Messingham Kelly A N, Onoh Amber, Vanderah Elizabeth M, Giudice George J, Fairley Janet A
Department of Dermatology, The University of Iowa, Iowa City, Iowa, USA.
Hybridoma (Larchmt). 2012 Apr;31(2):111-7. doi: 10.1089/hyb.2011.0102.
BP180 (collagen XVII) is the target antigen in several autoimmune diseases including bullous pemphigoid (BP). Both IgE and IgG class autoantibodies have been shown to be pathogenic in BP; however, studies designed to elucidate the patho-mechanisms mediated specifically by the IgE-class autoantibodies are limited by the low levels (ng/mL) of IgE in human sera. In this report, we developed mouse IgE class monoclonal antibodies (MAbs) against the immunodominant NC16A domain of the human BP180 protein and characterized two of the resultant MAbs, designated 395A5 and 395D2. Epitope mapping studies revealed that both MAbs target segment 2 of NC16A, as was described for IgE and IgG class BP autoantibodies. Also similar to BP IgE, MAb 395A5 showed indirect immunofluorescence labeling of the basement membrane zone (BMZ) of human skin, stimulated histamine release from mast cells when triggered with NC16A, and induced keratinocyte production of IL-8. The 395D2 MAb was also able to trigger antigen-specific histamine release from mast cells; however, in contrast to BP IgE and 395A5, 395D2 did not label the cutaneous BMZ, nor did it induce IL-8 production in keratinocytes. In summary, these studies underscore the importance of functionally characterizing MAbs generated for use in human disease models. The 395A5 IgE class murine MAb was shown to share several key functional properties with the pathogenically active IgE produced by BP patients. We therefore expect that this MAb will prove to be a useful tool for dissecting the mechanisms used by BP180-NC16A-specific IgE antibodies in the induction of BP skin lesions.
BP180(XVII型胶原蛋白)是包括大疱性类天疱疮(BP)在内的多种自身免疫性疾病中的靶抗原。IgE和IgG类自身抗体在BP中均已被证明具有致病性;然而,旨在阐明由IgE类自身抗体特异性介导的发病机制的研究受到人血清中IgE低水平(ng/mL)的限制。在本报告中,我们开发了针对人BP180蛋白免疫显性NC16A结构域的小鼠IgE类单克隆抗体(MAb),并对其中两种命名为395A5和395D2的所得MAb进行了表征。表位作图研究表明,这两种MAb均靶向NC16A的第2段,这与IgE和IgG类BP自身抗体的情况相同。同样与BP IgE相似,MAb 395A5显示出对人皮肤基底膜带(BMZ)的间接免疫荧光标记,当用NC16A触发时可刺激肥大细胞释放组胺,并诱导角质形成细胞产生IL-8。395D2 MAb也能够触发肥大细胞释放抗原特异性组胺;然而,与BP IgE和395A5不同,395D2未标记皮肤BMZ,也未在角质形成细胞中诱导IL-8产生。总之,这些研究强调了对用于人类疾病模型的MAb进行功能表征的重要性。395A5 IgE类鼠源MAb被证明与BP患者产生的具有致病活性的IgE具有几个关键的功能特性。因此,我们预计这种MAb将被证明是剖析BP180-NC16A特异性IgE抗体在诱导BP皮肤病变中所使用机制的有用工具。