Tsuzuki T, Yoshikai Y, Ito M, Mori N, Ohbayashi M, Asai J
Department of Pathology, Nagoya University School of Medicine, Japan.
Eur J Immunol. 1994 Mar;24(3):709-15. doi: 10.1002/eji.1830240333.
We examined the kinetics of intestinal intraepithelial lymphocytes (IEL) and the incidence of apoptosis at villus or crypt sites during the development of non-irradiated acute graft-versus-host disease (GVHD). The first IEL to increase were host-origin on day 3 and the donor-derived IEL appeared first on day 12 after GVHD induction. Unique CD3+CD4+CD8 alpha/alpha+ IEL were significantly increased on day 6 and an appreciable number of IEL bearing T cell receptor V beta capable of recognizing self-superantigen were detected on day 9. The sudden appearance of apoptosis and reduction of mitotic activity occurred on day 12, accompanied by a dramatic decrease of CD3+CD4-CD8 alpha/alpha+ IEL of host origin. CD8 alpha/alpha+ IEL of host origin, which expand and then decrease by apoptosis at the early stage of acute GVHD, may be associated with pathogenesis of the enteropathy occurring during acute GVHD.
我们研究了非照射性急性移植物抗宿主病(GVHD)发展过程中肠上皮内淋巴细胞(IEL)的动力学以及绒毛或隐窝部位的细胞凋亡发生率。最早增加的IEL是宿主来源的,在第3天出现,而供体来源的IEL在GVHD诱导后第12天首次出现。独特的CD3 + CD4 + CD8α/α + IEL在第6天显著增加,并且在第9天检测到相当数量的携带能够识别自身超抗原的T细胞受体Vβ的IEL。细胞凋亡的突然出现和有丝分裂活性的降低发生在第12天,同时宿主来源的CD3 + CD4 - CD8α/α + IEL显著减少。宿主来源的CD8α/α + IEL在急性GVHD早期扩增然后通过凋亡减少,可能与急性GVHD期间发生的肠病发病机制有关。