Streilein J W, Billingham R E
J Exp Med. 1970 Jul 1;132(1):163-80. doi: 10.1084/jem.132.1.163.
F(1) hybrid hamsters derived from genetically disparate strains develop a severe and often lethal cutaneous disorder when inoculated intracutaneously with immunologically competent lymphoid cells from either parental strain, The disease is characterized clinically by extensive epidermal necrolysis, and histologically by a complete dissolution of the dermal-epidermal junction. The requisites for elicitation of this syndrome were determined to be: (a) the parental strains must differ from each other at a major histocompatibility locus, and (b) the donor inoculum must contain immunologically competent parental strain cells. In addition it was found that specifically sensitized cells surpassed normal unsensitized ones in their ability to elicit the disease, and that the disease can be transferred adoptively from affected to normal F(1) hosts by means of lymphoid cells. On the basis of these observations, it was concluded that the disease was immunologic in nature, and graft-versus-host in type. However, a series of critical studies failed to demonstrate that the epidermolysis had an immunogenetically specific basis, thus invalidating the provisional assumption that this lesion resulted from a direct immunologic attack upon parenchymal cells of the epidermis and dermis. With the aid of radiation chimeras, it was clearly established that typical epidermolysis could be induced in skin of the same genetic constitution as the attacking donor lymphoid cells. This paradox was taken into account by the possibility that, amid the intense local cutaneous graft-versus-host reactions, "skin-specific" antigenic determinants are bared which incite a quasi autoimmune response that in turn is responsible for the epidermolytic lesions.
源自基因不同品系的F(1)杂种仓鼠,当皮内接种来自任一亲本品系的免疫活性淋巴细胞时,会发生一种严重且常常致命的皮肤疾病。该疾病临床上的特征是广泛的表皮坏死溶解,组织学上的特征是真皮-表皮连接完全溶解。引发该综合征的必要条件被确定为:(a)亲本品系在主要组织相容性位点上必须彼此不同,且(b)供体接种物必须含有免疫活性亲本品系细胞。此外,还发现特异性致敏细胞在引发疾病的能力上超过正常未致敏细胞,并且该疾病可通过淋巴细胞从患病的F(1)宿主过继转移至正常F(1)宿主。基于这些观察结果,得出结论:该疾病本质上是免疫性的,且属于移植物抗宿主类型。然而,一系列关键研究未能证明表皮溶解具有免疫遗传特异性基础,从而使这种病变是由对表皮和真皮实质细胞的直接免疫攻击导致的临时假设无效。借助辐射嵌合体,明确证实典型的表皮溶解可在与攻击的供体淋巴细胞具有相同基因构成的皮肤中诱导产生。考虑到在强烈的局部皮肤移植物抗宿主反应中,“皮肤特异性”抗原决定簇会暴露出来,从而引发一种准自身免疫反应,进而导致表皮溶解病变,这个矛盾就得到了解释。