The Anti-Inflammatory Peptide TnP Is a Candidate Molecule for Asthma Treatment

被引:3
|
作者
Lima, Carla [1 ]
Falcao, Maria Alice Pimentel [1 ]
Pinto, Felipe Justiniano [1 ]
Bernardo, Jefferson Thiago Goncalves [1 ]
Lopes-Ferreira, Monica [1 ]
机构
[1] Butantan Inst, Immunoregulat Unit, Lab Appl Toxinol CeTICs FAPESP, BR-05503900 Sao Paulo, Brazil
基金
巴西圣保罗研究基金会;
关键词
TnP; peptide drug; inflammatory diseases; asthma; lung remodeling;
D O I
10.3390/cells12060924
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Asthma is the most common chronic lung disease, with increasing morbidity and mortality worldwide. Accumulation of peribronchial leukocytes is the hallmark of asthma, in particular, eosinophils, which have been reported as the primary cell associated with the induction of airway hyperresponsiveness. Continued exacerbation and accumulation of other leukocytes, such as neutrophils, Th1, and Th17 cells correlate with many of the long-term effects of asthma, such as airway remodeling. We have patented the TnP family of synthetic cyclic peptides, which is in the preclinical phase of developmental studies for chronic inflammatory diseases. The aim of this work was to investigate whether TnP could show anti-inflammatory activity in a murine model of asthma that includes a mixed phenotype of eosinophilic and neutrophilic inflammation. For this, Balb/c mice, sensitized with OVA and exposed to 1% challenge with OVA aerosol, were submitted to prophylactic treatment, receiving TnP at 0.3 mg/kg orally, 1 h before each challenge. We found that sensitized mice challenged with OVA and treated with TnP showed no airway hyperreactivity or lung remodeling. TnP acts systemically in secondary lymphoid organs and locally in the lung, inhibiting the production of Th2/Th17 cytokines. Furthermore, TnP prevented the infiltration of eosinophils and neutrophils in the BAL and lung tissue, inhibited the production of IgE/IgG1, prevented hyperplasia of mucus-producing cells, and decreased the thickening and deposition of sub-epithelial collagen. Our results showed TnP as a candidate molecule for the treatment of airway remodeling associated with inflammatory diseases, such as asthma.
引用
收藏
页数:15
相关论文
共 50 条
  • [1] ANTI-INFLAMMATORY TREATMENT OF ASTHMA
    HAAHTELA, T
    PEDIATRIC PULMONOLOGY, 1988, 4 (02) : 123 - 123
  • [2] Minocycline as an anti-inflammatory agent in the treatment of asthma
    Joks, R
    Daoud, A
    Orloff, K
    Drew, H
    Taningco, G
    Homel, P
    Akerman, M
    Weiss, S
    Hammerschlag, M
    Josephson, AS
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1998, 101 (01) : S62 - S62
  • [3] Alternative agents for anti-inflammatory treatment of asthma
    Szefler, SJ
    Nelson, HS
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1998, 102 (04) : S23 - S35
  • [4] Shedding Light on the Drug-Target Prediction of the Anti-Inflammatory Peptide TnP with Bioinformatics Tools
    Lima, Carla
    Eto, Silas Fernandes
    Lopes-Ferreira, Monica
    PHARMACEUTICALS, 2022, 15 (08)
  • [5] ANTI-INFLAMMATORY THERAPY IN ASTHMA
    SMALL, P
    ANNALS OF ALLERGY, 1989, 62 (06): : 481 - 482
  • [6] Anti-inflammatory therapy for asthma
    Pawliczak, Rafal
    ALERGOLOGIA POLSKA-POLISH JOURNAL OF ALLERGOLOGY, 2014, 1 (01) : 38 - 42
  • [7] Adherence to anti-inflammatory treatment for asthma in clinical practice in France
    Latry, Philippe
    Pinet, Marion
    Labat, Anne
    Magand, Jean-Pierre
    Peter, Claude
    Robinson, Philip
    Martin-Latry, Karin
    Molimard, Mathieu
    CLINICAL THERAPEUTICS, 2008, 30 : 1058 - 1068
  • [8] EVALUATION OF ANTI-INFLAMMATORY AGENTS IN TREATMENT OF CHRONIC INFECTIOUS ASTHMA
    SIMON, SW
    ANNALS OF ALLERGY, 1962, 20 (07): : 460 - &
  • [9] Anti-inflammatory treatment of asthma: differentiation and trial-and-error
    Wolthers, Ole D.
    ACTA PAEDIATRICA, 2009, 98 (08) : 1237 - 1241
  • [10] Small-molecule anti-inflammatory drug compositions for the treatment of asthma: a patent review (2013-2014)
    Glossop, Paul
    Whitlock, Gavin
    Gibson, Karl
    EXPERT OPINION ON THERAPEUTIC PATENTS, 2015, 25 (07) : 743 - 754