Novel therapies for the treatment of pertussis disease

被引:22
作者
Scanlon, Karen M. [1 ]
Skerry, Ciaran [1 ]
Carbonetti, Nicholas. H. [1 ]
机构
[1] Univ Maryland, Sch Med, Dept Microbiol & Immunol, Baltimore, MD 21201 USA
来源
PATHOGENS AND DISEASE | 2015年 / 73卷 / 08期
基金
美国国家卫生研究院;
关键词
respiratory disease; sphingosine-1-phosphate; pendrin; acetazolamide; leucocytosis; ECMO; BORDETELLA-PARAPERTUSSIS INFECTION; ANION TRANSPORTER PENDRIN; VACCINE; SPHINGOSINE-1-PHOSPHATE; ACETAZOLAMIDE; INFANTS; ASTHMA; PERTACTIN; CELLS; IDENTIFICATION;
D O I
10.1093/femspd/ftv074
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Whooping cough, or pertussis, incidence has reached levels not seen since the 1950s. Previous studies have shown that antibiotics fail to improve the course of disease unless diagnosed early. Early diagnosis is complicated by the non-diagnostic presentation of disease early in infection. This review focuses on previous attempts at developing novel host-directed therapies for the treatment of pertussis. In addition, two novel approaches from our group are discussed. Manipulation of the signaling pathway of sphingosine-1-phosphate, a lipid involved in many immune processes, has shown great promise, but is in its infancy. Pendrin, a host epithelial anion exchanger upregulated in the airways with B. pertussis infection, appears to drive mucus production and dysregulation of airway surface liquid pH and salinity. In addition to detailing these potential new therapeutic targets, the need for greater focus on the neonatal model of disease is highlighted.
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页数:9
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