Iochmann S, Sagodira S, Mévélec M N, Répérant J M, Naciri M, Coursaget P, Bout D
Equipe INRA d>>Immunologie Parasitaire EA 2637, Laboratoire de Virologie, UFR des Sciences Pharmaceutiques, 31 avenue Monge, Tours, 37200, France.
Microb Pathog. 1999 Jun;26(6):307-15. doi: 10.1006/mpat.1999.0276.
This study compares the immune responses produced by immunising mice and rabbits with two preparations of the recombinant 15/60 kDa protein of Cryptosporidium parvum. Genomic C. parvum DNA was amplified and the recombinant protein was synthesized as a fusion protein with glutathione-S-transferase in Escherichia coli and in the eukaryotic system of baculovirus/insect cells. Both recombinant proteins induced similar levels of serum antibodies against the fusion recombinant protein, but the eukaryotic recombinant protein triggered a stronger humoral response to C. parvum. Similarly, increased lymphoproliferation occurred only after stimulation of spleen cells from mice immunised with the eukaryotic recombinant protein. This suggests that the eukaryotic protein is a better candidate for immunological studies on cryptosporidiosis.
本研究比较了用两种微小隐孢子虫重组15/60 kDa蛋白制剂免疫小鼠和兔子所产生的免疫反应。扩增微小隐孢子虫基因组DNA,并在大肠杆菌以及杆状病毒/昆虫细胞的真核系统中,将重组蛋白合成为与谷胱甘肽-S-转移酶的融合蛋白。两种重组蛋白诱导产生的针对融合重组蛋白的血清抗体水平相似,但真核重组蛋白引发了对微小隐孢子虫更强的体液反应。同样,仅在用真核重组蛋白免疫的小鼠的脾细胞受到刺激后,才出现淋巴细胞增殖增加的情况。这表明真核蛋白是隐孢子虫病免疫学研究的更好候选物。