Pavlovitch J H, Rizk-Rabin M, Picard F, Marussig M, Halbreich A
CNRS URA 583, Hôpital Necker, Paris, France.
Clin Exp Immunol. 1994 Apr;96(1):64-8. doi: 10.1111/j.1365-2249.1994.tb06231.x.
The effects of vaccination with RNA-free viral pseudoparticles, preinfection with non-pathogenic ecotropic virus, and induction of tolerance to viral proteins in newborns on the outcome of murine immunodeficiency syndrome (MAIDS) were studied. The parameters used to follow disease progression were: lymphopenia, circulating B and T8 cells, serum IgG and IgM levels, lymphoproliferation and skin graft rejection. Immunization with RNA-free viral pseudoparticles had no effect on any of these parameters. Preinfection of adults with ecotropic virus and the induction of tolerance in newborns to virus antigens both attenuated the early symptoms of viral infection and delayed the onset of immunodeficiency and lymphoproliferation in some mice, but did not significantly alter the number of deaths due to MAIDS. Failure of immune-based therapy to produce successful protection against MAIDS suggests that immune destruction caused by the persistent virus rather than hyperimmune activity is the main pathogenic factor in this disease.
研究了用无RNA病毒假颗粒进行疫苗接种、用非致病性亲嗜性病毒进行感染前处理以及诱导新生儿对病毒蛋白产生耐受性对小鼠免疫缺陷综合征(MAIDS)结局的影响。用于跟踪疾病进展的参数包括:淋巴细胞减少、循环B细胞和T8细胞、血清IgG和IgM水平、淋巴细胞增殖以及皮肤移植排斥反应。用无RNA病毒假颗粒进行免疫对这些参数均无影响。用亲嗜性病毒对成年动物进行感染前处理以及诱导新生儿对病毒抗原产生耐受性,均减轻了病毒感染的早期症状,并在一些小鼠中延迟了免疫缺陷和淋巴细胞增殖的发作,但并未显著改变MAIDS导致的死亡数量。基于免疫的疗法未能成功预防MAIDS,这表明由持续性病毒引起的免疫破坏而非超免疫活性是该疾病的主要致病因素。