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对旋盘尾丝虫(丝虫总科)的研究3. 体内抗体依赖性细胞介导的微丝蚴破坏作用

Studies on Dipetalonema viteae (Filarioidea) 3. Antibody-dependent cell-mediated destruction of microfilariae in vivo.

作者信息

Weiss N, Tanner M

出版信息

Tropenmed Parasitol. 1979 Mar;30(1):73-80.

PMID:375512
Abstract

Antibody-dependent cell-mediated destruction of Dipetalonema viteae microfilariae could be demonstrated in the golden hamster using a micropore chamber technique. Microfilariae were eliminated within 24 hours in chambers of 3.0 and 5.0 microm pore size when implanted into amicrofilaremic hamsters (week 30 post infection). At peak microfilaremia (week 12 post infection), only some hamsters could efficiently destroy microfilariae. In chambers with 0.3 microm pore size, microfilariae survived for more than 3 weeks in all hamsters. In uninfected hamsters, microfilariae could only be eliminated if they had been preincubated with serum or its 19S fraction containing antibodies to the cuticle of microfilariae. The opsonizing activity of the serum was abolished by 2-mercaptoethanol treatment. The composition of cells adhering to microfilariae was always significantly different from the composition of cells which migrated into a chamber. The adhesion patterns on individual microfilariae indicated that no single effector cell type was responsible for the destruction of microfilariae. The eosinophil was the predominant cell type but neutrophils, lymphocytes and monocytes also adhered to the microfilariae. Cellular adhesion led to the immobilization of microfilariae and subsequently to their disintegration within large cell clusters. During the final stages of destruction the contribution of the monocyte became more pronounced.

摘要

采用微孔小室技术,在金黄地鼠体内可证实抗体依赖的细胞介导的对旋盘尾丝虫微丝蚴的破坏作用。将孔径为3.0和5.0微米的小室植入无微丝蚴血症的地鼠(感染后30周)体内,微丝蚴在24小时内被清除。在微丝蚴血症高峰期(感染后12周),只有部分地鼠能有效破坏微丝蚴。在孔径为0.3微米的小室中,微丝蚴在所有地鼠体内存活超过3周。在未感染的地鼠中,只有当微丝蚴与含有抗微丝蚴角质层抗体的血清或其19S组分预孵育后,微丝蚴才能被清除。血清的调理活性经2-巯基乙醇处理后被消除。附着于微丝蚴的细胞组成与迁移至小室内的细胞组成始终存在显著差异。单个微丝蚴上的黏附模式表明,并非单一类型的效应细胞负责微丝蚴的破坏。嗜酸性粒细胞是主要的细胞类型,但中性粒细胞、淋巴细胞和单核细胞也会黏附于微丝蚴。细胞黏附导致微丝蚴固定,随后在大的细胞簇内崩解。在破坏的最后阶段,单核细胞的作用变得更加明显。

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