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氨曲南与其他β-内酰胺类抗生素的免疫交叉反应性研究。

Investigation into the immunologic cross-reactivity of aztreonam with other beta-lactam antibiotics.

作者信息

Saxon A, Swabb E A, Adkinson N F

出版信息

Am J Med. 1985 Feb 8;78(2A):19-26. doi: 10.1016/0002-9343(85)90198-6.

Abstract

The cross-reactivity between the monobactam antibiotic aztreonam and the commonly used beta-lactam antibiotics, penicillins, and cephalosporins was investigated. Antibodies to aztreonam, penicillin, and cephalothin were raised in rabbits. The ability of the homologous or heterologous drug or drug conjugates to inhibit antibody binding was assessed in a solid-phase radioimmunoassay. Aztreonam demonstrated very little ability to interact with anti-penicillin or anti-cephalothin antibodies as it required 10,000-fold higher concentrations than other beta-lactams to achieve equivalent blocking. Similarly, penicillin and cephalothin conjugates did not cross-react, to any significant degree, with anti-aztreonam rabbit antiserums. Interestingly, free aztreonam was as effective as conjugated aztreonam in reacting with antibodies raised against conjugated aztreonam. This result suggested that, in contrast to the other beta-lactams, antibodies to aztreonam recognize the side chain rather than the nuclear structures. Studies with other beta-lactam analogs confirmed that the IgG rabbit anti-aztreonam binding was indeed side chain-specific. Thirty-six volunteers were given a seven-day course of therapeutic doses of aztreonam and in none did any detectable IgE anti-aztreonam antibodies develop. Four of these subjects had evidence of preexisting IgG antibodies cross-reactive with aztreonam, but the levels rose in only one patient following drug exposure. This human IgG anti-aztreonam was also directed to the side chain and did not cross-react with cephalothin or penicillin. The ability of aztreonam to cross-react with human IgE to various penicillin determinants was also investigated. Aztreonam determinants analogous to the penicillin determinants (penicillin, penicilloyl, and penicilloate) were constructed and the maximal concentration that did not evoke false-positive skin test results was determined to be 6 X 10(-3) mol/liter. None of 41 patients with documented IgE-reactive skin tests to various penicillin determinants concurrently demonstrated reproducible reactivity to any aztreonam reagents. IgE anti-penicilloyl antibodies from three persons were also tested in vitro for their ability to cross-react with conjugated or free aztreonam. Minimal, if any, reactivity was observed between the IgE anti-penicilloyl and any of the aztreonam materials. These results indicate that there is very little cross-reactivity between the monobactam aztreonam and other beta-lactam antibiotics.

摘要

研究了单环β-内酰胺类抗生素氨曲南与常用β-内酰胺类抗生素、青霉素和头孢菌素之间的交叉反应性。在兔体内制备了针对氨曲南、青霉素和头孢噻吩的抗体。在固相放射免疫分析中评估同源或异源药物或药物偶联物抑制抗体结合的能力。氨曲南与抗青霉素或抗头孢噻吩抗体相互作用的能力非常小,因为它需要比其他β-内酰胺类药物高10000倍的浓度才能达到等效的阻断效果。同样,青霉素和头孢噻吩偶联物与抗氨曲南兔抗血清在任何显著程度上均无交叉反应。有趣的是,游离氨曲南与针对偶联氨曲南产生的抗体反应时与偶联氨曲南一样有效。该结果表明,与其他β-内酰胺类药物不同,针对氨曲南的抗体识别侧链而非核结构。对其他β-内酰胺类似物的研究证实,兔抗氨曲南IgG结合确实具有侧链特异性。36名志愿者接受了为期7天的治疗剂量氨曲南疗程,无一例出现可检测到的抗氨曲南IgE抗体。其中4名受试者有预先存在的与氨曲南交叉反应的IgG抗体证据,但只有1名患者在接触药物后抗体水平升高。这种人抗氨曲南IgG也针对侧链,且与头孢噻吩或青霉素无交叉反应。还研究了氨曲南与针对各种青霉素决定簇的人IgE的交叉反应能力。构建了与青霉素决定簇(青霉素、青霉噻唑酰基和青霉酸)类似的氨曲南决定簇,确定不引起假阳性皮肤试验结果的最大浓度为6×10⁻³mol/L。41例对各种青霉素决定簇有记录的IgE反应性皮肤试验的患者,均未同时对任何氨曲南试剂表现出可重复的反应性。还对来自3人的IgE抗青霉噻唑酰基抗体与偶联或游离氨曲南交叉反应的能力进行了体外测试。在IgE抗青霉噻唑酰基与任何氨曲南材料之间观察到最小的反应性(如果有的话)。这些结果表明,单环β-内酰胺类氨曲南与其他β-内酰胺类抗生素之间几乎没有交叉反应。

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