Zimecki M, Kapp J A
Institute of Immunology and Experimental Therapy, Polish Academy of Sciences, Wrocław, Poland.
Arch Immunol Ther Exp (Warsz). 1995;43(5-6):253-7.
In this communication we demonstrate that B cells from CBA/N mice with x chromosome-linked immunodeficiency and B cells from newborn mice, that have very limited ability to present antigen to antigen-specific T cells lines, acquire this function following preincubation with IL-7 or IL-10. These interleukins do not affect the antigen presenting function of B cells from normal, adult CBA mice. Incubation of B cells from xid and newborn mice with IL-7 or IL-10 but not with IL-2 induces expression of Lyb-5 marker on these cells. The study shows that the property of IL-7 and IL-10 to induce antigen presenting cell (APC) activity in immature B cells is associated with appearance of Lyb-5 antigen on these cells.
在本通讯中,我们证明,来自具有X染色体连锁免疫缺陷的CBA/N小鼠的B细胞以及来自新生小鼠的B细胞,它们向抗原特异性T细胞系呈递抗原的能力非常有限,但在与白细胞介素-7(IL-7)或白细胞介素-10(IL-10)预孵育后可获得此功能。这些白细胞介素不影响正常成年CBA小鼠B细胞的抗原呈递功能。用IL-7或IL-10而非IL-2孵育来自xid和新生小鼠的B细胞,可诱导这些细胞上Lyb-5标志物的表达。该研究表明,IL-7和IL-10在未成熟B细胞中诱导抗原呈递细胞(APC)活性的特性与这些细胞上Lyb-5抗原的出现有关。