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几种小鼠品系中铅对体内抗体介导免疫影响的分析。

Analysis of lead effects on in vivo antibody-mediated immunity in several mouse strains.

作者信息

Mudzinski S P, Rudofsky U H, Mitchell D G, Lawrence D A

出版信息

Toxicol Appl Pharmacol. 1986 Apr;83(2):321-30. doi: 10.1016/0041-008x(86)90309-1.

DOI:10.1016/0041-008x(86)90309-1
PMID:3515633
Abstract

The effect of administration of lead acetate (10 mM in the drinking water) for 8 weeks on the in vivo sheep red blood cell (SRBC) specific plaque-forming cell (PFC) responses of inbred A, BALB/c, C57Bl/6, DBA/1, SJL, and NZW/NZB F1 mice and outbred CFW mice was examined to determine if lead was immunomodulatory in a genetically related manner. Lead did not suppress the SRBC-specific PFC/10(6) splenocytes or PFC/spleen response in any mouse strain when compared to the responses of strain-matched control mice. In addition, 10 mM lead-treated BALB/c mice manifested augmented PFC/10(6) splenocytes (17%; p less than .05) but unchanged PFC/spleen responses. Correspondingly, serum concentrations of SRBC-specific antibody (measured by radioimmunoassay) and serum immunoglobulin G, M, or A isotypes were also unchanged by lead acetate treatment in all tested mouse strains. There were no observable lead-related histopathological changes or deposition of immune complexes or antibasement membrane antibody in the kidneys of treated mice. Further, splenocytes from lead-treated, SRBC-immunized mice cultured with T-independent antigens (TNP-LPS, TNP-Ficoll) or with a T-dependent antigen (SRBC) exhibited direct and indirect specific PFC responses that were unchanged from those of control mice. The H-2K/D haplotypes of the outbred CFW mice were determined by microcytotoxicity to include r, q, u, and s. These results suggest that lead acetate (10 mM) administered po for 8 weeks does not suppress the primary direct humoral immune response to SRBC in inbred and outbred mice of several H-2 haplotypes (k/d; d; b; q; d,z; s; r; and u).

摘要

研究了给予醋酸铅(饮用水中浓度为10 mM)8周对近交系A、BALB/c、C57Bl/6、DBA/1、SJL和NZW/NZB F1小鼠以及远交系CFW小鼠体内绵羊红细胞(SRBC)特异性空斑形成细胞(PFC)反应的影响,以确定铅是否以基因相关的方式具有免疫调节作用。与品系匹配的对照小鼠的反应相比,铅在任何小鼠品系中均未抑制SRBC特异性PFC/10⁶脾细胞或PFC/脾脏反应。此外,经10 mM铅处理的BALB/c小鼠表现出PFC/10⁶脾细胞增加(17%;p小于0.05),但PFC/脾脏反应未改变。相应地,在所有测试的小鼠品系中,醋酸铅处理也未改变SRBC特异性抗体(通过放射免疫测定)的血清浓度以及血清免疫球蛋白G、M或A同种型。在处理过的小鼠肾脏中未观察到与铅相关的组织病理学变化、免疫复合物沉积或抗基底膜抗体。此外,用非T依赖性抗原(TNP-LPS、TNP-Ficoll)或T依赖性抗原(SRBC)培养的经铅处理、SRBC免疫的小鼠的脾细胞表现出的直接和间接特异性PFC反应与对照小鼠的反应无变化。通过微量细胞毒性法确定远交系CFW小鼠的H-2K/D单倍型包括r、q、u和s。这些结果表明,经口给予醋酸铅(10 mM)8周不会抑制几种H-2单倍型(k/d;d;b;q;d,z;s;r;和u)的近交和远交小鼠对SRBC的初次直接体液免疫反应。

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