Safety of Interleukin-7 in HIV Infected People Currently Taking Anti-HIV Drugs

A Phase I, Randomized, Placebo-Controlled, Double-Blind Study Evaluating the Safety of Subcutaneous Single Dose Interleukin-7 in HIV-1-Infected Subjects Who Are Receiving Antiretroviral Treatment

The purpose of this study is to determine the safety of a single, under-the-skin dose of interleukin-7 (IL-7) in HIV infected people currently taking anti-HIV drugs.

Study Overview

• Status: Completed
• Conditions: HIV Infections
• Intervention / Treatment: Drug: Recombinant human interleukin-7

Detailed Description

CD4 count is the best predictor of HIV disease progression. IL-7 plays an important role in immune system function, especially in the development of T cells, including CD4 cells. IL-7 may improve HIV-specific immune responses by increasing the number of CD4 cells and boosting immune response. This study will evaluate the safety of a single IL-7 dose given under the skin in HIV infected patients who are currently on potent antiretroviral therapy (ART).

This study will last 13 weeks. Participants will be stratified into two groups by viral load: Stratum 1 participants will have viral loads of less than 50 copies/ml, and Stratum 2 participants will have viral loads between 50 and 50,000 copies/ml. Participants will receive one dose of either IL-7 or placebo at study entry. Five different dosing levels of IL-7 will be tested sequentially in both strata. Dose escalation will occur independently in each stratum and enrollment in a stratum will end when the maximum-tolerated dose is reached. As of 10/23/06, due to adverse events associated with the 60 mcg/kg dose level, all participants will receive up to the 30 mcg/kg dose level, with no further dose escalation. New participants will enroll in Stratum 2 only.

There will be 9 study visits; medical and medication history, a physical exam, lymph node and spleen assessment, and blood collection will occur at most visits. Participants will undergo an electrocardiogram at study entry and on Day 1, and a spleen ultrasound at Week 3. Urine collection will occur on Day 4 and at Weeks 2 and 3.

• Study Type: Interventional
• Enrollment (Actual): 25
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • California
    • Sacramento, California, United States, 95817
      • Univ. of California Davis Med. Ctr., ACTU
  • Florida
    • Miami, Florida, United States, 33136-1013
      • Univ. of Miami AIDS CRS
  • Illinois
    • Chicago, Illinois, United States, 60612-3806
      • Rush Univ. Med. Ctr. ACTG CRS
  • Ohio
    • Cleveland, Ohio, United States, 44106-5083
      • Case CRS
    • Cleveland, Ohio, United States, 44109-1998
      • MetroHealth CRS

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• HIV infected
• Currently on ART consisting of at least 3 antiretroviral drugs for at least 12 months prior to study entry and stable (no change in dose) on treatment for at least 3 months prior to study entry
• CD4 count of 100 cells/mm3 or more within 42 days of study entry
• Viral load of 50,000 copies/ml or less within 42 days of study entry
• Willing to use acceptable forms of contraception
• Participants with a Category C AIDS-defining illness during the 12 months prior to study entry may be eligible as long as their CD4 count is 200 cells/mm3 or more at screening. Participants with Kaposi's sarcoma may also be eligible for this study.

Exclusion Criteria:

• Lymphadenopathy greater than 2.0 cm
• Known allergy or sensitivity to study drug or its formulations
• Current drug or alcohol abuse
• Serious illness or hospitalization that, in the opinion of the site investigator, may interfere with the study results
• Prior use of any interleukins
• Systemic cancer chemotherapy, systemic investigational agents, or immunomodulators (e.g., growth factors, systemic corticosteroids, HIV vaccines, immune globulin, interferons) within 90 days prior to study entry
• Heparin within 96 hours prior to study entry, or anticipating the need for heparin within 96 hours after the study injection
• History of cancer (except basal carcinoma of the skin or Kaposi's sarcoma)
• Enlargement of spleen
• History of hypercoagulability (deep vein thrombosis or pulmonary embolism)
• History of seizure disorder
• History of extensive psoriasis, Crohn's disease, uveitis, or other autoimmune disease having induced severe complications
• Significant psychiatric, cardiac, pulmonary, thyroid, renal, or neurological disease requiring therapy
• Positive hepatitis B surface antigen or positive hepatitis C antibody at screening
• Plan to start new ART within 8 weeks after study entry
• Breastfeeding

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Safety, as assessed by dose-limiting toxicities

Secondary Outcome Measures

Outcome Measure
Change in IL-7 plasma level from study entry to Day 28
concentrations of recombinant human IL-7 (rhIL-7) at study entry (prior to dose) and at 0.5, 1.0, 1.5, 2.0, 2.5, 4, 8, 12, 24, 48, and 72 hours after dose
T-cell proliferation and activation status
lymphocyte subsets prior to study entry, study entry and on Days 1, 2, 4, 14, and 28
anti-IL-7 antibodies prior to study entry and on Days 28 and 56
HIV-1 viral load at baseline and on Days 1, 4, 14, and 28
nine-color advanced flow cytometry on stored peripheral blood mononuclear cells (PBMCs) at baseline and on Days 4 and 28
effect of age on laboratory outcomes

Collaborators and Investigators

• Sponsor: National Institute of Allergy and Infectious Diseases (NIAID)
• Investigators: Study Chair: Irini Sereti, MD, National Institute for Allergy and Infectious Diseases, National Institutes of Health; Study Chair: Michael M. Lederman, MD, Case Western Reserve University, University Hospitals of Cleveland

Publications and helpful links

General Publications

• Fry TJ, Mackall CL. Interleukin-7: master regulator of peripheral T-cell homeostasis? Trends Immunol. 2001 Oct;22(10):564-71. doi: 10.1016/s1471-4906(01)02028-2.
• Geiselhart LA, Humphries CA, Gregorio TA, Mou S, Subleski J, Komschlies KL. IL-7 administration alters the CD4:CD8 ratio, increases T cell numbers, and increases T cell function in the absence of activation. J Immunol. 2001 Mar 1;166(5):3019-27. doi: 10.4049/jimmunol.166.5.3019.
• Kedzierska K, Crowe SM. Cytokines and HIV-1: interactions and clinical implications. Antivir Chem Chemother. 2001 May;12(3):133-50. doi: 10.1177/095632020101200301.
• Pett SL, Kelleher AD. Cytokine therapies in HIV-1 infection: present and future. Expert Rev Anti Infect Ther. 2003 Jun;1(1):83-96. doi: 10.1586/14787210.1.1.83.
• Sereti I, Dunham RM, Spritzler J, Aga E, Proschan MA, Medvik K, Battaglia CA, Landay AL, Pahwa S, Fischl MA, Asmuth DM, Tenorio AR, Altman JD, Fox L, Moir S, Malaspina A, Morre M, Buffet R, Silvestri G, Lederman MM; ACTG 5214 Study Team. IL-7 administration drives T cell-cycle entry and expansion in HIV-1 infection. Blood. 2009 Jun 18;113(25):6304-14. doi: 10.1182/blood-2008-10-186601. Epub 2009 Apr 20.
• Vandergeeten C, Fromentin R, DaFonseca S, Lawani MB, Sereti I, Lederman MM, Ramgopal M, Routy JP, Sekaly RP, Chomont N. Interleukin-7 promotes HIV persistence during antiretroviral therapy. Blood. 2013 May 23;121(21):4321-9. doi: 10.1182/blood-2012-11-465625. Epub 2013 Apr 15.

Study record dates

Study Major Dates

• Study Start: April 1, 2005
• Primary Completion: December 7, 2022
• Study Completion (Actual): April 1, 2007

Study Registration Dates

• First Submitted: December 17, 2004
• First Submitted That Met QC Criteria: December 17, 2004
• First Posted (Estimate): December 20, 2004

Study Record Updates

• Last Update Posted (Actual): November 1, 2021
• Last Update Submitted That Met QC Criteria: October 28, 2021
• Last Verified: October 1, 2021

More Information

Terms related to this study

• Keywords: Treatment Experienced
• Additional Relevant MeSH Terms: RNA Virus Infections; Virus Diseases; Infections; Blood-Borne Infections; Communicable Diseases; Sexually Transmitted Diseases, Viral; Sexually Transmitted Diseases; Lentivirus Infections; Retroviridae Infections; Immunologic Deficiency Syndromes; Immune System Diseases; HIV Infections
• Other Study ID Numbers: A5214; 10022 (DAIDS ES Registry Number); ACTG A5214

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No