Neutrophil survival factors (TNF-alpha, GM-CSF, and G-CSF) produced by macrophages in cats infected with feline infectious peritonitis virus contribute to the pathogenesis of granulomatous lesions

被引:55
作者
Takano, Tomomi [1 ]
Azuma, Natsuko [1 ]
Satoh, Miyuki [1 ]
Toda, Ayako [1 ]
Hashida, Yoshikiyo [1 ]
Satoh, Ryoichi [1 ]
Hohdatsu, Tsutomu [1 ]
机构
[1] Kitasato Univ, Sch Vet Med, Lab Vet Infect Dis, Aomori 0348628, Japan
关键词
COLONY-STIMULATING FACTOR; ANTIBODY-DEPENDENT ENHANCEMENT; IMMUNODEFICIENCY-VIRUS; MONOCLONAL-ANTIBODIES; ENTERIC CORONAVIRUS; CANINE PARVOVIRUS; APOPTOSIS; CELL; SEQUENCE; DISEASE;
D O I
10.1007/s00705-009-0371-3
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Feline infectious peritonitis (FIP) is a feline coronavirus (FCoV)-induced fatal disease of domestic and wild cats. The infiltration of neutrophils into granulomatous lesions is unusual for a viral disease, but it is a typical finding of FIP. This study aimed to investigate the reason for the lesions containing neutrophils in cats with FIP. Neutrophils of cats with FIP were cultured, and changes in the cell survival rate were assessed. In addition, the presence or absence of neutrophil survival factors was investigated in specimens collected from cats with FIP. Furthermore, it was investigated whether macrophages, one of the target cells of FIPV infection, produce neutrophil survival factors (TNF-alpha, GM-CSF, and G-CSF). We showed that virus-infected macrophages overproduce neutrophil survival factors, and these factors act on neutrophils and up-regulate their survival. These observations suggest that sustained production of neutrophil survival factors by macrophages during FCoV infection is sufficient for neutrophil survival and contributes to development of granulomatous lesions.
引用
收藏
页码:775 / 781
页数:7
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