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淋球菌感染中的细胞介导免疫反应。

Cell-mediated immune response in gonococcal infections.

作者信息

Wyle F A, Rowlett C, Blumenthal T

出版信息

Br J Vener Dis. 1977 Dec;53(6):353-9. doi: 10.1136/sti.53.6.353.

Abstract

Peripheral blood lymphocyte (PBL) transformation stimulated by gonococcal and meningococcal antigens was studied in 29 men and 21 women with uncomplicated gonorrhoea. The blastogenic responses of PBLs from these men and women were substantially higher than from normal controls. Cross-reactivity between Neisseria gonorrhoeae and Neisseria meningitidis was manifested by the PBL transformation responses in patients with gonorrhoea to non-purified meningococcal antigen (MGC-I). In both male and female patients the PBLs were stimulated by non-purified gonococcal antigen (GC-I) and by non-purified meningococcal antigen. The extent of the blastogenic response in women was much greater than in men. Partial purification of these antigens by gel chromatography resulted in reduced cross-reactive responses to the semi-purified meningococcal antigen (MGC-II). Female patients demonstrated marked stimulation with the semi-purified gonococcal antigen (GC-II), while male patients showed slight stimulation with GC-II. It is possible that cell-mediated immunity may act to limit the spread of gonococcal infection beyond the genital mucous membranes.

摘要

对29名男性和21名无并发症淋病患者的外周血淋巴细胞(PBL)受淋球菌和脑膜炎球菌抗原刺激后的转化情况进行了研究。这些男性和女性的PBL的增殖反应明显高于正常对照组。淋病患者的PBL对未纯化的脑膜炎球菌抗原(MGC-I)的转化反应体现了淋病奈瑟菌和脑膜炎奈瑟菌之间的交叉反应性。在男性和女性患者中,PBL均受到未纯化的淋球菌抗原(GC-I)和未纯化的脑膜炎球菌抗原的刺激。女性患者的增殖反应程度远大于男性。通过凝胶色谱法对这些抗原进行部分纯化后,对半纯化的脑膜炎球菌抗原(MGC-II)的交叉反应性降低。女性患者对半纯化的淋球菌抗原(GC-II)表现出明显的刺激反应,而男性患者对GC-II的刺激反应较弱。细胞介导的免疫可能会限制淋球菌感染超出生殖器黏膜的传播范围。

相似文献

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Cell-mediated immune response in gonococcal infection.
Can J Microbiol. 1981 Jan;27(1):76-80. doi: 10.1139/m81-012.

本文引用的文献

1
Growth Requirements of the Meningococcus.脑膜炎球菌的生长需求
J Bacteriol. 1942 Jun;43(6):757-61. doi: 10.1128/jb.43.6.757-761.1942.
2
9
SEPARATION OF VIABLE LYMPHOCYTES FROM HUMAN BLOOD.从人血中分离活淋巴细胞
Lancet. 1964 Feb 29;1(7331):468-9. doi: 10.1016/s0140-6736(64)90799-8.

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