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Objective Comparison of ELISA for detection of Mycoplasmapneumoniae IgM(MP-IgM)and cold agglutination test for early diagnosis of Mycoplasma pneumoniae infection in clinical value. Methods ELISA and cold agglutination test were used to detect 500 cases of serum samples infected with Mycoplasma pneumoniae. Results The positive rate of ELISA(54.8%)was significantly higher than that of cold agglutination(28.4%), and there was significant difference(χ2=71.72,P<0.01).The positive rates of ELISA in Fever 3 days(44.2%), 4~7days(46.4%),8~14 days(71.3%),and 15 days(78.6%)were significantly higher than that of cold aggluti-nation 22.1%,25.4%,35.7%,35.7%.The positive rates were increased with fever days extended.These is no sig-nificant difference(P > 0.05)in 1 ~ 3 days and 4 ~ 7 days,8~14 days and more than 15 days(P > 0.05) by ELISA,while there was a significant difference(P < 0.05)in 8~14 days with 1 ~ 3 days and 4 ~ 7 days. Conclution ELISA of detection MP-IgM should be selected prior in clinical detection,especially in the fever 8~14 days.It can obviously improve the early detection rate of mycoplasma infection and give the most useful value for clinical diagnosis.
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Objective:To study the expression of CXCL 8 in the serum and CXCL8 mRNA in the peripheral blood mononuclear cells(PBMCs) of the children with Mycoplasma pneumoniae pneumonia (MPP) and its clinical significance.Methods: Forty-eight children(severe cases 12,light cases 36) with MPP were recruited from October 2013 to March 2015 in the Maternal and Child Health-Care Hospital of Huainan.The concentration of the CXCL8 in serum and the level of CXCL8 mRNA in the PBMCs were measured by enzyme linked immunosorbent assay ( ELISA) and polymerase chain reaction ( PCR).Taking GAPDH as the internal reference ,the ratio of lgcDNA/lgGAPDH was regarded as the extreme level of CXCL 8 mRNA.Results: The serum level of CXCL8 and expression of CXCL8 mRNA in PBMCs in the children with MPP were ( 298.917 ±51.860 ) pg/ml and ( 1.848 ±0.525 ) lgcDNA/lgGAPDH.Compared with the normal control ,there were significant differences between the two groups ( P0.05).However, the expression of CXCL8 mRNA in peripheral blood of the children with severe illness was significantly higher than those in light cases (P<0.05).Intravenous infusion of Erythromycin was provided in the acute phase for seven to ten days ,so that the children′s condition could be significantly controlled , and the symptoms of pulmonary inflammation were also relieved .Followed by the use of sequential therapy of Azithromycin for about two to three weeks ,the children′s condition were gradually from acute stage to recovery stage .At this time,the CXCL8 and its mRNA levels in peripheral blood of the sick children were all significantly decreased comparing with those in the acute stage(P<0.05).Conclusion: The expression of CXCL8 and its mRNA were increased in the peripheral blood of the sick children with Mycoplasma pneumonia ,and also correlated with the severity of the disease .CXCL8 can participate in the pathogenesis of Mycoplasma pneumonia ,and has a certain cue effect on the severity and prognosis of the disease .Azithromycin can reduce the content of CXCL8 in serum of the sick children via the pathway of inhibiting the proliferation of Mycoplasma pneumoniae ,and down regulate the expression of mRNA ,so that the immune injury mediated by Mycoplasma pneumoniae may be gradually inhibited .