Bradbury M G, Doherty K V, Parish C R, Lyons A B
Division of Cell Biology, John Curtin School of Medical Research, Canberra, Australia.
Immunology. 1996 Jan;87(1):80-5.
2-acetyl-4(5)-(1,2,3,4-tetrahydroxybutyl)imidazole (THI) is an immunosuppressive component of caramel food colouring that causes lymphopenia in mice and rats by an unknown mechanism. In this study we investigated some of the affects of THI on the murine immune system. Initially we showed that splenic T lymphocytes from mice treated with 50 mg/l THI in their drinking water were unable to launch a mixed lymphocyte reaction (MLR) against allogeneic stimulator cells, and had decreased and delayed interleukin-2 (IL-2) production. However, these T cells exhibited a normal proliferative response to concanavalin A (Con A), immobilized anti-CD3 monoclonal antibody (mAb) and anti-CD3 plus anti-CD28 mAb. Furthermore, the MLR response could be restored by the addition of IL-2 to the MLR culture. Homing studies using intravenous injection of fluorescence-labelled splenocytes showed that THI treatment decreased absolute numbers of labelled T and B lymphocytes in the blood and the spleen. Furthermore, these labelled cells reappeared in the blood and the spleen when mice were taken off THI, indicating that lymphocyte recirculation and splenic homing were modified reversibly by THI treatment. Cessation of THI treatment also resulted in a rapid reappearance of MLR responsiveness in the spleen, indicating that THI treatment does not functionally impair recirculating T cells. Collectively these data are compatible with the concept that a rapidly recirculating population of T cells, which produce IL-2 in an allogeneic MLR, are lost from the blood and spleen following THI treatment, and are sequestered in other, yet to be identified, tissues.
2-乙酰基-4(5)-(1,2,3,4-四羟基丁基)咪唑(THI)是焦糖色素中的一种免疫抑制成分,其通过未知机制导致小鼠和大鼠淋巴细胞减少。在本研究中,我们调查了THI对小鼠免疫系统的一些影响。最初,我们发现饮用含50 mg/l THI水的小鼠的脾T淋巴细胞无法对同种异体刺激细胞发起混合淋巴细胞反应(MLR),并且白细胞介素-2(IL-2)的产生减少且延迟。然而,这些T细胞对刀豆蛋白A(Con A)、固定化抗CD3单克隆抗体(mAb)以及抗CD3加抗CD28 mAb表现出正常的增殖反应。此外,通过向MLR培养物中添加IL-2可恢复MLR反应。使用静脉注射荧光标记脾细胞的归巢研究表明,THI处理降低了血液和脾脏中标记的T和B淋巴细胞的绝对数量。此外,当小鼠停止使用THI时,这些标记细胞重新出现在血液和脾脏中,表明淋巴细胞再循环和脾归巢通过THI处理被可逆地改变。停止THI处理还导致脾脏中MLR反应性迅速恢复,表明THI处理在功能上不会损害再循环T细胞。总体而言,这些数据与以下概念相符:在THI处理后,在同种异体MLR中产生IL-2的快速再循环T细胞群体从血液和脾脏中丢失,并被隔离在其他尚未确定的组织中。