| Literature DB >> 26675348 |
Virginia Sheikh1, Brian O Porter1, Rebecca DerSimonian1, Stephen B Kovacs2, William L Thompson1, Ainhoa Perez-Diez1, Alexandra F Freeman1, Gregg Roby1, JoAnn Mican1, Alice Pau1, Adam Rupert2, Joseph Adelsberger2, Jeanette Higgins2, Jeffrey S Bourgeois1, Stig M R Jensen1, David R Morcock3, Peter D Burbelo4, Leah Osnos1, Irina Maric5, Ven Natarajan2, Therese Croughs6, Michael D Yao1, Jacob D Estes3, Irini Sereti1.
Abstract
Idiopathic CD4 lymphopenia (ICL) is a rare syndrome defined by low CD4 T-cell counts (<300/µL) without evidence of HIV infection or other known cause of immunodeficiency. ICL confers an increased risk of opportunistic infections and has no established treatment. Interleukin-7 (IL-7) is fundamental for thymopoiesis, T-cell homeostasis, and survival of mature T cells, which provides a rationale for its potential use as an immunotherapeutic agent for ICL. We performed an open-label phase 1/2A dose-escalation trial of 3 subcutaneous doses of recombinant human IL-7 (rhIL-7) per week in patients with ICL who were at risk of disease progression. The primary objectives of the study were to assess safety and the immunomodulatory effects of rhIL-7 in ICL patients. Injection site reactions were the most frequently reported adverse events. One patient experienced a hypersensitivity reaction and developed non-neutralizing anti-IL-7 antibodies. Patients with autoimmune diseases that required systemic therapy at screening were excluded from the study; however, 1 participant developed systemic lupus erythematosus while on study and was excluded from further rhIL-7 dosing. Quantitatively, rhIL-7 led to an increase in the number of circulating CD4 and CD8 T cells and tissue-resident CD3 T cells in the gut mucosa and bone marrow. Functionally, these T cells were capable of producing cytokines after mitogenic stimulation. rhIL-7 was well tolerated at biologically active doses and may represent a promising therapeutic intervention in ICL. This trial was registered at www.clinicaltrials.gov as #NCT00839436.Entities:
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Year: 2015 PMID: 26675348 PMCID: PMC4768432 DOI: 10.1182/blood-2015-05-645077
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113