Migration inhibition of peritoneal macrophages by peptidoglycan.

B Bültmann, B Heymer, K H Schleifer, H P Seidl, O Haferkamp
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Abstract

Previous studies have shown that peptidoglycans from group A and B streptococci inhibit the migration of peritoneal exudate cells from non-sensitized rats and guinea pigs. In the present studies peptidoglycans from S. aureus and S. epidermidis were found to inhibit the migration of cells to the same extent as group A streptococcal peptidoglycan. In contrast, HSA-pentapeptide, an immunologically active synthetic analog of the peptide moiety of peptidoglycan which is free of the intrinsic toxicity of naturally occurring peptidoglycans, did not induce migration inhibition of peritoneal exudate cells from non-sensitized guinea pigs. Sensitization of animals with 200 mug HSA-pentapeptide emulsified in incomplete Freund's adjuvant significantly reduced the inhibitory effect of streptococcal and staphylococcal peptidoglycan; HSA-pentapeptide again showed no activity. However, when HSA-pentapeptide was tested against cells from animals sensitized with 200 mug HSA-pentapeptide incorporated in complete Freund's adjuvant, a strong inhibition of migration was evident. Skin tests performed in these animals, in contrast to the dermonecrotic reaction elicited by streptococcal or staphylococcal peptidoglycan, revealed a characteristic delay hypersensitivity to HSA-pentapeptide.

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肽聚糖对腹腔巨噬细胞迁移的抑制作用。
先前的研究表明,A组和B组链球菌的肽聚糖可抑制非致敏大鼠和豚鼠腹膜渗出细胞的迁移。在目前的研究中,发现金黄色葡萄球菌和表皮葡萄球菌的肽聚糖对细胞迁移的抑制程度与A组链球菌的肽聚糖相同。相比之下,一种具有免疫活性的肽聚糖肽段合成类似物HSA-pentapeptide没有天然肽聚糖的内在毒性,对非致敏豚鼠的腹膜渗出细胞没有迁移抑制作用。用不完全弗氏佐剂乳化的200杯hsa -五肽致敏动物可显著降低对链球菌和葡萄球菌肽聚糖的抑制作用;hsa -五肽再次显示无活性。然而,当hsa -五肽对被纳入完全弗氏佐剂的200马克杯hsa -五肽致敏的动物细胞进行测试时,明显有很强的迁移抑制作用。在这些动物身上进行的皮肤试验,与链球菌或葡萄球菌肽聚糖引起的皮肤坏死反应相反,显示出对hsa -五肽的特征性延迟超敏反应。
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