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不同制剂的正常多特异性免疫球蛋白G中针对链球菌超抗原的中和抗体滴度各异:对治疗效果的影响。

Varying titers of neutralizing antibodies to streptococcal superantigens in different preparations of normal polyspecific immunoglobulin G: implications for therapeutic efficacy.

作者信息

Norrby-Teglund A, Basma H, Andersson J, McGeer A, Low D E, Kotb M

机构信息

Research Service, Veterans Affairs Medical Center, Memphis, Tennessee 38104, USA.

出版信息

Clin Infect Dis. 1998 Mar;26(3):631-8. doi: 10.1086/514588.

Abstract

Inasmuch as normal intravenous polyspecific immunoglobulin G (IVIG) neutralizes the activity of a wide spectrum of superantigens, it may be an efficient adjunctive therapy for diseases associated with superantigen-producing organisms, including severe group A streptococcal diseases. The neutralizing activity against purified superantigens, streptococcal pyrogenic exotoxins (Spe), and a mixture of superantigens present in culture supernatant of clinical group A streptococcal isolates was determined for five IVIG preparations. A significant variation among different IVIG preparations (P < .05) and different lots of the same IVIG brand (P < .044) was found. Neutralization of SpeA activity was significantly lower than that of other streptococcal superantigens (P < .05); however, there was no correlation between SpeA binding and SpeA neutralizing activity in different IVIGs. Plasma samples obtained from patients after IVIG infusion varied in their titers of neutralizing antibodies to culture supernatants prepared from their respective isolates, and this variation paralleled differences in the neutralizing titer of the IVIG lot administered to each patient studied. The study suggests that complete neutralizing activity may be achieved by optimizing the type and/or dose of IVIG used in treatment.

摘要

由于正常静脉注射多特异性免疫球蛋白G(IVIG)可中和多种超抗原的活性,它可能是治疗与产生超抗原的生物体相关疾病(包括严重的A组链球菌疾病)的一种有效辅助疗法。测定了五种IVIG制剂对纯化超抗原、链球菌致热外毒素(Spe)以及临床A组链球菌分离株培养上清液中存在的超抗原混合物的中和活性。发现不同IVIG制剂之间(P <.05)以及同一IVIG品牌的不同批次之间(P <.044)存在显著差异。SpeA活性的中和作用明显低于其他链球菌超抗原(P <.05);然而,不同IVIG中SpeA结合与SpeA中和活性之间没有相关性。IVIG输注后从患者获得的血浆样本对各自分离株制备的培养上清液的中和抗体滴度各不相同,这种差异与给予每位研究患者的IVIG批次的中和滴度差异平行。该研究表明,通过优化治疗中使用的IVIG的类型和/或剂量,可能实现完全中和活性。

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