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体液和细胞因子对小鼠抵抗铜绿假单胞菌实验性感染的作用。II. 抗铜绿假单胞菌免疫球蛋白G抗体的调理、凝集和保护能力。

Contribution of humoral and cellular factors to the resistance to experimental infection by Pseudomonas aeruginosa in mice. II. Opsonic, agglutinative, and protective capacities of immunoglobulin G anti-Pseudomonas antibodies.

作者信息

Bjornson A B, Michael J G

出版信息

Infect Immun. 1972 May;5(5):775-82. doi: 10.1128/iai.5.5.775-782.1972.

Abstract

The opsonic, agglutinative, and mouse protective capacities of anti-Pseudomonas antibodies in immune and normal human immunoglobulin G (IgG) preparations were investigated. Opsonic activities of the immune IgG preparations correlated well with their protective activities. Antibodies present in normal IgG showed a substantial agglutinative activity but were poorly protective. Anti-Pseudomonas antibodies of both normal and immune IgG preparations were directed against the same serotype antigen as demonstrated by absorption experiments. Immune anti-Pseudomonas IgG antibodies fixed complement very efficiently as demonstrated by opsonophagocytic and hemolytic tests. Natural anti-Pseudomonas IgG antibodies fixed complement very poorly although they promoted phagocytic killing of bacteria only in the presence of heat-labile serum factors. It was concluded that, although agglutination can be used for qualitative measurement of antibacterial antibodies, it fails to measure their functional capacities.

摘要

对免疫和正常人免疫球蛋白G(IgG)制剂中抗假单胞菌抗体的调理、凝集及对小鼠的保护能力进行了研究。免疫IgG制剂的调理活性与其保护活性密切相关。正常IgG中存在的抗体表现出较强的凝集活性,但保护能力较差。吸收实验表明,正常和免疫IgG制剂中的抗假单胞菌抗体均针对相同的血清型抗原。调理吞噬和溶血试验表明,免疫抗假单胞菌IgG抗体能非常有效地固定补体。天然抗假单胞菌IgG抗体固定补体的能力很差,尽管它们仅在存在热不稳定血清因子的情况下才能促进细菌的吞噬杀伤。得出的结论是,虽然凝集可用于抗菌抗体的定性测量,但它无法测量其功能能力。

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Role of antibody in infections due to Pseudomonas aeruginosa.抗体在铜绿假单胞菌感染中的作用。
J Infect Dis. 1974 Nov;130 Suppl(0):S111-8. doi: 10.1093/infdis/130.supplement.s111.

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[A micro-method of immuno-electrophoresis].[免疫电泳的微量方法]
Int Arch Allergy Appl Immunol. 1955;7(2):103-10.
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Immunity to Pseudomonas pyocyanea in man.人类对绿脓杆菌的免疫力。
J Pathol Bacteriol. 1953 Apr;65(2):519-31. doi: 10.1002/path.1700650224.

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