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

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单位: [1]Division of Infectious Diseases, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA [2]Harvard Medical School, Boston, Massachusetts, USA [3]Division of Gastroenterology, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA [4]Department of Pharmacy Practice and Translational Research, University of Houston College of Pharmacy, Houston, Texas, USA [5]Department of Gastroenterology, Beijing Friendship Hospital, Capital Medical University, Beijing, China [6]College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi Province, China [7]Department of Laboratory Medicine, Boston Children’s Hospital, Boston, Massachusetts, USA
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关键词: C difficile toxins Clostridioides difficile infection humoral immunity immunosuppression

摘要:
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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出版当年[2020]版:
大类 | 3 区 医学
小类 | 3 区 免疫学 3 区 传染病学 3 区 微生物学
最新[2025]版:
大类 | 4 区 医学
小类 | 3 区 微生物学 4 区 免疫学 4 区 传染病学
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出版当年[2019]版:
Q2 IMMUNOLOGY Q2 MICROBIOLOGY Q2 INFECTIOUS DISEASES
最新[2023]版:
Q2 IMMUNOLOGY Q2 INFECTIOUS DISEASES Q2 MICROBIOLOGY

影响因子: 最新[2023版] 最新五年平均[2021-2025] 出版当年[2019版] 出版当年五年平均[2015-2019] 出版前一年[2018版] 出版后一年[2020版]

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第一作者单位: [1]Division of Infectious Diseases, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA [2]Harvard Medical School, Boston, Massachusetts, USA [*1]Division of Infectious Diseases, Department of Medicine, Beth Israel Deaconess Medical Center, 110 Francis Street, Suite GB, Boston, MA 02215, USA
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通讯机构: [1]Division of Infectious Diseases, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA [2]Harvard Medical School, Boston, Massachusetts, USA [*1]Division of Infectious Diseases, Department of Medicine, Beth Israel Deaconess Medical Center, 110 Francis Street, Suite GB, Boston, MA 02215, USA
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