Clerici M, DePalma L, Roilides E, Baker R, Shearer G M
Experimental Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
J Clin Invest. 1993 Jun;91(6):2829-36. doi: 10.1172/JCI116526.
The development of antigen-specific functional T lymphocyte immunity in infants and children is an area of immunology that needs elucidation. Leukocytes from cord blood (CBL) and from PBL of children of different ages who were in the hospital for minor surgical procedures were compared with PBL from healthy adults for their ability to generate T helper cell (Th) responses assessed by in vitro proliferation and IL-2 production after stimulation with: influenza A virus (FLU); tetanus toxoid (TET); adult allogeneic PBL that were either undepleted (ALLO) or depleted of adherent antigen presenting cells (ALLONW); and PHA. CBL generated Th responses to ALLONW, ALLO, and PHA, but not to FLU or TET. PBL from infants between 6 and 13 mo of age responded to ALLO and PHA; none responded to FLU or ALLONW, and two of four responded weakly to TET. PBL from children between 13 and 26 mo of age responded to all stimuli except FLU, to which only one child responded marginally. PBL from children older than 36 mo responded to all stimuli at levels comparable to those of PBL from adults. The use of undepleted and adherent cell-depleted CBL and PBL from children of different ages as allogeneic stimulators of responses generated by PBL from adults indicated that the antigen presenting function of CBL and PBL from children 13 mo or older are sufficiently developed to present alloantigen, whereas PBL from children younger than 13 mo are not. Therefore, our results indicate that age-dependent differences exist in both T helper and antigen-presenting functions of CBL and PBL from children of different ages. Surprisingly, CBL appear to be more efficient in antigen-presenting function than PBL from children younger than 13 mo. These findings are important for establishing developmental parameters of T helper cell immunity relevant for pediatric infection and transplantation in infants and children.
婴幼儿和儿童抗原特异性功能性T淋巴细胞免疫的发育是一个需要阐明的免疫学领域。将来自脐带血(CBL)以及因小手术住院的不同年龄儿童的外周血淋巴细胞(PBL)与健康成人的PBL进行比较,观察它们在受到以下刺激后通过体外增殖和白细胞介素-2产生来评估产生T辅助细胞(Th)反应的能力:甲型流感病毒(FLU);破伤风类毒素(TET);未去除贴壁抗原呈递细胞的成人同种异体PBL(ALLO)或去除贴壁抗原呈递细胞的成人同种异体PBL(ALLONW);以及植物血凝素(PHA)。CBL对ALLONW、ALLO和PHA产生Th反应,但对FLU或TET无反应。6至13个月大婴儿的PBL对ALLO和PHA有反应;对FLU或ALLONW均无反应,4例中有2例对TET反应微弱。13至26个月大儿童的PBL对除FLU外的所有刺激均有反应,只有1名儿童对FLU有轻微反应。36个月以上儿童的PBL对所有刺激的反应水平与成人PBL相当。使用不同年龄儿童未去除和去除贴壁细胞的CBL和PBL作为成人PBL产生反应的同种异体刺激物表明,13个月及以上儿童的CBL和PBL的抗原呈递功能已充分发育,足以呈递同种异体抗原,而13个月以下儿童的PBL则不然。因此,我们的结果表明,不同年龄儿童的CBL和PBL在T辅助和抗原呈递功能方面均存在年龄依赖性差异。令人惊讶的是,CBL在抗原呈递功能上似乎比13个月以下儿童的PBL更有效。这些发现对于确立与婴幼儿感染及移植相关的T辅助细胞免疫发育参数具有重要意义。