Kakai R, Bwayo J J, Wamola I A, Ndinya-Achola J O, Plummer F A
Department of Medical Microbiology, University of Nairobi, Kenya.
East Afr Med J. 1995 Nov;72(11):699-702.
The purpose of this study was to determine the relationship between intestinal mucosal immunity and diarrhoea. Stools were tested for total IgA by radial immunodiffusion, cultured for bacteria and examined for ova/cysts by microscopy. Peripheral blood was screened for HIV-1 antibody by ELISA, CD4 and CD8 enumerated by flow cytometry and phagocytic activity by C. albicans engulfment. A total of 271 children were enrolled with a mean age of 20.3 m (range 0.3-60.0 m). HIV exposed (born to HIV seropositive mothers) had more episodes of diarrhoea than HIV unexposed (born to HIV seronegative mothers) children in the first six months of life (26.0% versus 5.5%, p = 0.002). Exposed children had severe (16/44 versus 6/29, p = 0.02) and prolonged diarrhoea lasting more than nine days (11.0% versus 1.4%, p = 0.03) than unexposed. CD8 counts were significantly higher in exposed than unexposed children (1837.0 versus 1373.0 cells/mm3, p = p.01). Among children aged 15 months and over, HIV seropositive children had severe diarrhoea (4/6 versus 11/32, p<0.01), reduced phagocytic activity (phagocytic index 15.4 versus 28.9, p<0.01), total intestinal IgA (0.2 versus 0.7 mg/ml, p = 0.04) and CD4 counts (624.2 versus 1345.1 cells/mm3, p = 0.01) than seronegative. Reduction of CD4 was more significant in HIV seropositive children with severe diarrhoea (298.7 versus 1318.5 cells/mm3, p = 0.01). Isolation of enteric pathogens was independent of either maternal or child's HIV serostatus although E. coli was more frequent in children with low CD4 counts. These results highlight the importance of mucosal immunity in the intestinal infections. Exposure to HIV, reduced CD4 counts and IgA were associated with diarrhoea probably due to impaired intestinal mucosal immunity.
本研究的目的是确定肠道黏膜免疫与腹泻之间的关系。通过放射免疫扩散法检测粪便中的总IgA,对粪便进行细菌培养,并通过显微镜检查虫卵/包囊。采用酶联免疫吸附测定法筛查外周血中的HIV-1抗体,通过流式细胞术计数CD4和CD8,并通过白色念珠菌吞噬试验检测吞噬活性。共纳入271名儿童,平均年龄为20.3个月(范围0.3 - 60.0个月)。在出生后的前六个月,暴露于HIV的儿童(出生于HIV血清阳性母亲)比未暴露于HIV的儿童(出生于HIV血清阴性母亲)腹泻发作次数更多(26.0%对5.5%,p = 0.002)。与未暴露儿童相比,暴露儿童出现严重腹泻(16/44对6/29,p = 0.02)以及持续超过九天的长期腹泻(11.0%对1.4%,p = 0.03)的情况更多。暴露儿童的CD8计数显著高于未暴露儿童(1837.0对1373.0个细胞/mm³,p = 0.01)。在15个月及以上的儿童中,HIV血清阳性儿童出现严重腹泻(4/6对11/32,p<0.01)、吞噬活性降低(吞噬指数15.4对28.9,p<0.01)、肠道总IgA降低(0.2对0.7mg/ml,p = 0.04)以及CD4计数降低(624.2对1345.1个细胞/mm³,p = 0.01),与血清阴性儿童相比。在患有严重腹泻的HIV血清阳性儿童中,CD4的降低更为显著(298.7对1318.5个细胞/mm³,p = 0.01)。肠道病原体的分离与母亲或儿童的HIV血清学状态无关,尽管在CD4计数低的儿童中大肠杆菌更为常见。这些结果突出了黏膜免疫在肠道感染中的重要性。暴露于HIV、CD4计数降低和IgA降低与腹泻相关,可能是由于肠道黏膜免疫受损。