4.7 Article

A Polyclonal Antibody Raised against the Burkholderia cenocepacia OmpA-like Protein BCAL2645 Impairs the Bacterium Adhesion and Invasion of Human Epithelial Cells In Vitro

期刊

BIOMEDICINES
卷 9, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/biomedicines9121788

关键词

Burkholderia cenocepacia; OmpA-like protein; cystic fibrosis; human epithelial cells; immunotherapies; antibody

资金

  1. FCT [PTDC/BIA-MIC/1615/2014]
  2. FCT-Fundacao para a Ciencia e a Tecnologia, I.P. [UIDB/04565/2020, UIDP/04565/2020, LA/P/0140/2020]
  3. Fundação para a Ciência e a Tecnologia [UIDB/04565/2020, PTDC/BIA-MIC/1615/2014, UIDP/04565/2020] Funding Source: FCT

向作者/读者索取更多资源

This study focused on the cloning and functional characterization of the OmpA-like BCAL2645 protein, which was found to be immunoreactive against sera from CF patients with a history of Bcc infections. The results suggest that anti-BCAL2645 antibodies have the potential for developing passive immunization therapies to protect CF patients against Bcc infections.
Respiratory infections by bacteria of the Burkholderia cepacia complex (Bcc) remain a life threat to cystic fibrosis (CF) patients, due to the faster lung function decline and the absence of effective eradication strategies. Immunotherapies are regarded as an attractive alternative to control and reduce the damages caused by these infections. In this work, we report the cloning and functional characterization of the OmpA-like BCAL2645 protein, previously identified and found to be immunoreactive against sera from CF patients with a record of Bcc infections. The BCAL2645 protein is shown to play a role in biofilm formation, adherence to mucins and invasion of human lung epithelial cells. The expression of the BCAL2645 protein was found to be increased in culture medium, mimicking the lungs of CF patients and microaerophilic conditions characteristic of the CF lung. Moreover, a polyclonal antibody raised against BCAL2645 was found to inhibit, by about 75 and 85%, the ability of B. cenocepacia K56-2 to bind and invade in vitro CFBE41o- human bronchial epithelial cells. These results highlight the potential of anti-BCAL2645 antibodies for the development of passive immunization therapies to protect CF patients against Bcc infections.

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