Chipeta J, Komada Y, Zhang X L, Deguchi T, Sugiyama K, Azuma E, Sakurai M
Department of Pediatrics, Mie University School of Medicine, Japan.
Cell Immunol. 1998 Feb 1;183(2):149-56. doi: 10.1006/cimm.1998.1244.
The growing body of evidence suggestive of T helper types 1 and 2 (Th1/Th2) including their counterparts T cytotoxic types 1 and 2 (Tc1/Tc2) cell responses during various human disease states necessitates determination of normal T cell subsets' cytokine profiles. We show here, using intracellular cytokine staining and flow cytometry, that in healthy subjects interferon (IFN)-gamma producing CD4+ (Th1) and CD8+ (Tc1) cell populations progressively increase with age with strong correlation to CD45RO surface antigen expression. Meanwhile populations of cells capable of producing IL-4 (Th2 and Tc2) are comparably minimal across all age groups. Collectively, these results may reflect the maturation and expansion of Th1 and Tc1 cell populations from the neonatal period to adulthood, most probably dependent on antigen exposure.
越来越多的证据表明,在各种人类疾病状态下,1型和2型辅助性T细胞(Th1/Th2)及其对应的1型和2型细胞毒性T细胞(Tc1/Tc2)会发生细胞反应,因此有必要确定正常T细胞亚群的细胞因子谱。我们在此使用细胞内细胞因子染色和流式细胞术表明,在健康受试者中,产生干扰素(IFN)-γ的CD4+(Th1)和CD8+(Tc1)细胞群体随年龄增长而逐渐增加,且与CD45RO表面抗原表达密切相关。同时,在所有年龄组中,能够产生白细胞介素-4(IL-4)的细胞群体(Th2和Tc2)相对较少。总体而言,这些结果可能反映了从新生儿期到成年期Th1和Tc1细胞群体的成熟和扩增,很可能依赖于抗原暴露。