Synergistic effects between recombinant interleukin-2 and the synthetic immunomodulator murabutide: Selective enhancement of cytokine release and potentiation of antitumor activity

被引:16
作者
Bahr, GM
Darcissac, E
Pouillart, PR
Chedid, LA
机构
[1] Vacsyn S.A.
[2] Vacsyn S.A., 75015 Paris
关键词
D O I
10.1089/jir.1996.16.169
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The use of interleukin-2 (IL-2) in the treatment of cancer has shown limited efficacy and dose-limiting toxicity, Combination therapy with other cytokines and/or chemotherapeutic agents has been attempted to enhance the antitumor activity and to reduce the effective therapeutic dose of IL-2, We recently showed, in vitro and in vivo, a synergistic activity between the synthetic immunomodulator murabutide, which is in clinical stage of development, and another therapeutic cytokine, interferon-alpha (IFN-alpha). The present study was performed to assess a possible potentiation of the biologic activities of IL-2 by its association with murabutide. Human PBMC stimulated in vitro with IL-2 and murabutide showed synergistic levels of induced mRNA accumulation and protein secretion for IFN-gamma, HL-12, and colony-stimulating factors (CSFs). No such effects were obtained on the induction of most inflammatory cytokines, including IL-6, IL-8, and tumor necrosis factor alpha (TNF-alpha). Furthermore, the combined administration of murabutide with IL-2 into Meth-A sarcoma-bearing mice resulted in a very significant tumor inhibition as well as in complete tumor regression in nearly 70% of the treated mice, Under the same conditions, treatment with either compound separately had little or no antitumor effect, These preclinical findings will be pursued by the evaluation of the clinical tolerance and biologic activity of the murabutide/IL-2 combination therapy in cancer patients.
引用
收藏
页码:169 / 178
页数:10
相关论文
共 51 条
  • [1] IMMUNOPHARMACOLOGICAL ACTIVITIES AND CLINICAL DEVELOPMENT OF MURAMYL PEPTIDES WITH PARTICULAR EMPHASIS ON MURABUTIDE
    BAHR, GM
    DARCISSAC, E
    BEVEC, D
    DUKOR, P
    CHEDID, L
    [J]. INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1995, 17 (02): : 117 - 131
  • [2] BAHR GM, 1986, FASEB J, V45, P2541
  • [3] INHIBITION OF TUMOR-GROWTH IN A MOUSE FIBROSARCOMA AFTER INTERLEUKIN-2 APPLICATION
    BORBERG, H
    ABDALLAH, A
    SCHWULERA, U
    SONNEBORN, H
    [J]. IMMUNOBIOLOGY, 1986, 172 (3-5) : 383 - 390
  • [4] BOSCO MC, 1994, BLOOD, V83, P3462
  • [5] SEPARATION OF WHITE BLOOD CELLS
    BOYUM, A
    [J]. NATURE, 1964, 204 (496) : 793 - &
  • [6] BIOLOGICAL-ACTIVITY OF A NEW SYNTHETIC MURAMYL PEPTIDE ADJUVANT DEVOID OF PYROGENICITY
    CHEDID, LA
    PARANT, MA
    AUDIBERT, FM
    RIVEAU, GJ
    PARANT, FJ
    LEDERER, E
    CHOAY, JP
    LEFRANCIER, PL
    [J]. INFECTION AND IMMUNITY, 1982, 35 (02) : 417 - 424
  • [7] COLLINS M, 1985, ANAL BIOCHEM, V150, P218
  • [8] CONNOR J, 1993, J EXP MED, V177, P127
  • [9] A PHASE-II STUDY OF INTERLEUKIN-2 AND LYMPHOKINE-ACTIVATED KILLER CELLS IN PATIENTS WITH METASTATIC MALIGNANT-MELANOMA
    DUTCHER, JP
    CREEKMORE, S
    WEISS, GR
    MARGOLIN, K
    MARKOWITZ, AB
    ROPER, M
    PARKINSON, D
    CIOBANU, N
    FISHER, RI
    BOLDT, DH
    DOROSHOW, JH
    RAYNER, AA
    HAWKINS, M
    ATKINS, M
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1989, 7 (04) : 477 - 485
  • [10] EPLINGBURNETTE PK, 1993, BLOOD, V81, P3130