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  1. AU="Girmay, Tigisty"
  2. AU="Hain, Sofia"
  3. AU="de Kler, R C F"
  4. AU="Veness, R."

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  1. Article ; Online: Phase 1 Open-Label Dose Escalation Trial for the Development of a Human Bacillus Calmette-Guérin Challenge Model for Assessment of Tuberculosis Immunity In Vivo.

    Blazevic, Azra / Edwards, Rachel L / Xia, Mei / Eickhoff, Christopher S / Hamzabegovic, Fahreta / Meza, Krystal A / Ning, Huan / Tennant, Janice / Mosby, Karla J / Ritchie, James C / Girmay, Tigisty / Lai, Lilin / McCullough, Michele / Beck, Allison / Kelley, Colleen / Edupuganti, Srilatha / Kabbani, Sarah / Buchanan, Wendy / Makhene, Mamodikoe K /
    Voronca, Delia / Cherikh, Sami / Goll, Johannes B / Rouphael, Nadine G / Mulligan, Mark J / Hoft, Daniel F

    The Journal of infectious diseases

    2023  Volume 229, Issue 5, Page(s) 1498–1508

    Abstract: Background: A controlled human infection model for assessing tuberculosis (TB) immunity can accelerate new vaccine development.: Methods: In this phase 1 dose escalation trial, 92 healthy adults received a single intradermal injection of 2 × 106 to ... ...

    Abstract Background: A controlled human infection model for assessing tuberculosis (TB) immunity can accelerate new vaccine development.
    Methods: In this phase 1 dose escalation trial, 92 healthy adults received a single intradermal injection of 2 × 106 to 16 × 106 colony-forming units of Bacillus Calmette-Guérin (BCG). The primary endpoints were safety and BCG shedding as measured by quantitative polymerase chain reaction, colony-forming unit plating, and MGIT BACTEC culture.
    Results: Doses up to 8 × 106 were safe, and there was evidence for increased BCG shedding with dose escalation. The MGIT time-to-positivity assay was the most consistent and precise measure of shedding. Power analyses indicated that 10% differences in MGIT time to positivity (area under the curve) could be detected in small cohorts (n = 30). Potential biomarkers of mycobacterial immunity were identified that correlated with shedding. Transcriptomic analysis uncovered dose- and time-dependent effects of BCG challenge and identified a putative transcriptional TB protective signature. Furthermore, we identified immunologic and transcriptomal differences that could represent an immune component underlying the observed higher rate of TB disease incidence in males.
    Conclusions: The safety, reactogenicity, and immunogenicity profiles indicate that this BCG human challenge model is feasible for assessing in vivo TB immunity and could facilitate the vaccine development process.
    Clinical trials registration: NCT01868464 (ClinicalTrials.gov).
    MeSH term(s) Humans ; Male ; Adult ; Female ; BCG Vaccine/immunology ; BCG Vaccine/administration & dosage ; Tuberculosis/prevention & control ; Tuberculosis/immunology ; Young Adult ; Mycobacterium bovis/immunology ; Middle Aged ; Mycobacterium tuberculosis/immunology ; Injections, Intradermal ; Adolescent ; Dose-Response Relationship, Immunologic
    Language English
    Publishing date 2023-11-29
    Publishing country United States
    Document type Journal Article ; Clinical Trial, Phase I
    ZDB-ID 3019-3
    ISSN 1537-6613 ; 0022-1899
    ISSN (online) 1537-6613
    ISSN 0022-1899
    DOI 10.1093/infdis/jiad441
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Dose-Response of a Norovirus GII.2 Controlled Human Challenge Model Inoculum.

    Rouphael, Nadine / Beck, Allison / Kirby, Amy E / Liu, Pengbo / Natrajan, Muktha S / Lai, Lilin / Phadke, Varun / Winston, Juton / Raabe, Vanessa / Collins, Matthew H / Girmay, Tigisty / Alvarez, Alicarmen / Beydoun, Nour / Karmali, Vinit / Altieri-Rivera, Joanne / Lindesmith, Lisa C / Anderson, Evan J / Wang, Yuke / El-Khorazaty, Jill /
    Petrie, Carey / Baric, Ralph S / Baqar, Shahida / Moe, Christine L / Mulligan, Mark J

    The Journal of infectious diseases

    2022  Volume 226, Issue 10, Page(s) 1771–1780

    Abstract: Background: Genogroup II noroviruses are the most common cause of acute infectious gastroenteritis. We evaluated the use of a new GII.2 inoculum in a human challenge.: Methods: Forty-four healthy adults (36 secretor-positive and 8 secretor-negative ... ...

    Abstract Background: Genogroup II noroviruses are the most common cause of acute infectious gastroenteritis. We evaluated the use of a new GII.2 inoculum in a human challenge.
    Methods: Forty-four healthy adults (36 secretor-positive and 8 secretor-negative for histo-blood group antigens) were challenged with ascending doses of a new safety-tested Snow Mountain virus (SMV) GII.2 norovirus inoculum (1.2 × 104 to 1.2 × 107 genome equivalent copies [GEC]; n = 38) or placebo (n = 6). Illness was defined as diarrhea and/or vomiting postchallenge in subjects with evidence of infection (defined as GII.2 norovirus RNA detection in stool and/or anti-SMV immunoglobulin G [IgG] seroconversion).
    Results: The highest dose was associated with SMV infection in 90%, and illness in 70% of subjects with 10 of 12 secretor-positive (83%) and 4 of 8 secretor-negative (50%) becoming ill. There was no association between prechallenge anti-SMV serum IgG concentration, carbohydrate-binding blockade antibody, or salivary immunoglobulin A and infection. The median infectious dose (ID50) was 5.1 × 105 GEC.
    Conclusions: High rates of infection and illness were observed in both secretor-positive and secretor-negative subjects in this challenge study. However, a high dose will be required to achieve the target of 75% illness to make this an efficient model for evaluating potential norovirus vaccines and therapeutics.
    Clinical trials registration: NCT02473224.
    MeSH term(s) Adult ; Humans ; Norovirus/genetics ; Caliciviridae Infections ; Gastroenteritis ; Diarrhea ; Genotype ; Immunoglobulin G
    Chemical Substances Immunoglobulin G
    Language English
    Publishing date 2022-01-06
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 3019-3
    ISSN 1537-6613 ; 0022-1899
    ISSN (online) 1537-6613
    ISSN 0022-1899
    DOI 10.1093/infdis/jiac045
    Database MEDical Literature Analysis and Retrieval System OnLINE

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