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Evaluation for synergistic suppression of T cell responses to minor histocompatibility antigens by chloroquine in combination with tacrolimus and a rapamycin derivative, SDZ-RAD.

机译:氯喹联合他克莫司和雷帕霉素衍生物SDZ-RAD对T细胞对次要组织相容性抗原的T细胞应答的协同抑制作用进行评估。

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The 4-aminoquinolines, chloroquine and hydroxychloroquine, can suppress chronic graft-versus-host disease (GVHD) following blood and marrow transplantation (BMT) in mice and humans, respectively. We hypothesized that chloroquine in combination with tacrolimus and the rapamycin derivative SDZ-RAD can synergistically suppress T cell responses and antigen-presenting cell (APC) function in vitro. We used the APC-dependent C57BL/6 anti-BALB.B T cell response and APC-independent anti-CD3epsilon antibody-induced response to evaluate the role of synergism between chloroquine and tacrolimus or SDZ-RAD on each component of a T cell response to minor histocompatibility antigens. We found that chloroquine with tacrolimus had a greater synergistic suppression of APC-dependent compared to the APC-independent T cell responses, with a combination index (CIx) for 50% inhibition by mean effect analysis of 0.16 and 0.50, respectively (a lower number indicates greater suppression). By contrast, chloroquine with SDZ-RAD had a similar CIx between the two responsed 0.50 vs0.45) suggesting only T cell suppression. Synergy between chloroquine and SDZ-RAD involved a direct effect on T cell cytokine production, whereas synergism between chloroquine and tacrolimus was due to an effect on both T cells and APCs. We conclude that the renal-sparing 4-aminoquinolines may be used syneristically with immunosuppressive drugs currently used for BMT.
机译:4-氨基喹啉,氯喹和羟氯喹分别可以抑制小鼠和人类的血液和骨髓移植(BMT)后的慢性移植物抗宿主病(GVHD)。我们假设氯喹与他克莫司和雷帕霉素衍生物SDZ-RAD结合可以在体外协同抑制T细胞反应和抗原呈递细胞(APC)的功能。我们使用了APC依赖性C57BL / 6抗BALB.BT细胞应答和APC依赖性抗CD3epsilon抗体诱导的应答来评估氯喹和他克莫司或SDZ-RAD之间协同作用对T细胞应答的每个成分的作用次要的组织相容性抗原。我们发现,与他克莫司相比,氯喹与他克莫司比不依赖APC的T细胞应答具有更大的协同抑制作用,其均值分析分别为50%抑制的组合指数(CIx)为0.16和0.50(更低的数字表示更大的抑制)。相比之下,具有SDZ-RAD的氯喹在两个响应的0.50 vs.0.45之间具有相似的CIx,表明仅抑制了T细胞。氯喹和SDZ-RAD之间的协同作用直接影响T细胞细胞因子的产生,而氯喹和他克莫司之间的协同作用归因于对T细胞和APC的共同作用。我们得出结论,保肾的4-氨基喹啉可以与目前用于BMT的免疫抑制药物协同使用。

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