Le Gros G S, Prestidge R L, Watson J D
Immunology. 1983 Dec;50(4):537-46.
A procedure is described for the in vivo removal of all detectable T lymphocytes from spleen and lymph nodes in mice. A single intraperitoneal injection of monoclonal anti-Thy-1 antibody into mice leads to rapid depletion of functional T cells from peripheral lymphoid organs, but not thymus. The extent of T-cell depletion is dependent on the cytotoxic titre of the anti-Thy-1 antibody used. Antibody with a median cytotoxic titre greater than 10(6) causes the complete removal of cells bearing Thy-1, Lyt-1 and Lyt-2 surface antigens from peripheral lymphoid populations in 3 days. Eight days after treatment Thy-1+, Lyt-1+ and Lyt-2+ cells begin to reappear in these organs. Splenic B cells, assayed by the expression of surface immunoglobulin (sIg) and by mitogenic responsiveness to bacterial lipopolysaccharide (LPS), are not affected by this treatment. The monoclonal anti-Thy-1 antibody does not appear to penetrate thymus tissue and bind to thymocytes. Anti-Thy-1 antibody, but not F(ab')2 is required for in-vivo T-cell depletion. These findings indicate that anti-Thy-1 antibody causes the removal of Thy-1+ cells from peripheral lymphoid tissue, and as the circulating levels of anti-Thy-1 antibody decrease, cells from the thymus repopulate the thymus-dependent areas of the depleted lymphoid organs.
本文描述了一种在小鼠体内去除脾脏和淋巴结中所有可检测到的T淋巴细胞的方法。给小鼠腹腔内单次注射单克隆抗Thy-1抗体可导致外周淋巴器官中功能性T细胞迅速耗竭,但胸腺不受影响。T细胞耗竭的程度取决于所用抗Thy-1抗体的细胞毒性效价。细胞毒性效价中位数大于10(6)的抗体可在3天内使外周淋巴群体中携带Thy-1、Lyt-1和Lyt-2表面抗原的细胞完全清除。治疗8天后,Thy-1+、Lyt-1+和Lyt-2+细胞开始在这些器官中重新出现。通过表面免疫球蛋白(sIg)的表达和对细菌脂多糖(LPS)的促有丝分裂反应性检测的脾脏B细胞不受该治疗的影响。单克隆抗Thy-1抗体似乎不会穿透胸腺组织并与胸腺细胞结合。体内T细胞耗竭需要抗Thy-1抗体,而不是F(ab')2。这些发现表明,抗Thy-1抗体可导致外周淋巴组织中Thy-1+细胞的清除,并且随着抗Thy-1抗体循环水平的降低,胸腺细胞会重新填充耗尽的淋巴器官中依赖胸腺的区域。