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脾切除术后预防实验性b型流感嗜血杆菌菌血症所需的抗荚膜抗体

Anticapsular antibody requirements for protection against experimental Haemophilus influenzae type b bacteremia after splenectomy.

作者信息

Rubin L G

机构信息

Department of Pediatrics, Schneider Children's Hospital of Long Island Jewish Medical Center, New Hyde Park, New York 11042.

出版信息

Infect Immun. 1988 Apr;56(4):984-6. doi: 10.1128/iai.56.4.984-986.1988.

Abstract

Although asplenic individuals are at higher risk for infection with encapsulated bacteria, it is not known whether they require a higher concentration of anticapsular antibody than normal individuals do for protection against invasive disease caused by Haemophilus influenzae type b. At 21 days of age, rats were passively immunized with human hyperimmune serum globulin against H. influenzae b polysaccharide (or saline) after recovery from splenectomy or a sham operation. Starting at 18 h after immunization, rats received three intranasal inoculations of 10(7) CFU of H. influenzae b over the next 24 h. Of sham-operated rats given 0.75 or 3.0 micrograms of anticapsular antibody, 91 or 96%, respectively, were protected from bacteremia, whereas only 59 and 67% of similarly treated asplenic rats were protected (P less than 0.004, control versus asplenic rats). A 12-microgram antibody dose resulted in the complete protection of both groups. The magnitude of bacteria was significantly higher in the asplenic group at each dose of antibody. Thus, asplenic hosts may require a higher concentration of anticapsular antibody than normal individuals do for protection against invasive H. influenzae b disease.

摘要

尽管无脾个体感染包膜菌的风险更高,但尚不清楚他们是否比正常个体需要更高浓度的抗包膜抗体来预防由b型流感嗜血杆菌引起的侵袭性疾病。在21日龄时,大鼠在脾切除或假手术后恢复后,用针对b型流感嗜血杆菌多糖的人超免疫血清球蛋白(或生理盐水)进行被动免疫。从免疫后18小时开始,大鼠在接下来的24小时内接受三次鼻内接种10(7) CFU的b型流感嗜血杆菌。在给予0.75或3.0微克抗包膜抗体的假手术大鼠中,分别有91%或96%受到菌血症保护,而在接受类似治疗的无脾大鼠中,只有59%和67%受到保护(P小于0.004,对照组与无脾大鼠组)。12微克抗体剂量使两组均得到完全保护。在每个抗体剂量下,无脾组中的细菌数量均显著更高。因此,无脾宿主可能比正常个体需要更高浓度的抗包膜抗体来预防侵袭性b型流感嗜血杆菌疾病。

相似文献

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Postvaccination susceptibility to invasive Haemophilus influenzae type b disease in infant rats.
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