Todd R F, Meuer S C, Romain P L, Schlossman S F
Hum Immunol. 1984 May;10(1):23-40. doi: 10.1016/0198-8859(84)90083-1.
Previous studies using conventional hetero- or isoantisera have indicated the involvement of class II (Ia) molecules in presentation of soluble antigen by monocytes to inducer T lymphocytes, stimulation of inducer T cells in MLR, and recognition of Ia-bearing target cells by cytotoxic T lymphocytes (CTL). The experience in using monoclonal anti-Ia reagents capable of blocking these phenomena in the human system is limited. Recently, however, we have characterized a lytic IgG2a monoclonal antibody, 9-49, that binds to functionally significant class II molecules. This antibody blocks (in the absence of complement): (1) specific binding of peripheral blood lymphocytes (PBL) to antigen-pulsed monocyte monolayers, (2) proliferation of PBL in response to soluble antigen (tetanus toxoid or mumps) or cell surface class II antigen stimulation in allogeneic or autologous MLR, (3) proliferation of cloned T4+ (inducer) lymphocyte cell lines to class II antigens, (4) generation of cytotoxic lymphocytes during allogeneic MLR, and (5) recognition (and killing) of class II-bearing target cells by T4+ CTL clones. Proliferation and CTL activity of a T8+ clone is unaffected by the 9-49 antibody. These results indicate the usefulness of this monoclonal reagent in studies evaluating the functional role of Ia molecules in immune recognition phenomena.
以往使用传统的异种或同种抗血清进行的研究表明,Ⅱ类(Ia)分子参与单核细胞将可溶性抗原呈递给诱导性T淋巴细胞的过程、混合淋巴细胞反应(MLR)中诱导性T细胞的刺激以及细胞毒性T淋巴细胞(CTL)对携带Ia的靶细胞的识别。在人类系统中,使用能够阻断这些现象的单克隆抗Ia试剂的经验有限。然而,最近我们鉴定出一种溶细胞性IgG2a单克隆抗体9 - 49,它能与功能上重要的Ⅱ类分子结合。该抗体在无补体的情况下可阻断:(1)外周血淋巴细胞(PBL)与抗原脉冲单核细胞单层的特异性结合;(2)PBL对可溶性抗原(破伤风类毒素或腮腺炎病毒)或在同种异体或自体MLR中细胞表面Ⅱ类抗原刺激的增殖反应;(3)克隆的T4 +(诱导性)淋巴细胞系对Ⅱ类抗原的增殖反应;(4)同种异体MLR期间细胞毒性淋巴细胞的产生;(5)T4 + CTL克隆对携带Ⅱ类的靶细胞的识别(和杀伤)。T8 +克隆的增殖和CTL活性不受9 - 49抗体的影响。这些结果表明,这种单克隆试剂在评估Ia分子在免疫识别现象中的功能作用的研究中具有实用性。