Potential for anti-DNA immunoglobulin peptide therapy in systemic lupus erythematosus

被引:0
作者
Iikuni, Noriko [1 ]
Hahn, Bevra H. [1 ]
La Cava, Antonio [1 ]
机构
[1] Univ Calif Los Angeles, Div Rheumatol, Dept Med, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
anti DNA antibodies; peptide; immunotherapy; systemic lupus erythematosus; REGULATORY T-CELLS; COMPLEMENTARITY-DETERMINING REGION-1; BOUND SELF PEPTIDES; PHASE-II TRIAL; X NZW)F-1 MICE; MURINE LUPUS; MULTIPLE-SCLEROSIS; NUCLEOSOMAL PEPTIDES; AUTOIMMUNE-DISEASES; AMELIORATES LUPUS;
D O I
10.1517/14712590802681636
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
Background: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease with elevated morbidity and multi-organ involvement. While many strategies have shown efficacy and improved management of SLE, they have often been associated with adverse effects. Some patients may not respond well to some treatments because of inter-individual variability of the disease. More specific and safer therapies are needed. Objective/methods: To review literature on peptide-based therapy of SLE. Results/conclusions: Recently, emphasis has been placed on targeting molecules and pathways involved in the inflammatory response in SLE, including the use of immunogenic peptides derived from anti-DNA antibodies. Encouraging data from murine models of SLE have led to tests in initial clinical trials in humans - which have unfortunately not met the primary endpoints. The current challenge is to design improved strategies for immunotherapeutic use of anti-DNA peptides in SLE.
引用
收藏
页码:201 / 206
页数:6
相关论文
共 58 条
  • [1] Regulatory T cells in patients with systemic lupus erythematosus
    Alvarado-Sanchez, Brenda
    Hernandez-Castro, Berenice
    Portales-Perez, Diana
    Baranda, Lourdes
    Layseca-Espinosa, Esther
    Abud-Mendoza, Carlos
    Cubillas-Tejeda, Ana C.
    Gonzalez-Amaro, Roberto
    [J]. JOURNAL OF AUTOIMMUNITY, 2006, 27 (02) : 110 - 118
  • [2] Peptide-based immunotherapy of autoimmunity: a path of puzzles, paradoxes and possibilities
    Anderton, SM
    [J]. IMMUNOLOGY, 2001, 104 (04) : 367 - 376
  • [3] Encephalitogenic potential of the myelin basic protein peptide (amino acids 83-99) in multiple sclerosis: Results of a phase II clinical trial with an altered peptide ligand
    Bielekova, B
    Goodwin, B
    Richert, N
    Cortese, I
    Kondo, T
    Afshar, G
    Gran, B
    Eaton, J
    Antel, J
    Frank, JA
    McFarland, HF
    Martin, R
    [J]. NATURE MEDICINE, 2000, 6 (10) : 1167 - 1175
  • [4] How do CD4+CD25+ regulatory T cells control autoimmunity?
    Bluestone, JA
    Tang, QZ
    [J]. CURRENT OPINION IN IMMUNOLOGY, 2005, 17 (06) : 638 - 642
  • [5] Immune response of SLE patients to peptides based on the complementarity determining regions of a pathogenic anti-DNA monoclonal antibody
    Dayan, M
    Segal, R
    Sthoeger, Z
    Waisman, A
    Brosh, N
    Elkayam, O
    Eilat, E
    Fridkin, M
    Mozes, E
    [J]. JOURNAL OF CLINICAL IMMUNOLOGY, 2000, 20 (03) : 187 - 194
  • [6] MHC class II-bound self peptides from autoimmune MRL/lpr mice reveal potential T cell epitopes for autoantibody production in murine systemic lupus erythematosus
    Freed, JH
    Marrs, A
    VanderWall, J
    Cohen, PL
    Eisenberg, RA
    [J]. JOURNAL OF IMMUNOLOGY, 2000, 164 (09) : 4697 - 4705
  • [7] Garza K M, 2000, Rev Immunogenet, V2, P2
  • [8] Anti-DNA Ig peptides promote Treg cell activity in systemic lupus erythematosus patients
    Hahn, Bevra H.
    Anderson, Marissa
    Le, Elizabeth
    La Cava, Antonio
    [J]. ARTHRITIS AND RHEUMATISM, 2008, 58 (08): : 2488 - 2497
  • [9] Tolerogenic treatment of lupus mice with consensus peptide induces Foxp3-expressing, apoptosis-resistant, TGFβ-secreting CD8+ T cell suppressors
    Hahn, BH
    Singh, RP
    La Cava, A
    Ebling, FM
    [J]. JOURNAL OF IMMUNOLOGY, 2005, 175 (11) : 7728 - 7737
  • [10] Hahn BH, 2001, ARTHRITIS RHEUM-US, V44, P432, DOI 10.1002/1529-0131(200102)44:2<432::AID-ANR62>3.3.CO