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Table 1.

Characteristics of all subjects included in the study.

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Table 2.

Blood parameters for hemoglobin, thrombocytes, urea and creatinine of all patients included in the study.

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Figure 1.

CD55 and CD59 expression are increased on erythrocytes and leukocytes of former EAHEC-infected patients.

Erythrocytes and leukocytes were incubated with CD45-, CD55- and CD59-specific antibodies and analyzed via flow cytometry. The CD45 marker was used to exclude or include the leukocyte population whereas the leukocyte subsets were distinguished via FSC/SSC-plot. Patients were grouped according to their clinical course into 3 groups with either severe gastrointestinal symptoms (GI, n = 34), HUS without neurological symptoms (HUS, n = 23) and HUS with neurological symptoms only (HUS/N, n = 19). Healthy controls were also screened (HC, n = 12). A Erythrocytes, B Leukocytes, C Granulocytes, D Monocytes, E Lymphocytes. All values are given as mean fluorescence intensity (MFI) ± S.D. ANOVA, following symbols are used to pinpoint significant differences: vs. HC *, vs. GI #. One symbol equals 0.05, two symbols 0.01, three symbols 0.001.

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Table 3.

Pearson-Bravais correlation tests between CD55 and CD59 expression and hemoglobin, thrombocytes, urea and creatinine levels of all patients included in the study.

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Figure 2.

Plasma separation and ECU do not affect CD55 and CD59 expression on erythrocytes and leukocytes.

Erythrocytes and leukocytes were incubated with CD45-, CD55- and CD59-specific antibodies and analyzed via flow cytometry. The CD45 marker was used to exclude or include the leukocyte population whereas the leukocyte subsets were distinguished via FSC/SSC-plot. HUS patients were grouped according to their therapy into 4 groups with HUS patients who received plasma separation (n = 9), HUS patients who received plasma separation and ECU (n = 14), HUS/N patients who received plasma separation (n = 3) and HUS/N patients who received plasma separation and ECU (n = 16). Healthy controls were also screened (HC, n = 12). A Erythrocytes, B Leukocytes. All values are given as mean fluorescence intensity (MFI) ± S.D. ANOVA, following symbols are used to pinpoint significant differences: vs. HC *. One symbols equals 0.05, two symbols 0.01, three symbols 0.001.

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Figure 3.

Stx-2 does not reduce the expression of CD55 and CD59 on erythrocytes and leukocytes.

After incubating erythrocytes and leukocytes in whole blood with 0, 0.1 and 10/ml Shiga toxin 2 for 24 h the expression levels for CD55 and CD59 were analyzed via flow cytometry. Patients were grouped according to their clinical course into 3 groups with GI (n = 4), HUS (n = 4) and HUS/N (n = 4). Healthy controls were also screened (HC, n = 4) A CD55 expression, B CD59 expression on erythrocytes, C CD55 expression, D CD59 expression on leukocytes. All values are given as mean fluorescence intensity (MFI) ± S.D.

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