Valmori D, Romero J F, Men Y, Maryanski J L, Romero P, Corradin G
Institute of Biochemistry, University of Lausanne, Epalinges, Switzerland.
Eur J Immunol. 1994 Jun;24(6):1458-62. doi: 10.1002/eji.1830240633.
We have previously demonstrated that it is possible to induce a consistent and strong cytolytic T lymphocyte (CTL) response to synthetic peptides, corresponding to poorly immunogenic malaria CTL epitopes, by co-injecting them with peptides representing defined T helper (Th) epitopes in incomplete Freund's adjuvant (IFA). In this study we have tested different immunization protocols to improve further the elicitation of the CTL response. We show that the CTL response to a mixture of Th + CTL peptides administered in IFA was further enhanced by a previous injection of the Th epitope peptide in IFA. Moreover, we found that the response could be significantly augmented by a pre-injection of IFA alone. This enhancement was observed only if the Th epitope was also present in the second injection. The number of lymph node cells recovered was 2-3-fold higher in mice pre-injected with IFA, but the increase in specific CTL activity, expressed as lytic units per animal, by pre-injection of IFA was at least 10-20-fold. Thus, pre-injection of IFA clearly increases the magnitude of a subsequent CTL response.
我们之前已经证明,通过在不完全弗氏佐剂(IFA)中与代表特定T辅助(Th)表位的肽共同注射,能够诱导针对合成肽产生一致且强烈的细胞毒性T淋巴细胞(CTL)反应,这些合成肽对应免疫原性较差的疟疾CTL表位。在本研究中,我们测试了不同的免疫方案以进一步提高CTL反应的激发。我们发现,通过先前在IFA中注射Th表位肽,在IFA中给予Th + CTL肽混合物所引发的CTL反应会进一步增强。此外,我们发现单独预先注射IFA也能显著增强反应。只有当Th表位也存在于第二次注射中时,才会观察到这种增强。预先注射IFA的小鼠中回收的淋巴结细胞数量高出2 - 3倍,但通过预先注射IFA,以每只动物的裂解单位表示的特异性CTL活性增加至少10 - 20倍。因此,预先注射IFA明显增加了后续CTL反应的强度。