Hanna N, Kalderon R, Nelken D
Immunology. 1975 Sep;29(3):433-43.
Normal immunosuppressive protein (NIP) isolated from human plasma was studied in two well defined systems. (1) Spontaneous rosettes of sheep red blood cells with human peripheral blood lymphocytes and PHA-induced lymphocyte cytotoxicity as indicators for T-cell function. (2) Rosette formation tests of human lymphocytes with antibody-coated erythrocytes or erythrocytes coated with antibody and complement as well as antibody-induced lymphocyte-mediated cytotoxicity represented non-T-cell activity. While NIP did not inhibit the formation of any of the above mentioned rosettes, it practically prevented both PHA-induced and antibody-mediated lymphocyte cytotoxicity. Relatively small amounts of NIP inhibited PHA-induced cytotoxicity while higher doses were required for the inhibition of antibody-mediated lymphocyte cytotoxicity. Possible mechanisms of its suppressive activity are discussed. NIP was found to be heat-stable and did not show any species specificity, as NIP preparations from human plasma were immunosuppressive in human, mouse and guinea-pig systems.
从人血浆中分离出的正常免疫抑制蛋白(NIP)在两个明确的系统中进行了研究。(1)以绵羊红细胞与人外周血淋巴细胞的自发玫瑰花结形成以及PHA诱导的淋巴细胞细胞毒性作为T细胞功能的指标。(2)人淋巴细胞与抗体包被的红细胞或抗体和补体包被的红细胞的玫瑰花结形成试验以及抗体诱导的淋巴细胞介导的细胞毒性代表非T细胞活性。虽然NIP不抑制上述任何一种玫瑰花结的形成,但它实际上可阻止PHA诱导的和抗体介导的淋巴细胞细胞毒性。相对少量的NIP可抑制PHA诱导的细胞毒性,而抑制抗体介导的淋巴细胞细胞毒性则需要更高剂量。讨论了其抑制活性的可能机制。发现NIP具有热稳定性且不显示任何种属特异性,因为来自人血浆的NIP制剂在人、小鼠和豚鼠系统中均具有免疫抑制作用。