Hodge S, Hodge G, Flower R, Han P
Haematology Department, Women's and Children's Hospital, North Adelaide, South Australia.
Clin Exp Immunol. 1998 Jul;113(1):33-8. doi: 10.1046/j.1365-2249.1998.00626.x.
Diagnosis of perinatal infection in the newborn is difficult; there may be few clinical signs and current tests are slow or non-specific. Detection of organisms, antigen or specific antibody to common pathogens often requires repeat samples and does not give immediate results. Haematological parameters, although relied upon frequently to diagnose infection in the neonate prior to a positive bacterial isolation, are unreliable and insensitive. Indicators such as an increase in neutrophil band cell counts are highly variable between morphologists. Infection induces the expression of a number of T lymphocyte surface markers, including CD45RA/CD45RO and CD45RO. The use of changed expression of surface markers as a laboratory test for detection of infection in neonates was evaluated. We used multiparameter flow cytometry to detect expression of early (CD45RA/CD45RO) and late (CD45RO) activation markers. In the respective groups of 50 full term (including 25 normal vaginal deliveries and 25 caesarean deliveries) and 30 premature, i.e. < 36 weeks gestation (born by either normal vaginal delivery or caesarean delivery) the CD45RA isoform was brightly expressed on newborn 'naive' CD4+ T cells, whereas the CD45RO isoform (including both 'bright' and 'dim' populations) was present on < 19% of CD4+ T cells from these newborn infants. In a group of 37 infants, tested to evaluate possible effects of non-infective parameters such as respiratory distress and iso-immunization, no significant changes in surface marker expression were found and specificity of the test was confirmed. In 14 neonates with documented sepsis, up-regulation of dual staining CD45RA/CD45RO isoforms on CD4+ T cells was detected early in the infection. In addition, we found that CD45RO expression persisted for several weeks after bacterial infection, and up to several months in viral infection. In conclusion, detection of T cell activation by flow cytometry for the early diagnosis of neonatal infection is an easy test to carry out on small volumes of blood, is inexpensive, and may be a specific indicator of infection.
新生儿围产期感染的诊断较为困难;可能几乎没有临床症状,且目前的检测方法耗时较长或缺乏特异性。检测常见病原体的微生物、抗原或特异性抗体通常需要多次采样,且无法立即得出结果。血液学参数虽然在细菌培养结果呈阳性之前常被用于诊断新生儿感染,但并不可靠且不够灵敏。诸如中性粒细胞杆状核细胞计数增加等指标在不同形态学家之间差异很大。感染会诱导多种T淋巴细胞表面标志物的表达,包括CD45RA/CD45RO和CD45RO。我们评估了将表面标志物表达变化用作检测新生儿感染的实验室检测方法的可行性。我们使用多参数流式细胞术检测早期(CD45RA/CD45RO)和晚期(CD45RO)活化标志物的表达。在分别包含50例足月儿(其中25例为正常阴道分娩,25例为剖宫产)和30例早产儿(即孕周<36周,分娩方式为正常阴道分娩或剖宫产)的两组中,CD45RA亚型在新生儿“初始”CD4+T细胞上呈明亮表达,而CD45RO亚型(包括“明亮”和“暗淡”群体)在这些新生儿的CD4+T细胞中所占比例不到19%。在一组37例婴儿中,为评估呼吸窘迫和同种免疫等非感染性参数的可能影响而进行检测,结果发现表面标志物表达无显著变化,从而证实了该检测方法的特异性。在14例确诊为败血症的新生儿中,在感染早期就检测到CD4+T细胞上双染CD45RA/CD45RO亚型的上调。此外,我们发现细菌感染后CD45RO表达会持续数周,病毒感染时则可持续数月。总之,通过流式细胞术检测T细胞活化以早期诊断新生儿感染是一种易于对少量血液进行的检测方法,成本低廉,且可能是感染的特异性指标。