Cargando…
Intravenously administered interleukin-7 to reverse lymphopenia in patients with septic shock: a double-blind, randomized, placebo-controlled trial
BACKGROUND: Profound lymphopenia is an independent predictor of adverse clinical outcomes in sepsis. Interleukin-7 (IL-7) is essential for lymphocyte proliferation and survival. A previous phase II study showed that CYT107, a glycosylated recombinant human IL-7, administered intramuscularly reversed...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008152/ https://www.ncbi.nlm.nih.gov/pubmed/36906875 http://dx.doi.org/10.1186/s13613-023-01109-w |
_version_ | 1784905691738144768 |
---|---|
author | Daix, Thomas Mathonnet, Armelle Brakenridge, Scott Dequin, Pierre-François Mira, Jean-Paul Berbille, Frederique Morre, Michel Jeannet, Robin Blood, Teresa Unsinger, Jacqueline Blood, Jane Walton, Andrew Moldawer, Lyle L. Hotchkiss, Richard François, Bruno |
author_facet | Daix, Thomas Mathonnet, Armelle Brakenridge, Scott Dequin, Pierre-François Mira, Jean-Paul Berbille, Frederique Morre, Michel Jeannet, Robin Blood, Teresa Unsinger, Jacqueline Blood, Jane Walton, Andrew Moldawer, Lyle L. Hotchkiss, Richard François, Bruno |
author_sort | Daix, Thomas |
collection | PubMed |
description | BACKGROUND: Profound lymphopenia is an independent predictor of adverse clinical outcomes in sepsis. Interleukin-7 (IL-7) is essential for lymphocyte proliferation and survival. A previous phase II study showed that CYT107, a glycosylated recombinant human IL-7, administered intramuscularly reversed sepsis-induced lymphopenia and improved lymphocyte function. Thepresent study evaluated intravenous administration of CYT107. This prospective, double-blinded, placebo-controlled trial was designed to enroll 40 sepsis patients, randomized 3:1 to CYT107 (10 µg/kg) or placebo, for up to 90 days. RESULTS: Twenty-one patients were enrolled (fifteen CYT107 group, six placebo group) at eight French and two US sites. The study was halted early because three of fifteen patients receiving intravenous CYT107 developed fever and respiratory distress approximately 5–8 h after drug administration. Intravenous administration of CYT107 resulted in a two–threefold increase in absolute lymphocyte counts (including in both CD4(+) and CD8(+) T cells (all p < 0.05)) compared to placebo. This increase was similar to that seen with intramuscular administration of CYT107, was maintained throughout follow-up, reversed severe lymphopenia and was associated with increase in organ support free days (OSFD). However, intravenous CYT107 produced an approximately 100-fold increase in CYT107 blood concentration compared with intramuscular CYT107. No cytokine storm and no formation of antibodies to CYT107 were observed. CONCLUSION: Intravenous CYT107 reversed sepsis-induced lymphopenia. However, compared to intramuscular CYT107 administration, it was associated with transient respiratory distress without long-term sequelae. Because of equivalent positive laboratory and clinical responses, more favorable pharmacokinetics, and better patient tolerability, intramuscular administration of CYT107 is preferable. Trial registration: Clinicaltrials.gov, NCT03821038. Registered 29 January 2019, https://clinicaltrials.gov/ct2/show/NCT03821038?term=NCT03821038&draw=2&rank=1. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13613-023-01109-w. |
format | Online Article Text |
id | pubmed-10008152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-100081522023-03-13 Intravenously administered interleukin-7 to reverse lymphopenia in patients with septic shock: a double-blind, randomized, placebo-controlled trial Daix, Thomas Mathonnet, Armelle Brakenridge, Scott Dequin, Pierre-François Mira, Jean-Paul Berbille, Frederique Morre, Michel Jeannet, Robin Blood, Teresa Unsinger, Jacqueline Blood, Jane Walton, Andrew Moldawer, Lyle L. Hotchkiss, Richard François, Bruno Ann Intensive Care Research BACKGROUND: Profound lymphopenia is an independent predictor of adverse clinical outcomes in sepsis. Interleukin-7 (IL-7) is essential for lymphocyte proliferation and survival. A previous phase II study showed that CYT107, a glycosylated recombinant human IL-7, administered intramuscularly reversed sepsis-induced lymphopenia and improved lymphocyte function. Thepresent study evaluated intravenous administration of CYT107. This prospective, double-blinded, placebo-controlled trial was designed to enroll 40 sepsis patients, randomized 3:1 to CYT107 (10 µg/kg) or placebo, for up to 90 days. RESULTS: Twenty-one patients were enrolled (fifteen CYT107 group, six placebo group) at eight French and two US sites. The study was halted early because three of fifteen patients receiving intravenous CYT107 developed fever and respiratory distress approximately 5–8 h after drug administration. Intravenous administration of CYT107 resulted in a two–threefold increase in absolute lymphocyte counts (including in both CD4(+) and CD8(+) T cells (all p < 0.05)) compared to placebo. This increase was similar to that seen with intramuscular administration of CYT107, was maintained throughout follow-up, reversed severe lymphopenia and was associated with increase in organ support free days (OSFD). However, intravenous CYT107 produced an approximately 100-fold increase in CYT107 blood concentration compared with intramuscular CYT107. No cytokine storm and no formation of antibodies to CYT107 were observed. CONCLUSION: Intravenous CYT107 reversed sepsis-induced lymphopenia. However, compared to intramuscular CYT107 administration, it was associated with transient respiratory distress without long-term sequelae. Because of equivalent positive laboratory and clinical responses, more favorable pharmacokinetics, and better patient tolerability, intramuscular administration of CYT107 is preferable. Trial registration: Clinicaltrials.gov, NCT03821038. Registered 29 January 2019, https://clinicaltrials.gov/ct2/show/NCT03821038?term=NCT03821038&draw=2&rank=1. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13613-023-01109-w. Springer International Publishing 2023-03-12 /pmc/articles/PMC10008152/ /pubmed/36906875 http://dx.doi.org/10.1186/s13613-023-01109-w Text en © The Author(s) 2023 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/) . |
spellingShingle | Research Daix, Thomas Mathonnet, Armelle Brakenridge, Scott Dequin, Pierre-François Mira, Jean-Paul Berbille, Frederique Morre, Michel Jeannet, Robin Blood, Teresa Unsinger, Jacqueline Blood, Jane Walton, Andrew Moldawer, Lyle L. Hotchkiss, Richard François, Bruno Intravenously administered interleukin-7 to reverse lymphopenia in patients with septic shock: a double-blind, randomized, placebo-controlled trial |
title | Intravenously administered interleukin-7 to reverse lymphopenia in patients with septic shock: a double-blind, randomized, placebo-controlled trial |
title_full | Intravenously administered interleukin-7 to reverse lymphopenia in patients with septic shock: a double-blind, randomized, placebo-controlled trial |
title_fullStr | Intravenously administered interleukin-7 to reverse lymphopenia in patients with septic shock: a double-blind, randomized, placebo-controlled trial |
title_full_unstemmed | Intravenously administered interleukin-7 to reverse lymphopenia in patients with septic shock: a double-blind, randomized, placebo-controlled trial |
title_short | Intravenously administered interleukin-7 to reverse lymphopenia in patients with septic shock: a double-blind, randomized, placebo-controlled trial |
title_sort | intravenously administered interleukin-7 to reverse lymphopenia in patients with septic shock: a double-blind, randomized, placebo-controlled trial |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10008152/ https://www.ncbi.nlm.nih.gov/pubmed/36906875 http://dx.doi.org/10.1186/s13613-023-01109-w |
work_keys_str_mv | AT daixthomas intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT mathonnetarmelle intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT brakenridgescott intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT dequinpierrefrancois intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT mirajeanpaul intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT berbillefrederique intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT morremichel intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT jeannetrobin intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT bloodteresa intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT unsingerjacqueline intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT bloodjane intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT waltonandrew intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT moldawerlylel intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT hotchkissrichard intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial AT francoisbruno intravenouslyadministeredinterleukin7toreverselymphopeniainpatientswithsepticshockadoubleblindrandomizedplacebocontrolledtrial |