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对不可分型流感嗜血杆菌P6外膜蛋白的细胞免疫。

Cellular immunity to the P6 outer membrane protein of nontypeable Haemophilus influenzae.

作者信息

Kodama H, Faden H

机构信息

Department of Pediatrics, School of Medicine, State University of New York at Buffalo, USA.

出版信息

Infect Immun. 1995 Jul;63(7):2467-72. doi: 10.1128/iai.63.7.2467-2472.1995.

Abstract

Cellular immunity to nontypeable Haemophilus influenzae in a population of 10 healthy, immune adults was determined by measuring lymphocyte blast transformation and antibody secretion in response to the P6 outer membrane protein. P6 (200 microliters/ml) induced lymphocyte blast transformation that peaked on day 10 of incubation. The peak induction of antibody-secreting cells occurred on day 8 of incubation. In comparison with the response to tetanus toxoid stimulation, the peak lymphocyte blast transformation response to P6 was reduced (mean counts per minute +/- standard error of the mean [SEM], 3,457 +/- 503 versus 9,414 +/- 1,464; P = 0.0051) and delayed (mean days +/- SEM, 10.3 +/- 0.4 versus 8.4 +/- 0.5; P = 0.0169); however, P6 was a better stimulus of antibody secretion from lymphocytes, particularly antibody of the immunoglobulin M (IgM) class (mean peak numbers of antibody-secreting cells per 10(5) peripheral blood mononuclear cells +/- SEM: IgG, 85 +/- 29 versus 42 +/- 16 [P = 0.0469]; IgM, 81 +/- 20 versus 25 +/- 7 [P = 0.0125]; IgA, 24 +/- 8 versus 16 +/- 6 [P = 0.0526]). Thus, lymphocytes from immune individuals recognize P6 of nontypeable H. influenzae as an immunogen. These data provide a basis for future studies with otitis-prone children who fail to develop a normal antibody response to P6 antigen (N. Yamanaka and H. Faden, J. Pediatr. 122:212-218, 1993).

摘要

通过检测10名健康免疫成年人对P6外膜蛋白的淋巴细胞增殖转化和抗体分泌情况,确定了他们对不可分型流感嗜血杆菌的细胞免疫。P6(200微升/毫升)诱导的淋巴细胞增殖转化在培养第10天达到峰值。抗体分泌细胞的诱导峰值出现在培养第8天。与破伤风类毒素刺激的反应相比,对P6的淋巴细胞增殖转化峰值反应降低(平均每分钟计数±平均标准误差[SEM],3457±503对9414±1464;P = 0.0051)且延迟(平均天数±SEM,10.3±0.4对8.4±0.5;P = 0.0169);然而,P6是淋巴细胞抗体分泌的更好刺激物,尤其是免疫球蛋白M(IgM)类抗体(每10⁵外周血单个核细胞中抗体分泌细胞的平均峰值数量±SEM:IgG,85±29对42±16[P = 0.0469];IgM,81±20对25±7[P = 0.0125];IgA,24±8对16±6[P = 0.0526])。因此,免疫个体的淋巴细胞将不可分型流感嗜血杆菌的P6识别为免疫原。这些数据为未来对P6抗原未能产生正常抗体反应的易患中耳炎儿童的研究提供了基础(N. 山中伸弥和H. 法登,《儿科学杂志》122:212 - 218,1993年)。

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