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Humoral Immune Response to Clostridioides difficile Toxins A and B in Hospitalized Immunocompromised Patients With C difficile Infection

BACKGROUND: The humoral immune response to Clostridioides difficile toxins in C difficile infection (CDI) is incompletely characterized in immunocompromised hosts (ICHs). METHODS: We conducted a prospective study of hospitalized adults with CDI, with and without immunosuppression (hematologic malign...

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Autores principales: Alonso, Carolyn D, Papamichael, Konstantinos, Sprague, Rebecca, Barrett, Caitlin, Gonzales-Luna, Anne J, Daugherty, Kaitlyn, Garey, Kevin W, Villafuerte-Gálvez, Javier, Xu, Hua, Lin, Qianyun, Wang, Lamei, Chen, Xinhua, Pollock, Nira R, Kelly, Ciarán P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271131/
https://www.ncbi.nlm.nih.gov/pubmed/34258317
http://dx.doi.org/10.1093/ofid/ofab286
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author Alonso, Carolyn D
Papamichael, Konstantinos
Sprague, Rebecca
Barrett, Caitlin
Gonzales-Luna, Anne J
Daugherty, Kaitlyn
Garey, Kevin W
Villafuerte-Gálvez, Javier
Xu, Hua
Lin, Qianyun
Wang, Lamei
Chen, Xinhua
Pollock, Nira R
Kelly, Ciarán P
author_facet Alonso, Carolyn D
Papamichael, Konstantinos
Sprague, Rebecca
Barrett, Caitlin
Gonzales-Luna, Anne J
Daugherty, Kaitlyn
Garey, Kevin W
Villafuerte-Gálvez, Javier
Xu, Hua
Lin, Qianyun
Wang, Lamei
Chen, Xinhua
Pollock, Nira R
Kelly, Ciarán P
author_sort Alonso, Carolyn D
collection PubMed
description BACKGROUND: The humoral immune response to Clostridioides difficile toxins in C difficile infection (CDI) is incompletely characterized in immunocompromised hosts (ICHs). METHODS: We conducted a prospective study of hospitalized adults with CDI, with and without immunosuppression (hematologic malignancy, active solid tumor, solid organ or stem cell transplant, inflammatory bowel disease, autoimmune disease, congenital or acquired immunodeficiency, asplenia, chronic receipt of high-dose steroids, or receipt of immunosuppressing medications within 12 months). Serum and stool antibody concentrations of immunoglobulin (Ig)M, IgG, and IgA to C difficile toxins A and B at treatment days 0, 3, and 10–14 were compared. RESULTS: Ninety-eight subjects (47 ICH; 51 non-ICH) were enrolled. Baseline serum antitoxin A and B antibody levels were similar. At day 3, ICHs demonstrated lower serum levels of antitoxin A IgG, antitoxin A IgA, and antitoxin B IgA (all P < .05). At day 10–14, lower antitoxin A IgG concentrations were observed in ICHs (ICH, 21 enzyme-linked immunosorbent assay [ELISA] units; interquartile range [IQR], 16.4–44.6) compared with non-ICH subjects (49.0 ELISA units; IQR, 21.5–103; P = .045). In stool, we observed lower concentrations of antitoxin B IgA antibodies at baseline and at day 3 for ICH subjects, with a notable difference in concentrations of antitoxin B IgA at day 3 (ICH, 6.7 ELISA units [IQR, 1.9–13.9] compared with non-ICH, 18.1 ELISA units [IQR, 4.9–31.7]; P = .003). CONCLUSIONS: The ICHs with CDI demonstrated lower levels of C difficile antitoxin antibodies in serum and stool during early CDI therapy compared with non-ICHs. These data provide insight into the humoral response to CDI in ICHs.
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spelling pubmed-82711312021-07-12 Humoral Immune Response to Clostridioides difficile Toxins A and B in Hospitalized Immunocompromised Patients With C difficile Infection Alonso, Carolyn D Papamichael, Konstantinos Sprague, Rebecca Barrett, Caitlin Gonzales-Luna, Anne J Daugherty, Kaitlyn Garey, Kevin W Villafuerte-Gálvez, Javier Xu, Hua Lin, Qianyun Wang, Lamei Chen, Xinhua Pollock, Nira R Kelly, Ciarán P Open Forum Infect Dis Major Articles BACKGROUND: The humoral immune response to Clostridioides difficile toxins in C difficile infection (CDI) is incompletely characterized in immunocompromised hosts (ICHs). METHODS: We conducted a prospective study of hospitalized adults with CDI, with and without immunosuppression (hematologic malignancy, active solid tumor, solid organ or stem cell transplant, inflammatory bowel disease, autoimmune disease, congenital or acquired immunodeficiency, asplenia, chronic receipt of high-dose steroids, or receipt of immunosuppressing medications within 12 months). Serum and stool antibody concentrations of immunoglobulin (Ig)M, IgG, and IgA to C difficile toxins A and B at treatment days 0, 3, and 10–14 were compared. RESULTS: Ninety-eight subjects (47 ICH; 51 non-ICH) were enrolled. Baseline serum antitoxin A and B antibody levels were similar. At day 3, ICHs demonstrated lower serum levels of antitoxin A IgG, antitoxin A IgA, and antitoxin B IgA (all P < .05). At day 10–14, lower antitoxin A IgG concentrations were observed in ICHs (ICH, 21 enzyme-linked immunosorbent assay [ELISA] units; interquartile range [IQR], 16.4–44.6) compared with non-ICH subjects (49.0 ELISA units; IQR, 21.5–103; P = .045). In stool, we observed lower concentrations of antitoxin B IgA antibodies at baseline and at day 3 for ICH subjects, with a notable difference in concentrations of antitoxin B IgA at day 3 (ICH, 6.7 ELISA units [IQR, 1.9–13.9] compared with non-ICH, 18.1 ELISA units [IQR, 4.9–31.7]; P = .003). CONCLUSIONS: The ICHs with CDI demonstrated lower levels of C difficile antitoxin antibodies in serum and stool during early CDI therapy compared with non-ICHs. These data provide insight into the humoral response to CDI in ICHs. Oxford University Press 2021-06-01 /pmc/articles/PMC8271131/ /pubmed/34258317 http://dx.doi.org/10.1093/ofid/ofab286 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Articles
Alonso, Carolyn D
Papamichael, Konstantinos
Sprague, Rebecca
Barrett, Caitlin
Gonzales-Luna, Anne J
Daugherty, Kaitlyn
Garey, Kevin W
Villafuerte-Gálvez, Javier
Xu, Hua
Lin, Qianyun
Wang, Lamei
Chen, Xinhua
Pollock, Nira R
Kelly, Ciarán P
Humoral Immune Response to Clostridioides difficile Toxins A and B in Hospitalized Immunocompromised Patients With C difficile Infection
title Humoral Immune Response to Clostridioides difficile Toxins A and B in Hospitalized Immunocompromised Patients With C difficile Infection
title_full Humoral Immune Response to Clostridioides difficile Toxins A and B in Hospitalized Immunocompromised Patients With C difficile Infection
title_fullStr Humoral Immune Response to Clostridioides difficile Toxins A and B in Hospitalized Immunocompromised Patients With C difficile Infection
title_full_unstemmed Humoral Immune Response to Clostridioides difficile Toxins A and B in Hospitalized Immunocompromised Patients With C difficile Infection
title_short Humoral Immune Response to Clostridioides difficile Toxins A and B in Hospitalized Immunocompromised Patients With C difficile Infection
title_sort humoral immune response to clostridioides difficile toxins a and b in hospitalized immunocompromised patients with c difficile infection
topic Major Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271131/
https://www.ncbi.nlm.nih.gov/pubmed/34258317
http://dx.doi.org/10.1093/ofid/ofab286
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