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Pilot study of lithium to restore intestinal barrier function in severe graft-versus-host disease
Severe intestinal graft-vs-host disease (GVHD) after allogeneic hematopoietic cell transplantation (HCT) causes mucosal ulceration and induces innate and adaptive immune responses that amplify and perpetuate GVHD and the associated barrier dysfunction. Pharmacological agents to target mucosal barrie...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5560707/ https://www.ncbi.nlm.nih.gov/pubmed/28817727 http://dx.doi.org/10.1371/journal.pone.0183284 |
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author | Steinbach, Gideon Hockenbery, David M. Huls, Gerwin Furlong, Terry Myerson, David Loeb, Keith R. Fann, Jesse R. Castilla-Llorente, Christina McDonald, George B. Martin, Paul J. |
author_facet | Steinbach, Gideon Hockenbery, David M. Huls, Gerwin Furlong, Terry Myerson, David Loeb, Keith R. Fann, Jesse R. Castilla-Llorente, Christina McDonald, George B. Martin, Paul J. |
author_sort | Steinbach, Gideon |
collection | PubMed |
description | Severe intestinal graft-vs-host disease (GVHD) after allogeneic hematopoietic cell transplantation (HCT) causes mucosal ulceration and induces innate and adaptive immune responses that amplify and perpetuate GVHD and the associated barrier dysfunction. Pharmacological agents to target mucosal barrier dysfunction in GVHD are needed. We hypothesized that induction of Wnt signaling by lithium, an inhibitor of glycogen synthase kinase (GSK3), would potentiate intestinal crypt proliferation and mucosal repair and that inhibition of GSK3 in inflammatory cells would attenuate the deregulated inflammatory response to mucosal injury. We conducted an observational pilot study to provide data for the potential design of a randomized study of lithium. Twenty patients with steroid refractory intestinal GVHD meeting enrollment criteria were given oral lithium carbonate. GVHD was otherwise treated per current practice, including 2 mg/kg per day of prednisone equivalent. Seventeen patients had extensive mucosal denudation (extreme endoscopic grade 3) in the duodenum or colon. We observed that 8 of 12 patients (67%) had a complete remission (CR) of GVHD and survived more than 1 year (median 5 years) when lithium administration was started promptly within 3 days of endoscopic diagnosis of denuded mucosa. When lithium was started promptly and less than 7 days from salvage therapy for refractory GVHD, 8 of 10 patients (80%) had a CR and survived more than 1 year. In perspective, a review of 1447 consecutive adult HCT patients in the preceding 6 years at our cancer center showed 0% one-year survival in 27 patients with stage 3–4 intestinal GVHD and grade 3 endoscopic appearance in the duodenum or colon. Toxicities included fatigue, somnolence, confusion or blunted affect in 50% of the patients. The favorable outcomes in patients who received prompt lithium therapy appear to support the future conduct of a randomized study of lithium for management of severe GVHD with extensive mucosal injury. Trial Registration: ClinicalTrials.gov NCT00408681 |
format | Online Article Text |
id | pubmed-5560707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55607072017-08-25 Pilot study of lithium to restore intestinal barrier function in severe graft-versus-host disease Steinbach, Gideon Hockenbery, David M. Huls, Gerwin Furlong, Terry Myerson, David Loeb, Keith R. Fann, Jesse R. Castilla-Llorente, Christina McDonald, George B. Martin, Paul J. PLoS One Research Article Severe intestinal graft-vs-host disease (GVHD) after allogeneic hematopoietic cell transplantation (HCT) causes mucosal ulceration and induces innate and adaptive immune responses that amplify and perpetuate GVHD and the associated barrier dysfunction. Pharmacological agents to target mucosal barrier dysfunction in GVHD are needed. We hypothesized that induction of Wnt signaling by lithium, an inhibitor of glycogen synthase kinase (GSK3), would potentiate intestinal crypt proliferation and mucosal repair and that inhibition of GSK3 in inflammatory cells would attenuate the deregulated inflammatory response to mucosal injury. We conducted an observational pilot study to provide data for the potential design of a randomized study of lithium. Twenty patients with steroid refractory intestinal GVHD meeting enrollment criteria were given oral lithium carbonate. GVHD was otherwise treated per current practice, including 2 mg/kg per day of prednisone equivalent. Seventeen patients had extensive mucosal denudation (extreme endoscopic grade 3) in the duodenum or colon. We observed that 8 of 12 patients (67%) had a complete remission (CR) of GVHD and survived more than 1 year (median 5 years) when lithium administration was started promptly within 3 days of endoscopic diagnosis of denuded mucosa. When lithium was started promptly and less than 7 days from salvage therapy for refractory GVHD, 8 of 10 patients (80%) had a CR and survived more than 1 year. In perspective, a review of 1447 consecutive adult HCT patients in the preceding 6 years at our cancer center showed 0% one-year survival in 27 patients with stage 3–4 intestinal GVHD and grade 3 endoscopic appearance in the duodenum or colon. Toxicities included fatigue, somnolence, confusion or blunted affect in 50% of the patients. The favorable outcomes in patients who received prompt lithium therapy appear to support the future conduct of a randomized study of lithium for management of severe GVHD with extensive mucosal injury. Trial Registration: ClinicalTrials.gov NCT00408681 Public Library of Science 2017-08-17 /pmc/articles/PMC5560707/ /pubmed/28817727 http://dx.doi.org/10.1371/journal.pone.0183284 Text en © 2017 Steinbach et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Steinbach, Gideon Hockenbery, David M. Huls, Gerwin Furlong, Terry Myerson, David Loeb, Keith R. Fann, Jesse R. Castilla-Llorente, Christina McDonald, George B. Martin, Paul J. Pilot study of lithium to restore intestinal barrier function in severe graft-versus-host disease |
title | Pilot study of lithium to restore intestinal barrier function in severe graft-versus-host disease |
title_full | Pilot study of lithium to restore intestinal barrier function in severe graft-versus-host disease |
title_fullStr | Pilot study of lithium to restore intestinal barrier function in severe graft-versus-host disease |
title_full_unstemmed | Pilot study of lithium to restore intestinal barrier function in severe graft-versus-host disease |
title_short | Pilot study of lithium to restore intestinal barrier function in severe graft-versus-host disease |
title_sort | pilot study of lithium to restore intestinal barrier function in severe graft-versus-host disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5560707/ https://www.ncbi.nlm.nih.gov/pubmed/28817727 http://dx.doi.org/10.1371/journal.pone.0183284 |
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