Increase of circulating CD8+CD57+ lymphocytes after measles infection but not after measles vaccination.

B Aronsson, M Troye-Blomberg, L Smedman
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Abstract

Natural measles virus infection is recognised to induce immunosuppression, contributing to an increased susceptibility to other infections. A cell population that could be involved in this process is the CD8CD57 double-positive lymphocyte subset (CD8+CD57+), known to be significantly expanded in some viral infections, e.g. human immunodeficiency virus (HIV) infection. We therefore studied the level of CD8+CD57+ lymphocytes during measles infection and measles vaccination. Twenty-two measles patients were examined 5-57 days after the onset of fever and several months later. Healthy, age-matched controls were examined twice. Eleven children receiving measles-mumps-rubella (MMR) vaccination were examined before, 9-19 days and 5-9 months afterwards. Blood samples were analysed for the proportion of peripheral blood mononuclear cells carrying both CD8 and CD57, and for other cell surface markers (CD4, CD14, CD3, CD16(CD56) or CD20). Elevated proportions of CD8CD57 double-positive cells were found in the peripheral blood of children with natural measles early after infection (p < 0.05), whereas the proportion of other cell surface markers remained stable. No corresponding change in CD8+CD57+ lymphocytes was noted in MMR-vaccinated children or in healthy controls. Since CD8+CD57+ lymphocytes could be related to the immunosuppression seen in some viral infections, our finding of elevated CD8CD57 double-positive lymphocytes during acute measles infection would suggest that this population of lymphocytes is involved in measles-induced immunosuppression. The absence of an increase of CD8CD57 in children vaccinated with the conventional live attenuated measles vaccine, in contrast to children with natural measles infection, would thus indicate that the vaccine does not induce immunosuppression as measured in our in vitro system.

麻疹感染后循环CD8+CD57+淋巴细胞增加,而麻疹疫苗接种后没有。
自然麻疹病毒感染被认为会引起免疫抑制,从而增加对其他感染的易感性。可能参与这一过程的细胞群是CD8CD57双阳性淋巴细胞亚群(CD8+CD57+),已知在某些病毒感染中显著扩增,例如人类免疫缺陷病毒(HIV)感染。因此,我们研究了麻疹感染和麻疹疫苗接种期间CD8+CD57+淋巴细胞的水平。22例麻疹患者在发热后5-57天和几个月后接受检查。健康的、年龄匹配的对照组被检查了两次。在接种麻疹-腮腺炎-风疹(MMR)疫苗前、9-19天和5-9个月对11名儿童进行了检查。分析血液样本中同时携带CD8和CD57的外周血单个核细胞比例,以及其他细胞表面标志物(CD4、CD14、CD3、CD16(CD56)或CD20)。自然麻疹患儿感染后早期外周血CD8CD57双阳性细胞比例升高(p < 0.05),其他细胞表面标志物比例保持稳定。在接种mmr疫苗的儿童或健康对照中,CD8+CD57+淋巴细胞没有相应的变化。由于CD8+CD57+淋巴细胞可能与某些病毒感染中的免疫抑制有关,我们在急性麻疹感染中发现CD8CD57双阳性淋巴细胞升高,这表明这群淋巴细胞参与了麻疹诱导的免疫抑制。与自然麻疹感染的儿童相比,接种常规麻疹减毒活疫苗的儿童中CD8CD57没有增加,这表明在我们的体外系统中,疫苗不会诱导免疫抑制。
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