Sanchez M E, Maki D V, McLaren L C, Bankhurst A D
Prostaglandins. 1979 Jul;18(1):35-41. doi: 10.1016/s0090-6980(79)80021-0.
Prostaglandins of the E series (PGE) may serve as important regulators of human immune responsiveness. The present study was designed to examine the possibility that PGE may effect human lymphocyte function by the modulation of surface receptors. The presence of surface binding sites on human lymphocytes for measles virus antigens was studied using a rosette adherence assay. We observed that the addition of PGE1 increased the proportion of measles-infected cells (Hela-Kll) with adherent lymphocytes (75% increase at 3 x 10(-6) M PGE1). PGE was observed to enhance the adherence of purified normal peripheral T cells (87%) and T lymphoid cells (Molt 3) (27%). In contrast, no significant change in normal peripheral B cell or B lymphoid cell (Raji) adherence was observed with the addition of PGE. These results are consistent with a selective modulation of surface measles virus binding sites by PGE1 on T and not B lymphoid cells.
E系列前列腺素(PGE)可能是人类免疫反应的重要调节因子。本研究旨在探讨PGE是否可能通过调节表面受体来影响人类淋巴细胞功能。使用玫瑰花结粘附试验研究了人类淋巴细胞上麻疹病毒抗原表面结合位点的存在情况。我们观察到,添加PGE1会增加感染麻疹的细胞(Hela-Kll)与粘附淋巴细胞的比例(在3×10⁻⁶M PGE1时增加75%)。观察到PGE可增强纯化的正常外周T细胞(87%)和T淋巴细胞(Molt 3)(27%)的粘附。相比之下,添加PGE后,正常外周B细胞或B淋巴细胞(Raji)的粘附未观察到显著变化。这些结果与PGE1对T淋巴细胞而非B淋巴细胞表面麻疹病毒结合位点的选择性调节一致。