Cargando…
Analysis of sex-based differences in clinical and molecular responses to ischemia reperfusion after lung transplantation
BACKGROUND: Sex and hormones influence immune responses to ischemia reperfusion (IR) and could, therefore, cause sex-related differences in lung transplantation (LTx) outcomes. We compared men’s and women’s clinical and molecular responses to post-LTx IR. METHODS: In 203 LTx patients, we used the 20...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693497/ https://www.ncbi.nlm.nih.gov/pubmed/34937545 http://dx.doi.org/10.1186/s12931-021-01900-y |
_version_ | 1784619152208560128 |
---|---|
author | Chacon-Alberty, Lourdes Ye, Shengbin Daoud, Daoud Frankel, William C. Virk, Hassan Mase, Jonathan Hochman-Mendez, Camila Li, Meng Sampaio, Luiz C. Taylor, Doris A. Loor, Gabriel |
author_facet | Chacon-Alberty, Lourdes Ye, Shengbin Daoud, Daoud Frankel, William C. Virk, Hassan Mase, Jonathan Hochman-Mendez, Camila Li, Meng Sampaio, Luiz C. Taylor, Doris A. Loor, Gabriel |
author_sort | Chacon-Alberty, Lourdes |
collection | PubMed |
description | BACKGROUND: Sex and hormones influence immune responses to ischemia reperfusion (IR) and could, therefore, cause sex-related differences in lung transplantation (LTx) outcomes. We compared men’s and women’s clinical and molecular responses to post-LTx IR. METHODS: In 203 LTx patients, we used the 2016 International Society for Heart and Lung Transplantation guidelines to score primary graft dysfunction (PGD). In a subgroup of 40 patients with blood samples collected before LTx (T0) and 6, 24, 48 (T48), and 72 h (T72) after lung reperfusion, molecular response to IR was examined through serial analysis of circulating cytokine expression. RESULTS: After adjustment, women had less grade 3 PGD than men at T48, but not at T72. PGD grade decreased from T0 to T72 more often in women than men. The evolution of PGD (the difference in mean PGD between T72 and T0) was greater in men. However, the evolution of IL-2, IL-7, IL-17a, and basic fibroblast growth factor levels was more often sustained throughout the 72 h in women. In the full cohort, we noted no sex differences in secondary clinical outcomes, but women had significantly lower peak lactate levels than men across the 72 h. CONCLUSIONS: Men and women differ in the evolution of PGD and cytokine secretion after LTx: Women have a more sustained proinflammatory response than men despite a greater reduction in PGD over time. This interaction between cytokine and PGD responses warrants investigation. Additionally, there may be important sex-related differences that could be used to tailor treatment during or after transplantation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-021-01900-y. |
format | Online Article Text |
id | pubmed-8693497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86934972021-12-23 Analysis of sex-based differences in clinical and molecular responses to ischemia reperfusion after lung transplantation Chacon-Alberty, Lourdes Ye, Shengbin Daoud, Daoud Frankel, William C. Virk, Hassan Mase, Jonathan Hochman-Mendez, Camila Li, Meng Sampaio, Luiz C. Taylor, Doris A. Loor, Gabriel Respir Res Research BACKGROUND: Sex and hormones influence immune responses to ischemia reperfusion (IR) and could, therefore, cause sex-related differences in lung transplantation (LTx) outcomes. We compared men’s and women’s clinical and molecular responses to post-LTx IR. METHODS: In 203 LTx patients, we used the 2016 International Society for Heart and Lung Transplantation guidelines to score primary graft dysfunction (PGD). In a subgroup of 40 patients with blood samples collected before LTx (T0) and 6, 24, 48 (T48), and 72 h (T72) after lung reperfusion, molecular response to IR was examined through serial analysis of circulating cytokine expression. RESULTS: After adjustment, women had less grade 3 PGD than men at T48, but not at T72. PGD grade decreased from T0 to T72 more often in women than men. The evolution of PGD (the difference in mean PGD between T72 and T0) was greater in men. However, the evolution of IL-2, IL-7, IL-17a, and basic fibroblast growth factor levels was more often sustained throughout the 72 h in women. In the full cohort, we noted no sex differences in secondary clinical outcomes, but women had significantly lower peak lactate levels than men across the 72 h. CONCLUSIONS: Men and women differ in the evolution of PGD and cytokine secretion after LTx: Women have a more sustained proinflammatory response than men despite a greater reduction in PGD over time. This interaction between cytokine and PGD responses warrants investigation. Additionally, there may be important sex-related differences that could be used to tailor treatment during or after transplantation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-021-01900-y. BioMed Central 2021-12-22 2021 /pmc/articles/PMC8693497/ /pubmed/34937545 http://dx.doi.org/10.1186/s12931-021-01900-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Chacon-Alberty, Lourdes Ye, Shengbin Daoud, Daoud Frankel, William C. Virk, Hassan Mase, Jonathan Hochman-Mendez, Camila Li, Meng Sampaio, Luiz C. Taylor, Doris A. Loor, Gabriel Analysis of sex-based differences in clinical and molecular responses to ischemia reperfusion after lung transplantation |
title | Analysis of sex-based differences in clinical and molecular responses to ischemia reperfusion after lung transplantation |
title_full | Analysis of sex-based differences in clinical and molecular responses to ischemia reperfusion after lung transplantation |
title_fullStr | Analysis of sex-based differences in clinical and molecular responses to ischemia reperfusion after lung transplantation |
title_full_unstemmed | Analysis of sex-based differences in clinical and molecular responses to ischemia reperfusion after lung transplantation |
title_short | Analysis of sex-based differences in clinical and molecular responses to ischemia reperfusion after lung transplantation |
title_sort | analysis of sex-based differences in clinical and molecular responses to ischemia reperfusion after lung transplantation |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693497/ https://www.ncbi.nlm.nih.gov/pubmed/34937545 http://dx.doi.org/10.1186/s12931-021-01900-y |
work_keys_str_mv | AT chaconalbertylourdes analysisofsexbaseddifferencesinclinicalandmolecularresponsestoischemiareperfusionafterlungtransplantation AT yeshengbin analysisofsexbaseddifferencesinclinicalandmolecularresponsestoischemiareperfusionafterlungtransplantation AT daouddaoud analysisofsexbaseddifferencesinclinicalandmolecularresponsestoischemiareperfusionafterlungtransplantation AT frankelwilliamc analysisofsexbaseddifferencesinclinicalandmolecularresponsestoischemiareperfusionafterlungtransplantation AT virkhassan analysisofsexbaseddifferencesinclinicalandmolecularresponsestoischemiareperfusionafterlungtransplantation AT masejonathan analysisofsexbaseddifferencesinclinicalandmolecularresponsestoischemiareperfusionafterlungtransplantation AT hochmanmendezcamila analysisofsexbaseddifferencesinclinicalandmolecularresponsestoischemiareperfusionafterlungtransplantation AT limeng analysisofsexbaseddifferencesinclinicalandmolecularresponsestoischemiareperfusionafterlungtransplantation AT sampaioluizc analysisofsexbaseddifferencesinclinicalandmolecularresponsestoischemiareperfusionafterlungtransplantation AT taylordorisa analysisofsexbaseddifferencesinclinicalandmolecularresponsestoischemiareperfusionafterlungtransplantation AT loorgabriel analysisofsexbaseddifferencesinclinicalandmolecularresponsestoischemiareperfusionafterlungtransplantation |