Antonaci S, Polignano A, Tortorella C, Garofalo A R, Jirillo E, Bonomo L
Patologia Medica, University of Bari Medical Faculty, Policlinico, Italy.
Cytobios. 1992;70(281):77-85.
There is evidence for an impaired T cell-mediated B cell response during senescence. In thirty aged donors, pokeweed mitogen (PWM)-driven immunoglobulin (Ig) synthesis by B cells co-cultured with autologous enriched CD4+ lymphocytes and low amounts of monocytes, was evaluated. Under such experimental conditions, elderly cultures displayed a reduced IgG and/or IgM production when compared with the younger counterpart. Moreover, interleukin (IL)-2 and/or IL-5 addition to cultures led to an enhancement of Ig release. In contrast, IL-4 supplementation failed to positively modulate B cell differentiation. At the same time, aged cells cultured in the presence of IL-2 + IL-5 exhibited an increased Ig synthesis, while the addition of IL-2 + IL-4 or IL-4 + IL-5 mixtures did not induce any significant effect in comparison with homologous untreated samples. The results suggest a critical role for IL-2, IL-4 and IL-5 in the modulation of T helper cell-driven B cell polyclonal responsiveness in the elderly.
有证据表明衰老过程中T细胞介导的B细胞反应受损。对30名老年供体,评估了与自体富集的CD4 +淋巴细胞和少量单核细胞共培养的B细胞由商陆有丝分裂原(PWM)驱动的免疫球蛋白(Ig)合成。在这种实验条件下,与年轻对照相比,老年培养物中IgG和/或IgM产生减少。此外,向培养物中添加白细胞介素(IL)-2和/或IL-5导致Ig释放增强。相反,补充IL-4未能对B细胞分化产生正向调节作用。同时,在IL-2 + IL-5存在下培养的老年细胞表现出Ig合成增加,而与同源未处理样品相比,添加IL-2 + IL-4或IL-4 + IL-5混合物未诱导任何显著影响。结果表明IL-2、IL-4和IL-5在调节老年人T辅助细胞驱动的B细胞多克隆反应性中起关键作用。