Miyagawa Y, Kawasaki A, Komiyama A, Akabane T
Microbiol Immunol. 1978;22(11):701-10. doi: 10.1111/j.1348-0421.1978.tb00423.x.
Transfer factor (TF) causes nonimmune lymphocytes to produce leukocyte migration inhibitory factor (LMIF) in the presence of purified protein derivative (PPD). The activity of TF was measured by leukocyte migration inhibitory test (LMIT). The LMIT was a modification of the conventional agarose droplet method. To express the activity of LMIF quantitatively and simply, LMIF titer was introduced. The LMIF titer was obtained from the combination of two factors, LMIF dilution and cell migration diameter, and therefore this made the LMIT much more sensitive as compared to the conventional LMIT. The responsiveness of lymphocytes from acute lymphoblastic leukemia (ALL) and from cell-mediated immunodeficiency in children to TF was assayed by LMIT. In ALL, the lymphocyte responsiveness was poor in relapse but improved with remission. The responsiveness was remarkably well in 3 patients with cell-mediated immunodeficiency. This method appears useful for the in vitro evaluation of responsiveness of lymphocytes to TF.
转移因子(TF)可使非免疫淋巴细胞在纯化蛋白衍生物(PPD)存在的情况下产生白细胞移动抑制因子(LMIF)。通过白细胞移动抑制试验(LMIT)测定TF的活性。LMIT是对传统琼脂糖滴法的改良。为了简单定量地表达LMIF的活性,引入了LMIF效价。LMIF效价由LMIF稀释度和细胞移动直径这两个因素共同得出,因此与传统的LMIT相比,这使得LMIT更加灵敏。通过LMIT检测急性淋巴细胞白血病(ALL)患儿以及细胞介导免疫缺陷患儿的淋巴细胞对TF的反应性。在ALL中,淋巴细胞反应性在复发时较差,但在缓解期有所改善。3例细胞介导免疫缺陷患者的反应性明显良好。该方法似乎有助于体外评估淋巴细胞对TF的反应性。