Nickoloff B J, Basham T Y, Merigan T C, Torseth J W, Morhenn V B
J Invest Dermatol. 1986 Jul;87(1):11-8. doi: 10.1111/1523-1747.ep12523513.
To extend our observation that recombinant gamma interferon (r-IFN-gamma) induces the synthesis and expression of HLA-DR antigen we have investigated 2 major areas including the modulation of r-IFN-gamma-induced HLA-DR expression and the possible immunologic consequences of keratinocyte HLA-DR expression in vitro. The induction of keratinocyte HLA-DR expression was greater for continuous compared with pulse dosage (0.5-24 h) of r-IFN-gamma and was markedly decreased after trypsinization of attached monolayers into single cell suspensions. The r-IFN-gamma caused induction of HLA-DR and this was not influenced by either pretreatment with irradiation, PGE2, or indomethacin. Both HLA-DR+ and HLA-DR- cultured keratinocytes induced RNA synthesis and gamma interferon production by allogeneic peripheral blood mononuclear leukocytes (PBMLs) indicating mononuclear cell activation. However, this activation was not followed by significant mitogenesis and only slightly increased levels of [3H]thymidine incorporation (maximal = 5800 cpm) by the PBMLs was observed. Cultured keratinocytes apparently inhibit both lectin-driven and mixed-lymphocyte reactions by producing a soluble mediator which is not dialyzable, or inhibited by pretreatment with indomethacin or anti-alpha, -beta, -gamma interferon antibodies. These results suggest that lymphocyte-keratinocyte reactions in vitro are complex and may be mediated by a variety of cytokines, lymphokines, and prostaglandins.
为了扩展我们关于重组γ干扰素(r-IFN-γ)诱导HLA-DR抗原合成及表达的观察结果,我们研究了两个主要方面,包括r-IFN-γ诱导的HLA-DR表达的调节,以及角质形成细胞HLA-DR表达在体外可能产生的免疫后果。与r-IFN-γ的脉冲剂量(0.5 - 24小时)相比,持续给药时角质形成细胞HLA-DR表达的诱导作用更强,并且当贴壁单层细胞经胰蛋白酶消化成单细胞悬液后,其表达明显降低。r-IFN-γ可诱导HLA-DR的产生,且这一过程不受照射、前列腺素E2或吲哚美辛预处理的影响。HLA-DR+和HLA-DR-培养的角质形成细胞均可诱导同种异体外周血单个核白细胞(PBMLs)的RNA合成和γ干扰素产生,表明单核细胞被激活。然而,这种激活并未伴随显著的有丝分裂,并且仅观察到PBMLs的[3H]胸腺嘧啶核苷掺入水平略有增加(最大值 = 5800 cpm)。培养的角质形成细胞显然通过产生一种不可透析的可溶性介质来抑制凝集素驱动反应和混合淋巴细胞反应,该介质可被吲哚美辛预处理或抗α、β、γ干扰素抗体抑制。这些结果表明,体外淋巴细胞与角质形成细胞的反应是复杂的,可能由多种细胞因子、淋巴因子和前列腺素介导。