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Interleukin-7 restores lymphocytes in septic shock: the IRIS-7 randomized clinical trial
Bruno Francois, Robin Jeannet, Thomas Daix, Andrew H. Walton, Matthew S. Shotwell, Jacqueline Unsinger, Guillaume Monneret, Thomas Rimmelé, Teresa Blood, Michel Morre, Anne Gregoire, Gail A. Mayo, Jane Blood, Scott K. Durum, Edward R. Sherwood, Richard S. Hotchkiss
Bruno Francois, Robin Jeannet, Thomas Daix, Andrew H. Walton, Matthew S. Shotwell, Jacqueline Unsinger, Guillaume Monneret, Thomas Rimmelé, Teresa Blood, Michel Morre, Anne Gregoire, Gail A. Mayo, Jane Blood, Scott K. Durum, Edward R. Sherwood, Richard S. Hotchkiss
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Clinical Research and Public Health Immunology

Interleukin-7 restores lymphocytes in septic shock: the IRIS-7 randomized clinical trial

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Abstract

BACKGROUND. A defining pathophysiologic feature of sepsis is profound apoptosis-induced death and depletion of CD4+ and CD8+ T cells. Interleukin-7 (IL-7) is an antiapoptotic common γ-chain cytokine that is essential for lymphocyte proliferation and survival. Clinical trials of IL-7 in over 390 oncologic and lymphopenic patients showed that IL-7 was safe, invariably increased CD4+ and CD8+ lymphocyte counts, and improved immunity. METHODS. We conducted a prospective, randomized, double-blind, placebo-controlled trial of recombinant human IL-7 (CYT107) in patients with septic shock and severe lymphopenia. Twenty-seven patients at academic sites in France and the United States received CYT107 or placebo for 4 weeks. Primary aims were to determine the safety of CYT107 in sepsis and its ability to reverse lymphopenia. RESULTS. CYT107 was well tolerated without evidence of inducing cytokine storm or worsening inflammation or organ dysfunction. CYT107 caused a 3- to 4-fold increase in absolute lymphocyte counts and in circulating CD4+ and CD8+ T cells that persisted for weeks after drug administration. CYT107 also increased T cell proliferation and activation. CONCLUSIONS. This is the first trial of an immunoadjuvant therapy targeting defects in adaptive immunity in patients with sepsis. CYT107 reversed the marked loss of CD4+ and CD8+ immune effector cells, a hallmark of sepsis and a likely key mechanism in its morbidity and mortality. CYT107 represents a potential new way forward in the treatment of patients with sepsis by restoring adaptive immunity. Such immune-based therapy should be broadly protective against diverse pathogens including multidrug resistant bacteria that preferentially target patients with impaired immunity. TRIAL REGISTRATION. Trials registered at clinicaltrials.gov: NCT02640807 and NCT02797431. FUNDING. Revimmune, NIH National Institute of General Medical Sciences GM44118.

Authors

Bruno Francois, Robin Jeannet, Thomas Daix, Andrew H. Walton, Matthew S. Shotwell, Jacqueline Unsinger, Guillaume Monneret, Thomas Rimmelé, Teresa Blood, Michel Morre, Anne Gregoire, Gail A. Mayo, Jane Blood, Scott K. Durum, Edward R. Sherwood, Richard S. Hotchkiss

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Figure 7

CYT107 decreased IL-7 receptor α (CD127) expression.

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CYT107 decreased IL-7 receptor α (CD127) expression.
(A) The IL-7 recept...
(A) The IL-7 receptor is composed of a common γ chain and the IL-7 receptor α (CD127). CD127 is known to be transiently downregulated after administration of IL-7. Flow cytometry showed that there was a decrease in CD4+ and CD8+ T cell expression of IL-7 receptor α in patients treated with both low- and high-frequency treatment regimens of CYT107 versus placebo at day 4. *P < 0.05. Statistical tests were conducted using a Wald-type multiple-degree-of-freedom method. Values reported are mean ± SEM for the 3 different treatment groups, i.e., placebo, low-frequency CYT107, and high-frequency CYT107. n = 10, 8, and 9 for placebo, low-frequency CYT107, and high-frequency CYT107-treated patients, respectively. (B) The lower left and lower right panels depict the percentages of CD4+ and CD8+ T cells positive for the IL-7 receptor α respectively for each patient in the 3 treatment groups, i.e., placebo, low-frequency CYT107 group, and high-frequency CYT107 group. US study patients had flow cytometric quantification of Ki67 for 6 weeks, while French study patients had flow cytometric quantification out to 4 weeks only. Baseline adjustment reflects the difference between study day values and the predosing values.

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