Dysbiosis, defined as an imbalance in the gut microbiota caused by too few beneficial bacteria and an overgrowth of bad bacteria, yeast, and/or parasites, is now being associated with several diseases, including the development of colorectal carcinoma (CRC). In this study, the potential association of (formerly ) with CRC was investigated. Plasma samples obtained from preoperative histologically confirmed CRC patients (=39) and their age- and sex-matched clinically healthy controls (=39) were analyzed for antibodies to toxin B of (anti-tcdB) by enzyme-linked immunosorbent assay (ELISA). A significantly greater number (p=0.012) of CRC cases (=26/39, 66.7%) had anti-tcdB IgG levels above the cutoff value compared with controls (=12/39, 30.8%). Eight cases (8/39, 20.5%) and none of the controls registered anti-tcdB IgA levels above the cutoff value (p=0.0039). Anti-tcdB IgG and IgA levels were not shown to be significantly associated with tumor grade or tumor stage. Anti-tcdB IgG showed 66.7% sensitivity and 69.2% specificity. For anti-tcdB IgA, sensitivity and specificity were 20.5% and 100%, respectively. The positive predictive values for anti-tcdB IgA and IgG were 100% and 68.4%, respectively. The anti-tcdB IgA and IgG negative predictive values were 55.7% and 67.5%, respectively. The results suggest the potential association of with CRC and anti-tcdB levels, particularly the IgA level. Hence, anti-tcdB antibodies can be candidate serologic markers for CRC.
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http://dx.doi.org/10.12938/bmfh.2020-010 | DOI Listing |
Biosci Microbiota Food Health
February 2020
The Graduate School, University of Santo Tomas, España Blvd., Manila, Philippines.
Dysbiosis, defined as an imbalance in the gut microbiota caused by too few beneficial bacteria and an overgrowth of bad bacteria, yeast, and/or parasites, is now being associated with several diseases, including the development of colorectal carcinoma (CRC). In this study, the potential association of (formerly ) with CRC was investigated. Plasma samples obtained from preoperative histologically confirmed CRC patients (=39) and their age- and sex-matched clinically healthy controls (=39) were analyzed for antibodies to toxin B of (anti-tcdB) by enzyme-linked immunosorbent assay (ELISA).
View Article and Find Full Text PDFAnaerobe
October 2016
Institut für Medizinische Mikrobiologie und Hygiene Universitätsmedizin der Johannes Gutenberg-Universität Mainz, Hochhaus am Augustusplatz, Obere Zahlbacher Str. 67, D-55131 Mainz, Germany; tgcBIOMICS GmbH, Franz-Kirsten-Str. 1, 55411 Bingen, Germany. Electronic address:
According to the literature Clostridium difficile antitoxins are present in up to 66% of humans. In a survey of ∼400 plasma samples from healthy blood donors we found that less than 6% were positive for anti-TcdA or anti-TcdB antitoxins. Using the same standard immunoassay protocol, we looked for IgG and IgA antitoxins in the blood and stool samples from 25 patients with C.
View Article and Find Full Text PDFClin Microbiol Infect
December 2014
Department of Infectious Diseases, Centre for Infectious Diseases, Leiden University Medical Centre, Leiden, The Netherlands.
Low serum concentrations of antibodies directed against the toxins TcdA and TcdB have been associated with a higher risk of recurrence of Clostridium difficile infection (CDI) after successful antibiotic treatment. However, there are conflicting reports. Herein, we compared serum levels of antibodies of patients with a single episode of CDI with those of patients who subsequently suffered a recurrence.
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