Potential use of IL-2/anti-IL-2 antibody immune complexes for the treatment of cancer and autoimmune disease

被引:113
作者
Boyman, Onur [1 ]
Surh, Charles D. [1 ]
Sprent, Jonathan [1 ]
机构
[1] CHU Vaudois, Div Immunol & Allergy, CH-1011 Lausanne, Switzerland
关键词
activation-induced cell death; autoimmune disease; autoimmunity; cancer; cytokine-binding protein(s); IL-2; immune complexes; immune modulation; memory T cell; T regulatory cell;
D O I
10.1517/14712598.6.12.1323
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Initially discovered as a potent T cell proliferation factor, IL-2 was soon used for cancer immunotherapy, especially for metastatic melanoma and renal cell carcinoma; however, the severe side effects of IL-2 therapy, plus the negative role of IL-2 in maintaining of CD4(+) CD25(+) T regulatory cells (Tregs), has somewhat dampened enthusiasm for using IL-2 in immunotherapy. This opinion article discusses the possibility of combining IL-2 with certain anti-IL-2 antibodies for reducing the dose of IL-2 needed and preferentially stimulating effector T cells, but not Tregs, an approach that might provide an improved strategy for anticancer immunotherapy. Alternatively, complexes of IL-2 with other anti-IL-2 antibodies can selectively stimulate Tregs and could, therefore, be useful for treating autoimmune diseases.
引用
收藏
页码:1323 / 1331
页数:9
相关论文
共 72 条
  • [1] Fusokine interleukin-2/interleukin-18, a novel potent innate and adaptive immune stimulator with decreased toxicity
    Acres, B
    Gantzer, M
    Remy, C
    Futin, N
    Accart, N
    Chaloin, O
    Hoebeke, J
    Balloul, JM
    Paul, S
    [J]. CANCER RESEARCH, 2005, 65 (20) : 9536 - 9546
  • [2] IL-2 administration increases CD4+CD25hi Foxp3+ regulatory T cells in cancer patients
    Ahmadzadeh, M
    Rosenberg, ST
    [J]. BLOOD, 2006, 107 (06) : 2409 - 2414
  • [3] ANDERSON PM, 1992, J IMMUNOTHER, V12, P19
  • [4] ANDERSON TD, 1988, LAB INVEST, V59, P598
  • [5] CD4+CD25+ T regulatory cells, immunotherapy of cancer, and interleukin-2
    Antony, PA
    Restifo, NP
    [J]. JOURNAL OF IMMUNOTHERAPY, 2005, 28 (02) : 120 - 128
  • [6] CD8+T cell immunity against a tumor/self-antigen is augmented by CD4+ T helper cells and hindered by naturally occurring T regulatory cells
    Antony, PA
    Piccirillo, CA
    Akpinarli, A
    Finkelstein, SE
    Speiss, PJ
    Surman, DR
    Palmer, DC
    Chan, CC
    Klebanoff, CA
    Overwijk, WW
    Rosenberg, SA
    Restifo, NP
    [J]. JOURNAL OF IMMUNOLOGY, 2005, 174 (05) : 2591 - 2601
  • [7] Interleukin 2-dependent mechanisms of tolerance and immunity in vivo
    Antony, Paul A.
    Paulos, Chrystal M.
    Ahmadzadeh, Mojgan
    Akpinarli, Akgul
    Palmer, Douglas C.
    Sato, Noriko
    Kaiser, Andrew
    Heinrichs, Christian
    Klebanoff, Christopher A.
    Tagaya, Yutaka
    Restifo, Nicholas P.
    [J]. JOURNAL OF IMMUNOLOGY, 2006, 176 (09) : 5255 - 5266
  • [8] NK cells and polymorphonuclear neutrophils are both critical for IL-2-induced pulmonary vascular leak syndrome
    Assier, E
    Jullien, V
    Lefort, J
    Moreau, JL
    Di Santo, JP
    Vargaftig, BB
    Silva, JRLE
    Thèze, J
    [J]. JOURNAL OF IMMUNOLOGY, 2004, 172 (12) : 7661 - 7668
  • [9] High-dose recombinant interleukin 2 therapy for patients with metastatic melanoma: Analysis of 270 patients treated between 1985 and 1993
    Atkins, MB
    Lotze, MT
    Dutcher, JP
    Fisher, RI
    Weiss, G
    Margolin, K
    Abrams, J
    Sznol, M
    Parkinson, D
    Hawkins, M
    Paradise, C
    Kunkel, L
    Rosenberg, SA
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (07) : 2105 - 2116
  • [10] Evidence for a structural motif in toxins and interleukin-2 that may be responsible for binding to endothelial cells and initiating vascular leak syndrome
    Baluna, R
    Rizo, J
    Gordon, BE
    Ghetie, V
    Vitetta, ES
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) : 3957 - 3962