Instituto de Investigaciones Hematológicas, Academia Nacional de Medicina, Buenos Aires, Argentina.
Clin Immunol. 2011 Dec;141(3):357-64. doi: 10.1016/j.clim.2011.09.007. Epub 2011 Sep 22.
Peripheral blood mononuclear cells with T(FH) phenotype from two asymptomatic XLP patients were studied. Normal/high numbers of CXCR5+, CD4+ T cells coexpressing PD-1 were demonstrated. Peripheral blood mononuclear cells (PBMC) from these patients responded to sub-optimal PHA/IL-2 stimulation upregulating ICOS and CD40L and increasing intracellular expression of IL-10, IL-21 and IL-4 by CD4+ T(FH) cells. However when compared to N, the time profile of activation and cytokine synthesis was different in XLP and N. While ICOS and CD40L expression in N decreased after 6-8 days, it continued to increase or was maintained in XLP cultures. Intracellular IL-10, IL-21 and IL-4 reached higher values in XLP than N after 8 days. Rather than the absence of T(FH) cells or their intrinsic inability to respond to stimuli, differences in the time profile of their response could contribute to impair their role as helpers of B lymphocytes.
对两名无症状 XLP 患者的外周血单个核细胞(PBMC)进行了研究。结果显示,CXCR5+、CD4+T 细胞的表达水平正常/偏高,且这些细胞共表达 PD-1。这些患者的 PBMC 在亚最佳 PHA/IL-2 刺激下反应良好,可上调 ICOSL 和 CD40L,并增加 CD4+T(FH)细胞内的 IL-10、IL-21 和 IL-4 的表达。然而,与正常对照组(N)相比,XLP 患者和 N 组的细胞激活和细胞因子合成的时间进程不同。在 N 组中,ICOSL 和 CD40L 的表达在 6-8 天后下降,但在 XLP 培养物中,其表达继续增加或维持不变。在 XLP 组中,细胞内的 IL-10、IL-21 和 IL-4 在 8 天后达到比 N 组更高的值。导致这种差异的原因不是 T(FH)细胞的缺失,或是其对刺激的固有反应能力不足,而是它们反应时间进程的差异,这可能会影响其作为 B 淋巴细胞辅助者的作用。