Campbell D, Vose B M
Immunology. 1985 Sep;56(1):81-91.
The capacity of T cells from different sites to augment IgA production by LPS-stimulated B cells has been investigated. Peyer's patch T lymphocytes activated with Con A induced up to a 20-fold increase in IgA production. The effect was isotype-specific, in that no consistent effect on IgG and a diminution of IgM synthesis were observed. Less activity was recorded in spleen and mesenteric lymph node T cells. Optimal activation of the Thy 1+ Lyt 1+2- helper cells required the addition of splenic adherent cells and the elimination of Thy 1+ Lyt 2+ suppressor cells prior to activation. T lymphocytes maintained regulatory activity for several months after expansion in medium supplemented with IL-2 and are now being cloned. We conclude that IgA production is under control of T cells sited preferentially, but not exclusively, in gut-associated lymphoid tissue, and that these T cells can augment IgA production by B lymphocytes from sites with low commitment to production of this isotype.
已对来自不同部位的T细胞增强LPS刺激的B细胞产生IgA的能力进行了研究。用伴刀豆球蛋白A激活的派尔集合淋巴结T淋巴细胞可使IgA产生增加多达20倍。该效应具有同种型特异性,因为未观察到对IgG有一致的效应,且IgM合成减少。在脾脏和肠系膜淋巴结T细胞中记录到的活性较低。Thy 1⁺Lyt 1⁺2⁻辅助细胞的最佳激活需要添加脾黏附细胞,并在激活前消除Thy 1⁺Lyt 2⁺抑制细胞。在补充有白细胞介素-2的培养基中扩增后,T淋巴细胞维持调节活性数月,目前正在进行克隆化。我们得出结论,IgA的产生受T细胞的控制,这些T细胞优先但非唯一地位于肠道相关淋巴组织中,并且这些T细胞可以增强来自对该同种型产生低倾向部位的B淋巴细胞产生IgA的能力。