treg DLI) from the original stem cell donor with in vivo Treg expansion using LD IL-2 (1 × 10(6) IU/m(2) per day for 8 weeks) in 25 adult patients with SR-cGVHD. Treg were not expanded ex vivo. Treg DLI was initiated at 0.1 × 10(6) cells per kg patient and escalated to a maximum dose of 1 × 10(6) cells per kg. Treg DLI plus LD IL-2 was well tolerated and led to partial responses (PR) in 5 of 25 patients (20%) after 8 weeks of therapy. Ten additional patients (40%) had stable disease with minor responses not meeting PR criteria. Patients at all dose levels had similar Treg expansion without significant changes in CD4(+) conventional T cells or CD8(+) T cells. High-throughput sequencing of the T-cell receptor β locus showed selective improvement of Treg diversity. A subset of DLI-derived Treg clones showed preferential expansion at week 8 and long-term persistence 1-year postinfusion. We demonstrate for the first time that infusion of polyclonal healthy donor Tregs followed by expansion with LD IL-2 is safe in patients with SR-cGVHD, thus establishing a foundation for future adoptive Treg therapies in the posttransplant setting. This trial was registered at www.clinicaltrials.gov as #NCT01937468. The American Society of Hematology 2022-04-29 /pmc/articles/PMC9647832/ /pubmed/35475885 http://dx.doi.org/10.1182/bloodadvances.2021006625 Text en © 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Whangbo, Jennifer S.
Nikiforow, Sarah
Kim, Haesook T.
Wahl, Jonathan
Reynolds, Carol G.
Rai, Sharmila C.
Kim, Soomin
Burden, Andrew
Alho, Ana C.
Lacerda, João F.
Alyea, Edwin P.
Cutler, Corey S.
Ho, Vincent T.
Antin, Joseph H.
Soiffer, Robert J.
Ritz, Jerome
Koreth, John
A phase 1 study of donor regulatory T-cell infusion plus low-dose interleukin-2 for steroid-refractory chronic graft-vs-host disease
title A phase 1 study of donor regulatory T-cell infusion plus low-dose interleukin-2 for steroid-refractory chronic graft-vs-host disease
title_full A phase 1 study of donor regulatory T-cell infusion plus low-dose interleukin-2 for steroid-refractory chronic graft-vs-host disease
title_fullStr A phase 1 study of donor regulatory T-cell infusion plus low-dose interleukin-2 for steroid-refractory chronic graft-vs-host disease
title_full_unstemmed A phase 1 study of donor regulatory T-cell infusion plus low-dose interleukin-2 for steroid-refractory chronic graft-vs-host disease
title_short A phase 1 study of donor regulatory T-cell infusion plus low-dose interleukin-2 for steroid-refractory chronic graft-vs-host disease
title_sort phase 1 study of donor regulatory t-cell infusion plus low-dose interleukin-2 for steroid-refractory chronic graft-vs-host disease
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9647832/
https://www.ncbi.nlm.nih.gov/pubmed/35475885
http://dx.doi.org/10.1182/bloodadvances.2021006625
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