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补体途径在鼠伤寒沙门氏菌突变株调理作用中的活性。

Complement pathway activity in the opsonization of mutant strains of Salmonella typhimurium.

作者信息

Shaio M F, Rowland H

出版信息

Zhonghua Min Guo Wei Sheng Wu Ji Mian Yi Xue Za Zhi. 1986 May;19(2):137-52.

PMID:3102176
Abstract

Two separate complement pathway activities and their interaction in the opsonization of mutant strains of Salmonella typhimurium by human neutrophils were investigated in 1% and 10% sera. In the absence of antibody, all mutant strains of S. typhimurium could activate complement by either the classical or the alternative pathway. The presence of antibody did not alter alternative pathway activity but enhanced the classical pathway activity, especially for those strains possessing intact core structure and in the presence of 10% serum. This effect of antibody on classical pathway activation decreased as the lipopolysaccharide chain length decreased. The finding that the presence of antibody reduced the classical pathway activity in the opsonization of SL 1032 (Rd1) strain in 10% serum was unexpected. This suggests that if complement activity in the absence of antibody is already marked, the presence of antibody cannot increase it further. Inhibition was also found in the interaction between classical and alternative pathways. For SL 1032 (Rd1) strain, in the absence of antibody, either classical or alternative pathway activity alone could be maximally activated in 10% serum and when present together were in competition with each other. The interaction, either enhancement or inhibition, was not only dependent on the individual strain but also on the concentration of serum. In general, enhancement occurred in the presence of 1% serum while inhibition was observed in the presence of 10% serum. Such antagonistic interaction has not previously been reported.

摘要

在1%和10%的血清中,研究了两种独立的补体途径活性及其在人中性粒细胞对鼠伤寒沙门氏菌突变株调理作用中的相互作用。在无抗体存在的情况下,所有鼠伤寒沙门氏菌突变株均可通过经典途径或替代途径激活补体。抗体的存在并未改变替代途径活性,但增强了经典途径活性,尤其是对于那些具有完整核心结构的菌株,且在10%血清存在的情况下。随着脂多糖链长度的缩短,抗体对经典途径激活的这种作用减弱。在10%血清中,抗体的存在降低了SL 1032(Rd1)菌株调理作用中的经典途径活性,这一发现出乎意料。这表明,如果在无抗体时补体活性已经显著,抗体的存在并不能进一步增强它。在经典途径和替代途径之间的相互作用中也发现了抑制现象。对于SL 1032(Rd1)菌株,在无抗体时,单独的经典途径或替代途径活性在10%血清中均可被最大程度激活,当两者同时存在时则相互竞争。这种增强或抑制的相互作用不仅取决于单个菌株,还取决于血清浓度。一般来说,在1%血清存在时发生增强作用,而在10%血清存在时观察到抑制作用。这种拮抗相互作用此前尚未见报道。

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